| Literature DB >> 25527293 |
Cheng-Guo Duan1, Huiming Zhang1, Kai Tang1, Xiaohong Zhu1, Weiqiang Qian2, Yueh-Ju Hou1, Bangshing Wang1, Zhaobo Lang1, Yang Zhao3, Xingang Wang1, Pengcheng Wang1, Jianping Zhou4, Gaimei Liang5, Na Liu6, Chunguo Wang7, Jian-Kang Zhu8.
Abstract
Argonaute (AGO) family proteins are conserved key components of small RNA-induced silencing pathways. In the RNA-directed DNA methylation (RdDM) pathway in Arabidopsis, AGO6 is generally considered to be redundant with AGO4. In this report, our comprehensive, genomewide analyses of AGO4- and AGO6-dependent DNA methylation revealed that redundancy is unexpectedly negligible in the genetic interactions between AGO4 and AGO6. Immunofluorescence revealed that AGO4 and AGO6 differ in their subnuclear co-localization with RNA polymerases required for RdDM. Pol II and AGO6 are absent from perinucleolar foci, where Pol V and AGO4 are co-localized. In the nucleoplasm, AGO4 displays a strong co-localization with Pol II, whereas AGO6 co-localizes with Pol V. These patterns suggest that RdDM is mediated by distinct, spatially regulated combinations of AGO proteins and RNA polymerases. Consistently, Pol II physically interacts with AGO4 but not AGO6, and the levels of Pol V-dependent scaffold RNAs and Pol V chromatin occupancy are strongly correlated with AGO6 but not AGO4. Our results suggest that AGO4 and AGO6 mainly act sequentially in mediating small RNA-directed DNA methylation.Entities:
Keywords: DNA methylation; RNA polymerases; RdDM; argonautes; epigenetics
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Year: 2014 PMID: 25527293 PMCID: PMC4365029 DOI: 10.15252/embj.201489453
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598