细菌染色体组织进化过程中超卷曲介导的调节网络的出现。

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
PLoS Computational Biology Pub Date : 2025-09-29 eCollection Date: 2025-09-01 DOI:10.1371/journal.pcbi.1013482
Théotime Grohens, Sam Meyer, Guillaume Beslon
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引用次数: 0

摘要

DNA超卷曲——DNA分子在自身周围的扭曲水平——通过调节启动子活性在细菌基因表达调控中起着重要作用。DNA超卷曲水平是染色体的一种动态特性,它在局部和全局尺度上都有变化,既受环境扰动等外部因素的影响,也受基因转录等内部因素的影响。因此,从理论上讲,超卷曲的局部变异可以通过在转录水平上产生反馈回路来耦合邻近基因的表达水平。然而,这种超卷曲介导的相互作用对基因表达调控的影响仍然不确定。在这项工作中,我们研究了转录和超卷曲之间的耦合如何塑造基因组组织并帮助调节基因转录。我们提出了一种基因组进化模型,其中基因转录率与局部超卷曲相耦合的个体必须适应诱导不同全球超卷曲水平的两种环境。在这个模型中,我们观察了全基因组调控网络的进化,该网络通过利用转录-超卷曲耦合来控制基因表达,并表明这些网络的结构是由染色体上的基因组织在几个尺度上支撑的。因此,DNA超卷曲的局部变异可能有助于共同塑造进化过程中的基因调控和基因组组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emergence of supercoiling-mediated regulatory networks through the evolution of bacterial chromosome organization.

DNA supercoiling-the level of twisting and writhing of the DNA molecule around itself-plays an important role in the regulation of gene expression in bacteria by modulating promoter activity. The level of DNA supercoiling is a dynamic property of the chromosome which varies both at local and global scales, in response to both external factors such as environmental perturbations and internal factors including gene transcription. As such, local variations in supercoiling could in theory couple the expression levels of neighboring genes by creating feedback loops at the transcriptional level. However, the impact of such supercoiling-mediated interactions on the regulation of gene expression still remains uncertain. In this work, we study how this coupling between transcription and supercoiling could shape genome organization and help regulate gene transcription. We present a model of genome evolution in which individuals whose gene transcription rates are coupled to local supercoiling must adapt to two environments that induce different global supercoiling levels. In this model, we observe the evolution of whole-genome regulatory networks that provide control over gene expression by leveraging the transcription-supercoiling coupling, and show that the structure of these networks is underpinned by the organization of genes along the chromosome at several scales. Local variations in DNA supercoiling could therefore help jointly shape both gene regulation and genome organization during evolution.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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