PURIFICATION, SEQUENCE, AND CELLULAR-LOCALIZATION OF A NOVEL CHROMOSOMAL PROTEIN THAT BINDS TO METHYLATED DNA

被引:1093
作者
LEWIS, JD
MEEHAN, RR
HENZEL, WJ
MAURERFOGY, I
JEPPESEN, P
KLEIN, F
BIRD, A
机构
[1] RES INST MOLEC PATHOL,A-1030 VIENNA,AUSTRIA
[2] GENENTECH INC,S SAN FRANCISCO,CA 94080
[3] ERNST BOEHRINGER INST ARZNEIMITTELFORSCH,A-1121 VIENNA,AUSTRIA
[4] WESTERN GEN HOSP,MRC,HUMAN GENET UNIT,EDINBURGH EH4 2XU,MIDLOTHIAN,SCOTLAND
[5] UNIV VIENNA,INST BOT,A-1010 VIENNA,AUSTRIA
基金
英国惠康基金;
关键词
D O I
10.1016/0092-8674(92)90610-O
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 of mammalian DNA can lead to repression of transcription and alteration of chromatin structure. Recent evidence suggests that both effects are the result of an interaction between the methylated sites and methyl-CpG-binding proteins (MeCPs). MeCP1 has previously been detected in crude nuclear extracts. Here we report the identification, purification, and cDNA cloning of a novel MeCP called MeCP2. Unlike MeCP1, the new protein is able to bind to DNA that contains a single methyl-CpG pair. By staining with an antibody, we show that the distribution of MeCP2 along the chromosomes parallels that of methyl-CpG. In mouse, for example, MeCP2 is concentrated in pericentromeric heterochromatin, which contains a large fraction (about 40%) of all genomic 5-methylcytosine.
引用
收藏
页码:905 / 914
页数:10
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