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中国仓鼠卵巢细胞中染色体整合基因的自发突变和甲磺酸乙酯诱导突变中的DNA碱基序列变化

DNA base sequence changes in spontaneous and ethyl methanesulfonate-induced mutations of a chromosomally-integrated gene in Chinese hamster ovary cells.

作者信息

Ashman C R

机构信息

Department of Radiation and Cellular Oncology, University of Chicago, IL 60637.

出版信息

Mutat Res. 1992 Nov 16;270(2):115-24. doi: 10.1016/0027-5107(92)90122-i.

Abstract

A series of spontaneous and ethyl methanesulfonate-induced 6-thioguanine-resistant mutants were isolated in the CHO-10T5 cell line. This cell line was constructed by the introduction of a shuttle vector containing the Escherichia coli gpt gene into a hypoxanthine-guanine phosphoribosyltransferase deficient derivative of the Chinese hamster cell line CHO-K1. Shuttle vector sequences were recovered from many of the mutant cell lines by the COS cell fusion technique and the DNA base sequence of the gpt genes was determined whenever possible. The base sequences were determined for gpt genes recovered from 29 spontaneous mutants. Of these 29 mutants, 9 have single base substitutions, 1 has a small duplication, 17 have simple deletions, 1 has a deletion with additional bases inserted at the deletion site, and 1 has no change in the gpt coding sequence. Many of the deletions were less than 20 basepairs in length and several occurred in a region previously observed to be a hotspot for spontaneous deletions. The generation of the deletion/insertion mutation may have involved a quasi-palindromic intermediate. A total of 59 ethyl methansesulfonate-induced mutants were isolated and vector sequences were recovered from 50 mutants. All 50 mutants sequenced had single base substitutions and most (45) were G:C to A:T transitions. While there were no strong hotspots in this collection of mutations, the site distribution was obviously nonrandom. Many of the G:C to A:T transitions either produced a nonsense codon or occurred at glycine codons.

摘要

在CHO-10T5细胞系中分离出一系列自发的和经甲磺酸乙酯诱导的6-硫鸟嘌呤抗性突变体。该细胞系是通过将含有大肠杆菌gpt基因的穿梭载体导入中国仓鼠细胞系CHO-K1的次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺陷衍生物中构建而成的。通过COS细胞融合技术从许多突变细胞系中回收穿梭载体序列,并尽可能确定gpt基因的DNA碱基序列。测定了从29个自发突变体中回收的gpt基因的碱基序列。在这29个突变体中,9个有单碱基替换,1个有小的重复,17个有简单缺失,1个在缺失位点有额外碱基插入的缺失,1个gpt编码序列无变化。许多缺失长度小于20个碱基对,有几个发生在先前观察到的自发缺失热点区域。缺失/插入突变的产生可能涉及一个准回文中间体。总共分离出59个甲磺酸乙酯诱导的突变体,并从50个突变体中回收了载体序列。所有测序的50个突变体都有单碱基替换,大多数(45个)是G:C到A:T的转换。虽然在这组突变中没有强烈的热点,但位点分布明显是非随机的。许多G:C到A:T的转换要么产生一个无义密码子,要么发生在甘氨酸密码子处。

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