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天蓝色链霉菌A3(2)中groEL基因的转录分析

Transcriptional analysis of groEL genes in Streptomyces coelicolor A3(2).

作者信息

Duchêne A M, Thompson C J, Mazodier P

机构信息

Unité de Biochimie Microbienne, Institut Pasteur, Paris, France.

出版信息

Mol Gen Genet. 1994 Oct 17;245(1):61-8. doi: 10.1007/BF00279751.

Abstract

In Streptomyces coelicolor A3(2), synthesis of the groES, groES-groEL1 and groEL2 transcripts is induced either by heat shock or by undefined physiological stress signals present at a certain stage of growth. Under all conditions tested, transcription of groES and groES-groEL1 originated from a unique start site upstream of groES, whereas transcription of groEL2 originated from a unique site upstream of groEL2. RNA polymerase isolated either from heat-shocked or control mycelia allowed in vitro transcription from the P1 promoter of groES/EL1 and the P2 promoter of groEL2. The fact that these two RNA polymerase preparations both initiated transcription with equal efficiency from the same sites suggested that a heat shock-specific sigma factor is not responsible for the temperature-induced transcription of groE genes. Instead, regulation of these genes from vegetative-type promoters may be effected by a DNA-binding protein observed in gel retardation assays, which recognizes a motif found in the groE and dnaK promoter regions of many prokaryotic genes.

摘要

在天蓝色链霉菌A3(2)中,groES、groES-groEL1和groEL2转录本的合成可由热休克或生长特定阶段存在的未明确的生理应激信号诱导。在所有测试条件下,groES和groES-groEL1的转录起始于groES上游的一个独特起始位点,而groEL2的转录起始于groEL2上游的一个独特位点。从热休克或对照菌丝体中分离的RNA聚合酶可在体外从groES/EL1的P1启动子和groEL2的P2启动子进行转录。这两种RNA聚合酶制剂都能从相同位点以相同效率起始转录,这一事实表明热休克特异性σ因子并不负责groE基因的温度诱导转录。相反,这些基因从营养型启动子的调控可能受凝胶阻滞试验中观察到的一种DNA结合蛋白影响,该蛋白识别许多原核基因的groE和dnaK启动子区域中发现的一个基序。

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