Affiliation:
1. Research Institute of Molecular Pathology (IMP), A-1030 Vienna, Austria, 1 and
2. Wellcome/CRC Institute of Cancer and Developmental Biology, Cambridge CB21QR, United Kingdom2
Abstract
ABSTRACT
Polycomb
-group (Pc-G) genes are required for the stable repression of the homeotic selector genes and other developmentally regulated genes, presumably through the modulation of chromatin domains. Among the
Drosophila
Pc-G genes,
Enhancer of zeste
[
E(z)
] merits special consideration since it represents one of the Pc-G genes most conserved through evolution. In addition, the E(Z) protein family contains the SET domain, which has recently been linked with histone methyltransferase (HMTase) activity. Although E(Z)-related proteins have not (yet) been directly associated with HMTase activity, mammalian Ezh2 is a member of a histone deacetylase complex. To investigate its in vivo function, we generated mice deficient for
Ezh2
. The
Ezh2
null mutation results in lethality at early stages of mouse development.
Ezh2
mutant mice either cease developing after implantation or initiate but fail to complete gastrulation. Moreover,
Ezh2
-deficient blastocysts display an impaired potential for outgrowth, preventing the establishment of
Ezh2-
null embryonic stem cells. Interestingly,
Ezh2
is up-regulated upon fertilization and remains highly expressed at the preimplantation stages of mouse development. Together, these data suggest an essential role for
Ezh2
during early mouse development and genetically link
Ezh2
with
eed
and
YY1
, the only other early-acting Pc-G genes.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
792 articles.
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