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  1. 原著論文

Accumulation of Ku80 proteins at DNA double-strand breaks in living cells

https://repo.qst.go.jp/records/45132
https://repo.qst.go.jp/records/45132
622e989b-485f-420a-803b-82f65159d458
Item type 学術雑誌論文 / Journal Article(1)
公開日 2008-04-02
タイトル
タイトル Accumulation of Ku80 proteins at DNA double-strand breaks in living cells
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 Koike, Manabu

× Koike, Manabu

WEKO 448167

Koike, Manabu

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Koike, Aki

× Koike, Aki

WEKO 448168

Koike, Aki

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小池 学

× 小池 学

WEKO 448169

en 小池 学

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小池 亜紀

× 小池 亜紀

WEKO 448170

en 小池 亜紀

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抄録
内容記述タイプ Abstract
内容記述 Ku plays a key role in multiple nuclear processes, e.g., DNA double-strand break (DSB) repair. The regulation mechanism of the localizations of Ku70 and Ku80 plays a key role in regulating the multiple functions of Ku. Although numerous biochemical studies in vitro have elucidated the DNA binding mechanism of Ku, no accumulation mechanisms of Ku70 and Ku80 at DSBs have been clarified in detail in vivo. In this study, we examined the accumulation mechanism of Ku80 at DSBs in living cells. EGFP-Ku80 accumulation at DSBs began immediately after irradiation. On the other hand, our data show that Ku70 alone, which has DNA binding activity independent of Ku80, cannot accumulate at the DSBs, whereas Ku70 bound to Ku80 can. The deletion of the C-terminal DNA-PKcs-binding domain and the mutation at the SUMOylation site of Ku80 had no effect on Ku80 accumulation. Unexpectedly, N-terminal deletion mutants of Ku80 fully lost their accumulation activity, although the mutants retained their Ku70 binding activity. Altogether, these data demonstrate that Ku80 is essential for Ku70 accumulation at DSBs. Furthermore, three domains of Ku80, i.e., the N-terminal alpha/beta, the DNA-binding, and Ku70-binding domains, seem to necessary for the accumulation at or recognition of DSBs in the early stage after irradiation.
書誌情報 Experimental Cell Research

巻 314, 号 5, p. 1061-1070, 発行日 2007-11
ISSN
収録物識別子タイプ ISSN
収録物識別子 0014-4827
DOI
識別子タイプ DOI
関連識別子 10.1016/j.yexcr.2007.11.014
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