首页> 外文期刊>Journal of bacteriology >Role of the Anti-Sigma Factor SpoIIAB in Regulation of σG during Bacillus subtilis Sporulation
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Role of the Anti-Sigma Factor SpoIIAB in Regulation of σG during Bacillus subtilis Sporulation

机译:抗Sigma因子SpoIIAB在枯草芽孢杆菌孢子形成过程中对σG调控的作用

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RNA polymerase sigma factor σF initiates the prespore-specific program of gene expression during Bacillus subtilis sporulation. σF governs transcription of spoIIIG, encoding the late prespore-specific regulator σG. However, transcription of spoIIIG is delayed relative to other genes under the control of σF, and after synthesis, σG is initially kept in an inactive form. Activation of σG requires the complete engulfment of the prespore by the mother cell and expression of the spoIIIA and spoIIIJ loci. We screened for random mutations in spoIIIG that bypassed the requirement for spoIIIA for the activation of σG. We found a mutation (spoIIIGE156K) that resulted in an amino acid substitution at position 156, which is adjacent to the position of a mutation (E155K) previously shown to prevent interaction of SpoIIAB with σG. Comparative modelling techniques and in vivo studies suggested that the spoIIIGE156K mutation interferes with the interaction of SpoIIAB with σG. The σGE156K isoform restored σG-directed gene expression to spoIIIA mutant cells. However, expression of sspE-lacZ in the spoIIIA spoIIIGE156K double mutant was delayed relative to completion of the engulfment process and was not confined to the prespore. Rather, β-galactosidase accumulated throughout the entire cell at late times in development. This suggests that the activity of σGE156K is still regulated in the prespore of a spoIIIA mutant, but not by SpoIIAB. In agreement with this suggestion, we also found that expression of spoIIIGE156K from the promoter for the early prespore-specific gene spoIIQ still resulted in sspE-lacZ induction at the normal time during sporulation, coincidently with completion of the engulfment process. In contrast, transcription of spoIIIGE156K, but not of the wild-type spoIIIG gene, from the mother cell-specific spoIID promoter permitted the rapid induction of sspE-lacZ expression. Together, the results suggest that SpoIIAB is either redundant or has no role in the regulation of σG in the prespore.
机译:RNA聚合酶西格玛因子σ F 启动枯草芽孢杆菌(Bacillus subtilis)孢子形成过程中孢子特异性基因表达程序。 σ F 控制 spoIIIG 的转录,编码晚期孢子特异性调节子σ G 。但是, spoIIIG 的转录相对于其他基因在σ F 的控制下有所延迟,并且在合成后,σ G 最初保持在一个非活动形式。 σ G 的激活需要母细胞完全包被芽孢,并表达 spoIIIA spoIIIJ 位点。我们筛选了 spoIIIG 中的随机突变,该突变忽略了 spoIIIA 激活σ G 的要求。我们发现了一个突变( spoIIIGE156K ),该突变导致在位置156处发生了氨基酸取代,该位置与先前显示可防止SpoIIAB与σ G相互作用的突变(E155K)的位置相邻。比较建模技术和体内研究表明, spoIIIGE156K 突变会干扰SpoIIAB与σ G 的相互作用。 σ GE156K 同工型将σ G 导向的基因表达恢复到 spoIIIA 突变细胞。但是, sspE - lacZ spoIIIA spoIIIGE156K 双重突变体中的表达相对于吞噬过程的完成是延迟的,并且不仅限于孢子。而是,β-半乳糖苷酶在发育的晚期积累在整个细胞中。这表明σ GE156K 的活性仍在 spoIIIA 突变体的孢子中被调节,但不受SpoIIAB的调节。与此建议相一致,我们还发现,从早期孢子特异性基因 spoIIQ 的启动子表达 spoIIIGE156K 仍会导致 sspE-lacZ 在孢子形成的正常时间诱导,与吞噬过程完成同时发生。相反,从母细胞特异性的 spoIID 启动子转录 spoIIIGE156K 而不是野生型 spoIIIG 基因,可以快速诱导sspE-lacZ 表达式的形式。总之,结果表明SpoIIAB是多余的,或在孢子中对σ G 的调节中没有作用。

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