MORF9 - Plant Editosome Database - BIG Data Center

Summary

Editing Factor: MORF9
Synonym: MULTIPLE ORGANELLAR RNA EDITING FACTOR 9; RIP9; OsMORF9
Description: Encoding an editing factor involved at almost all RNA editing sites in chloroplasts; MORF2-MORF9 heterodimer is the core members of editosomes in chloroplasts, while they are not responsible for RNA editing site recognition; MORF9-mediated RNA editing is tissue-dependent and the resultant organelle proteomes are pertinent to the specific tissue functions; Loss of MORF9 function impaired PSII efficiency, NDH activity, and carbohydrate production, rapidly promoted nuclear gene expression including sucrose transporter and sugar/energy responsive genes, and attenuated root growth under sugar starvation conditions; Sugar repletion increased MORF9 and MORF2 expression in wild-type seedlings and reduced RNA editing of matK-706, accD-794, ndhD-383 and ndhF-290 in the morf9 mutant; RNA editing efficiency of ndhD-383 and ndhF-290 sites was diminished in the gin2/morf9 double mutants, and that of matK-706, accD-794, ndhD-383 and ndhF-290 sites were significantly diminished in the snrk1/morf9 double mutants; In contrast, overexpressing HXK1 or SnRK1 promoted RNA editing rate of matK-706, accD-794, ndhD-383 and ndhF-290 in leaves of morf9 mutants, suggesting that HXK1 partially impacts MORF9 mediated ndhD-383 and ndhF-290 editing, while SnRK1 may only affect MORF9-mediated ndhF-290 site editing
Protein Family: MORF
Subclass: NA
Construct Structure: NA
Gene ID & Species: AT1G11430 (Arabidopsis thaliana)
LOC_Os08g04450 (Oryza sativa)
Edited Gene(s): ndhB    ndhD    psbF    atpF    clpP    accD    matK    ndhF    ndhG    petL    rpoB    rps14    rpoA    psbZ    rps12    rpl23    rpoC1    psbE    clpP1    atpA    ndhA    rpl2    rps8    rpoC2    ycf3
Editing Type(s): C-to-U (369)
Publication(s): [1] MORF9-dependent specific plastid RNA editing inhibits root growth under sugar starvation in Arabidopsis., Plant, cell & environment, 2024. [PMID=38357785]
[2] OsMORF9 is necessary for chloroplast development and seedling survival in rice., Plant science : an international journal of experimental plant biology, 2021. [PMID=33902846]
[3] MORF9 Functions in Plastid RNA Editing with Tissue Specificity., International journal of molecular sciences, 2019. [PMID=31546885]
[4] MORF2 tightly associates with MORF9 to regulate chloroplast RNA editing in Arabidopsis., Plant science : an international journal of experimental plant biology, 2019. [PMID=30471730]
[5] Multiple organellar RNA editing factor (MORF) family proteins are required for RNA editing in mitochondria and plastids of plants., Proceedings of the National Academy of Sciences of the United States of America, 2012. [PMID=22411807]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
accD 794 CDS C-to-U UCG=>UUG
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products4.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products89.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Leaf21 daysBulk-cDNA sequencing80.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Flower56 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Root21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing89.89%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WTmockSugar starvationNo mutantNormalRootNASequencing PCR products100.00%CompleteNone38357785
Columbia (Col-0)WTSucrose exposure2% sucrose exposureNo mutantNARootNASequencing PCR products100.00%CompleteNone38357785
Columbia (Col-0)morf9mockMutant; Sugar starvationHomozygousA dwarfed seedling characterized by pale yellow leaves and highly reduced root length, diminished photosynthetic fluorescence intensity, derangements in thylakoid membrane structure in the chloroplasts, and decreased PSII chemical quantum efficiency (Fv/Fm) and NDH activity relative to wild type plants (WT); Furthermore, sucrose content was significantly decreased in 28-day-old morf9 plants compared with WT when grown in absence of glucose in the medium, although glucose content remained stable in the morf9 mutant leaves; Roots of morf9 mutant plants were significantly shorter and associated with a slower root elongation rate relative to WT in sugar deficiency medium; Propidium iodide staining revealed smaller root meristems (i.e., fewer epidermal cells between the QC and the meristem–elongation zone boundary), and shorter mature epidermal cells in morf9 mutants compared with WT plantsLeaf; RootNASequencing PCR products90.00%HighDecreased38357785
Columbia (Col-0)morf9Sucrose exposureMutant; 2% sucrose exposureHomozygousNALeaf; RootNASequencing PCR products90.00%HighDecreased38357785
Columbia (Col-0)gin2mockMutant; Sugar starvationNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)gin2Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteSimilar38357785
Columbia (Col-0)snrk1mockMutant; Sugar starvationNANALeafNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)snrk1Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteSimilar38357785
Columbia (Col-0)gin2morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)gin2morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteSimilar38357785
Columbia (Col-0)oeHXK1morf9mockOverexpressing HXK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oeHXK1morf9Sucrose exposureOverexpressing HXK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)snrk1morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)snrk1morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteSimilar38357785
Columbia (Col-0)oesnRK1morf9mockOverexpressing SnRK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oesnRK1morf9Sucrose exposureOverexpressing SnRK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Arabidopsis thaliana AT1G11430 Chloroplast accD NA 3'UTR C-to-U NA=>NA NA=>NA NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products40.00%MediumIncreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products20.00%LowNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
atpF 92 CDS C-to-U CCA=>CUA
NA=>NA
