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三种转录因子对vvpS表达的稳定期诱导:LeuO的抑制作用以及SmcR和CRP的激活作用。

Stationary-phase induction of vvpS expression by three transcription factors: repression by LeuO and activation by SmcR and CRP.

作者信息

Kim Jeong-A, Park Jin Hwan, Lee Mi-Ae, Lee Hyun-Jung, Park Soon-Jung, Kim Kun-Soo, Choi Sang-Ho, Lee Kyu-Ho

机构信息

Department of Life Science, Sogang University, Seoul, 121-742, South Korea.

National Research Laboratory of Molecular Microbiology and Toxicology, Department of Agricultural Biotechnology, Seoul National University, Seoul, 151-921, South Korea.

出版信息

Mol Microbiol. 2015 Jul;97(2):330-46. doi: 10.1111/mmi.13028. Epub 2015 May 9.

DOI:10.1111/mmi.13028
PMID:25869813
Abstract

An exoprotease of Vibrio vulnificus, VvpS, exhibits an autolytic function during the stationary phase. To understand how vvpS expression is controlled, the regulators involved in vvpS transcription and their regulatory mechanisms were investigated. LeuO was isolated in a ligand-fishing experiment, and experiments using a leuO-deletion mutant revealed that LeuO represses vvpS transcription. LeuO bound the extended region including LeuO-binding site (LBS)-I and LBS-II. Further screening of additional regulators revealed that SmcR and cyclic adenosine monophosphate-receptor protein (CRP) play activating roles in vvpS transcription. SmcR and CRP bound the regions overlapping LBS-I and -II, respectively. In addition, the LeuO occupancy of LBS-I and LBS-II was competitively exchanged by SmcR and CRP, respectively. To examine the mechanism of stationary-phase induction of vvpS expression, in vivo levels of three transcription factors were monitored. Cellular level of LeuO was maximal at exponential phase, while those of SmcR and CRP were maximal at stationary phase and relatively constant after the early-exponential phase, respectively. Thus, vvpS transcription was not induced during the exponential phase by high cellular content of LeuO. When entering the stationary phase, however, LeuO content was significantly reduced and repression by LeuO was relieved through simultaneous binding of SmcR and CRP to LBS-I and -II, respectively.

摘要

创伤弧菌的一种外蛋白酶VvpS在稳定期表现出自溶功能。为了解vvpS表达是如何被调控的,对参与vvpS转录的调控因子及其调控机制进行了研究。在配体垂钓实验中分离出了LeuO,使用leuO缺失突变体的实验表明LeuO抑制vvpS转录。LeuO结合包括LeuO结合位点(LBS)-I和LBS-II的延伸区域。对其他调控因子的进一步筛选表明,SmcR和环磷酸腺苷受体蛋白(CRP)在vvpS转录中起激活作用。SmcR和CRP分别结合与LBS-I和-II重叠的区域。此外,LBS-I和LBS-II上的LeuO占据分别被SmcR和CRP竞争性置换。为了研究vvpS表达在稳定期诱导的机制,监测了三种转录因子的体内水平。LeuO的细胞水平在指数期最高,而SmcR和CRP的细胞水平分别在稳定期最高且在指数早期后相对恒定。因此,在指数期,高细胞含量的LeuO不会诱导vvpS转录。然而,当进入稳定期时,LeuO含量显著降低,通过SmcR和CRP分别同时结合到LBS-I和-II上,LeuO的抑制作用得以解除。

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