GRS1 - Plant Editosome Database - BIG Data Center

Summary

Editing Factor: GRS1
Synonym: GROWING SLOWLY 1
Description: GRS1 is a mitochondrial PLS-type PRR protein required for RNA editing and plant development
Protein Family: PPR
Subclass: DYW,E+
Construct Structure: PLS-E1-E2-DYW, NA
Gene ID & Species: NA (Arabidopsis thaliana)
AT4G32430 (Arabidopsis thaliana)
Edited Gene(s): nad1    nad4L    nad6    rps4
Editing Type(s): C-to-U (32)
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] Growing Slowly 1 locus encodes a PLS-type PPR protein required for RNA editing and plant development in Arabidopsis., Journal of experimental botany, 2016. [PMID=27670716]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana AT4G32430 Mitochondrion nad1 265 CDS C-to-U CGG=>UGG R=>W Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NAgrs1-1T-DNA InsertionT-DNA is located at 1325 bp downstream of the ATG start codonKnockoutgrs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedAbsent27670716
NAgrs1-2T-DNA InsertionT-DNA is inserted at 850 bp downstream of the ATG start codonKnockoutHomozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedNone27670716
qrt 1WTControlControlControlNormalSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteNone27670716
NAgrs1-1 complemented linesComplementationGenomic complemented linesHomozygousNo obvious differences compared to the wild-typeSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteRestored27670716
Arabidopsis thaliana NA Mitochondrion nad1 265 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
Col-0WTControlControlControlNANANARNA-seq99.05%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteNone28761003
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 (BlueTract32.00%LowDecreased28761003
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 (BlueTract11.00%PoorDecreased28761003
Arabidopsis thaliana AT4G32430 Mitochondrion nad4L 55 CDS C-to-U CGG=>UGG R=>W Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NAgrs1-1T-DNA InsertionT-DNA is located at 1325 bp downstream of the ATG start codonKnockoutgrs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedAbsent27670716
NAgrs1-2T-DNA InsertionT-DNA is inserted at 850 bp downstream of the ATG start codonKnockoutHomozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedNone27670716
qrt 1WTControlControlControlNormalSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteNone27670716
NAgrs1-1 complemented linesComplementationGenomic complemented linesHomozygousNo obvious differences compared to the wild-typeSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteRestored27670716
Arabidopsis thaliana NA Mitochondrion nad4L 55 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
Col-0WTControlControlControlNANANARNA-seq94.28%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract95.00%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 (BlueTract32.00%LowDecreased28761003
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 (BlueTract17.00%PoorDecreased28761003
Arabidopsis thaliana AT4G32430 Mitochondrion nad6 103 CDS C-to-U CGC=>UGC R=>C Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NAgrs1-1T-DNA InsertionT-DNA is located at 1325 bp downstream of the ATG start codonKnockoutgrs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedAbsent27670716
NAgrs1-2T-DNA InsertionT-DNA is inserted at 850 bp downstream of the ATG start codonKnockoutHomozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedNone27670716
qrt 1WTControlControlControlNormalSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteNone27670716
NAgrs1-1 complemented linesComplementationGenomic complemented linesHomozygousNo obvious differences compared to the wild-typeSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteRestored27670716
Arabidopsis thaliana NA Mitochondrion nad6 103 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
Col-0WTControlControlControlNANANARNA-seq98.34%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract98.00%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 (BlueTract21.00%LowDecreased28761003
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 (BlueTract1.00%PoorDecreased28761003
Arabidopsis thaliana AT4G32430 Mitochondrion rps4 377 CDS C-to-U CCG=>CUG 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
NAgrs1-1T-DNA InsertionT-DNA is located at 1325 bp downstream of the ATG start codonKnockoutgrs1-1 homozygotes are either lethal or exhibited growth retardation; cell division activity is reduced dramatically in the roots of grs1 plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedAbsent27670716
NAgrs1-2T-DNA InsertionT-DNA is inserted at 850 bp downstream of the ATG start codonKnockoutHomozygous grs1-2 plants are found to phenocopy grs1-1 homozygous plantsSeedling20 daysDirect Sequencing of PCR Products0.00%UneditedNone27670716
qrt 1WTControlControlControlNormalSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteNone27670716
NAgrs1-1 complemented linesComplementationGenomic complemented linesHomozygousNo obvious differences compared to the wild-typeSeedling20 daysDirect Sequencing of PCR Products100.00%CompleteRestored27670716
Arabidopsis thaliana NA Mitochondrion rps4 377 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
Col-0WTControlControlControlNANANARNA-seq87.31%HighNone32098170
Col-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract100.00%CompleteNone28761003
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 (BlueTract2.00%PoorDecreased28761003
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 (BlueTract0.00%UneditedAbsent28761003
Last update: Jul 2021 (version 1.0)