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  1. 原著論文

Human SIRT2 and SIRT3 deacetylases function in DNA homologous recombinational repair

https://repo.qst.go.jp/records/82248
https://repo.qst.go.jp/records/82248
d7c1fe26-8794-4ad3-8c92-63efe8cd0f61
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-03-18
タイトル
タイトル Human SIRT2 and SIRT3 deacetylases function in DNA homologous recombinational repair
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 Takeshi, Yasuda

× Takeshi, Yasuda

WEKO 1018820

Takeshi, Yasuda

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Kazuya, Takizawa

× Kazuya, Takizawa

WEKO 1018821

Kazuya, Takizawa

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Ui, Ayako

× Ui, Ayako

WEKO 1018822

Ui, Ayako

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Michio, Hama

× Michio, Hama

WEKO 1018823

Michio, Hama

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Kagawa, Wataru

× Kagawa, Wataru

WEKO 1018824

Kagawa, Wataru

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Sugasawa, Kaoru

× Sugasawa, Kaoru

WEKO 1018825

Sugasawa, Kaoru

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Katsushi, Tajima

× Katsushi, Tajima

WEKO 1018826

Katsushi, Tajima

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Takeshi, Yasuda

× Takeshi, Yasuda

WEKO 1018827

en Takeshi, Yasuda

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Kazuya, Takizawa

× Kazuya, Takizawa

WEKO 1018828

en Kazuya, Takizawa

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Michio, Hama

× Michio, Hama

WEKO 1018829

en Michio, Hama

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Katsushi, Tajima

× Katsushi, Tajima

WEKO 1018830

en Katsushi, Tajima

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抄録
内容記述タイプ Abstract
内容記述 SIRT2 and SIRT3 protein deacetylases maintain genome integrity and stability. However, their mechanisms for maintaining the genome remain unclear. To examine the roles of SIRT2 and SIRT3 in DSB repair, I‐SceI‐based GFP reporter assays for HR, single‐strand annealing (SSA), and non‐homologous end joining (NHEJ) repair were performed under SIRT2‐ or SIRT3‐depleted conditions. SIRT2 or SIRT3 depletion inhibited HR repair equally to RAD52 depletion, but did not affect SSA and NHEJ repairs. SIRT2 or SIRT3 depletion disturbed the recruitment of RAD51 to DSB sites, an essential step for RAD51‐dependent HR repair, but not directly through RAD52 deacetylation. SIRT2 or SIRT3 depletion decreased the colocalization of γH2AX foci with RPA1, and thus they might be involved in initiating DSB end resection for the recruitment of RAD51 to DSB sites at an early step in HR repair. These results reveal the novel underlying mechanism of the SIRT2 and SIRT3 functions in HR for genome stability.
書誌情報 Genes to Cells

巻 26, 号 5, p. 328-335, 発行日 2021-03
出版者
出版者 Wiley
ISSN
収録物識別子タイプ ISSN
収録物識別子 1356-9597
DOI
識別子タイプ DOI
関連識別子 10.1111/gtc.12842
関連サイト
識別子タイプ URI
関連識別子 https://onlinelibrary.wiley.com/doi/10.1111/gtc.12842
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