Suppr超能文献

多个顺式作用位点正向调控大肠杆菌nrd基因的表达。

Multiple cis-acting sites positively regulate Escherichia coli nrd expression.

作者信息

Jacobson B A, Fuchs J A

机构信息

Department of Biochemistry, University of Minnesota, St. Paul 55108, USA.

出版信息

Mol Microbiol. 1998 Jun;28(6):1315-22. doi: 10.1046/j.1365-2958.1998.00897.x.

Abstract

Regulation of nrd expression in Escherichia coli by cis-acting elements was found to be more complex than previously reported. At least five upstream sites appear to positively regulate nrd expression including a Fis binding site, a DnaA binding site, an AT-rich region, an inverted repeat and a 10 bp site between the AT-rich region and the inverted repeat. Double mutants defective in these sites indicate that all sites tested act independently when regulating nrd expression. As the decrease in nrd expression in exponentially growing cultures paralleled the decrease observed in DNA synthesis-inhibited cultures for all single and double mutants, we concluded that nrd is regulated by the same mechanism in these physiological states. As mutants unable to induce nrd expression during inhibition of DNA synthesis also fail to exhibit cell cycle-regulated nrd expression, we conclude that cell cycle nrd regulation is controlled by these same sites. Site-directed mutagenesis was used to show that the absence of an increase in nrd expression during DNA inhibition previously observed for deletion of the AT-rich region results from deletion of both the Fis binding site and the AT-rich region.

摘要

人们发现,大肠杆菌中顺式作用元件对nrd表达的调控比之前报道的更为复杂。至少有五个上游位点似乎对nrd表达起正向调控作用,包括一个Fis结合位点、一个DnaA结合位点、一个富含AT的区域、一个反向重复序列以及富含AT区域与反向重复序列之间的一个10bp位点。这些位点存在缺陷的双突变体表明,在调控nrd表达时,所有测试位点都是独立起作用的。由于在指数生长培养物中nrd表达的降低与所有单突变体和双突变体在DNA合成受抑制培养物中观察到的降低情况相似,我们得出结论,在这些生理状态下,nrd受相同机制的调控。由于在DNA合成受抑制期间无法诱导nrd表达的突变体也未能表现出细胞周期调控的nrd表达,我们得出结论,细胞周期nrd调控受这些相同位点的控制。定点诱变用于表明,先前观察到的因富含AT区域缺失而导致DNA抑制期间nrd表达未增加,是由于Fis结合位点和富含AT区域均缺失所致。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验