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Studies on a role of XRCC4 in human cells

https://repo.qst.go.jp/records/67424
https://repo.qst.go.jp/records/67424
eb372b90-9c83-4cc9-95f9-5369cc94d246
Item type 会議発表用資料 / Presentation(1)
公開日 2003-08-25
タイトル
タイトル Studies on a role of XRCC4 in human 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_c94f
資源タイプ conference object
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 Mori, Masahiko

× Mori, Masahiko

WEKO 662774

Mori, Masahiko

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Itsukaichi, Hiromi

× Itsukaichi, Hiromi

WEKO 662775

Itsukaichi, Hiromi

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Kanda, Reiko

× Kanda, Reiko

WEKO 662776

Kanda, Reiko

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Nakamura, Atsuko

× Nakamura, Atsuko

WEKO 662777

Nakamura, Atsuko

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Shiomi, Naoko

× Shiomi, Naoko

WEKO 662778

Shiomi, Naoko

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Aizawa, Shirou

× Aizawa, Shirou

WEKO 662779

Aizawa, Shirou

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Shiomi, Tadahiro

× Shiomi, Tadahiro

WEKO 662780

Shiomi, Tadahiro

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森 雅彦

× 森 雅彦

WEKO 662781

en 森 雅彦

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五日市 ひろみ

× 五日市 ひろみ

WEKO 662782

en 五日市 ひろみ

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神田 玲子

× 神田 玲子

WEKO 662783

en 神田 玲子

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中村 篤子

× 中村 篤子

WEKO 662784

en 中村 篤子

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塩見 尚子

× 塩見 尚子

WEKO 662785

en 塩見 尚子

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相澤 志郎

× 相澤 志郎

WEKO 662786

en 相澤 志郎

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塩見 忠博

× 塩見 忠博

WEKO 662787

en 塩見 忠博

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抄録
内容記述タイプ Abstract
内容記述 Ionizing radiation produces a variety of lesions in DNA including single-strand breaks, double strand breaks and base damage. The repair of DNA double-strand breaks in essential for the maintenance of genomic integrity. Failure to repair DNA double-strand breaks result in loss of genetic information, chromosome translocations, carcinogenesis and cell death. XRCC4 is a member of non-homologous end-joining proteins that functioned in DNA double-strand break repair in eukaryote including human. XRCC4 is a DNA ligase IV accessory factor and required for the rejoining of DNA double- strand breaks. Both XRCC4 and DNA ligase IV deficient mice have been generated. Both deficient mice are not viable because of neuronal degeneration caused by p53-induced apoptosis. Cells obtained from XRCC4 or DNA ligase IV deficient embryo are viable, but show reduced cell proliferation and hypersensitivity to ionizing radiation. To study the role of XRCC4 in human cells, we tried to inactivate XRCC4 gene by using gene targeting technology in human colon cancer cell line, HCT116. We have succeeded to disrupt both alleles of XRCC4 gene. Heterozygous (XRCC4+/-)cells showed reduced cell proliferation but normal X Ray-sensitivity, indicating haploinsufficiency in cell proliferation but not in X ray-sensitivity. Homozygous (XRCC4-/-) cells show reduced cell proliferation and increased chromosome aberrations, and are highly sensitive to X-rays.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 12th International Congress of Radiation Research
発表年月日
日付 2003-08-22
日付タイプ Issued
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