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
相关论文
共 45 条
[1]   Leucine auxotrophy restricts growth of Mycobacterium bovis BCG in macrophages [J].
Bange, FC ;
Brown, AM ;
Jacobs, WR .
INFECTION AND IMMUNITY, 1996, 64 (05) :1794-1799
[2]   The Ic1R-type transcriptional repressor LtbR regulates the expression of leucine and tryptophan biosynthesis genes in the amino acid producer Corynebacterium glutamicum [J].
Brune, Iris ;
Jochmann, Nina ;
Brinkrolf, Karina ;
Hueser, Andrea T. ;
Gerstmeir, Robert ;
Eikmanns, Bernhard J. ;
Kalinowski, Joern ;
Puehler, Alfred ;
Tauch, Andreas .
JOURNAL OF BACTERIOLOGY, 2007, 189 (07) :2720-2733
[3]   Reconstitution of the biochemical activities of the AttJ repressor and the AttK, AttL, and AttM catabolic enzymes of Agrobacterium tumefaciens [J].
Chai, Yunrong ;
Tsai, Ching Sung ;
Cho, Hongbaek ;
Winans, Stephen C. .
JOURNAL OF BACTERIOLOGY, 2007, 189 (09) :3674-3679
[4]   Signalling early developmental events in two highly diverged Streptomyces species [J].
Chater, KF ;
Horinouchi, S .
MOLECULAR MICROBIOLOGY, 2003, 48 (01) :9-15
[5]   REGULATION OF TRANSCRIPTION OF GENES REQUIRED FOR FATTY-ACID TRANSPORT AND UNSATURATED FATTY-ACID BIOSYNTHESIS IN ESCHERICHIA-COLI BY FADR [J].
DIRUSSO, CC ;
METZGER, AK ;
HEIMERT, TL .
MOLECULAR MICROBIOLOGY, 1993, 7 (02) :311-322
[6]  
DIRUSSO CC, 1992, J BIOL CHEM, V267, P8685
[7]   Preparation and properties of pure, full-length IclR protein of Escherichia coli. Use of time-of-flight mass spectrometry to investigate the problems encountered [J].
Donald, LJ ;
Chernushevich, IV ;
Zhou, J ;
Verentchikov, A ;
PoppeSchriemer, N ;
Hosfield, DJ ;
Westmore, JB ;
Ens, W ;
Duckworth, HW ;
Standing, KG .
PROTEIN SCIENCE, 1996, 5 (08) :1613-1624
[8]   Mass spectrometric study of the Escherichia coli repressor proteins, Iclr and GclR, and their complexes with DNA [J].
Donald, LJ ;
Hosfield, DJ ;
Cuvelier, SL ;
Ens, W ;
Standing, KG ;
Duckworth, HW .
PROTEIN SCIENCE, 2001, 10 (07) :1370-1380
[9]   Intramolecular signal transmission in a tetrameric repressor of the IclR family [J].
Fillet, Sandy ;
Krell, Tino ;
Morel, Bertrand ;
Lu, Duo ;
Zhang, Xiaodong ;
Ramos, Juan L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (37) :15372-15377
[10]   Ethionamide Boosters: Synthesis, Biological Activity, and Structure-Activity Relationships of a Series of 1,2,4-Oxadiazole EthR Inhibitors [J].
Flipo, Marion ;
Desroses, Matthieu ;
Lecat-Guillet, Nathalie ;
Dirie, Bertrand ;
Carette, Xavier ;
Leroux, Florence ;
Piveteau, Catherine ;
Demirkaya, Fatma ;
Lens, Zoe ;
Rucktooa, Prakash ;
Villeret, Vincent ;
Christophe, Thierry ;
Jeon, Hee Kyoung ;
Locht, Camille ;
Brodin, Priscille ;
Deprez, Benoit ;
Baulard, Alain R. ;
Willand, Nicolas .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (08) :2994-3010