ISWI chromatin remodeling complexes recruit NSD2 and H3K36me2 in pericentromeric heterochromatin

Author:

Goto Naoki1ORCID,Suke Kazuma2ORCID,Yonezawa Nao2ORCID,Nishihara Hidenori13ORCID,Handa Tetsuya4ORCID,Sato Yuko14ORCID,Kujirai Tomoya5ORCID,Kurumizaka Hitoshi5ORCID,Yamagata Kazuo2ORCID,Kimura Hiroshi14ORCID

Affiliation:

1. School of Life Science and Technology, Tokyo Institute of Technology 1 , Yokohama, Japan

2. Faculty of Biology-Oriented Science and Technology, Kindai University 2 , Kinokawa, Japan

3. Graduate School of Agriculture, Kindai University 3 Department of Advanced Bioscience, , Nara, Japan

4. Cell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology 4 , Yokohama, Japan

5. Institute for Quantitative Biosciences, The University of Tokyo 5 , Tokyo, Japan

Abstract

Histone H3 lysine36 dimethylation (H3K36me2) is generally distributed in the gene body and euchromatic intergenic regions. However, we found that H3K36me2 is enriched in pericentromeric heterochromatin in some mouse cell lines. We here revealed the mechanism of heterochromatin targeting of H3K36me2. Among several H3K36 methyltransferases, NSD2 was responsible for inducing heterochromatic H3K36me2. Depletion and overexpression analyses of NSD2-associating proteins revealed that NSD2 recruitment to heterochromatin was mediated through the imitation switch (ISWI) chromatin remodeling complexes, such as BAZ1B-SMARCA5 (WICH), which directly binds to AT-rich DNA via a BAZ1B domain-containing AT-hook-like motifs. The abundance and stoichiometry of NSD2, SMARCA5, and BAZ1B could determine the localization of H3K36me2 in different cell types. In mouse embryos, H3K36me2 heterochromatin localization was observed at the two- to four-cell stages, suggesting its physiological relevance.

Funder

Japan Society for the Promotion of Science

Japan Science and Technology Agency

Japan Agency for Medical Research and Development

Publisher

Rockefeller University Press

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3