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MucR 作为一种类似于 H-NS 的蛋白,可使毒力基因沉默并对核基质进行结构重塑。

MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid.

机构信息

Department of Microbiology and Immunology, Brody School of Medicine, East Carolina University, Greenville, North Carolina, USA.

Department of Biology, Indiana University, Bloomington, Indiana, USA.

出版信息

mBio. 2023 Dec 19;14(6):e0220123. doi: 10.1128/mbio.02201-23. Epub 2023 Oct 17.

DOI:10.1128/mbio.02201-23
PMID:37847580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10746212/
Abstract

Histone-like nucleoid structuring (H-NS) and H-NS-like proteins coordinate host-associated behaviors in many pathogenic bacteria, often through forming silencer/counter-silencer pairs with signal-responsive transcriptional activators to tightly control gene expression. and related bacteria do not encode H-NS or homologs of known H-NS-like proteins, and it is unclear if they have other proteins that perform analogous functions during pathogenesis. In this work, we provide compelling evidence for the role of MucR as a novel H-NS-like protein in . We show that MucR possesses many of the known functions attributed to H-NS and H-NS-like proteins, including the formation of silencer/counter-silencer pairs to control virulence gene expression and global structuring of the nucleoid. These results uncover a new role for MucR as a nucleoid structuring protein and support the importance of temporal control of gene expression in and related bacteria.

摘要

组蛋白样核小体结构(H-NS)和 H-NS 样蛋白在许多致病性细菌中协调与宿主相关的行为,通常通过与信号响应转录激活子形成沉默子/反沉默子对来紧密控制基因表达。然而, 和相关细菌不编码 H-NS 或已知 H-NS 样蛋白的同源物,也不清楚它们是否在发病过程中有其他具有类似功能的蛋白质。在这项工作中,我们提供了令人信服的证据证明 MucR 是 中的一种新型 H-NS 样蛋白。我们表明 MucR 具有许多已知归因于 H-NS 和 H-NS 样蛋白的功能,包括形成沉默子/反沉默子对以控制毒力基因表达和核小体的全局结构。这些结果揭示了 MucR 作为核小体结构蛋白的新作用,并支持了 在 和相关细菌中基因表达的时间控制的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/9bbf9da233d5/mbio.02201-23.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/fb81c78d592a/mbio.02201-23.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/c2654b1220b8/mbio.02201-23.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/88dd7f9cd0bf/mbio.02201-23.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/413710e94ebc/mbio.02201-23.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/cb77d321722d/mbio.02201-23.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/6a50872f057b/mbio.02201-23.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/9bbf9da233d5/mbio.02201-23.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/fb81c78d592a/mbio.02201-23.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/c2654b1220b8/mbio.02201-23.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/88dd7f9cd0bf/mbio.02201-23.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/413710e94ebc/mbio.02201-23.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/cb77d321722d/mbio.02201-23.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/6a50872f057b/mbio.02201-23.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/944d/10746212/9bbf9da233d5/mbio.02201-23.f007.jpg

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