ISOLATION AND CHARACTERIZATION OF MOUSE XRCC-1, A DNA-REPAIR GENE AFFECTING LIGATION

被引:21
作者
BROOKMAN, KW
TEBBS, RS
ALLEN, SA
TUCKER, JD
SWIGER, RR
LAMERDIN, JE
CARRANO, AV
THOMPSON, LH
机构
[1] Lawrence Livermore National Laboratory, Livermore, CA 94551-0808
关键词
D O I
10.1006/geno.1994.1359
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human DNA repair gene XRCC1 complements the strand-break rejoining defect in Chinese hamster mutant EM9 and encodes a protein that is apparently required for optimal activity of DNA ligase III. Toward the goal of producing transgenic mice that carry a mutation in the Xrcc-1 locus, the murine homolog of XRCC1 was cloned from both cosmid genomic and cDNA libraries. Upon transfection into EM9 cells, cosmids containing the functional mouse gene efficiently corrected (94-100%) the high sister-chromatid-exchange defect. Mouse Xrcc-1 is 26 kb in length, contains 17 exons, and maps by metaphase in situ hybridization to the 7A3-7B2 region of mouse chromosome 7. Isolated cDNA clones were highly truncated and were extended by anchored polymerase chain reactions. The 1893-bp open reading frame of mouse Xrcc-1 encodes 631 amino acids, compared with 633 for the human homolog. The predicted mouse Xrcc-1 protein of 69.1 kDa and pI of 5.95 is 86% identical and 93% similar to human XRCC1. (C) 1994 Academic Press, Inc.
引用
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页码:180 / 188
页数:9
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