Cited 2 time in
Cited 3 time in
Arabidopsis VIM Proteins Regulate Epigenetic Silencing by Modulating DNA Methylation and Histone Modification in Cooperation with MET1
- Arabidopsis VIM Proteins Regulate Epigenetic Silencing by Modulating DNA Methylation and Histone Modification in Cooperation with MET1
- Kim, Jeongsik; Kim, Jin Hee; Richards, Eric J.; Chung, Kyung Min; Woo, Hye Ryun
- DGIST Authors
- Kim, Jeongsik; Kim, Jin Hee; Woo, Hye Ryun
- Issue Date
- Molecular Plant, 7(9), 1470-1485
- Article Type
- Animalia; Arabidopsis; Arabidopsis Protein; Arabidopsis Proteins; DNA (Cytosine-5-)-Methyltransferase; DNA Methylation; Epigenetic Silencing; Gene Locus; Gene Silencing; Genetic Loci; Genetic Transcription; Genetics; Genome, Plant; Heterochromatin; Histone; Histone Modification; Histones; MET1; MET1 Protein, Arabidopsis; Metabolism; Mutation; Plant Genome; Promoter Region; Promoter Regions, Genetic; SRA; Transcription, Genetic; VIM/ORTH
- Methylcytosine-binding proteins containing SRA (SET- and RING-Associated) domain are required for the establishment and/or maintenance of DNA methylation in both plants and animals. We previously proposed that Arabidopsis VIM/ORTH proteins with an SRA domain maintain DNA methylation and epigenetic gene silencing in heterochromatic regions. However, their endogenous targets of epigenetic gene silencing have not been analyzed globally and the mechanisms by which VIM proteins coordinate DNA methylation and epigenetic silencing are largely unknown. In this study, a genome-wide transcript profiling analysis revealed 544 derepressed genes in a vim1/2/3 triple mutant, including 133 known genes. VIM1 bound to promoter and transcribed regions of the up-regulated genes in vim1/2/3 and VIM deficiency caused severe DNA hypomethylation in all sequence contexts at direct VIM1 targets. We found a drastic loss of H3K9me2 at heterochromatic chromocenters in vim1/2/3 nuclei. Furthermore, aberrant changes in transcriptionally active and repressive histone modifications were observed at VIM1 targets in vim1/2/3. VIM1-binding capacity to target genes was significantly reduced in the met1 background, indicating that VIM1 primarily recognizes CG methylation deposited by MET1. Overall, our data indicate that VIM proteins regulate genome-wide epigenetic gene silencing through coordinated modulation of DNA methylation and histone modification status in collaboration with MET1. © 2014 The Authors. All rights reserved.
- Cell Press
- Related Researcher
Woo, Hye Ryun
CBRG(Complex Biology Research Group)
There are no files associated with this item.
- New BiologyCBRG(Complex Biology Research Group)1. Journal Articles
New BiologyETC1. Journal Articles
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.