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转录偶联修复缺陷与人类错配修复基因中的突变。

Transcription-coupled repair deficiency and mutations in human mismatch repair genes.

作者信息

Mellon I, Rajpal D K, Koi M, Boland C R, Champe G N

机构信息

Department of Pathology, Program in Toxicology, Markey Cancer Center, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Science. 1996 Apr 26;272(5261):557-60. doi: 10.1126/science.272.5261.557.

Abstract

Deficiencies in mismatch repair have been linked to a common cancer predisposition syndrome in humans, hereditary nonpolyposis colorectal cancer (HNPCC), and a subset of sporadic cancers. Here, several mismatch repair-deficient tumor cell lines and HNPCC-derived lymphoblastoid cell lines were found to be deficient in an additional DNA repair process termed transcription-coupled repair (TCR). The TCR defect was corrected in a mutant cell line whose mismatch repair deficiency had been corrected by chromosome transfer. Thus, the connection between excision repair and mismatch repair previously described in Escherichia coli extends to humans. These results imply that deficiencies in TCR and exposure to carcinogens present in the environment may contribute to the etiology of tumors associated with genetic defects in mismatch repair.

摘要

错配修复缺陷与人类一种常见的癌症易感性综合征——遗传性非息肉病性结直肠癌(HNPCC)以及一部分散发性癌症有关。在此,发现几种错配修复缺陷的肿瘤细胞系和源自HNPCC的淋巴母细胞系在另一种称为转录偶联修复(TCR)的DNA修复过程中存在缺陷。在一个错配修复缺陷已通过染色体转移得到纠正的突变细胞系中,TCR缺陷也得到了纠正。因此,先前在大肠杆菌中描述的切除修复与错配修复之间的联系延伸到了人类。这些结果表明,TCR缺陷以及暴露于环境中的致癌物可能促成了与错配修复基因缺陷相关的肿瘤的病因。

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