MBD family proteins: reading the epigenetic code

被引:92
作者
Fatemi, Mehrnaz [1 ]
Wade, Paul A. [1 ]
机构
[1] Natl Inst Environm Hlth Sci, Lab Mol Carcinogenesis, Res Triangle Pk, NC 27709 USA
关键词
DNA methylation; transcriptional repression; epigenetics; methyl CpG binding protein;
D O I
10.1242/jcs.03099
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Methylation of DNA in mammalian cells serves to demarcate functionally specialized regions of the genome and is strongly associated with transcriptional repression. A highly conserved family of DNA-binding proteins characterized by a common sequence motif is widely believed to convert the information represented by methylation patterns into the appropriate functional state. This family, the MBD family, has been characterized at both the biochemical and genetic levels. A key issue, given their highly similar DNA-binding surfaces, is whether the individual MBD proteins bind differentially to distinct regions within the genome and, if so, by what mechanism. Somewhat surprisingly, some MBD family members, such as MeCP2, have considerable selectivity for specific sequences. Other family members, such as MBD2, appear to bind with somewhat relaxed specificity to methylated DNA. Recent genetic and molecular experiments have shed considerable light on these and other issues relevant to the chromosomal biology of this interesting protein family.
引用
收藏
页码:3033 / 3037
页数:5
相关论文
共 54 条
[1]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[2]   REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis [J].
Ballas, N ;
Grunseich, C ;
Lu, DD ;
Speh, JC ;
Mandel, G .
CELL, 2005, 121 (04) :645-657
[3]   Methyl-CpG binding proteins identify novel sites of epigenetic inactivation in human cancer [J].
Ballestar, E ;
Paz, MF ;
Valle, L ;
Wei, S ;
Fraga, MF ;
Espada, J ;
Cigudosa, JC ;
Huang, THM ;
Esteller, M .
EMBO JOURNAL, 2003, 22 (23) :6335-6345
[4]   DNA METHYLATION - EVOLUTION OF A BACTERIAL IMMUNE FUNCTION INTO A REGULATOR OF GENE-EXPRESSION AND GENOME STRUCTURE IN HIGHER EUKARYOTES [J].
BESTOR, TH .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1990, 326 (1235) :179-187
[5]   Methylation-induced repression - Belts, braces, and chromatin [J].
Bird, AP ;
Wolffe, AP .
CELL, 1999, 99 (05) :451-454
[6]   Methyl CpG-binding proteins induce large-scale chromatin reorganization during terminal differentiation [J].
Brero, A ;
Easwaran, HP ;
Nowak, D ;
Grunewald, I ;
Cremer, T ;
Leonhardt, H ;
Cardoso, MC .
JOURNAL OF CELL BIOLOGY, 2005, 169 (05) :733-743
[7]   The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA [J].
Chandler, SP ;
Guschin, D ;
Landsberger, N ;
Wolffe, AP .
BIOCHEMISTRY, 1999, 38 (22) :7008-7018
[8]   Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice [J].
Chen, RZ ;
Akbarian, S ;
Tudor, M ;
Jaenisch, R .
NATURE GENETICS, 2001, 27 (03) :327-331
[9]   Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2 [J].
Chen, WG ;
Chang, Q ;
Lin, YX ;
Meissner, A ;
West, AE ;
Griffith, EC ;
Jaenisch, R ;
Greenberg, ME .
SCIENCE, 2003, 302 (5646) :885-889
[10]   A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins [J].
Cross, SH ;
Meehan, RR ;
Nan, XS ;
Bird, A .
NATURE GENETICS, 1997, 16 (03) :256-259