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  1. 原著論文

Novel characteristics of CtIP at damage-induced foci following the initiation of DNA end resection

https://repo.qst.go.jp/records/47073
https://repo.qst.go.jp/records/47073
4092d774-228e-4b36-adbc-670b55099c88
Item type 学術雑誌論文 / Journal Article(1)
公開日 2015-04-02
タイトル
タイトル Novel characteristics of CtIP at damage-induced foci following the initiation of DNA end resection
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 Fujisawa, Hiroshi

× Fujisawa, Hiroshi

WEKO 470121

Fujisawa, Hiroshi

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Fujimori, Akira

× Fujimori, Akira

WEKO 470122

Fujimori, Akira

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Okayasu, Ryuichi

× Okayasu, Ryuichi

WEKO 470123

Okayasu, Ryuichi

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Uesaka, Mitsuru

× Uesaka, Mitsuru

WEKO 470124

Uesaka, Mitsuru

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Yajima, Hirohiko

× Yajima, Hirohiko

WEKO 470125

Yajima, Hirohiko

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藤澤 寛

× 藤澤 寛

WEKO 470126

en 藤澤 寛

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藤森 亮

× 藤森 亮

WEKO 470127

en 藤森 亮

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岡安 隆一

× 岡安 隆一

WEKO 470128

en 岡安 隆一

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上坂 充

× 上坂 充

WEKO 470129

en 上坂 充

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矢島 浩彦

× 矢島 浩彦

WEKO 470130

en 矢島 浩彦

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抄録
内容記述タイプ Abstract
内容記述 Homologous recombination (HR) is a major repair pathway for DNA double strand breaks (DSBs), and end resection, which generates a 3’-single strand DNA tail at the DSB, is an early step in the process. Resection is initiated by the Mre11 nuclease together with CtIP. Here, we describe novel characteristics of CtIP at DSBs. At early times following exposure of human cells to ionizing radiation, CtIP localized to the DSB, became hyperphosphorylated and formed foci in an ATM-dependent manner. At later times, when the initiation of resection had occurred, CtIP foci persist but CtIP is maintained in a hypophosphorylated state, which is dependent on ATM and ATR. Exposure to cycloheximide revealed that CtIP turns over at DSB sites downstream of resection. Our findings provide strong evidence that CtIP is continuously recruited to DSBs downstream of both the initiation and extension step of resection, strongly suggesting that CtIP has functions in addition to promoting the initiation of resection during HR.
書誌情報 Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis

巻 771, p. 36-44, 発行日 2014-12
出版者
出版者 Elsevier Ltd.
ISSN
収録物識別子タイプ ISSN
収録物識別子 0027-5107
DOI
識別子タイプ DOI
関連識別子 doi:10.1016/j.mrfmmm.2014.12.001
関連サイト
識別子タイプ URI
関連識別子 http://www.sciencedirect.com/science/article/pii/S0027510714002073
関連名称 http://www.sciencedirect.com/science/article/pii/S0027510714002073
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