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大肠杆菌thrS-infC-rplT操纵子的转录模式。

Transcriptional patterns for the thrS-infC-rplT operon of Escherichia coli.

作者信息

Wertheimer S J, Klotsky R A, Schwartz I

机构信息

Department of Biochemistry, New York Medical College, Valhalla 10595.

出版信息

Gene. 1988 Mar 31;63(2):309-20. doi: 10.1016/0378-1119(88)90534-3.

Abstract

The genes coding for threonyl-tRNA synthetase (thrS), translation initiation factor 3 (infC) and ribosomal protein L20 (rplT) are clustered in the Escherichia coli genome. Previous studies had suggested the possibility that the expression of these genes is coupled. The transcriptional events in this operon have now been examined by S1 nuclease mapping and promoter fusion studies. The results indicate that infC-containing mRNAs are initiated from three separate promoters. Two of these are located in the protein-coding region of thrS and one, P12, is the major promoter at all growth rates tested. In addition, there is co-transcription of thrS and infC from the thrS promoter (PT). A single promoter for thrS has been mapped approx. 170 nucleotides upstream from its translation initiation site. Another promoter has been located within the infC-coding region. It is separated from the next downstream gene, rplT, by a transcription end point. However, termination at this region is only 50-70% efficient and transcripts starting at this promoter can read through into rplT. These findings demonstrate that the pattern of transcription in this operon is highly complex and the mRNA levels for each of the genes is determined by a variety of factors, including multiple promoters, co-transcription and readthrough of transcription termination signals.

摘要

编码苏氨酰 - tRNA合成酶(thrS)、翻译起始因子3(infC)和核糖体蛋白L20(rplT)的基因在大肠杆菌基因组中是成簇排列的。先前的研究表明这些基因的表达可能是偶联的。现在已经通过S1核酸酶图谱分析和启动子融合研究对该操纵子中的转录事件进行了检测。结果表明,含infC的mRNA由三个不同的启动子起始转录。其中两个位于thrS的蛋白质编码区内,另一个P12在所有测试的生长速率下都是主要启动子。此外,thrS和infC从thrS启动子(PT)共同转录。已确定thrS的一个单一启动子位于其翻译起始位点上游约170个核苷酸处。另一个启动子位于infC编码区内。它与下游的下一个基因rplT之间有一个转录终点。然而,该区域的终止效率仅为50 - 70%,从这个启动子起始的转录本可以通读进入rplT。这些发现表明该操纵子中的转录模式非常复杂,每个基因的mRNA水平由多种因素决定,包括多个启动子、共同转录以及转录终止信号的通读。

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