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编码翻译起始因子IF1的infA操纵子的结构与表达。生长速率对转录的调控。

Structure and expression of the infA operon encoding translational initiation factor IF1. Transcriptional control by growth rate.

作者信息

Cummings H S, Sands J F, Foreman P C, Fraser J, Hershey J W

机构信息

Department of Biological Chemistry, School of Medicine, University of California, Davis 95616.

出版信息

J Biol Chem. 1991 Sep 5;266(25):16491-8.

PMID:1909328
Abstract

The cellular levels of the three translational initiation factors, IF1, IF2, and IF3, increase as a function of growth rate in parallel with those of ribosomes. Therefore both ribosomal and initiation factor gene expression is under metabolic control. To address how expression of the Escherichia coli gene for IF1, infA, is regulated, a 3-kilobase region of the genome surrounding infA was sequenced. The 5' and 3' termini of in vivo infA transcripts were defined by S1 nuclease mapping, and mRNA size was measured by Northern blot hybridization. The infA gene is transcribed by two promoters, P1 and P2, which generate transcripts of 525 and 330 nucleotides, apparently ending at the same rho-independent terminator. Analyses of operon and protein fusions to lacZ demonstrate that neither infA transcription nor translation is affected by high cellular levels of IF1. However, P2, but not P1, increases in activity as a function of the growth rate of the cell and is the dominant promoter in rich medium. Therefore, metabolic control of infA expression occurs exclusively at the level of transcription by the P2 promoter.

摘要

三种翻译起始因子IF1、IF2和IF3的细胞水平随着生长速率的变化而增加,与核糖体的细胞水平变化平行。因此,核糖体和起始因子基因的表达都受到代谢调控。为了研究大肠杆菌IF1基因(infA)的表达是如何调控的,对infA周围3千碱基的基因组区域进行了测序。通过S1核酸酶作图确定了体内infA转录本的5'和3'末端,并通过Northern印迹杂交测量了mRNA的大小。infA基因由两个启动子P1和P2转录,产生525和330个核苷酸的转录本,显然终止于同一个不依赖于ρ因子的终止子。对与lacZ的操纵子和蛋白质融合体的分析表明,IF1的高细胞水平既不影响infA的转录也不影响其翻译。然而,P2而不是P1的活性随着细胞生长速率的变化而增加,并且是丰富培养基中的主要启动子。因此,infA表达的代谢调控仅发生在P2启动子的转录水平。

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