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两个跨膜转录调节因子协同激活霍乱弧菌中几丁质诱导的自然转化。

Two transmembrane transcriptional regulators coordinate to activate chitin-induced natural transformation in Vibrio cholerae.

作者信息

Hullinger Allison C, Green Virginia E, Klancher Catherine A, Dalia Triana N, Dalia Ankur B

机构信息

Department of Biology, Indiana University, Bloomington, Indiana, United States of America.

出版信息

PLoS Genet. 2025 Feb 18;21(2):e1011606. doi: 10.1371/journal.pgen.1011606. eCollection 2025 Feb.

Abstract

Transcriptional regulators are a broad class of proteins that alter gene expression in response to environmental stimuli. Transmembrane transcriptional regulators (TTRs) are a subset of transcriptional regulators in bacteria that can directly regulate gene expression while remaining anchored in the membrane. Whether this constraint impacts the ability of TTRs to bind their DNA targets remains unclear. Vibrio cholerae uses two TTRs, ChiS and TfoS, to activate horizontal gene transfer by natural transformation in response to chitin by inducing the tfoR promoter (PtfoR). While TfoS was previously shown to bind and regulate PtfoR directly, the role of ChiS in PtfoR activation remains unclear. Here, we show that ChiS directly binds PtfoR upstream of TfoS, and that ChiS directly interacts with TfoS. By independently disrupting ChiS-PtfoR and ChiS-TfoS interactions, we show that ChiS-PtfoR interactions play the dominant role in PtfoR activation. Correspondingly, we show that in the absence of ChiS, recruitment of the PtfoR locus to the membrane is sufficient for PtfoR activation when TfoS is expressed at native levels. Finally, we show that the overexpression of TfoS can bypass the need for ChiS for PtfoR activation. All together, these data suggest a model whereby ChiS both (1) recruits the PtfoR DNA locus to the membrane for TfoS and (2) directly interacts with TfoS, thereby recruiting it to the membrane-proximal promoter. This work furthers our understanding of the molecular mechanisms that drive chitin-induced responses in V. cholerae and more broadly highlights how the membrane-embedded localization of TTRs can impact their activity.

摘要

转录调节因子是一类广泛的蛋白质,可响应环境刺激改变基因表达。跨膜转录调节因子(TTRs)是细菌转录调节因子的一个子集,它们可以在锚定在膜上的同时直接调节基因表达。这种限制是否会影响TTRs与其DNA靶点结合的能力仍不清楚。霍乱弧菌利用两种TTRs,即ChiS和TfoS,通过诱导tfoR启动子(PtfoR)来响应几丁质,从而通过自然转化激活水平基因转移。虽然之前已证明TfoS可直接结合并调节PtfoR,但ChiS在PtfoR激活中的作用仍不清楚。在这里,我们表明ChiS直接结合在TfoS上游的PtfoR,并且ChiS直接与TfoS相互作用。通过独立破坏ChiS-PtfoR和ChiS-TfoS相互作用,我们表明ChiS-PtfoR相互作用在PtfoR激活中起主导作用。相应地,我们表明在没有ChiS的情况下,当TfoS以天然水平表达时,将PtfoR基因座募集到膜上就足以激活PtfoR。最后,我们表明TfoS的过表达可以绕过激活PtfoR对ChiS的需求。总之,这些数据表明了一种模型,即ChiS既(1)将PtfoR DNA基因座募集到膜上以供TfoS作用,又(2)直接与TfoS相互作用,从而将其募集到膜近端启动子。这项工作进一步加深了我们对驱动霍乱弧菌几丁质诱导反应的分子机制的理解,并更广泛地突出了TTRs的膜嵌入定位如何影响其活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f60c/11856585/d8b266033feb/pgen.1011606.g001.jpg

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