Arrand J E, Bone N M, Johnson R T
Department of Zoology, University of Cambridge, United Kingdom.
Proc Natl Acad Sci U S A. 1989 Sep;86(18):6997-7001. doi: 10.1073/pnas.86.18.6997.
A hamster DNA repair gene has been isolated by cosmid rescue after two rounds of transfection of an immortalized xeroderma pigmentosum (XP) complementation group D cell line with neomycin-resistance gene (neo)-tagged normal hamster DNA and selection with G418 and ultraviolet irradiation. The functional length of the sequence has been defined as 11.5 kilobase pairs by measurement of the region of overlap between two hamster DNA-containing cosmids, cloned by selection for the integrated neo gene, that are able to confer an increase in resistance to ultraviolet irradiation on two XP-D cell line but not on an XP-A line. Detailed molecular characterization of the hamster repair gene has revealed no obvious similarities to two human excision repair genes (ERCC1 and ERCC2) that correct repair-defective hamster cells but have no effect on XP cells. Hybridization analyses of normal human and XP cell genomic DNAs and mRNAs, using a cosmid-clone probe from which repeated sequences have been removed, show that homologues are present and expressed in all cases.
通过两轮转染永生化的着色性干皮病(XP)互补组D细胞系,用新霉素抗性基因(neo)标记的正常仓鼠DNA,并用G418和紫外线照射进行筛选,经黏粒拯救分离出一个仓鼠DNA修复基因。通过测量两个含仓鼠DNA的黏粒之间的重叠区域,将该序列的功能长度定义为11.5千碱基对,这两个黏粒是通过选择整合的neo基因克隆得到的,它们能够使两个XP-D细胞系对紫外线照射的抗性增加,但对XP-A细胞系无效。对仓鼠修复基因的详细分子特征分析表明,它与两个人类切除修复基因(ERCC1和ERCC2)没有明显相似性,这两个人类基因可纠正修复缺陷的仓鼠细胞,但对XP细胞无效。使用去除了重复序列的黏粒克隆探针,对正常人及XP细胞基因组DNA和mRNA进行杂交分析,结果表明在所有情况下均存在同源物并表达。