| Literature DB >> 31363048 |
Wen-Feng Nie1,2,3, Mingguang Lei1,2, Mingxuan Zhang1,4, Kai Tang1,2, Huan Huang1, Cuijun Zhang1,2, Daisuke Miki1, Pan Liu1, Yu Yang1, Xingang Wang2, Heng Zhang1, Zhaobo Lang1, Na Liu5, Xuechen Xu3, Ramesh Yelagandula6, Huiming Zhang1, Zhidan Wang1, Xiaoqiang Chai1, Andrea Andreucci7, Jing-Quan Yu3, Frederic Berger6, Rosa Lozano-Duran1, Jian-Kang Zhu8,2.
Abstract
Active DNA demethylation is critical for controlling the DNA methylomes in plants and mammals. However, little is known about how DNA demethylases are recruited to target loci, and the involvement of chromatin marks in this process. Here, we identify 2 components of the SWR1 chromatin-remodeling complex, PIE1 and ARP6, as required for ROS1-mediated DNA demethylation, and discover 2 SWR1-associated bromodomain-containing proteins, AtMBD9 and nuclear protein X1 (NPX1). AtMBD9 and NPX1 recognize histone acetylation marks established by increased DNA methylation 1 (IDM1), a known regulator of DNA demethylation, redundantly facilitating H2A.Z deposition at IDM1 target loci. We show that at some genomic regions, H2A.Z and DNA methylation marks coexist, and H2A.Z physically interacts with ROS1 to regulate DNA demethylation and antisilencing. Our results unveil a mechanism through which DNA demethylases can be recruited to specific target loci exhibiting particular histone marks, providing a conceptual framework to understand how chromatin marks regulate DNA demethylation.Entities:
Keywords: DNA demethylation pathway; bromodomain; chromatin remodeling; gene silencing; histone variant
Year: 2019 PMID: 31363048 PMCID: PMC6697875 DOI: 10.1073/pnas.1906023116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205