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  1. 原著論文

The C-terminal region of Rad52 is essential for Rad52 nuclear and nucleolar localization, and accumulation at DNA damage sites immediately after irradiation.

https://repo.qst.go.jp/records/46912
https://repo.qst.go.jp/records/46912
1278f5e5-b011-427b-976c-4458b47d5bc2
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-11-10
タイトル
タイトル The C-terminal region of Rad52 is essential for Rad52 nuclear and nucleolar localization, and accumulation at DNA damage sites immediately after irradiation.
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 468153

Koike, Manabu

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Yutoku, Yasutomo

× Yutoku, Yasutomo

WEKO 468154

Yutoku, Yasutomo

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Koike, Aki

× Koike, Aki

WEKO 468155

Koike, Aki

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小池 学

× 小池 学

WEKO 468156

en 小池 学

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湯徳 靖友

× 湯徳 靖友

WEKO 468157

en 湯徳 靖友

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小池 亜紀

× 小池 亜紀

WEKO 468158

en 小池 亜紀

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抄録
内容記述タイプ Abstract
内容記述 Rad52 plays essential roles in homologous recombination (HR) and repair of DNA double-strand breaks (DSBs) in Saccharomyces cerevisiae. However, in vertebrates, knockouts of the Rad52 gene show no hypersensitivity to agents that induce DSBs. Rad52 localizes in the nucleus and forms foci at a late stage following irradiation. Ku70 and Ku80, which play an essential role in nonhomologous DNA-end-joining (NHEJ), are essential for the accumulation of other core NHEJ factors, e.g., XRCC4, and a HR-related factor, e.g., BRCA1. Here, we show that the subcellular localization of EYFP-Rad52(1-418) changes dynamically during the cell cycle. In addition, EYFP-Rad52(1-418) accumulates rapidly at microirradiated sites and colocalizes with the DSB sensor protein Ku80. Moreover, the accumulation of EYFP-Rad52(1-418) at DSB sites is independent of the core NHEJ factors, i.e., Ku80 and XRCC4. Furthermore, we observed that EYFP-Rad52(1-418) localizes in nucleoli in CHO-K1 cells and XRCC4-deficient cells, but not in Ku80-deficient cells. We also found that Rad52 nuclear localization, nucleolar localization, and accumulation at DSB sites are dependent on eight amino acids (411-418) at the end of the C-terminal region of Rad52 (Rad52 CTR). Furthermore, basic amino acids on Rad52 CTR are highly conserved among mammalian, avian, and fish homologues, suggesting that Rad52 CTR is important for the regulation and function of Rad52 in vertebrates. These findings also suggest that the mechanism underlying the regulation of subcellular localization of Rad52 is important for the physiological function of Rad52 not only at a late stage following irradiation, but also at an early stage.
書誌情報 Biochemical and biophysical research communications

巻 435, 号 2, p. 260-266, 発行日 2013-05
出版者
出版者 Academic Press
ISSN
収録物識別子タイプ ISSN
収録物識別子 0006-291X
PubMed番号
識別子タイプ PMID
関連識別子 23639616
DOI
識別子タイプ DOI
関連識別子 10.1016/j.bbrc.2013.04.067
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