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The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

TitleThe methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.
Publication TypeJournal Article
Year of Publication1996
AuthorsTate P, Skarnes W, Bird A
JournalNat Genet
Volume12
Issue2
Pagination205-8
Date Published1996 Feb
ISSN1061-4036
KeywordsAnimals, beta-Galactosidase, Chimera, Chromosomal Proteins, Non-Histone, DNA-Binding Proteins, Embryonic and Fetal Development, Gene Targeting, Genetic Linkage, Male, Methyl-CpG-Binding Protein 2, Mice, Recombinant Fusion Proteins, Repressor Proteins, RNA, Messenger, Stem Cells, X Chromosome
Abstract

Vertebrate genomes are heavily methylated at cytosines in the sequence CpG. The biological role of this modification is probably mediated by DNA binding proteins that are either attracted to or repelled by methyl-CpG. MeCP2 is an abundant chromosomal protein that binds specifically to methylated DNA in vitro, and depends upon methyl-CpG for its chromosomal distribution in vivo. To assess the functional significance of MeCP2, the X-linked gene was mutated in male mouse embryonic stem (ES) cells using a promoterless gene-targeting construct containing a lacZ reporter gene. Mutant ES cells lacking MeCP2 grew with the same vigour as the parental line and were capable of considerable differentiation. Chimaeric embryos derived from several independent mutant lines, however, exhibited developmental defects whose severity was positively correlated with the contribution of mutant cells. The results demonstrate that MeCP2, like DNA methyltransferase, is dispensable in stem cells, but essential for embryonic development.

DOI10.1038/ng0296-205
Alternate JournalNat. Genet.
PubMed ID8563762