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枯草芽孢杆菌染色体克隆片段中的发育调控转录

Developmentally regulated transcription in a cloned segment of the Bacillus subtilis chromosome.

作者信息

Ollington J F, Haldenwang W G, Huynh T V, Losick R

出版信息

J Bacteriol. 1981 Aug;147(2):432-42. doi: 10.1128/jb.147.2.432-442.1981.

DOI:10.1128/jb.147.2.432-442.1981
PMID:6790515
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC216062/
Abstract

We describe a model system for studying developmentally regulated transcription during spore formation in Bacillus subtilis. This model system is a cloned cluster of genes known as 0.4 kb, ctc, and veg from the purA-cysA region of the B. subtilis chromosome. Each gene exhibited a distinct pattern of transcription in cells growing in glucose medium and in cells deprived of nutrients in sporulation medium. The 0.4 kb gene was transcribed at a low level in growing cells but was actively transcribed during nutrient deprivation in sporulation medium. This ribonucleic acid (RNA) synthesis was dependent upon the products of five B. subtilis genes that are involved in the initiation of spore formation:spo0A, spo0A, spo0E, spo0F, and spo0H. A mutation in any one of these regulatory genes severely restricted transcription of the 0.4 kb sequence. Transcription of the ctc gene was also turned on by nutrient deprivation, but this RNA synthesis was not impaired in spo0 mutants. Although not under spo0 control, the ctc gene probably corresponds to a locus, spoVC, whose product is required at a late stage of sporulation. Finally, the veg gene was actively transcribed both in growing cells and in nutrient-deprived cells. Like ctc RNA synthesis, transcription of the veg gene was not dependent upon the spo0 gene products. We propose that the spo0A, spo0B, spo0E, spo0F, and spo0H gene products are components of a pathway(s) that senses nutrient deprivation in B. subtilis and translates this environmental signal into the transcriptional activation of a subset of developmental genes.

摘要

我们描述了一种用于研究枯草芽孢杆菌孢子形成过程中发育调控转录的模型系统。该模型系统是一个克隆的基因簇,来自枯草芽孢杆菌染色体的purA - cysA区域,包含0.4 kb、ctc和veg基因。每个基因在葡萄糖培养基中生长的细胞以及在孢子形成培养基中缺乏营养的细胞中都表现出独特的转录模式。0.4 kb基因在生长细胞中低水平转录,但在孢子形成培养基中营养缺乏期间被积极转录。这种核糖核酸(RNA)合成依赖于参与孢子形成起始的五个枯草芽孢杆菌基因的产物:spo0A、spo0B、spo0E、spo0F和spo0H。这些调控基因中任何一个发生突变都会严重限制0.4 kb序列的转录。ctc基因的转录也因营养缺乏而开启,但这种RNA合成在spo0突变体中并未受损。尽管不受spo0控制,但ctc基因可能对应于一个位点spoVC,其产物在孢子形成后期是必需的。最后,veg基因在生长细胞和营养缺乏的细胞中都被积极转录。与ctc RNA合成一样,veg基因的转录不依赖于spo0基因产物。我们提出,spo0A、spo0B、spo0E、spo0F和spo0H基因产物是一条途径的组成部分,该途径感知枯草芽孢杆菌中的营养缺乏,并将这种环境信号转化为一组发育基因的转录激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/d1da4fc298f0/jbacter00267-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/94cf82da0b89/jbacter00267-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/6bd28ccbc99c/jbacter00267-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/875928b672d1/jbacter00267-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/f446e83227f3/jbacter00267-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/b5291383ac8f/jbacter00267-0172-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/d1da4fc298f0/jbacter00267-0173-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/94cf82da0b89/jbacter00267-0169-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/6bd28ccbc99c/jbacter00267-0170-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/875928b672d1/jbacter00267-0171-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/f446e83227f3/jbacter00267-0172-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/b5291383ac8f/jbacter00267-0172-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7196/216062/d1da4fc298f0/jbacter00267-0173-a.jpg

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本文引用的文献

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