P=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Leaf21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Flower56 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Root21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast clpP 559 CDS C-to-U CAU=>UAU H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products40.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products80.00%HighNone22411807
Arabidopsis thaliana AT1G11430 Plastid clpP1 559 CDS C-to-U NA=>NA H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing70.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Leaf21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Flower56 daysBulk-cDNA sequencing45.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Root21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing79.90%HighNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
matK 706 CDS C-to-U CAU=>UAU
NA=>NA
H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products70.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing80.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Leaf21 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing80.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Flower56 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing80.44%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing80.41%HighNone31546885
Columbia (Col-0)WTmockSugar starvationNo mutantNormalRootNASequencing PCR products90.00%HighNone38357785
Columbia (Col-0)WTSucrose exposure2% sucrose exposureNo mutantNARootNASequencing PCR products90.00%HighNone38357785
Columbia (Col-0)morf9mockMutant; Sugar starvationHomozygousA dwarfed seedling characterized by pale yellow leaves and highly reduced root length, diminished photosynthetic fluorescence intensity, derangements in thylakoid membrane structure in the chloroplasts, and decreased PSII chemical quantum efficiency (Fv/Fm) and NDH activity relative to wild type plants (WT); Furthermore, sucrose content was significantly decreased in 28-day-old morf9 plants compared with WT when grown in absence of glucose in the medium, although glucose content remained stable in the morf9 mutant leaves; Roots of morf9 mutant plants were significantly shorter and associated with a slower root elongation rate relative to WT in sugar deficiency medium; Propidium iodide staining revealed smaller root meristems (i.e., fewer epidermal cells between the QC and the meristem–elongation zone boundary), and shorter mature epidermal cells in morf9 mutants compared with WT plantsLeaf; RootNASequencing PCR products70.00%HighDecreased38357785
Columbia (Col-0)morf9Sucrose exposureMutant; 2% sucrose exposureHomozygousNALeaf; RootNASequencing PCR products55.00%MediumDecreased38357785
Columbia (Col-0)gin2mockMutant; Sugar starvationNANALeafNASequencing PCR products70.00%HighDecreased38357785
Columbia (Col-0)gin2Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)snrk1mockMutant; Sugar starvationNANALeafNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)snrk1Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products90.00%HighSimilar38357785
Columbia (Col-0)gin2morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products70.00%HighDecreased38357785
Columbia (Col-0)gin2morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)oeHXK1morf9mockOverexpressing HXK1; Sugar starvationNANALeafNASequencing PCR products95.00%HighRestored38357785
Columbia (Col-0)oeHXK1morf9Sucrose exposureOverexpressing HXK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)snrk1morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products30.00%LowDecreased38357785
Columbia (Col-0)snrk1morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products90.00%HighSimilar38357785
Columbia (Col-0)oesnRK1morf9mockOverexpressing SnRK1; Sugar starvationNANALeafNASequencing PCR products95.00%HighRestored38357785
Columbia (Col-0)oesnRK1morf9Sucrose exposureOverexpressing SnRK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Arabidopsis thaliana AT1G11430 Chloroplast ndhB 1255 CDS C-to-U CAU=>UAU H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products15.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast ndhB 1481 CDS C-to-U CCA=>CUA P=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast ndhB 149 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products90.00%HighNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 467 CDS C-to-U CCA=>CUA
NA=>NA
P=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products15.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products90.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Leaf21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Flower56 daysBulk-cDNA sequencing20.00%LowDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Root21 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 586 CDS C-to-U CAU=>UAU
NA=>NA
H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Leaf21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Flower56 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Root21 daysBulk-cDNA sequencing80.00%HighDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 746 CDS C-to-U UCU=>UUU
NA=>NA
S=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Leaf21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Flower56 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Root21 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 830 CDS C-to-U UCA=>UUA
NA=>NA
S=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Leaf21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Flower56 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Root21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 836 CDS C-to-U UCA=>UUA
NA=>NA
S=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Leaf21 daysBulk-cDNA sequencing35.00%LowDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Flower56 daysBulk-cDNA sequencing30.00%LowDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Root21 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhB 872 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products85.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Leaf21 daysBulk-cDNA sequencing80.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Flower56 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Root21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast ndhD 2 CDS C-to-U ACG=>AUG T=>M Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products45.00%MediumNone22411807
