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对在严谨反应中发生改变的大肠杆菌RNA聚合酶突变体进行的体内研究。

Studies in vivo on Escherichia coli RNA polymerase mutants altered in the stringent response.

作者信息

Baracchini E, Glass R, Bremer H

机构信息

Biology Programs, University of Texas at Dallas, Richardson 75083-0688.

出版信息

Mol Gen Genet. 1988 Aug;213(2-3):379-87. doi: 10.1007/BF00339606.

Abstract

Previous studies on two Escherichia coli rpoB mutants, carrying single amino acid substitutions at approximate amino acid positions 736 and 906 in the beta subunit, showed that these alterations in the RNA polymerase resulted in an apparent reduced response to valine-induced amino acid starvation in vivo and prevented ppGpp-mediated inhibition of transcriptional initiation at stable RNA promoters in vitro. These observations suggested that the mutations had altered either the ppGpp binding site or the promoter selectivity of the enzyme. The in vivo analysis presented here indicates that these mutants encode an RNA polymerase that responds normally to changes in the level of ppGpp; their apparent relaxedness is due to a reduced accumulation of ppGpp during isoleucine starvation. Thus, there is no indication that the mutations have altered ppGpp binding sites. These observations and the difference between in vitro and in vivo results can be explained by the assumption that the mutations produce an extended ppGpp-dependent pausing of RNA polymerase during the transcription of unstable RNA. Comparison of the vivo and in vitro effects of ppGpp on rrn transcription further suggests that these reflect different phenomena, although in both cases ppGpp inhibits rrn transcription.

摘要

先前对两种大肠杆菌rpoB突变体的研究表明,它们在β亚基中大约氨基酸位置736和906处携带单个氨基酸替换,这些RNA聚合酶的改变导致体内对缬氨酸诱导的氨基酸饥饿的反应明显降低,并在体外阻止了ppGpp介导的对稳定RNA启动子转录起始的抑制。这些观察结果表明,这些突变改变了ppGpp结合位点或酶的启动子选择性。此处进行的体内分析表明,这些突变体编码的RNA聚合酶对ppGpp水平的变化反应正常;它们明显的松弛是由于在异亮氨酸饥饿期间ppGpp的积累减少。因此,没有迹象表明这些突变改变了ppGpp结合位点。这些观察结果以及体外和体内结果之间的差异可以通过以下假设来解释,即这些突变在不稳定RNA转录过程中产生了RNA聚合酶的ppGpp依赖性延长暂停。ppGpp对rrn转录的体内和体外作用的比较进一步表明,尽管在两种情况下ppGpp都抑制rrn转录,但它们反映了不同的现象。

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