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Updated: Jul 15, 2026

Derivation of Mouse Trophoblast Stem Cells from Blastocysts
Published on: June 8, 2010
RETRACTED: Cdx2 gene expression and trophectoderm lineage specification in mouse embryos
Kaushik Deb1, Mayandi Sivaguru, Hwan Yul Yong
1Department of Animal Sciences, Columbia, MO 65211, USA.
The late-dividing cell in two-cell mouse embryos is the trophectoderm precursor, identified by Cdx2 expression. Asymmetrical Cdx2 distribution in the oocyte and embryo dictates this lineage.
Area of Science:
- Developmental Biology
- Genetics
- Cell Biology
Background:
- The developmental potential and fate of individual blastomeres in early mammalian embryos remain a subject of debate.
- Understanding cell lineage determination is crucial for early embryonic development.
Purpose of the Study:
- To investigate whether blastomeres from two-cell-stage mouse embryos possess identical developmental properties.
- To identify the specific blastomere that serves as the precursor to trophectoderm.
Main Methods:
- Lineage tracing experiments in mouse embryos.
- RNA interference (RNAi) knock-down of the Cdx2 gene.
- Analysis of Cdx2 transcription factor and mRNA localization.
Main Results:
- Cdx2 expression was detected in the nuclei of cells originating from the late-dividing blastomere of two-cell embryos.
- Lineage tracing and RNAi experiments confirmed the late-dividing cell as the trophectoderm precursor.
- Asymmetrical localization of Cdx2 mRNA in oocytes and its reorientation post-fertilization concentrate it in the late-dividing blastomere.
Conclusions:
- The asymmetrical distribution of Cdx2 gene products establishes the trophectoderm lineage.
- Cdx2 acts as a key determinant for trophectoderm specification in early mouse embryos.
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