NAWTWild TypeWild TypeNo mutantNormalNANANANANANA30471730
Salk_013483morf9A T-DNA insertionThe T-DNA was inserted in the 5′-untranslated region of the MORF9 gene.HomozygousA dwarf phenotype and green leaves with an albino marginNANANANANANA30471730
Columbia (Col-0)ProMORF9: MORF9-4xMYCComplementationWe then created transgenic complemented morf9 plants expressing a gene encoding a 4xMYC-tagged MORF9 fusion protein (MORF9-4xMYC) under the control of the native MORF9 promoter.HomozygousNormalNANANANANANA30471730
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhD 383 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products40.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products90.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Leaf21 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Flower56 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WTmockSugar starvationNo mutantNormalRootNASequencing PCR products100.00%CompleteNone38357785
Columbia (Col-0)WTSucrose exposure2% sucrose exposureNo mutantNARootNASequencing PCR products90.00%HighNone38357785
Columbia (Col-0)morf9mockMutant; Sugar starvationHomozygousA dwarfed seedling characterized by pale yellow leaves and highly reduced root length, diminished photosynthetic fluorescence intensity, derangements in thylakoid membrane structure in the chloroplasts, and decreased PSII chemical quantum efficiency (Fv/Fm) and NDH activity relative to wild type plants (WT); Furthermore, sucrose content was significantly decreased in 28-day-old morf9 plants compared with WT when grown in absence of glucose in the medium, although glucose content remained stable in the morf9 mutant leaves; Roots of morf9 mutant plants were significantly shorter and associated with a slower root elongation rate relative to WT in sugar deficiency medium; Propidium iodide staining revealed smaller root meristems (i.e., fewer epidermal cells between the QC and the meristem–elongation zone boundary), and shorter mature epidermal cells in morf9 mutants compared with WT plantsLeaf; RootNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)morf9Sucrose exposureMutant; 2% sucrose exposureHomozygousNALeaf; RootNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)gin2mockMutant; Sugar starvationNANALeafNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)gin2Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)snrk1mockMutant; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteSimilar38357785
Columbia (Col-0)snrk1Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)gin2morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)gin2morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products65.00%HighDecreased38357785
Columbia (Col-0)oeHXK1morf9mockOverexpressing HXK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oeHXK1morf9Sucrose exposureOverexpressing HXK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)snrk1morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products60.00%HighDecreased38357785
Columbia (Col-0)snrk1morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products95.00%HighSimilar38357785
Columbia (Col-0)oesnRK1morf9mockOverexpressing SnRK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oesnRK1morf9Sucrose exposureOverexpressing SnRK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhD 674 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products80.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Flower56 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Root21 daysBulk-cDNA sequencing100.00%CompleteIncreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing90.06%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing89.48%HighNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhD 878 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products80.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Flower56 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing60.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Root21 daysBulk-cDNA sequencing60.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhD 887 CDS C-to-U CCC=>CUC
NA=>NA
P=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing60.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Leaf21 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing50.00%MediumNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Flower56 daysBulk-cDNA sequencing50.00%MediumSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing10.00%PoorNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf14) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf14 mutant.Root21 daysBulk-cDNA sequencing10.00%PoorSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhF 290 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products40.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Flower56 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing20.00%LowNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Root21 daysBulk-cDNA sequencing20.00%LowSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing90.02%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WTmockSugar starvationNo mutantNormalRootNASequencing PCR products100.00%CompleteNone38357785
Columbia (Col-0)WTSucrose exposure2% sucrose exposureNo mutantNARootNASequencing PCR products95.00%HighNone38357785
Columbia (Col-0)morf9mockMutant; Sugar starvationHomozygousA dwarfed seedling characterized by pale yellow leaves and highly reduced root length, diminished photosynthetic fluorescence intensity, derangements in thylakoid membrane structure in the chloroplasts, and decreased PSII chemical quantum efficiency (Fv/Fm) and NDH activity relative to wild type plants (WT); Furthermore, sucrose content was significantly decreased in 28-day-old morf9 plants compared with WT when grown in absence of glucose in the medium, although glucose content remained stable in the morf9 mutant leaves; Roots of morf9 mutant plants were significantly shorter and associated with a slower root elongation rate relative to WT in sugar deficiency medium; Propidium iodide staining revealed smaller root meristems (i.e., fewer epidermal cells between the QC and the meristem–elongation zone boundary), and shorter mature epidermal cells in morf9 mutants compared with WT plantsLeaf; RootNASequencing PCR products70.00%HighDecreased38357785
