Dynamics of bacterial operons during genome-wide stresses is influenced by premature terminations and internal promoters

IF 11.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Rahul Jagadeesan, Suchintak Dash, Cristina S. D. Palma, Ines S. C. Baptista, Vatsala Chauhan, Jarno Mäkelä, Andre S. Ribeiro
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Abstract

Bacterial gene networks have operons, each coordinating several genes under a primary promoter. Half of the operons in Escherichia coli have been reported to also contain internal promoters. We studied their role during genome-wide stresses targeting key transcription regulators, RNA polymerase (RNAP) and gyrase. Our results suggest that operons’ responses are influenced by stress-related changes in premature elongation terminations and internal promoters’ activity. Globally, this causes the responses of genes in the same operon to differ with the distance between them in a wave-like pattern. Meanwhile, premature terminations are affected by positive supercoiling buildup, collisions between elongating and promoter-bound RNAPs, and local regulatory elements. We report similar findings in E. coli under other stresses and in evolutionarily distant bacteria Bacillus subtilis, Corynebacterium glutamicum, and Helicobacter pylori. Our results suggest that the strength, number, and positioning of operons’ internal promoters might have evolved to compensate for premature terminations, providing distal genes similar response strengths.
细菌操纵子在全基因组胁迫过程中的动力学受到过早终止和内部启动子的影响
细菌基因网络有操纵子,每个操纵子在一个初级启动子下协调几个基因。据报道,大肠杆菌中一半的操纵子也含有内部启动子。我们研究了它们在针对关键转录调控因子、RNA聚合酶(RNAP)和回转酶的全基因组胁迫中的作用。我们的研究结果表明,操纵子的反应受到应力相关的早伸长终止和内部启动子活性变化的影响。从整体上看,这导致同一操纵子上的基因的反应随着它们之间的距离而不同,呈波浪状。与此同时,过早终止受正向超卷曲形成、伸长和启动子结合rnap之间的碰撞以及局部调控元件的影响。我们报告了在其他压力下的大肠杆菌和进化上遥远的细菌枯草芽孢杆菌、谷氨酸棒状杆菌和幽门螺杆菌中类似的发现。我们的研究结果表明,操纵子内部启动子的强度、数量和位置可能已经进化为补偿过早终止,为远端基因提供类似的响应强度。
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来源期刊
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
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