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[DNA的稳定性和局部协同性分析:关于大肠杆菌RNA聚合酶启动噬菌体T7基因A3转录的分子机制的提议]

[Analysis of the stability and local cooperativity of DNA: proposal of a molecular mechanism for the initiation of the transcription of gene A3 of bacteriophage T7 by the RNA polymerase from E. coli].

作者信息

Ehrlich R, Marín M, Gabarró-Arpa J, Rodier F, Schmitt B, Reiss C

出版信息

C R Seances Acad Sci III. 1981 Jan 12;292(2):177-80.

PMID:6783340
Abstract

RNA polymerase (RNAP) complexed to the A3 promoter of bacteriophage T7 is known to unwind a DNA segment located downstream of the Pribnow box. This finding can be accounted for if it is assumed that the subunit sigma of RNAP unstabilizes three GC base pairs located just upstream of the transcription start. As a consequence, the rate of promoter utilisation might be related to the relative stability of the DNA between the "Pribnow box" and the transcription start.

摘要

已知与噬菌体T7的A3启动子复合的RNA聚合酶(RNAP)会解开位于普里布诺框下游的一段DNA。如果假设RNAP的σ亚基使位于转录起始点上游的三个GC碱基对不稳定,那么这一发现就可以得到解释。因此,启动子的利用速率可能与“普里布诺框”和转录起始点之间DNA的相对稳定性有关。

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