VAC1 - Plant Editosome Database - CNCB-NGDC

Summary

Editing Factor: VAC1
Synonym: VAC1
Description: Homologous to mammalian VAC14s, which is involved in the production of phosphatidylinositol 3,5-bisphosphate. Mutants are male gametophyte lethal
Protein Family: PPR
Subclass: DYW
Physical Interaction: NA
Construct Structure: PLS-E-DYW, NA
Gene ID & Species: NA (Arabidopsis thaliana)
AT1G15510 (Arabidopsis thaliana)
Edited Gene(s): accD    ndhF
Editing Type(s): C-to-U (15)
Publication(s): [1] 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]
[2] Editing of accD and ndhF chloroplast transcripts is partially affected in the Arabidopsis vanilla cream1 mutant., Plant molecular biology, 2010. [PMID=20143129]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Nuclear Genome Organelle Genome Other Position Region Other Position Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana NA Chloroplast accD 1568 CDS NA NA NA NA 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-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract85.00%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 (BlueTract94.00%HighSimilar28761003
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 (BlueTract89.00%HighSimilar28761003
Arabidopsis thaliana AT1G15510 Chloroplast accD 794 CDS NA NA NA NA 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
ACR3p-GUS 73heterozygous vac1T-DNA InsertionNAHeterozygous; Null alleleAlbino to pale yellow phenotypeSeedling2 weeksDirect Sequencing of PCR Products62.00%HighDecreased20143129
Col-0WTControlControlControlNormalSeedling2 weeksDirect Sequencing of PCR Products100.00%CompleteNone20143129
Arabidopsis thaliana NA Chloroplast accD 794 CDS NA NA NA NA 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-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract94.00%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%CompleteSimilar28761003
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%CompleteSimilar28761003
Arabidopsis thaliana AT1G15510 Chloroplast accD NA 3'UTR NA NA NA 1568 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
ACR3p-GUS 73heterozygous vac1T-DNA InsertionNAHeterozygous; Null alleleAlbino to pale yellow phenotypeSeedling2 weeksDirect Sequencing of PCR Products8.00%PoorDecreased20143129
Col-0WTControlControlControlNormalSeedling2 weeksDirect Sequencing of PCR Products55.00%MediumNone20143129
Arabidopsis thaliana AT1G15510 Chloroplast ndhF 290 CDS NA NA NA NA 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
ACR3p-GUS 73heterozygous vac1T-DNA InsertionNAHeterozygous; Null alleleAlbino to pale yellow phenotypeSeedling2 weeksDirect Sequencing of PCR Products49.00%MediumDecreased20143129
Col-0WTControlControlControlNormalSeedling2 weeksDirect Sequencing of PCR Products95.00%HighNone20143129
Arabidopsis thaliana NA Chloroplast ndhF 290 CDS NA NA NA NA 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-0WTControlControlControlNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract48.00%MediumNone28761003
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 (BlueTract78.00%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 (BlueTract61.00%HighIncreased28761003
Last update: Feb 2026 (version 2.0)