CRR28 - Plant Editosome Database - BIG Data Center

Summary

Editing Factor: CRR28
Synonym: CHLORORESPIRATORY REDUCTION28
Description: Encoding a PPR-DYW protein with endonuclease activity required for editing of multiple plastid transcripts
Protein Family: PPR
Subclass: DYW
Construct Structure: PLS-E-DYW
Gene ID & Species: AT1G59720 (Arabidopsis thaliana)
Edited Gene(s): ndhB    ndhD
Editing Type(s): C-to-U (26)
Publication(s): [1] The Analysis of the Editing Defects in the Mutant Provides New Clues for the Prediction of RNA Targets of Arabidopsis E+-Class PPR Proteins., Plants (Basel, Switzerland), 2020. [PMID=32098170]
[2] Multiple PPR protein interactions are involved in the RNA editing system in mitochondria and plastids., Proceedings of the National Academy of Sciences of the United States of America, 2017. [PMID=28761003]
[3] Pentatricopeptide repeat proteins with the DYW motif have distinct molecular functions in RNA editing and RNA cleavage in Arabidopsis chloroplasts., The Plant cell, 2009. [PMID=19182104]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana AT1G59720 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
Col-0Col-0ControlControlControlNormalLeaf4 weeksPoisoned Primer Extension (PPE) Assay100.00%CompleteNone19182104
Lercrr28-1Ds InsertionNARecessive mutationImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
Lercrr28-1+CRR28DYW2Complementationcrr28-1 is transformed with CRR28, in which the DYW motif is replaced by that of CRR2NANALeaf4 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent19182104
Lercrr28-1+CRR28DYW22Complementationcrr28-1 is transformed with CRR28, in which the DYW motif is replaced by that of CRR22NANALeaf4 weeksDirect Sequencing of PCR Products100.00%CompleteRestored19182104
Lercrr28-1+CRR28△DYWComplementationcrr28-1 is transformed with CRR28 lacking the DYW motifNANALeaf4 weeksDirect Sequencing of PCR Products100.00%CompleteRestored19182104
Lercrr28-1+CRR28△E/DYWComplementationcrr28-1 is transformed with CRR28 lacking the E and DYW motifsNANALeaf4 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent19182104
SALK_115133crr28-2T-DNA InsertionNANAImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
SALK_012455crr28-3T-DNA InsertionNANAImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
LerLerControlControlControlNormalLeaf4 weeksPoisoned Primer Extension (PPE) Assay100.00%CompleteNone19182104
Col-0WTControlControlControlNANANARNA-seq87.52%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract82.00%HighNone28761003
Col-0DYW2-GFP-OE1Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract99.00%HighIncreased28761003
Col-0DYW2-GFP-OE2Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract99.00%HighIncreased28761003
Arabidopsis thaliana AT1G59720 Chloroplast
Plastid
ndhD 878 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
Col-0Col-0ControlControlControlNormalLeaf4 weeksPoisoned Primer Extension (PPE) Assay100.00%CompleteNone19182104
Lercrr28-1Ds InsertionNARecessive mutationImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
Lercrr28-1+CRR28DYW2Complementationcrr28-1 is transformed with CRR28, in which the DYW motif is replaced by that of CRR2NANALeaf4 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent19182104
Lercrr28-1+CRR28DYW22Complementationcrr28-1 is transformed with CRR28, in which the DYW motif is replaced by that of CRR22NANALeaf4 weeksDirect Sequencing of PCR Products100.00%CompleteRestored19182104
Lercrr28-1+CRR28△DYWComplementationcrr28-1 is transformed with CRR28 lacking the DYW motifNANALeaf4 weeksDirect Sequencing of PCR Products100.00%CompleteRestored19182104
Lercrr28-1+CRR28△E/DYWComplementationcrr28-1 is transformed with CRR28 lacking the E and DYW motifsNANALeaf4 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent19182104
SALK_115133crr28-2T-DNA InsertionNANAImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
SALK_012455crr28-3T-DNA InsertionNANAImpaired NDH activityLeaf4 weeksPoisoned Primer Extension (PPE) Assay0.00%UneditedAbsent19182104
LerLerControlControlControlNormalLeaf4 weeksPoisoned Primer Extension (PPE) Assay100.00%CompleteNone19182104
Col-0WTControlControlControlNANANARNA-seq83.91%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract88.00%HighNone28761003
Col-0DYW2-GFP-OE1Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteIncreased28761003
Col-0DYW2-GFP-OE2Generating Arabidopsis plants overexpressing the GFP-tagged DYW2 geneCol-0 A. thaliana plants were transformed with the 35S::DYW2-GFP plasmids (in pK7WGF2 backbone) by the floral-dip method. Transformed plants were selected based on Kanamycin resistance. Two independenNASlow growthLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteIncreased28761003
Last update: Jul 2021 (version 1.0)