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新月柄杆菌中鞭毛基因转录调控所需的顺式和反式作用元件。

Cis- and trans-acting elements required for regulation of flagellar gene transcription in the bacterium Caulobacter crescentus.

作者信息

Mullin D A, Mullin A H

机构信息

Department of Cell and Molecular Biology, Tulane University, New Orleans, LA 70118-5698.

出版信息

Cell Mol Biol Res. 1993;39(4):361-9.

PMID:8312972
Abstract

The flagellar genes of the bacterium Caulobacter crescentus are organized into a regulatory hierarchy that consists of four classes or levels of genes, and expression of these genes is restricted to a discrete interval in the cell cycle that begins just prior to flagellum assembly. This paper summarizes data on the promoters and other cis-acting elements that are required for transcription of the level II gene fliF and the level III genes flaN and flbG. Regulated expression of flaN and flbG requires sigma 54 promoters, enhancer-like sequences called ftr, and sequences called ihf that conform to the consensus binding sequence for Escherichia coli integration host factor protein. The fliF regulatory region contains a new type of promoter sequence that is different from other known promoter motifs, and it has a sequence called ftr4 that is a site of negative regulation. ftr4 appears to function as part of a developmental switch that turns fliF transcription off at the correct time in the cell cycle. flbD, the last gene in the fliF operon is a negative regulator of fliF and an activator of both flaN and flbG expression. Evidence that FlbD protein plays a direct role as a transcriptional regulator comes from the finding that it has a DNA binding activity within its carboxy terminus that specifically recognizes ftr4 in fliF and four ftr elements in the flaN-flbG promoter region.

摘要

新月柄杆菌的鞭毛基因被组织成一个调控层级结构,该结构由四类或四个水平的基因组成,并且这些基因的表达被限制在细胞周期中的一个离散区间,这个区间刚好在鞭毛组装之前开始。本文总结了关于II级基因fliF以及III级基因flaN和flbG转录所需的启动子和其他顺式作用元件的数据。flaN和flbG的调控表达需要σ54启动子、称为ftr的增强子样序列以及与大肠杆菌整合宿主因子蛋白的共有结合序列相符的称为ihf的序列。fliF调控区域包含一种新型启动子序列,它不同于其他已知的启动子基序,并且它有一个称为ftr4的序列,该序列是负调控位点。ftr4似乎作为发育开关的一部分发挥作用,在细胞周期的正确时间关闭fliF转录。flbD是fliF操纵子中的最后一个基因,是fliF的负调控因子以及flaN和flbG表达的激活因子。FlbD蛋白作为转录调控因子发挥直接作用的证据来自于以下发现:它在其羧基末端具有DNA结合活性,可特异性识别fliF中的ftr4以及flaN - flbG启动子区域中的四个ftr元件。

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