Suppr超能文献

枯草芽孢杆菌中通过 SinR/SlrR 与响应调节子基因 degU 的结合以及 DegU 对 SinR/SlrR 的排除来调节响应调节子基因 degU。

Regulation of the response regulator gene degU through the binding of SinR/SlrR and exclusion of SinR/SlrR by DegU in Bacillus subtilis.

机构信息

Institute of Oceanic Research and Development, Tokai University, Shizuoka, Japan.

出版信息

J Bacteriol. 2014 Feb;196(4):873-81. doi: 10.1128/JB.01321-13. Epub 2013 Dec 6.

Abstract

Bacillus subtilis DegU is a response regulator of the DegS-DegU two-component regulatory system. Phosphorylated DegU (DegU-P) controls many genes and biological processes, such as exoprotease and γ-polyglutamic acid production, in addition to the degU gene, by binding to target gene promoters. Nonphosphorylated DegU and low levels of DegU-P are required for swarming motility and genetic competence. The DNA-binding repressors SinR and SlrR are part of a double-negative feedback loop and comprise the epigenetic switch governing biofilm formation. In this study, we found that SinR repressed degU. Furthermore, SlrR, which interacts with SinR through protein-protein interaction, seems to have an active role in degU expression in in vivo lacZ analysis. An in vitro transcription assay supported this observation. An electrophoretic mobility shift assay (EMSA) showed that SinR bound to the degU promoter and that SlrR formed a complex with SinR on the degU promoter. In EMSA, DegU-P excluded the SinR/SlrR complex but not SinR from the degU promoter in the presence of RNA polymerase. These findings suggest that DegU-P interacts with SlrR. In support of this hypothesis, disruption of the slrR gene resulted in decreased degU expression. This newly identified regulatory mechanism for degU is considered to be sequential transcription factor replacement.

摘要

枯草芽孢杆菌 DegU 是 DegS-DegU 双组分调控系统的响应调节剂。磷酸化的 DegU(DegU-P)通过与靶基因启动子结合,控制许多基因和生物过程,如外蛋白酶和 γ-多谷氨酸的产生,除了 degU 基因。非磷酸化的 DegU 和低水平的 DegU-P 是 swarm 运动和遗传能力所必需的。DNA 结合抑制剂 SinR 和 SlrR 是双负反馈回路的一部分,构成了控制生物膜形成的表观遗传开关。在这项研究中,我们发现 SinR 抑制了 degU。此外,SlrR 通过蛋白-蛋白相互作用与 SinR 相互作用,似乎在体内 lacZ 分析中 degU 表达中具有积极作用。体外转录测定支持了这一观察结果。电泳迁移率变动分析(EMSA)表明 SinR 结合在 degU 启动子上,SlrR 在 degU 启动子上与 SinR 形成复合物。在 EMSA 中,在存在 RNA 聚合酶的情况下,DegU-P 将 SinR/SlrR 复合物但不是 SinR 从 degU 启动子中排除。这些发现表明 DegU-P 与 SlrR 相互作用。支持这一假设,slrR 基因的破坏导致 degU 表达减少。这种新发现的 degU 调控机制被认为是顺序转录因子替代。

相似文献

7
Involvement of nitrogen regulation in Bacillus subtilis degU expression.枯草芽孢杆菌degU表达中氮调节的参与
J Bacteriol. 2008 Aug;190(15):5162-71. doi: 10.1128/JB.00368-08. Epub 2008 May 23.
9
Characterization of DegU-dependent expression of bpr in Bacillus subtilis.枯草芽孢杆菌中bpr的DegU依赖性表达的表征
FEMS Microbiol Lett. 2008 Mar;280(1):8-13. doi: 10.1111/j.1574-6968.2007.01019.x. Epub 2008 Jan 7.

引用本文的文献

1
Differential expression of the operon in a biofilm.操纵子在生物膜中的差异表达。
Appl Environ Microbiol. 2024 Nov 20;90(11):e0136224. doi: 10.1128/aem.01362-24. Epub 2024 Oct 22.
7
The structure and regulation of flagella in Bacillus subtilis.枯草芽孢杆菌中鞭毛的结构与调控
Annu Rev Genet. 2014;48:319-40. doi: 10.1146/annurev-genet-120213-092406. Epub 2014 Sep 10.

本文引用的文献

6
Sticking together: building a biofilm the Bacillus subtilis way.黏附在一起:构建枯草芽孢杆菌生物膜的方式。
Nat Rev Microbiol. 2013 Mar;11(3):157-68. doi: 10.1038/nrmicro2960. Epub 2013 Jan 28.
10
Bacillus subtilis RNA polymerase incorporates digoxigenin-labeled nucleotide in vitro.
J Gen Appl Microbiol. 2011;57(3):153-7. doi: 10.2323/jgam.57.153.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验