Chromatin crosstalk in development and disease: lessons from REST

被引:304
作者
Ooi, Lezanne [1 ]
Wood, Ian C. [1 ]
机构
[1] Univ Leeds, Inst Membrane & Syst Biol, Fac Biol Sci, Leeds, W Yorkshire, England
关键词
7;
D O I
10.1038/nrg2100
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Protein complexes that contain chromatin-modifying enzymes have an important role in regulating gene expression. Recent studies have shown that a single transcription factor, the repressor element 1-silencing transcription factor (REST), can act as a hub for the recruitment of multiple chromatin-modifying enzymes, uncovering interdependencies among individual enzymes that affect gene regulation. Research into the function of REST and its corepressors has provided novel insight into how chromatin-modifying proteins cooperate, and how alterations in this function cause disease. These mechanisms will be relevant to the combinatorial functioning of modular transcriptional regulators that work together to regulate a common promoter; they should also identify targets for potential therapies for a range of human diseases.
引用
收藏
页码:544 / 554
页数:11
相关论文
共 128 条
[61]   Studies on the interaction of REST4 with the cholinergic repressor element-1/neuron restrictive silencer element [J].
Lee, JH ;
Shimojo, M ;
Chai, YG ;
Hersh, LB .
MOLECULAR BRAIN RESEARCH, 2000, 80 (01) :88-98
[62]   An essential role for CoREST in nucleosomal histone 3 lysine 4 demethylation [J].
Lee, MG ;
Wynder, C ;
Cooch, N ;
Shiekhattar, R .
NATURE, 2005, 437 (7057) :432-435
[63]   One nucleotide in a κB site can determine cofactor specificity for NF-κB dimers [J].
Leung, TH ;
Hoffmann, A ;
Baltimore, D .
CELL, 2004, 118 (04) :453-464
[64]   The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells [J].
Loh, YH ;
Wu, Q ;
Chew, JL ;
Vega, VB ;
Zhang, WW ;
Chen, X ;
Bourque, G ;
George, J ;
Leong, B ;
Liu, J ;
Wong, KY ;
Sung, KW ;
Lee, CWH ;
Zhao, XD ;
Chiu, KP ;
Lipovich, L ;
Kuznetsov, VA ;
Robson, P ;
Stanton, LW ;
Wei, CL ;
Ruan, YJ ;
Lim, B ;
Ng, HH .
NATURE GENETICS, 2006, 38 (04) :431-440
[65]   Cell type-specific regulation of choline acetyltransferase gene expression - Role of the neuron-restrictive silencer element and cholinergic-specific enhancer sequences [J].
Lonnerberg, P ;
Schoenherr, CJ ;
Anderson, DJ ;
Ibanez, CF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (52) :33358-33365
[66]   Corepressor-dependent silencing of chromosomal regions encoding neuronal genes [J].
Lunyak, VV ;
Burgess, R ;
Prefontaine, GG ;
Nelson, C ;
Sze, SH ;
Chenoweth, J ;
Schwartz, P ;
Pevzner, PA ;
Glass, C ;
Mandel, G ;
Rosenfeld, MG .
SCIENCE, 2002, 298 (5599) :1747-1752
[67]   RE-1 silencing transcription factor-4 (REST4) is neither a transcriptional repressor nor a de-repressor [J].
Magin, A ;
Lietz, M ;
Cibelli, G ;
Thiel, G .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (03) :195-202
[68]   REST in good times and bad - Roles in tumor suppressor and oncogenic activities [J].
Majumder, Sadhan .
CELL CYCLE, 2006, 5 (17) :1929-1935
[69]   Expression of the rat m4 muscarinic acetylcholine receptor gene is regulated by the neuron-restrictive silencer element/repressor element 1 [J].
Mieda, M ;
Haga, T ;
Saffen, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (09) :5854-5860
[70]   Covalent modification of DNA regulates memory formation [J].
Miller, Courtney A. ;
Sweatt, J. David .
NEURON, 2007, 53 (06) :857-869