Green J, Guest J R
Krebs Institute for Biomolecular Research, Department of Molecular Biology & Biotechnology, University of Sheffield, Western Bank, UK.
FEBS Lett. 1993 Aug 23;329(1-2):55-8. doi: 10.1016/0014-5793(93)80192-w.
FNR is a transcriptional regulator which controls the expression of target genes in response to anoxia in Escherichia coli. The mechanism by which FNR senses and responds to anaerobiosis is unknown but indirect evidence suggests that an iron cofactor is involved. Using KMnO4 as a probe for DNA melting at active promoters, footprinting studies have now shown that the ferrous iron chelator, ferrozine, inhibits open complex formation in vivo, and that FNR with a high iron-content is essential for open complex formation in vitro. Since open complex formation is an essential pre-requisite for transcription, it is concluded that transcriptional activation by FNR is mediated by a ferrous iron cofactor.
FNR是一种转录调节因子,可控制大肠杆菌中靶基因对缺氧的响应表达。FNR感知和响应厌氧的机制尚不清楚,但间接证据表明涉及铁辅因子。使用高锰酸钾作为活性启动子处DNA解链的探针,足迹研究现已表明,亚铁螯合剂二氮杂菲在体内抑制开放复合物的形成,而高铁含量的FNR对于体外开放复合物的形成至关重要。由于开放复合物的形成是转录的必要先决条件,因此得出结论,FNR的转录激活是由亚铁辅因子介导的。