细菌染色质蛋白、转录和 DNA 拓扑:基因表达控制中不可分割的伙伴。

IF 2.6 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Microbiology Pub Date : 2024-07-01 Epub Date: 2024-06-07 DOI:10.1111/mmi.15283
Christine M Hustmyer, Robert Landick
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引用次数: 0

摘要

细菌染色体中的 DNA 被称为核仁相关蛋白(NAPs)或细菌染色质蛋白(BCPs)的 DNA 结合蛋白组织成高阶结构。BCPs 通常与 RNA 聚合酶(RNAP)转录的 DNA 位点结合或靠近 DNA 位点,可以增加或减少基因表达。要了解 BCPs 改变转录的机制,必须同时考虑立体效应和 DNA 偏离其完全松弛的双螺旋结构时产生的拓扑力。当 RNAP 和 DNA 无法自由旋转时,转录 RNAP 会在上游产生 DNA 负(-)超卷,在下游产生正(+)超卷。这种(-)和(+)超螺旋会产生拓扑力,阻碍 DNA 通过 RNAP 向前转移,除非超螺旋受到 BCP 的限制或拓扑异构酶的缓解。BCPs 还可增强拓扑压力,总体上可抑制或帮助转录。在此,我们回顾了目前对 RNAP、BCPs 和 DNA 拓扑如何相互作用控制基因表达的理解。
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Bacterial chromatin proteins, transcription, and DNA topology: Inseparable partners in the control of gene expression.

DNA in bacterial chromosomes is organized into higher-order structures by DNA-binding proteins called nucleoid-associated proteins (NAPs) or bacterial chromatin proteins (BCPs). BCPs often bind to or near DNA loci transcribed by RNA polymerase (RNAP) and can either increase or decrease gene expression. To understand the mechanisms by which BCPs alter transcription, one must consider both steric effects and the topological forces that arise when DNA deviates from its fully relaxed double-helical structure. Transcribing RNAP creates DNA negative (-) supercoils upstream and positive (+) supercoils downstream whenever RNAP and DNA are unable to rotate freely. This (-) and (+) supercoiling generates topological forces that resist forward translocation of DNA through RNAP unless the supercoiling is constrained by BCPs or relieved by topoisomerases. BCPs also may enhance topological stress and overall can either inhibit or aid transcription. Here, we review current understanding of how RNAP, BCPs, and DNA topology interplay to control gene expression.

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来源期刊
Molecular Microbiology
Molecular Microbiology 生物-生化与分子生物学
CiteScore
7.20
自引率
5.60%
发文量
132
审稿时长
1.7 months
期刊介绍: Molecular Microbiology, the leading primary journal in the microbial sciences, publishes molecular studies of Bacteria, Archaea, eukaryotic microorganisms, and their viruses. Research papers should lead to a deeper understanding of the molecular principles underlying basic physiological processes or mechanisms. Appropriate topics include gene expression and regulation, pathogenicity and virulence, physiology and metabolism, synthesis of macromolecules (proteins, nucleic acids, lipids, polysaccharides, etc), cell biology and subcellular organization, membrane biogenesis and function, traffic and transport, cell-cell communication and signalling pathways, evolution and gene transfer. Articles focused on host responses (cellular or immunological) to pathogens or on microbial ecology should be directed to our sister journals Cellular Microbiology and Environmental Microbiology, respectively.
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