首页> 美国卫生研究院文献>Genetics >Genetic Analysis of Bacillus subtilis spo Mutations Generated by Tn917-Mediated Insertional Mutagenesis
【2h】

Genetic Analysis of Bacillus subtilis spo Mutations Generated by Tn917-Mediated Insertional Mutagenesis

机译: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。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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 Tn 917 insertions, this should significantly facilitate efforts to understand the regulation of these gene sets.
机译:引起孢子形成缺陷的突变(spo突变)通常会识别发育受调控的转录单位或基因,其产物是表达孢子特异性调节子所必需的。我们在这里报告了通过转座子Tn917的插入诱变产生的spo突变的分离,遗传分析和表型特征,Tn917是一种诱变形式,可通过多种方式促进突变基因的遗传和物理操纵。详细研究了二十四个插入spo突变。根据转化介导的和转导介导的连锁分析以及一系列的表型测试,将这些突变分配给20个不同的基因座,其中至少9个不同于先前描述的40个基因座。插入突变导致在孢子形成的各种不同阶段受阻,因此可能鉴定出在孢子形成期间在不同时间有活性的基因。除了大大增加已知基因位点的总数外,我们预计该集合将包括许多时间调控基因的代表,这些基因包括枯草芽孢杆菌中孢子特异性基因激活的总体程序。考虑到被Tn 917插入破坏的基因可能进行的各种操作,这将极大地促进人们努力理解这些基因集的调控。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号