DEK48 - Plant Editosome Database - CNCB-NGDC

Summary

Editing Factor: DEK48
Synonym: Defective Kernel 48
Description: DEK48 loss of function abolishes the C-to-U editing at nad3-185, -215, and nad4-376, -977 sites and decreases the editing at 11 other sites, resulting in the alteration of the corresponding amino acids; Consequently, the absence of editing caused reduced assembly and activity of complex I in dek48
Protein Family: PPR
Subclass: DYW
Physical Interaction: NA
Construct Structure: PLS-E1-E2-E+-DYW
Gene ID & Species: GRMZM2G017197 (Zea mays)
Edited Gene(s): nad3    nad4    nad9
Editing Type(s): C-to-U (48)
Publication(s): [1] DEK48 Is Required for RNA Editing at Multiple Mitochondrial Sites and Seed Development in Maize., International journal of molecular sciences, 2022. [PMID=35328485]

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
Zea mays GRMZM2G017197 Mitochondrion nad3 146 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments82.35%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments29.03%LowDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments44.44%MediumDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments45.71%MediumDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 185 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 190 NA NA NA NA NA C-to-U CCU=>UCU P=>S Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments87.80%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments46.90%MediumDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments47.86%MediumDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments61.08%HighDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 208 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments78.43%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments25.68%LowDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments42.86%MediumDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments43.23%MediumDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 209 NA NA NA NA NA C-to-U CCU/UCU=>CUU/UUU P/L=>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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments44.79%MediumDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments66.91%HighDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments69.94%HighDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 215 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 230 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments64.71%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments20.98%LowDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments31.76%LowDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments31.09%LowDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 247 NA NA NA NA NA C-to-U CCU=>UCU P=>S Recoding
Experiment Details
Genotype (Ecotype) Allele Treatment Treatment Detail Mutant Type Phenotype Tissue Development Stage Detection Method Editing Frequency Editing Extent Mutant Effect PMID
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments75.18%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments25.00%LowDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments39.73%LowDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments49.11%MediumDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 251 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments65.89%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments20.29%LowDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments31.34%LowDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments33.33%LowDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 275 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments65.28%HighNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments0.00%UneditedDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments32.87%LowDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments32.07%LowDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad3 317 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments47.10%MediumDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments71.62%HighDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments72.13%HighDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad4 376 NA NA NA NA NA C-to-U CGU=>UGU 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
Zea mays GRMZM2G017197 Mitochondrion nad4 977 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
Zea mays GRMZM2G017197 Mitochondrion nad9 311 NA NA NA NA NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments68.75%HighDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments62.96%HighDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments67.07%HighDecreased35328485
Zea mays GRMZM2G017197 Mitochondrion nad9 398 NA 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
NAWTControlControlNo mutantNormalKernel12 DAPSequencing of RT-PCR fragments100.00%CompleteNone35328485
UFMu-06548dek48-1Mu insertionThe Mutator (Mu) insertional mutant (dek48-1) was isolated from the UniformMu population.Recessive; HeterozygousKernels are smaller at maturity; the embryo and endosperm development were severely defective.Kernel12 DAPSequencing of RT-PCR fragments63.83%HighDecreased35328485
EMS3-024001dek48-2EMS mutagenizationCausing a mutation of C-to-T at +784 bp, resulting in a stop codon (from CAA to TAA) that leads to a truncation of 605 amino acid residues in the C-terminus of DEK48.Recessive; HeterozygousDefective kernelKernel12 DAPSequencing of RT-PCR fragments60.45%HighDecreased35328485
EMS3-0b2fabdek48-3EMS mutagenizationLeading to a mutation of G-to-A at + 2595 bp, causing a stop codon (TGG to TGA) that generates a loss of only the last tryptophan (W) residue in the DYW triplet of DEK48.Recessive; HeterozygousSmall kernelKernel12 DAPSequencing of RT-PCR fragments58.19%MediumDecreased35328485
Last update: Feb 2026 (version 2.0)