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Developmental Biology
Article
License: Elsevier Non-Commercial
Data sources: UnpayWall
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Developmental Biology
Article . 2008
License: Elsevier Non-Commercial
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Developmental Biology
Article . 2008 . Peer-reviewed
License: Elsevier Non-Commercial
Data sources: Crossref
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Cdx2 acts downstream of cell polarization to cell-autonomously promote trophectoderm fate in the early mouse embryo

Authors: Ralston, Amy; Rossant, Janet;

Cdx2 acts downstream of cell polarization to cell-autonomously promote trophectoderm fate in the early mouse embryo

Abstract

The first lineage decision during mouse development is the establishment of trophectoderm and inner cell mass lineages, morphologically distinguishable at the blastocyst stage. The Caudal-like transcription factor Cdx2 is required for repression of inner cell mass genes Oct4 and Nanog in the trophectoderm. Expression of Cdx2 in the trophectoderm is thus one of the earliest known events in lineage determination. However, it is not clear whether the Cdx2 expression pattern is the cause or the consequence of this first lineage decision. Here, we show that Cdx2 is initially ubiquitously expressed, and becomes progressively upregulated in outside, future trophectoderm cells prior to blastocyst formation. Ubiquitous Cdx2 expression begins around the time of cell polarization, but we show that cell polarization is independent of zygotic Cdx2. Finally, we show functionally that Cdx2 is downstream of lineage allocation since Cdx2 mutant cells, which show cell-autonomous defects in expression of Oct4, Nanog, and the trophectoderm marker Eomesodermin, do not preferentially contribute to inner cell mass in chimeric blastocysts. Cdx2 therefore appears to act downstream of the first lineage decision, suggesting that processes influencing lineage allocation or morphogenesis may regulate Cdx2 expression along the inside/outside axis of the embryo.

Related Organizations
Keywords

Embryonic Development, Morula, Models, Biological, aPKC, Lineage specification, Mice, Ectoderm, Animals, CDX2 Transcription Factor, Cell Lineage, Preimplantation, Molecular Biology, Homeodomain Proteins, Mice, Knockout, Krt8, Mice, Inbred ICR, Trophoblast, Cell Polarity, Gene Expression Regulation, Developmental, EndoA, Cell Biology, Nanog Homeobox Protein, Embryo, Mammalian, Tbr2, DNA-Binding Proteins, Blastocyst, Mutation, T-Box Domain Proteins, Octamer Transcription Factor-3, Biomarkers, Troma, Developmental Biology

  • BIP!
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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    318
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
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    influence
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
318
Top 1%
Top 1%
Top 1%
hybrid