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CRP与Sxy特异性相互作用以激活……中的转录。

CRP Interacts Specifically With Sxy to Activate Transcription in .

作者信息

Søndberg Emilie, Sinha Anurag Kumar, Gerdes Kenn, Semsey Szabolcs

机构信息

Centre for Bacterial Stress Response and Persistence, Department of Biology, University of Copenhagen, Copenhagen, Denmark.

出版信息

Front Microbiol. 2019 Aug 30;10:2053. doi: 10.3389/fmicb.2019.02053. eCollection 2019.

Abstract

Horizontal gene transfer through natural competence is an important driving force of bacterial evolution and antibiotic resistance development. In several Gram-negative pathogens natural competence is regulated by the concerted action of cAMP receptor protein (CRP) and the transcriptional co-regulator Sxy through a subset of CRP-binding sites (CRP-S sites) at genes encoding competence factors. Despite the wealth of knowledge on CRP's structure and function it is not known how CRP and Sxy act together to activate transcription. In order to get an insight into the regulatory mechanism by which these two proteins activate gene expression, we performed a series of mutational analyses on CRP and Sxy. We found that CRP contains a previously uncharacterized region necessary for Sxy dependent induction of CRP-S sites, here named "Sxy Interacting Region" (SIR) encompassing residues Q194 and L196. Lost promoter induction in SIR mutants could be restored in the presence of specific complementary Sxy mutants, presenting evidence for a direct interaction of CRP and Sxy proteins in transcriptional activation. Moreover, we identified constitutive mutants of Sxy causing higher levels of CRP-S site promoter activation than wild-type Sxy. Both suppressor and constitutive mutations are located within the same area of Sxy.

摘要

通过自然感受态进行的水平基因转移是细菌进化和抗生素耐药性发展的重要驱动力。在几种革兰氏阴性病原体中,自然感受态受环磷酸腺苷受体蛋白(CRP)和转录共调节因子Sxy的协同作用调控,通过编码感受态因子的基因上的一部分CRP结合位点(CRP-S位点)来实现。尽管对CRP的结构和功能已有丰富的了解,但尚不清楚CRP和Sxy如何共同作用来激活转录。为了深入了解这两种蛋白质激活基因表达的调控机制,我们对CRP和Sxy进行了一系列突变分析。我们发现CRP含有一个以前未被表征的区域,该区域是Sxy依赖诱导CRP-S位点所必需的,这里命名为“与Sxy相互作用区域”(SIR),包含第194位谷氨酰胺和第196位亮氨酸残基。在存在特定互补Sxy突变体的情况下,SIR突变体中丧失的启动子诱导可以恢复,这为CRP和Sxy蛋白在转录激活中的直接相互作用提供了证据。此外,我们鉴定出Sxy的组成型突变体,其导致CRP-S位点启动子激活水平高于野生型Sxy。抑制突变和组成型突变均位于Sxy的同一区域内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adb7/6728893/0909c6620a5b/fmicb-10-02053-g001.jpg

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