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Mutational Properties at the Hprt Locus of Xrcc4-defective Mouse LX830 cells

https://repo.qst.go.jp/records/67669
https://repo.qst.go.jp/records/67669
dd471423-56b8-4a52-99a0-eb647679114e
Item type 会議発表用資料 / Presentation(1)
公開日 2003-12-04
タイトル
タイトル Mutational Properties at the Hprt Locus of Xrcc4-defective Mouse LX830 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 Furuno-Fukushi, Ikuko

× Furuno-Fukushi, Ikuko

WEKO 665030

Furuno-Fukushi, Ikuko

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M., Jones Irene

× M., Jones Irene

WEKO 665031

M., Jones Irene

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Tatsumi, Kouichi

× Tatsumi, Kouichi

WEKO 665032

Tatsumi, Kouichi

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福士 育子

× 福士 育子

WEKO 665033

en 福士 育子

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巽 紘一

× 巽 紘一

WEKO 665034

en 巽 紘一

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内容記述タイプ Abstract
内容記述 The radiosensitive mutant LX830, a derivative of the mouse leukemia L5178Y cell, is defective in DNA double-strand break rejoining ability. This cell line belongs to the XRCC4 deficiency group. LX830 cells were hypersensitive to cell killing and mutation induction by gamma rays compared to the parental cells. No dose-rate dependence was found for mutation induction in this cell line. To characterize the structural alterations at the Hprt locus in LX830 cells, we have developed the primer sets for multiplex PCR analysis of the gene. The cells were employed after the removal of pre-existing 6-thioguanine resistant (TGr) mutants by THMG (Thymidine-Hypoxanthine-Methotrexate-Glycine) treatment. Independent TGr mutant clones were isolated from unirradiated and gamma-irradiated cultures of both LX830 and L5178Y cells. The proportion of mutants with deletions, together with the size and distribution of deletions are determined by the multiplex PCR method. How the deficiency of XRCC4 protein affects the molecular nature of TGr mutants will be discussed.
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 日本放射線影響学会第46回大会
発表年月日
日付 2003-10-08
日付タイプ Issued
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