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pSV2gpt转化细胞中缺失突变的检测。

Detection of deletion mutations in pSV2gpt-transformed cells.

作者信息

Tindall K R, Stankowski L F, Machanoff R, Hsie A W

出版信息

Mol Cell Biol. 1984 Jul;4(7):1411-5. doi: 10.1128/mcb.4.7.1411-1415.1984.

Abstract

We have developed a system to study mutations that affect xanthine-guanine phosphoribosyltransferase gene (gpt) expression in hypoxanthine-guanine phosphoribosyltransferase-deficient CHO cells that have been transformed by the plasmid vector pSV2gpt. One isolated transformant, designated AS52, carries a single copy of the Escherichia coli gpt gene stably integrated into the high-molecular-weight DNA and expresses the bacterial gene for the enzyme xanthine-guanine phosphoribosyltransferase. Mutants deficient in this enzyme can be induced in the AS52 cell line by a variety of mutagens, and spontaneous or induced mutants can be selected for resistance to 6-thioguanine (Tgr). Two Tgr clones derived from the AS52 line were analyzed by Southern blot hybridization and were found to contain deletions involving at least a portion of the gpt gene. Because of the small size and stability of the integrated pSV2gpt plasmid, and the well-defined selection protocol for mutant isolation, the AS52 line offers promise as a system suitable for the study of mutation at the molecular level in CHO cells.

摘要

我们开发了一个系统,用于研究影响次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶基因(gpt)表达的突变,该研究在已被质粒载体pSV2gpt转化的次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶缺陷型CHO细胞中进行。一个分离得到的转化体,命名为AS52,携带单个拷贝的大肠杆菌gpt基因,该基因稳定整合到高分子量DNA中,并表达黄嘌呤 - 鸟嘌呤磷酸核糖转移酶的细菌基因。该酶缺陷的突变体可在AS52细胞系中由多种诱变剂诱导产生,并且自发或诱导的突变体可通过对6 - 硫鸟嘌呤(Tgr)的抗性进行筛选。通过Southern印迹杂交分析了源自AS52系的两个Tgr克隆,发现它们含有涉及至少一部分gpt基因的缺失。由于整合的pSV2gpt质粒的小尺寸和稳定性,以及用于突变体分离的明确选择方案,AS52系有望成为适合在CHO细胞中进行分子水平突变研究的系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce4b/368924/cbed88c82258/molcellb00149-0230-a.jpg

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