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大肠杆菌RNA聚合酶E sigma 38对重叠启动子的选择性以及支持CRP激活的能力。

Selectivity of the Escherichia coli RNA polymerase E sigma 38 for overlapping promoters and ability to support CRP activation.

作者信息

Kolb A, Kotlarz D, Kusano S, Ishihama A

机构信息

Unité de Physicochimie des Macromolécules Biologiques, URA 1149 du CNRS, Paris, France.

出版信息

Nucleic Acids Res. 1995 Mar 11;23(5):819-26. doi: 10.1093/nar/23.5.819.

Abstract

A series of gal promoter mutants has been used to compare the in vitro selectivities of the two forms of Escherichia coli RNA polymerase, E sigma 38 and E sigma 70. In the absence of the CRP-cAMP complex, E sigma 38 shows a strong preference for the ga/P1 promoter, whereas E sigma 70 preferentially initiates transcription from the ga/P2 promoter. E sigma 38 selectivity is not affected by the nature and position of the upstream sequences or by the phasing between synthetic upstream curved sequences and the -10 regions. In fact, all effects of mutations in the extended -10 region can be accounted for without evoking strong new sequence preferences for E sigma 38. Finally, both E sigma 38 and E sigma 70 initiate transcription from the ga/P1 promoter in the presence of CRP-cAMP complex and support direct cAMP-CRP activation at several CRP-dependent promoters.

摘要

一系列gal启动子突变体已被用于比较两种形式的大肠杆菌RNA聚合酶E sigma 38和E sigma 70的体外选择性。在没有CRP-cAMP复合物的情况下,E sigma 38对ga/P1启动子表现出强烈偏好,而E sigma 70优先从ga/P2启动子起始转录。E sigma 38的选择性不受上游序列的性质和位置或合成上游弯曲序列与-10区域之间相位的影响。事实上,在不引发E sigma 38强烈新序列偏好的情况下,可以解释延伸-10区域突变的所有影响。最后,在存在CRP-cAMP复合物的情况下,E sigma 38和E sigma 70都从ga/P1启动子起始转录,并在几个CRP依赖性启动子处支持直接的cAMP-CRP激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b4/306765/a1aebb0af8f7/nar00005-0106-a.jpg

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