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Genome-wide analysis of temporally regulated and compartment-specific gene expression in sporulating cells of Bacillus subtilis

机译:枯草素枯草芽孢杆菌孢子细胞中颞下调节和舱室特异性基因表达的基因组分析

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Temporal and compartment-specific control of gene expression during sporulation in Bacillus subtilis is governed by a cascade of four RNA polymerase subunits. σF in the prespore and σE in the mother cell control early stages of development, and are replaced at later stages by σG and σK, respectively. Ultimately, a comprehensive description of the molecular mechanisms underlying spore morphogenesis requires the knowledge of all the intervening genes and their assignment to specific regulons. Here, in an extension of earlier work, DNA macroarrays have been used, and members of the four compartment-specific sporulation regulons have been identified. Genes were identified and grouped based on: i) their temporal expression profile and ii) the use of mutants for each of the four sigma factors and a bofA allele, which allows σK activation in the absence of σG. As a further test, artificial production of active alleles of the sigma factors in non-sporulating cells was employed. A total of 439 genes were found, including previously characterized genes whose transcription is induced during sporulation: 55 in the σF regulon, 154 σE-governed genes, 113 σG-dependent genes, and 132 genes under σK control. The results strengthen the view that the activities of σF, σE, σG and σK are largely compartmentalized, both temporally as well as spatially, and that the major vegetative sigma factor (σA) is active throughout sporulation. The results provide a dynamic picture of the changes in the overall pattern of gene expression in the two compartments of the sporulating cell, and offer insight into the roles of the prespore and the mother cell at different times of spore morphogenesis.
机译:在枯草芽孢杆菌中孢子症期间基因表达的时间和隔室特异性控制受到四个RNA聚合酶亚基的级联来控制。 ΣF在母细胞中的Prespore和ΣE中控制早期的发育阶段,并分别在σg和σk的后续阶段被替换。最终,孢子形态发生的分子机制的综合描述需要对所有干预基因的知识及其对特定调节子的作用。这里,在较早工作的延伸中,已经使用了DNA Macroarrays,并且已经确定了四个隔室特异性孢子化调节器的构件。基于以下:i)鉴定基因并分组它们的时间表达谱和II)用于四种Sigma因子和BOFA等位基因中的每一个的突变体,这允许σk激活在不存在σg中。作为进一步的测试,采用了非孢子化细胞中Sigma因子的活性等位质的人工生产。发现总共439个基因,包括先前表征的基因,其转录在孢子期间诱导:55在ΣF调节件,154ΣE治理的基因,113σg依赖性基因和132个基因下进行σk控制。结果加强了ΣF,σe,σg和σk的活性在很大程度上划分的,在时间上以及空间上的情况下,主要植物σ因子(σa)在整个孢子中有效。结果提供了孢子用细胞的两个隔间中基因表达的整体模式的变化的动态图片,并在不同时间的孢子形态发生时提供了对Prespore和母细胞的作用的洞察。

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