Methyl-CpG binding proteins in the nervous system

被引:71
作者
Fan, GP
Hutnick, L
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Interdept Program Neurosci, Los Angeles, CA 90095 USA
关键词
MeCP2; MBD proteins; DNA methylation; neuronal differentiation; chromatin remodeling; gene silencing; histone modification;
D O I
10.1038/sj.cr.7290294
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Classical methyl-CpG binding proteins contain the conserved DNA binding motif methyl-cytosine binding domain (MBD), which preferentially binds to methylated CpG dinucleotides. These proteins serve as transcriptional repressors, mediating gene silencing via DNA cytosine methylation. Mutations in methyl-CpG binding protein 2 (MeCP2) have been linked to the human mental retardation disorder Rett syndrome, suggesting an important role for methyl-CpG binding proteins in brain development and function. This mini-review summarizes the recent advances in studying the diverse functions of MeCP2 as a prototype for other methyl-CpG binding proteins in the development and function of the vertebrate nervous system.
引用
收藏
页码:255 / 261
页数:7
相关论文
共 67 条
  • [1] Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    Amir, RE
    Van den Veyver, IB
    Wan, M
    Tran, CQ
    Francke, U
    Zoghbi, HY
    [J]. NATURE GENETICS, 1999, 23 (02) : 185 - 188
  • [2] A mammalian protein with specific demethylase activity for mCpG DNA
    Bhattacharya, SK
    Ramchandani, S
    Cervoni, N
    Szyf, M
    [J]. NATURE, 1999, 397 (6720) : 579 - 583
  • [3] Chromosomal regulation by MeCP2: structural and enzymatic considerations
    Bowen, NJ
    Palmer, MB
    Wade, PA
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (17) : 2163 - 2167
  • [4] Brooks PJ, 1996, J NEUROSCI, V16, P939
  • [5] Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study
    Cassel, S
    Revel, MO
    Kelche, C
    Zwiller, J
    [J]. NEUROBIOLOGY OF DISEASE, 2004, 15 (02) : 206 - 211
  • [6] Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
    Chen, RZ
    Akbarian, S
    Tudor, M
    Jaenisch, R
    [J]. NATURE GENETICS, 2001, 27 (03) : 327 - 331
  • [7] Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2
    Chen, WG
    Chang, Q
    Lin, YX
    Meissner, A
    West, AE
    Griffith, EC
    Jaenisch, R
    Greenberg, ME
    [J]. SCIENCE, 2003, 302 (5646) : 885 - 889
  • [8] Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis
    Cohen, DRS
    Matarazzo, V
    Palmer, AM
    Tu, Y
    Jeon, OH
    Pevsner, J
    Ronnett, GV
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 22 (04) : 417 - 429
  • [9] Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
    Collins, AL
    Levenson, JM
    Vilaythong, AP
    Richman, R
    Armstrong, DL
    Noebels, JL
    Sweatt, JD
    Zoghbi, HY
    [J]. HUMAN MOLECULAR GENETICS, 2004, 13 (21) : 2679 - 2689
  • [10] A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins
    Cross, SH
    Meehan, RR
    Nan, XS
    Bird, A
    [J]. NATURE GENETICS, 1997, 16 (03) : 256 - 259