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Effects of plasmid propagation of a sporulation promoter on promoter utilization and sporulation in Bacillus subtilis.

机译:孢子形成启动子的质粒繁殖对枯草芽孢杆菌中启动子利用和孢子形成的影响。

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摘要

Transcription of the sporulation gene spoVG of Bacillus subtilis is induced at the onset of spore formation and depends on the products of the regulatory genes spoOA, spoOB, and spoOH. We describe two effects of propagating the promoter region of spoVG on a multicopy plasmid replicon in B. subtilis cells. One effect is that transcription from the plasmid-borne spoVG promoter is altered with respect to the time of its induction and the dependence on spoO gene products. An example of this effect is that plasmid propagation was observed to relieve substantially the inhibitory effect of a mutation in spoOH, the spoO gene upon which spoVG promoter activity is most strongly dependent. We present results which suggest that propagation on a plasmid replicon causes an alteration in the conformation of spoVG promoter DNA which somehow compensates for the defective spoOH gene product. Plasmid propagation did not, however, entirely eliminate the requirement for the spoOH gene product; little or no spoVG-directed RNA synthesis was observed in cells bearing a putative spoOH deletion mutation, a finding which indicates that SpoOH protein plays an indispensable role in spoVG promoter utilization. Another effect of propagating the promoter region of spoVG on a multicopy plasmid is to inhibit sporulation. S1 nuclease mapping experiments suggest that amplification of spoVG on a multicopy plasmid causes the titration of a transcription factor or minor form of RNA polymerase holoenzyme required for utilization of one of the two overlapping promoters which comprise the spoVG transcription initiation region.
机译:枯草芽孢杆菌的孢子形成基因spoVG的转录在孢子形成开始时被诱导,并取决于调节基因spoOA,spoOB和spoOH的产物。我们描述了在枯草芽孢杆菌细胞中多拷贝质粒复制子上传播spoVG启动子区域的两种作用。一种效果是,质粒诱导的spoVG启动子的转录就其诱导时间和对spoO基因产物的依赖性而改变。这种作用的一个例子是观察到质粒的繁殖基本上减轻了spoOH突变的抑制作用,spoOH是spoVG启动子活性最强烈依赖的spoO基因。我们提出的结果表明,在质粒复制子上的繁殖会引起spoVG启动子DNA构象的改变,从而以某种方式补偿了有缺陷的spoOH基因产物。然而,质粒的繁殖并不能完全消除对spoOH基因产物的需求。在携带推定的spoOH缺失突变的细胞中,几乎没有观察到spoVG定向的RNA合成,这一发现表明SpoOH蛋白在spoVG启动子的利用中起着不可或缺的作用。在多拷贝质粒上传播spoVG启动子区域的另一种作用是抑制孢子形成。 S1核酸酶作图实验表明,多拷贝质粒上spoVG的扩增引起滴定转录因子或利用构成spoVG转录起始区的两个重叠启动子之一所需的RNA聚合酶全酶的次要形式。

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