Columbia (Col-0)morf9Sucrose exposureMutant; 2% sucrose exposureHomozygousNALeaf; RootNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)gin2mockMutant; Sugar starvationNANALeafNASequencing PCR products40.00%MediumDecreased38357785
Columbia (Col-0)gin2Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products55.00%MediumDecreased38357785
Columbia (Col-0)snrk1mockMutant; Sugar starvationNANALeafNASequencing PCR products70.00%HighDecreased38357785
Columbia (Col-0)snrk1Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products30.00%LowDecreased38357785
Columbia (Col-0)gin2morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products20.00%LowDecreased38357785
Columbia (Col-0)gin2morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products40.00%MediumDecreased38357785
Columbia (Col-0)oeHXK1morf9mockOverexpressing HXK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oeHXK1morf9Sucrose exposureOverexpressing HXK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)snrk1morf9mockMutant; Sugar starvationNANALeafNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)snrk1morf9Sucrose exposureMutant; 2% sucrose exposureNANALeafNASequencing PCR products50.00%MediumDecreased38357785
Columbia (Col-0)oesnRK1morf9mockOverexpressing SnRK1; Sugar starvationNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Columbia (Col-0)oesnRK1morf9Sucrose exposureOverexpressing SnRK1; 2% sucrose exposureNANALeafNASequencing PCR products100.00%CompleteRestored38357785
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
ndhG 50 CDS C-to-U UCC=>UUC
NA=>NA
S=>F
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast petL 5 CDS C-to-U CCU=>CUU P=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Arabidopsis thaliana AT1G11430 Plastid psbE 214 CDS C-to-U NA=>NA NA=>NA NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Leaf21 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Flower56 daysBulk-cDNA sequencing100.00%CompleteSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
psbF 65 CDS C-to-U NA=>NA NA=>NA
S=>F
NA
Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products70.00%HighDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf13) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf13 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing90.30%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
psbZ 50 CDS C-to-U UCA=>UUA
NA=>NA
S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products30.00%LowDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Flower56 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
rpl23 89 CDS C-to-U UCA=>UUA
NA=>NA
S=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products70.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Leaf21 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Flower56 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Root21 daysBulk-cDNA sequencing80.00%HighDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing80.37%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing90.16%HighNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
rpoA 200 CDS C-to-U UCU=>UUU
NA=>NA
S=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products0.00%UneditedAbsent22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products50.00%MediumNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing70.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Leaf21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Flower56 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf10) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf10 mutant.Root21 daysBulk-cDNA sequencing90.00%HighSimilar31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing80.05%HighNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing70.78%HighNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast rpoB 2432 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products80.00%HighDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast rpoB 338 CDS C-to-U UCU=>UUU S=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products70.00%HighDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products90.00%HighNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast rpoB 551 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products60.00%HighDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products90.00%HighNone22411807
Arabidopsis thaliana AT1G11430 Plastid rpoC1 488 CDS C-to-U NA=>NA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing20.00%LowNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Leaf21 daysBulk-cDNA sequencing20.00%LowSimilar31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing50.00%MediumNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Flower56 daysBulk-cDNA sequencing30.00%LowDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing50.00%MediumNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf9) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf9 mutant.Root21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing20.07%LowNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing20.21%LowNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast rps12 NA Intron C-to-U NA=>NA NA=>NA NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products10.00%PoorDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products20.00%LowNone22411807
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
rps14 149 CDS C-to-U CCA=>CUA
NA=>NA
P=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products95.00%HighNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Leaf21 daysBulk-cDNA sequencing50.00%MediumDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Flower56 daysBulk-cDNA sequencing30.00%LowDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing80.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf12) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf12 mutant.Root21 daysBulk-cDNA sequencing40.00%MediumDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing40.24%MediumNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Arabidopsis thaliana AT1G11430 Chloroplast
