Complex sporulation-specific expression of transcription termination factor Rho highlights its involvement in Bacillus subtilis cell differentiation.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Biological Chemistry Pub Date : 2024-10-19 DOI:10.1016/j.jbc.2024.107905
Vladimir Bidnenko, Arnaud Chastanet, Christine Péchoux, Yulia Redko-Hamel, Olivier Pellegrini, Sylvain Durand, Ciarán Condon, Marc Boudvillain, Matthieu Jules, Elena Bidnenko
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Abstract

Termination factor Rho, responsible for the main factor-dependent pathway of transcription termination and the major inhibitor of antisense transcription, is an emerging regulator of various physiological processes in microorganisms. In Gram-positive bacterium Bacillus subtilis, Rho is involved in the control of cell adaptation to starvation and, in particular, in the control of sporulation, a complex differentiation program leading to the formation of a highly resistant dormant spore. While the initiation of sporulation requires a decrease in Rho protein levels during the transition to stationary phase, the mechanisms regulating the expression of rho gene throughout the cell cycle remain largely unknown. Here we show that a drop in the activity of the vegetative SigA-dependent rho promoter causes the inhibition of rho expression in stationary phase. However, after the initiation of sporulation, rho gene is specifically reactivated in two compartments of the sporulating cell using distinct mechanisms. In the mother cell, rho expression occurs by read-through transcription initiated at the SigH-dependent promoter of the distal spo0F gene. In the forespore, rho gene is transcribed from the intrinsic promoter recognized by the alternative sigma factor SigF. These regulatory elements ensure the activity of Rho during sporulation, which appears important for the proper formation of spores. We provide experimental evidence that disruption of the spatiotemporal expression of rho during sporulation affects the resistance properties of spores, their morphology, and the ability to return to vegetative growth under favorable growth conditions.

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转录终止因子 Rho 的复杂孢子特异性表达突显了它在枯草杆菌细胞分化中的参与。
终止因子 Rho 是转录终止的主要依赖因子途径,也是反义转录的主要抑制因子,是微生物各种生理过程的新兴调节因子。在革兰氏阳性细菌枯草杆菌(Bacillus subtilis)中,Rho 参与控制细胞对饥饿的适应,尤其是对孢子化的控制,孢子化是一种复杂的分化程序,可形成具有高度抵抗力的休眠孢子。孢子形成的启动需要在向静止期过渡时降低 Rho 蛋白水平,但整个细胞周期中 Rho 基因表达的调控机制在很大程度上仍不为人所知。在这里,我们发现依赖于 SigA 的无性繁殖期 rho 启动子活性的下降会导致 rho 在静止期的表达受到抑制。然而,在孢子形成开始后,rho 基因会通过不同的机制在孢子细胞的两个区室中特异性地重新激活。在母细胞中,rho 的表达是通过远端 spo0F 基因的 SigH 依赖性启动子启动的直读转录进行的。在前孢子中,rho 基因由替代 sigma 因子 SigF 识别的内在启动子转录。这些调控元件确保了 Rho 在孢子形成过程中的活性,这似乎对孢子的正常形成非常重要。我们提供的实验证据表明,在孢子形成过程中破坏 rho 的时空表达会影响孢子的抗性、形态以及在有利生长条件下恢复无性生殖的能力。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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