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FNR在体外激活并抑制转录。

FNR activates and represses transcription in vitro.

作者信息

Sharrocks A D, Green J, Guest J R

机构信息

Krebs Institute for Biomolecular Research, Department of Molecular Biology and Biotechnology, University of Sheffield, U.K.

出版信息

Proc Biol Sci. 1991 Sep 23;245(1314):219-26. doi: 10.1098/rspb.1991.0113.

Abstract

FNR is an iron-binding transcriptional regulator for anaerobic gene expression in Escherichia coli. Footprinting studies with the purified protein have confirmed that it is a site-specific DNA-binding protein. Transcription tests with the positively-regulated FFmelR promoter and the negatively-regulated ndh promoter likewise demonstrated that FNR can activate or repress transcription in vitro. Reducing conditions were not required but activity was abolished by substituting an essential cysteine residue with alanine (C122A) and the affinity for DNA was reduced by iron-depletion. The start point(s) for transcription of the FNR-repressed NADH dehydrogenase II gene (ndh) were identified by transcript mapping and the corresponding promoter (-35 and -10 sequences) was located immediately downstream of the FNR-binding site.

摘要

FNR是大肠杆菌中负责厌氧基因表达的一种铁结合转录调节因子。对纯化蛋白进行的足迹分析研究证实,它是一种位点特异性DNA结合蛋白。对正向调控的FFmelR启动子和负向调控的ndh启动子进行的转录测试同样表明,FNR在体外可激活或抑制转录。不需要还原条件,但用丙氨酸替代一个必需的半胱氨酸残基(C122A)会使活性丧失,并且铁缺乏会降低对DNA的亲和力。通过转录图谱确定了FNR抑制的NADH脱氢酶II基因(ndh)的转录起始点,相应的启动子(-35和-10序列)位于FNR结合位点的紧邻下游。

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