Regulation of gene expression in the nervous system

被引:44
作者
Ooi, Lezanne [1 ]
Wood, Ian C. [1 ]
机构
[1] Univ Leeds, Fac Biol Sci, Inst Membrane & Syst Biol, Leeds LS2 9JT, W Yorkshire, England
关键词
chromatin; gene expression; microRNA; nervous system; synaptic plasticity; transcription;
D O I
10.1042/BJ20080963
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nervous system contains a multitude of cell types which are specified during development by cascades of transcription factors acting combinatorially. Some of these transcription factors are only active during development, whereas others continue to function in the mature nervous system to maintain appropriate gene-expression patterns in differentiated cells. Underpinning the function of the nervous system is its plasticity in response to external stimuli, and many transcription factors are involved in regulating gene expression in response to neuronal activity, allowing Lis to learn, remember and make complex decisions. Here we review some of the recent findings that have uncovered the molecular mechanisms that underpin the control of gene regulatory networks within the nervous system. We highlight some recent insights into the gene-regulatory circuits in the development and differentiation of cells within the nervous system and discuss some of the mechanisms by which synaptic transmission influences transcription-factor activity in the mature nervous system. Mutations in genes that are important in epigenetic regulation (by influencing DNA methylation and post-translational historic modifications) have long been associated with neuronal disorders in humans such as Rett syndrome, Huntington's disease and some forms of mental retardation, and recent work has focused oil unravelling their mechanisms of action. Finally, the discovery of microRNAs has produced a paradigm shift in gene expression, and we provide some examples and discuss the contribution of microRNAs to maintaining dynamic gene regulatory networks in the brain.
引用
收藏
页码:327 / 341
页数:15
相关论文
共 174 条
[71]   The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases [J].
Iwase, Shigeki ;
Lan, Fei ;
Bayliss, Peter ;
de la Torre-Ubieta, Luis ;
Huarte, Maite ;
Qi, Hank H. ;
Whetstine, Johnathan R. ;
Bonni, Azad ;
Roberts, Thomas M. ;
Shi, Yang .
CELL, 2007, 128 (06) :1077-1088
[72]   Transcriptional repression coordinates the temporal switch from motor to serotonergic neurogenesis [J].
Jacob, John ;
Ferri, Anna L. ;
Milton, Christopher ;
Prin, Fabrice ;
Pla, Patrick ;
Lin, Wei ;
Gavalas, Anthony ;
Ang, Siew-Lan ;
Briscoe, James .
NATURE NEUROSCIENCE, 2007, 10 (11) :1433-1439
[73]   Stem cells, the molecular circuitry of pluripotency and nuclear reprogramming [J].
Jaenisch, Rudolf ;
Young, Richard .
CELL, 2008, 132 (04) :567-582
[74]   Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation [J].
Jensen, LR ;
Amende, M ;
Gurok, U ;
Moser, B ;
Gimmel, V ;
Tzschach, A ;
Janecke, AR ;
Tariverdian, G ;
Chelly, J ;
Fryns, JP ;
Van Esch, H ;
Kleefstra, T ;
Hamel, B ;
Moraine, C ;
Gécz, J ;
Turner, G ;
Reinhardt, R ;
Kalscheuer, VM ;
Ropers, HH ;
Lenzner, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 2005, 76 (02) :227-236
[75]   GADD45A does not promote DNA demethylation [J].
Jin, Seung-Gi ;
Guo, Cai ;
Pfeifer, Gerd P. .
PLOS GENETICS, 2008, 4 (03)
[76]   Regulation of chromatin structure by histone H3S10 phosphorylation [J].
Johansen, Kristen M. ;
Johansen, Jorgen .
CHROMOSOME RESEARCH, 2006, 14 (04) :393-404
[77]   Genome-wide mapping of in vivo protein-DNA interactions [J].
Johnson, David S. ;
Mortazavi, Ali ;
Myers, Richard M. ;
Wold, Barbara .
SCIENCE, 2007, 316 (5830) :1497-1502
[78]   A microRNA-based gene dysregulation pathway in Huntington's disease [J].
Johnson, Rory ;
Zuccato, Chiara ;
Belyaev, Nikolai D. ;
Guest, Deborah J. ;
Cattaneo, Elena ;
Buckley, Noel J. .
NEUROBIOLOGY OF DISEASE, 2008, 29 (03) :438-445
[79]   Identification of the REST regulon reveals extensive transposable element-mediated binding site duplication [J].
Johnson, Rory ;
Gamblin, Richard J. ;
Ooi, Lezanne ;
Bruce, Alexander W. ;
Donaldson, Ian J. ;
Westhead, David R. ;
Wood, Ian C. ;
Jackson, Richard M. ;
Buckley, Noel J. .
NUCLEIC ACIDS RESEARCH, 2006, 34 (14) :3862-3877
[80]   Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription [J].
Jones, PL ;
Veenstra, GJC ;
Wade, PA ;
Vermaak, D ;
Kass, SU ;
Landsberger, N ;
Strouboulis, J ;
Wolffe, AP .
NATURE GENETICS, 1998, 19 (02) :187-191