Identification and characterization of a family of mammalian methyl-CpG binding proteins

被引:1031
作者
Hendrich, B [1 ]
Bird, A [1 ]
机构
[1] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
基金
英国惠康基金;
关键词
D O I
10.1128/MCB.18.11.6538
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
Methylation at the DNA sequence 5'-CpG is required for mouse development. MeCP2 and MBD1 (formerly PCM1) are two known proteins that bind specifically to methylated DNA via a related amino acid motif and that can repress transcription. We describe here three novel human and mouse proteins (MBD2, MBD3, and MBD4) that contain the methyl-CpG binding domain. MBD2 and MBD4 bind specifically to methylated DNA in vitro. Expression of MBD2 and MBD4 tagged with green fluorescent protein in mouse cells shows that both proteins colocalize with foci of heavily methylated satellite DNA. Localization is disrupted in cells that have greatly reduced levels of CpG methylation. MBD3 does not bind methylated DNA in vivo or in vitro. MBD1, MBD2, MBD3, and MBD4 are expressed in somatic tissues, but MBD1 and MBD2 expression is reduced or absent in embryonic stem cells which are known to be deficient in MeCP1 activity, The data demonstrate that MBD2 and MBD4 bind specifically to methyl-CpG in vitro and in vivo and are therefore likely to be mediators of the biological consequences of the methylation signal.
引用
收藏
页码:6538 / 6547
页数:10
相关论文
共 49 条
[1]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[2]   HIGH-LEVELS OF DENOVO METHYLATION AND ALTERED CHROMATIN STRUCTURE AT CPG ISLANDS IN CELL-LINES [J].
ANTEQUERA, F ;
BOYES, J ;
BIRD, A .
CELL, 1990, 62 (03) :503-514
[3]   Genomic imprinting in mammals [J].
Bartolomei, MS ;
Tilghman, SM .
ANNUAL REVIEW OF GENETICS, 1997, 31 :493-525
[4]   COMPARATIVE GENOMICS, GENOME CROSS-REFERENCING AND XREFDB [J].
BASSET, DE ;
BOGUSKI, MS ;
SPENCER, F ;
REEVES, R ;
GOEBL, M ;
HIETER, P .
TRENDS IN GENETICS, 1995, 11 (09) :372-373
[5]   LOSS OF METHYLATION ACTIVATES XIST IN SOMATIC BUT NOT IN EMBRYONIC-CELLS [J].
BEARD, C ;
LI, E ;
JAENISCH, R .
GENES & DEVELOPMENT, 1995, 9 (19) :2325-2334
[6]  
Bird AP, 1996, CANCER SURV, V28, P87
[7]   GENE NUMBER, NOISE-REDUCTION AND BIOLOGICAL COMPLEXITY [J].
BIRD, AP .
TRENDS IN GENETICS, 1995, 11 (03) :94-100
[8]   CPG-RICH ISLANDS AND THE FUNCTION OF DNA METHYLATION [J].
BIRD, AP .
NATURE, 1986, 321 (6067) :209-213
[9]   DNA METHYLATION INHIBITS TRANSCRIPTION INDIRECTLY VIA A METHYL-CPG BINDING-PROTEIN [J].
BOYES, J ;
BIRD, A .
CELL, 1991, 64 (06) :1123-1134
[10]   REPRESSION OF GENES BY DNA METHYLATION DEPENDS ON CPG DENSITY AND PROMOTER STRENGTH - EVIDENCE FOR INVOLVEMENT OF A METHYL-CPG BINDING-PROTEIN [J].
BOYES, J ;
BIRD, A .
EMBO JOURNAL, 1992, 11 (01) :327-333