Plastid
rps14 80 CDS C-to-U UCA=>UUA
NA=>NA
S=>L
NA=>NA
Recoding
NA
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
SALK_013483 (E) (R)morf9-1T-DNA InsertionNAHomozygousDefects in greening in lightLeafNADirect Sequencing of PCR Products50.00%MediumDecreased22411807
ColWTControlControlControlNormalLeafNADirect Sequencing of PCR Products100.00%CompleteNone22411807
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing100.00%CompleteNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Leaf21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalFlower56 daysBulk-cDNA sequencing80.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Flower56 daysBulk-cDNA sequencing60.00%HighDecreased31546885
Columbia (Col-0)WTWild TypeWild TypeNo mutantNormalRoot21 daysBulk-cDNA sequencing90.00%HighNone31546885
Columbia (Col-0)morf9A T-DNA insertionT-DNA insertion lines SALK_013483 (morf11) were provided by NASC.HomozygousPhenotypically, morf9 seedlings grown in sugar-free 1/2 MS medium showed a stunted plant, short roots, and yellow leaves. These plants exhibited retarded growth with yellow variegated leaves after they were transferred to soil for 35 days. At 12 days after germination (dag), the average root length of the morf9 seedlings was one-sixth shorter than that of WT ones, whereas the average root length of plants overexpressing MORF9-GFP did not differ significantly from that of WT plants. Both yellowish rosette leaves and shortened roots during sugar-free germination were obvious in morf11 mutant.Root21 daysBulk-cDNA sequencing70.00%HighDecreased31546885
Columbia (Col-0)WT-leaf-12dWild TypeWild TypeNo mutantNormalLeaf12 daysBulk-cDNA sequencing45.31%MediumNone31546885
Columbia (Col-0)WT-leaf-21dWild TypeWild TypeNo mutantNormalLeaf21 daysBulk-cDNA sequencing90.00%HighNone31546885
Oryza sativa LOC_Os08g04450 Chloroplast atpA 1148 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhA 1070 CDS C-to-U UCC=>UUC S=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products73.91%HighNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products20.00%LowDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products17.86%PoorDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 467 CDS C-to-U CCA=>CUA P=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products40.54%MediumDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products32.43%LowDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 586 CDS C-to-U CAU=>UAU H=>Y Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products20.69%LowDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products28.57%LowDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 611 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products30.77%LowDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products17.95%PoorDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 704 CDS C-to-U UCC=>UUC S=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products91.67%HighNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products44.68%MediumDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products32.50%LowDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 737 CDS C-to-U CCA=>CUA P=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products62.22%HighNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products11.76%PoorDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 830 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products32.00%LowDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products83.67%HighDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhB 836 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products35.42%LowDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products77.78%HighDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhD 878 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products80.00%HighNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast ndhG 10 CDS C-to-U CUU=>UUU L=>F Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products57.14%MediumDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products55.56%MediumDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast rpl2 2 CDS C-to-U ACG=>AUG T=>M Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products50.00%MediumNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast rpoB 467 CDS C-to-U UCG=>UUG S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast rpoB 545 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products80.77%HighNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products16.67%PoorDecreased33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products19.61%PoorDecreased33902846
Oryza sativa LOC_Os08g04450 Chloroplast rpoC2 4106 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast rps14 80 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast rps8 182 CDS C-to-U UCA=>UUA S=>L Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Oryza sativa LOC_Os08g04450 Chloroplast ycf3 185 CDS C-to-U ACG=>AUG T=>M Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NipponbareWTControlControlNo mutantNormalLeafNASequencing RT-PCR products100.00%CompleteNone33902846
Nipponbareosmorf9-1DeletionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Nipponbareosmorf9-2InsertionSequence analysis showed that the osmorf9-1 and osmorf9-2 mutants had a 1 bp deletion and 2 bp insertion, respectively, at the target site.KnockoutPhenotypic analysis showed that both mutants exhibited albino phenotypes and died after about one month. Thereafter, the study measured the levels of chlorophyll a (Chl a) and b (Chl b). The findings revealed that there was a significant decrease in the levels of both Chl a and Chl b in the osmorf9 mutants. Furthermore, the Fv/Fm ratio was also significantly decreased in the osmorf9-1 and osmorf9-2 mutants compared to the WT. In addition, the ultrastructure of chloroplast in WT, osmorf9-1 and osmorf9-2 mutant plants were observed through TEM. When compared with WT, abnormal chloroplasts which lacked stacked grana and thylakoid membranes were observed in the leaves of the osmorf9-1 and osmorf9-2 mutants.LeafNASequencing RT-PCR products0.00%UneditedAbsent33902846
Last update: Jul 2021 (version 1.0)