Molecular mechanisms underlying the function diversity of transcriptional factor IclR family

被引:22
作者
Zhou, Yexin [1 ]
Huang, Hairong [2 ]
Zhou, Peifu [1 ]
Xie, Jianping [1 ]
机构
[1] Southwest Univ, Inst Modern Biopharmaceut, State Key Lab Breeding Base Ecoenvironm & Bioreso, Three Gorges Area,Sch Life Sci, Chongqing 400715, Peoples R China
[2] Beijing TB & Thorac Tumor Res Inst, Beijing 101149, Peoples R China
关键词
Mycobacterium tuberculosis; The IclR family; Function; Molecular mechanism; STREPTOMYCES-COELICOLOR A3(2); ESCHERICHIA-COLI; MYCOBACTERIUM-TUBERCULOSIS; AGROBACTERIUM-TUMEFACIENS; PSEUDOMONAS-PUTIDA; GLYOXYLATE SHUNT; ETHR INHIBITORS; GNTR FAMILY; IN-VIVO; REPRESSOR;
D O I
10.1016/j.cellsig.2012.02.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The IclR family transcriptional factor is widespread and involves in diverse bacterial physio-pathological events, such as primary and secondary metabolism, virulence, quorum sensing, sporulation. Unlike other transcriptional factors which function as either activators or repressors. IclR can assume both role simutaneously. Its N-terminal domain possesses a helix-turn-helix DNA binding motif which can dimerize or tetramerize to bind target promoters, while the C-terminal domain is for the effector binding. The function of IclR varies with the effectors bound. Escherichia coli transcription factor IclR is the archetype of this family, which regulates the aceBAK operon responsible for the glyoxylate shunt The sophisticated regulatory mechanisms underlying iclR was largely based on E. coli iclR. Information concerning the pathogen IclR, especially those of Mycobacterium tuberculosis is poor, and is pivotal to our understanding of its biology and development of new effective TB control measures. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1270 / 1275
页数:6
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