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大肠杆菌uvrD基因的转录受lexA阻遏物和衰减作用的控制。

Transcription of the uvrD gene of Escherichia coli is controlled by the lexA repressor and by attenuation.

作者信息

Easton A M, Kushner S R

出版信息

Nucleic Acids Res. 1983 Dec 20;11(24):8625-40. doi: 10.1093/nar/11.24.8625.

Abstract

The nucleotide sequence of the control region and the presumptive N-terminal portion of the uvrD gene of Escherichia coli K-12 has been determined. The 1190 base pairs of DNA examined include the likely coding sequence for the first 258 amino acids of the uvrD protein. The transcription promoter for the uvrD gene was identified upstream of the protein coding region. Synthesis of messenger RNA in vitro from this promoter was inhibited by purified lexA protein. The lexA protein was found to bind downstream from the promoter at a sequence, CTGTATATATACCCAG, which is homologous to other known lexA protein binding sites. In the absence of the lexA protein, approximately half of the messages initiated in vitro at the uvrD promoter terminate after about 60 nucleotides at a sequence which resembles a rho-independent terminator. These results indicate that the uvrD gene is induced during the SOS response, and that the expression of the gene may also be regulated by transcription attenuation.

摘要

已测定大肠杆菌K-12的uvrD基因控制区及推测的N端部分的核苷酸序列。所检测的1190个碱基对的DNA包括uvrD蛋白前258个氨基酸的可能编码序列。uvrD基因的转录启动子在蛋白质编码区上游被鉴定出来。从该启动子体外合成信使RNA受到纯化的lexA蛋白的抑制。发现lexA蛋白在启动子下游的CTGTATATATACCCAG序列处结合,该序列与其他已知的lexA蛋白结合位点同源。在没有lexA蛋白的情况下,大约一半在uvrD启动子处体外起始的信使RNA在大约60个核苷酸后于一个类似不依赖ρ因子终止子的序列处终止。这些结果表明uvrD基因在SOS应答期间被诱导,并且该基因的表达也可能受转录衰减调控。

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