A structural-maintenance-of-chromosomes hinge domain–containing protein is required for RNA-directed DNA methylation View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2008-04-20

AUTHORS

Tatsuo Kanno, Etienne Bucher, Lucia Daxinger, Bruno Huettel, Gudrun Böhmdorfer, Wolfgang Gregor, David P Kreil, Marjori Matzke, Antonius J M Matzke

ABSTRACT

RNA-directed DNA methylation (RdDM) is a process in which dicer-generated small RNAs guide de novo cytosine methylation at the homologous DNA region1,2. To identify components of the RdDM machinery important for Arabidopsis thaliana development, we targeted an enhancer active in meristems for methylation, which resulted in silencing of a downstream GFP reporter gene. This silencing system also features secondary siRNAs, which trigger methylation that spreads beyond the targeted enhancer region. A screen for mutants defective in meristem silencing and enhancer methylation retrieved six dms complementation groups, which included the known factors DRD1 (ref. 3; a SNF2-like chromatin-remodeling protein) and Pol IVb subunits4,5. Additionally, we identified a previously unknown gene DMS3 (At3g49250), encoding a protein similar to the hinge-domain region of structural maintenance of chromosomes (SMC) proteins. This finding implicates a putative chromosome architectural protein that can potentially link nucleic acids6 in facilitating an RNAi-mediated epigenetic modification involving secondary siRNAs and spreading of DNA methylation. More... »

PAGES

670-675

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ng.119

DOI

http://dx.doi.org/10.1038/ng.119

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1020980808

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/18425128


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