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  1. 原著論文

Nuclear localization of mouse Ku70 in interphase cells, and focus formation of mouse Ku70 at DNA damage sites immediately after irradiation.

https://repo.qst.go.jp/records/48177
https://repo.qst.go.jp/records/48177
ea4be7df-8c58-4830-ba67-23f140531968
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-07-25
タイトル
タイトル Nuclear localization of mouse Ku70 in interphase cells, and focus formation of mouse Ku70 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 小池, 学

× 小池, 学

WEKO 483911

小池, 学

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湯徳, 靖友

× 湯徳, 靖友

WEKO 483912

湯徳, 靖友

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小池, 亜紀

× 小池, 亜紀

WEKO 483913

小池, 亜紀

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小池 学

× 小池 学

WEKO 483914

en 小池 学

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湯徳 靖友

× 湯徳 靖友

WEKO 483915

en 湯徳 靖友

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小池 亜紀

× 小池 亜紀

WEKO 483916

en 小池 亜紀

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抄録
内容記述タイプ Abstract
内容記述 To elucidate the mechanisms of DNA repair pathway is critical for developing next-generation radiotherapies and chemotherapeutic drugs for cancer. Ionizing radiation and many chemotherapeutic drugs kill tumor cells mainly by inducing DNA double-strand breaks (DSBs). The classical nonhomologous DNA-end joining (NHEJ) (C-NHEJ) pathway repairs a predominant fraction of DSBs in mammalian cells. The C-NHEJ pathway appears to start with the binding of Ku (heterodimer of Ku70 and Ku80) to DNA break ends. Therefore, recruitment of Ku to DSB sites might play a critical role in regulating NHEJ activity. Indeed, human Ku70 and Ku80 localize in the nuclei and accumulate at microirradiated DSB sites. However, the localization and regulation mechanisms of Ku70 and Ku80 homologues in animal models, such as mice and other species, have not been elucidated in detail, particularly in cells immediately after microirradiation. Here, we show that EYFP-tagged mouse Ku70 localizes in the interphase nuclei of mouse fibroblasts and epithelial cells. Furthermore, our findings indicate that EYFP-mouse Ku70 accumulates with its heterodimeric partner Ku80 immediately at laser-microirradiated DSB sites. We also confirmed that the structure of Ku70 nuclear localization signal (NLS) is highly conserved among various rodent species, such as the mouse, rat, degu and ground squirrel, supporting the idea that NLS is important for the regulation of rodent Ku70 function. Collectively, these results suggest that the mechanisms of regulating the localization and accumulation of Ku70 at DSBs might be well conserved between the mouse and human species.
書誌情報 The Journal of veterinary medical science / the Japanese Society of Veterinary Science

巻 77, 号 9, p. 1137-1142, 発行日 2015-08
出版者
出版者 日本獣医学会
関連サイト
識別子タイプ URI
関連識別子 10.1292/jvms.14-0651
関連名称 10.1292/jvms.14-0651
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