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构巢曲霉诱变敏感nuv突变体的分离及其对有丝分裂重组的影响。

The isolation of mutagen-sensitive nuv mutants of Aspergillus nidulans and their effects on mitotic recombination.

作者信息

Osman F, Tomsett B, Strike P

机构信息

Department of Genetics and Microbiology, University of Liverpool, England.

出版信息

Genetics. 1993 Jun;134(2):445-54. doi: 10.1093/genetics/134.2.445.

Abstract

More than 200 mutants of Aspergillus nidulans were isolated as hypersensitive to the monofunctional alkylating agent MNNG and/or UV-irradiation (designated nuv mutants). Of these, 23 were selected for further characterization. All were markedly hypersensitive to both MNNG and the quasi-UV-mimetic mutagen 4-NQO. The hypersensitive phenotype of each mutant was shown to result from mutation of a single gene. The nuv mutants exhibited a diverse range of growth responses on solid media containing various concentrations of MNNG or 4-NQO. This suggested that they represented many nonallelic mutations. Analysis to determine the dominance/recessiveness of the nuv mutations with respect to hypersensitivity revealed that most were fully recessive, although several appeared to be semidominant. A novel system to assay homologous mitotic recombination using simple plating tests was developed. The system was exploited to determine the effects of the nuv mutations on mitotic recombination. Of the 23 mutations tested, 10 caused a hypo-recombination phenotype and three a hyper-recombination phenotype, while 10 appeared to have no effect on recombination. The hypo-rec effect of one of the mutations, nuv-117, appeared to be semidominant. Transcomplementation analysis between seven of the nuv mutations defined at least six nonallelic loci.

摘要

分离出200多个构巢曲霉突变体,它们对单功能烷化剂MNNG和/或紫外线照射敏感(命名为nuv突变体)。其中,选择了23个进行进一步表征。所有突变体对MNNG和准紫外线模拟诱变剂4-NQO均表现出明显的超敏反应。每个突变体的超敏表型显示是由单个基因突变引起的。nuv突变体在含有不同浓度MNNG或4-NQO的固体培养基上表现出多种生长反应。这表明它们代表了许多非等位基因突变。分析nuv突变在超敏反应方面的显性/隐性,发现大多数是完全隐性的,尽管有几个似乎是半显性的。开发了一种使用简单平板试验检测同源有丝分裂重组的新系统。利用该系统确定nuv突变对有丝分裂重组的影响。在测试的23个突变中,10个导致重组减少表型,3个导致重组增加表型,而10个似乎对重组没有影响。其中一个突变体nuv-117的重组减少效应似乎是半显性的。对7个nuv突变进行的互补分析确定了至少6个非等位基因座。

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