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大肠杆菌uvrC基因单元的多个控制元件。

Multiple control elements for the uvrC gene unit of Escherichia coli.

作者信息

Sharma S, Stark T F, Beattie W G, Moses R E

出版信息

Nucleic Acids Res. 1986 Mar 11;14(5):2301-18. doi: 10.1093/nar/14.5.2301.

Abstract

We have sequenced the control region of the uvrC protein including two open reading frames (ORF) encoding polypeptides of 28 kd and 23 kd molecular weight. The uvrC gene is preceded by five promoters. The P1, P2a and P2b promoter sequences are 5' to the 28 kd and the 23 kd proteins respectively. The P3 and P4 promoters are located within the structural gene for the 23 kd protein. The P3 promoter is required for adequate in vivo expression. There are three putative lexA protein binding sites, detected at the 3' end of the 28 kd protein (lexA1), within the coding sequences for the 23 kd protein (lexA2) and within the P3 promoter (lexA3). Promoter P2 is responsible for transcription of the uvrC gene, producing transcripts of 2.8 and 1.6 kb. The upstream region including the 28 kd protein is required for enhanced expression under non-induced conditions. These results show that the uvrC gene is controlled by multiple promoters and is transcribed as part of a multigene unit.

摘要

我们已对uvrC蛋白的调控区进行了测序,该调控区包括两个开放阅读框(ORF),分别编码分子量为28kd和23kd的多肽。uvrC基因之前有五个启动子。P1、P2a和P2b启动子序列分别位于28kd和23kd蛋白编码序列的5'端。P3和P4启动子位于23kd蛋白的结构基因内。P3启动子是体内充分表达所必需的。在28kd蛋白的3'端(lexA1)、23kd蛋白的编码序列内(lexA2)以及P3启动子内(lexA3)检测到三个假定的lexA蛋白结合位点。启动子P2负责uvrC基因的转录,产生2.8kb和1.6kb的转录本。包括28kd蛋白在内的上游区域是在非诱导条件下增强表达所必需的。这些结果表明,uvrC基因受多个启动子调控,并作为多基因单位的一部分进行转录。

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