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仓鼠细胞中次黄嘌呤磷酸核糖转移酶(hprt)基因自发及甲磺酸乙酯诱导突变的分子分析

Molecular analysis of spontaneous and ethyl methanesulphonate-induced mutations of the hprt gene in hamster cells.

作者信息

Thacker J, Ganesh A N

机构信息

MRC Radiobiology Unit, Chilton, Didcot, Oxon, Great Britain.

出版信息

Mutat Res. 1989 Jan;210(1):103-12. doi: 10.1016/0027-5107(89)90049-3.

Abstract

Independent spontaneous or ethyl methanesulphonate (EMS)-induced mutants lacking HPRT enzyme activity were analysed for changes in hprt gene structure. Of 21 spontaneous mutants, 6 had total gene deletions, 2 had partial gene deletions, and 13 were indistinguishable from wild-type by Southern analysis. In contrast a sample of 23 EMS-induced mutants, each of which showed potentially interesting characteristics (e.g. high reversion frequency, X-chromosome rearrangement), showed no detectable hprt gene changes. RNA isolated from 59 mutants with presumptive point mutations (13 spontaneous, 46 EMS-induced) was analysed on dot blots for changes in the amount of hprt mRNA. A wide range of mRNA levels was found, from mutants with undetectable amounts to those with more than wild-type amounts. However, Northern blots of all these mutant RNAs revealed only one (EMS-induced) mutation with a change in hprt mRNA size. Taken with our previously-published data on these mutants, it is argued that they represent a broad range of mutational types, and that the hprt gene mutation system provides a sensitive means of distinguishing mutational spectra of different DNA-damaging agents.

摘要

对缺乏次黄嘌呤磷酸核糖转移酶(HPRT)酶活性的独立自发突变体或甲磺酸乙酯(EMS)诱导的突变体进行了hprt基因结构变化分析。在21个自发突变体中,6个发生了整个基因缺失,2个发生了部分基因缺失,通过Southern分析,13个与野生型无差异。相比之下,23个EMS诱导的突变体样本,每个都表现出潜在有趣的特征(如高回复频率、X染色体重排),但未检测到hprt基因变化。从59个推定有碱基突变的突变体(13个自发突变体、46个EMS诱导的突变体)中分离的RNA,在斑点印迹上分析hprt mRNA量的变化。发现了广泛的mRNA水平范围,从无法检测到的量到超过野生型量的突变体。然而,所有这些突变体RNA的Northern印迹仅显示一个(EMS诱导的)突变体的hprt mRNA大小发生了变化。结合我们之前发表的关于这些突变体的数据,认为它们代表了广泛的突变类型,并且hprt基因突变系统提供了一种区分不同DNA损伤剂突变谱的灵敏方法。

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