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大肠杆菌的uvrB基因既有受lexA抑制的启动子,也有不依赖lexA的启动子。

The uvrB gene of Escherichia coli has both lexA-repressed and lexA-independent promoters.

作者信息

Sancar G B, Sancar A, Little J W, Rupp W D

出版信息

Cell. 1982 Mar;28(3):523-30. doi: 10.1016/0092-8674(82)90207-0.

Abstract

We have found that the uvrB gene of Escherichia coli is transcribed from at least two promoters, which we call P1 and P2. Transcription from P1 begins with an ATP at +1, and transcription from P2 begins primarily with a GTP at -31. A binding site for the lexA protein (LEXA), located between the -35 sequence and Pribnow box of P2, regulates transcription from this promoter. In vitro, LEXA inhibits transcription from P2 but has no detectable effect on transcription from P1. A third promoter, P3, was also detected at -341; transcription from P3 is toward uvrB but terminates in vitro in the region of the LEXA binding site. The binding of LEXA to P2 inhibits transcription from the P3 promoter even though several hundred nucleotides separate the two promoters. The data suggest that a transcribing RNA polymerase stalls when it reaches the repressor-operator complex but remains bound to the DNA, causing a jamming of RNA polymerases between P3 and the repressor-operator complex at P2. The physiological significance of P3 is unknown.

摘要

我们发现大肠杆菌的uvrB基因至少从两个启动子转录,我们将其称为P1和P2。从P1开始的转录在+1处起始于一个ATP,而从P2开始的转录主要在-31处起始于一个GTP。位于P2的-35序列和Pribnow框之间的lexA蛋白(LEXA)的结合位点调节该启动子的转录。在体外,LEXA抑制从P2的转录,但对从P1的转录没有可检测到的影响。在-341处还检测到第三个启动子P3;从P3开始的转录朝向uvrB,但在体外在LEXA结合位点区域终止。尽管两个启动子相隔数百个核苷酸,但LEXA与P2的结合抑制了P3启动子的转录。数据表明,正在转录的RNA聚合酶在到达阻遏物-操纵子复合物时会停滞,但仍与DNA结合,导致P3和P2处的阻遏物-操纵子复合物之间的RNA聚合酶发生阻塞。P3的生理意义尚不清楚。

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