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  1. 原著論文

Investigating the Influence of Arginine Dimethylation on Nucleosome Dynamics Using All-Atom Simulations and Kinetic Analysis

https://repo.qst.go.jp/records/49433
https://repo.qst.go.jp/records/49433
dd949a92-38ec-4343-bbad-ed5af2df3962
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-10-11
タイトル
タイトル Investigating the Influence of Arginine Dimethylation on Nucleosome Dynamics Using All-Atom Simulations and Kinetic Analysis
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Li, Zhenhai

× Li, Zhenhai

WEKO 734372

Li, Zhenhai

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Kono, Hidetoshi

× Kono, Hidetoshi

WEKO 734373

Kono, Hidetoshi

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Li, Zhenhai

× Li, Zhenhai

WEKO 734374

en Li, Zhenhai

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Kono, Hidetoshi

× Kono, Hidetoshi

WEKO 734375

en Kono, Hidetoshi

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抄録
内容記述タイプ Abstract
内容記述 The dimethylation of Arg at the 42nd position (R42me2) of H3 histone, a post-translational modification (PTM) in nucleosomes close to the DNA entry/exit region, showed controversial gene regulations. To address this discrepancy, we performed comprehensive all-atom replicaexchange molecular dynamics simulations with and without a single PTM, either symmetric (R42me2s) or asymmetric (R42me2a) dimethylation. Together with a kinetics analysis, our simulations showed that DNA at the entry/exit region in the R42me2a nucleosome adopts a relatively more open conformation than that in the unmodified nucleosome,whereas R42me2s exhibits significantly weaker or even negligible effects on DNA dynamics and structures, which may provide clues of the discrepancy of gene regulation by R42me2. Our approach will be useful to study the mechanism of nucleosome dynamical change induced by a subtle modification.
書誌情報 The Journal of Physical Chemistry B

巻 122, 号 42, p. 9625-9634, 発行日 2018-10
ISSN
収録物識別子タイプ ISSN
収録物識別子 1520-6106
DOI
識別子タイプ DOI
関連識別子 10.1021/acs.jpcb.8b05067
関連サイト
識別子タイプ DOI
関連識別子 https://doi.org/10.1021/acs.jpcb.8b05067
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