Atypical RNA polymerase subunits required for RNA-directed DNA methylation View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-05-29

AUTHORS

Tatsuo Kanno, Bruno Huettel, M Florian Mette, Werner Aufsatz, Estelle Jaligot, Lucia Daxinger, David P Kreil, Marjori Matzke, Antonius J M Matzke

ABSTRACT

RNA-directed DNA methylation, one of several RNA interference–mediated pathways in the nucleus1, has been documented in plants2,3 and in human cells4,5. Despite progress in identifying the DNA methyltransferases, histone-modifying enzymes and RNA interference proteins needed for RNA-directed DNA methylation1, the mechanism remains incompletely understood. We screened for mutants defective in RNA-directed DNA methylation and silencing of a transgene promoter in Arabidopsis thaliana and identified three drd complementation groups6. DRD1 is a SNF2-like protein6 required for RNA-directed de novo methylation. We report here that DRD2 and DRD3 correspond to the second-largest subunit and largest subunit, respectively, of a fourth class of DNA-dependent RNA polymerase (polymerase IV) that is unique to plants. DRD3 is a functionally diversified homolog of NRPD1a or SDE4, identified in a separate screen for mutants defective in post-transcriptional gene silencing7,8. The identical DNA methylation patterns observed in all three drd mutants suggest that DRD proteins cooperate to create a substrate for RNA-directed de novo methylation. More... »

PAGES

761-765

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ng1580

DOI

http://dx.doi.org/10.1038/ng1580

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1034310095

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/15924141


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