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创伤弧菌putAP操纵子通过环磷酸腺苷受体蛋白(cAMP受体蛋白)和PutR协同结合重叠位点实现共激活。

Coactivation of Vibrio vulnificus putAP operon by cAMP receptor protein and PutR through cooperative binding to overlapping sites.

作者信息

Lee Jeong Hyun, Choi Sang Ho

机构信息

Department of Food Science and Technology, School of Agricultural Biotechnology, and Center for Agricultural Biomaterials, Seoul National University, Seoul 151-742, South Korea.

出版信息

Mol Microbiol. 2006 Apr;60(2):513-24. doi: 10.1111/j.1365-2958.2006.05115.x.

Abstract

The cAMP receptor protein (CRP) positively regulates the expression of Vibrio vulnificus putAP genes encoding a proline dehydrogenase and a proline permease. In the present study, an open reading frame encoding PutR was identified downstream of the putAP genes and a mutational analysis revealed that the PutR protein was also involved in regulating the putAP transcription by activating Pput promoter. Although CRP acts as a primary activator and the influence of PutR on Pput is mediated by CRP, the level of Pput activity observed when PutR and CRP functioned together was greater than the sum of Pput activities achieved by each activator alone. Western blot analyses demonstrated that the cellular levels of PutR and CRP were not significantly affected by each other, indicating that PutR and CRP coactivate Pput rather than function sequentially in a regulatory cascade. Two adjacent binding sites for PutR mapped by in vitro DNase I protection assays were found to overlap the CRP binding sites and were centred -91.5 (PCBI) and -133.5 bp (PCBII) upstream of the transcription start site of Pput respectively. PutR and CRP bind to the sites cooperatively and a dissection of the role of the binding sites revealed that CRP at PCBI plays the most crucial role in the activation of Pput. Accordingly, the present results revealed that PutR and CRP coactivate the expression of Pput and exert their effect by cooperatively binding to the promoter.

摘要

环磷酸腺苷受体蛋白(CRP)正向调控创伤弧菌putAP基因的表达,该基因编码脯氨酸脱氢酶和脯氨酸通透酶。在本研究中,在putAP基因下游鉴定出一个编码PutR的开放阅读框,突变分析表明PutR蛋白也通过激活Pput启动子参与调控putAP转录。尽管CRP作为主要激活剂,PutR对Pput的影响是由CRP介导的,但当PutR和CRP共同发挥作用时观察到的Pput活性水平高于单独由每种激活剂所达到的Pput活性之和。蛋白质免疫印迹分析表明,PutR和CRP的细胞水平彼此之间没有显著影响,这表明PutR和CRP共同激活Pput,而不是在调控级联反应中依次发挥作用。通过体外DNase I保护试验定位的两个相邻的PutR结合位点与CRP结合位点重叠,分别位于Pput转录起始位点上游-91.5(PCBI)和-133.5 bp(PCBII)处。PutR和CRP协同结合到这些位点,对结合位点作用的剖析表明,PCBI处的CRP在Pput激活中起最关键作用。因此,本研究结果表明,PutR和CRP共同激活Pput的表达,并通过协同结合到启动子发挥作用。

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