SLO1 - Plant Editosome Database - CNCB-NGDC

Summary

Editing Factor: SLO1
Synonym: SLOW GROWTH 1
Description: SLO1 protein may indirectly regulate plant growth and development via affecting mitochondrial RNA editing and gene expression
Protein Family: Pentatricopeptide repeat (PPR) protein
Subclass: E
Physical Interaction: NA
Construct Structure: PLS-E
Gene ID & Species: AT2G22410 (Arabidopsis thaliana)
Edited Gene(s): nad4    nad9
Editing Type(s): C-to-U (12)
Publication(s): [1] Multiple PPR Protein Interactions Are Involved in the RNA Editing System in Arabidopsis Mitochondria and Plastids, Proc Natl Acad Sci U S A, 2017. [doi:10.1073/pnas.1705815114]
[2] The SLO1 PPR protein is required for RNA editing at multiple sites with similar upstream sequences in Arabidopsis mitochondria, The Plant Journal, 2010. [doi:10.1111/j.1365-313X.2010.04258.x]

Editing Details

Species Gene ID Organelle Edited Gene Position Region Nuclear Genome Organelle Genome Other Region Other Position Editing Type Codon Amino Acid Molecular Effect Experiment Details
Arabidopsis thaliana AT2G22410 Mitochondrion nad4 449 CDS NA Y08501
NA
NA NA 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-0slo1-1T-DNA InsertionT-DNA is located at -38 bpRecessiveLate germination, slow growth and delayed development; Small plantSeedling2 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent20497377
SALK_071273slo1-2T-DNA InsertionT-DNA is inserted in the coding regionNALate germination, slow growth and delayed development; Small plantSeedling2 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent20497377
Col-0WTControlControlNo mutantNormalSeedling2 weeksDirect Sequencing of PCR Products100.00%CompleteNone20497377
Col-0WTControlControlNo mutantNormalLeafNART-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 (BlueTract27.00%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 (BlueTract21.00%LowDecreased28761003
Arabidopsis thaliana AT2G22410 Mitochondrion nad9 328 CDS NA Y08501
NA
NA NA C-to-U CGG=>UGG
NA=>NA
R=>W
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-0slo1-1T-DNA InsertionT-DNA is located at -38 bpRecessiveLate germination, slow growth and delayed development; Small plantSeedling2 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent20497377
SALK_071273slo1-2T-DNA InsertionT-DNA is inserted in the coding regionNALate germination, slow growth and delayed development; Small plantSeedling2 weeksDirect Sequencing of PCR Products0.00%UneditedAbsent20497377
Col-0WTControlControlNo mutantNormalSeedling2 weeksDirect Sequencing of PCR Products81.00%HighNone20497377
Col-0WTControlControlNo mutantNormalLeafNART-PCR and calculated with the DNADynamo software (BlueTract97.00%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 (BlueTract20.00%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 (BlueTract20.00%LowDecreased28761003
Last update: Sep 2026 (version 2.0)