Interaction between Oct3/4 and Cdx2 determines trophectoderm differentiation

被引:926
作者
Niwa, H
Toyooka, T
Shimosato, D
Strumpf, D
Takahashi, K
Yagi, R
Rossant, J
机构
[1] RIKEN, Lab Pluripotent Cell Studies, Ctr Dev Biol, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Kobe Univ, Grad Sch Med, Lab Dev & Regenerat Med, Chuo Ku, Kobe, Hyogo 6500017, Japan
[3] CREST, Core Res Evolut Sci & Technol, Japn Sci & Technol Agcy, Kawaguchi, Saitama 3320012, Japan
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
基金
日本科学技术振兴机构;
关键词
D O I
10.1016/j.cell.2005.08.040
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
Trophectoderm (TE), the first differentiated cell lineage of mammalian embryogenesis, forms the placenta, a structure unique to mammalian development. The differentiation of TE is a hallmark event in early mammalian development, but molecular mechanisms underlying this first differentiation event remain obscure. Embryonic stem (ES) cells can be induced to differentiate into the TE lineage by forced repression of the POU-family transcription factor, Oct3/4. We show here that this event can be mimicked by overexpression of Caudal-related homeobox 2 (Cdx2), which is sufficient to generate proper trophoblast stem (T) cells. Cdx2 is dispensable for trophectoderm differentiation induced by Oct3/4 repression but essential for TS cell self-renewal. In preimplantation embryos, Cdx2 is initially coexpressed with Oct3/4 and they form a complex for the reciprocal repression of their target genes in ES cells. This suggests that reciprocal inhibition between lineagespecific transcription factors might be involved in the first differentiation event of mammalian development.
引用
收藏
页码:917 / 929
页数:13
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