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同源RNA聚合酶与大肠杆菌DNA的结合:稳定结合位点分布的研究

Homologous RNA polymerase binding to Escherichia coli DNA: a study of the distribution of stable binding sites.

作者信息

Pedone F, Ballario P, Di Mauro E

出版信息

Eur J Biochem. 1978 Jul 3;87(3):445-51. doi: 10.1111/j.1432-1033.1978.tb12394.x.

Abstract

The number and the distribution of the sites of Escherichia coli DNA that form stable complexes with the homologous RNA polymerase (class A sites according to Hinkle and Chamberlin [3]) have been investigated. Almost all the DNA can bind RNA polymerase, even when fragmented at short (undergenic) size; this general non-promoter-specific binding is highly labile and is not temperature-dependent. The range of RNA polymerase/DNA ratios that give rise to the stable temperature-dependent complexes was examined. The amount and the distribution of class A complexes were studied analysing the dissociation of complexes formed by RNA polymerase on DNA fragments of various length. The E. coli genome appears to form 3.8 X 10(3) stable complexes; the majority of these complexes shows a short-range distribution (800-1200 base pairs). The rest is more widely spaced (1200-6000 base pairs).

摘要

已对与同源RNA聚合酶形成稳定复合物的大肠杆菌DNA位点的数量和分布进行了研究(根据欣克尔和钱伯林[3]的分类为A类位点)。几乎所有的DNA都能结合RNA聚合酶,即使在短片段(低于基因长度)时也是如此;这种一般的非启动子特异性结合非常不稳定,且不依赖于温度。研究了产生稳定的温度依赖性复合物的RNA聚合酶/DNA比率范围。通过分析RNA聚合酶与各种长度DNA片段形成的复合物的解离,研究了A类复合物的数量和分布。大肠杆菌基因组似乎形成了3.8×10³个稳定复合物;这些复合物中的大多数呈短程分布(800 - 1200个碱基对)。其余的分布则更为分散(1200 - 6000个碱基对)。

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