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通过Tn917介导的插入诱变产生的枯草芽孢杆菌spo突变的遗传分析。

Genetic analysis of Bacillus subtilis spo mutations generated by Tn917-mediated insertional mutagenesis.

作者信息

Sandman K, Losick R, Youngman P

机构信息

Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.

出版信息

Genetics. 1987 Dec;117(4):603-17. doi: 10.1093/genetics/117.4.603.

Abstract

Mutations that cause sporulation defects (spo mutations) often identify developmentally regulated transcription units or genes whose products are required for the expression of sporulation-specific regulons. We report here the isolation, genetic analysis and phenotypic characterization of spo mutations produced by insertional mutagenesis with transposon Tn917, a form of mutagenesis that facilitates genetic and physical manipulation of mutated genes in many ways. Twenty-four insertional spo mutations were studied in detail. On the basis of transformation-mediated and transduction-mediated linkage analysis and a range of phenotypic tests, these mutations were assigned to 20 distinct loci, at least 9 of which are different from the 40 previously described spo loci. The insertional mutations caused blocks at a variety of different stages of sporulation, and therefore probably identify genes active at different times during sporulation. In addition to increasing substantially the total of known spo loci, we anticipate that this collection will include representatives of many of the temporally regulated sets of genes that comprise the overall program of sporulation-specific gene activation in Bacillus subtilis. Given the kinds of manipulations that are possible with genes disrupted by Tn917 insertions, this should significantly facilitate efforts to understand the regulation of these gene sets.

摘要

导致芽孢形成缺陷的突变(spo突变)常常能鉴定出发育调控的转录单元或基因,其产物是芽孢形成特异性调控子表达所必需的。我们在此报告通过转座子Tn917进行插入诱变产生的spo突变的分离、遗传分析及表型特征,这种诱变形式在许多方面有助于对突变基因进行遗传和物理操作。我们详细研究了24个插入性spo突变。基于转化介导和转导介导的连锁分析以及一系列表型测试,这些突变被定位到20个不同的位点,其中至少9个与先前描述的40个spo位点不同。插入突变在芽孢形成的各种不同阶段造成阻断,因此可能鉴定出在芽孢形成过程中不同时间活跃的基因。除了大幅增加已知spo位点的总数外,我们预计这个集合将包括许多时间调控基因集的代表,这些基因集构成了枯草芽孢杆菌芽孢形成特异性基因激活的总体程序。鉴于通过Tn917插入破坏的基因可以进行各种操作,这应该会显著促进对这些基因集调控的理解。

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