EVEN-SKIPPED HOMEOBOX 1 controls human ES cell differentiation by directly repressing GOOSECOID expression

被引:23
作者
Kalisz, Mark [1 ,2 ]
Winzi, Maria [1 ]
Bisgaard, Hanne Cathrine [2 ]
Serup, Palle [1 ]
机构
[1] Hagedorn Res Inst, Dept Dev Biol, DK-2820 Gentofte, Denmark
[2] Univ Copenhagen, Fac Hlth Sci, Dept Cellular & Mol Med, Copenhagen, Denmark
关键词
EVX1; GSC; Brachyury; TGFbeta; Human ES cells; EMBRYONIC STEM-CELLS; DEFINITIVE ENDODERM; TRANSCRIPTIONAL REPRESSION; SPEMANNS ORGANIZER; MESODERM FORMATION; GRADED EXPRESSION; XENOPUS EMBRYOS; SELF-RENEWAL; GENE XHOX3; M-TWIST;
D O I
10.1016/j.ydbio.2011.11.017
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TGF beta signaling patterns the primitive streak, yet little is known about transcriptional effectors that mediate the cell fate choices during streak-like development in mammalian embryos and in embryonic stem (ES) cells. Here we demonstrate that cross-antagonistic actions of EVEN-SKIPPED HOMEOBOX 1 (EVX1) and GOOSECOID (CSC) regulate cell fate decisions in streak-like progenitors derived from human ES cells exposed to BMP4 and/or activin. We found that EVX1 repressed GSC expression and promoted formation of posterior streak-like progeny in response to BMP4, and conversely that GSC repressed EVX1 expression and was required for development of anterior streak-like progeny in response to activin. Chromatin immunoprecipitation assays showed that EVX1 bound to the GSC5'-flanking region in BMP4 treated human ES cells, and band shift assays identified two EVX1 binding sites in the GSC 5'-region. Significantly, we found that intact EVX1 binding sites were required for BMP4-mediated repression of GSC reporter constructs. We conclude that BMP4-induced EVX1 repress GSC directly and the two genes form the core of a gene regulatory network (GRN) controlling cell fates in streak-like human ES cell progeny. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:94 / 103
页数:10
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