Chromosome remodeling and differentiation of tetraploid embryos during preimplantation development

Dev Dyn. 2011 Jul;240(7):1660-9. doi: 10.1002/dvdy.22653. Epub 2011 May 5.

Abstract

Although it is known that the tetraploid embryo contributes only to the placenta, the question of why tetraploid embryos differentiate into placenta remains unclear. To study the effect of electrofusion on the development of mouse tetraploid oocytes, mouse two-cell embryos were fused and cultured in vitro in Chatot-Ziomek-Bavister medium. After electrofusion, two chromosome sets from the tetraploid blastomere were individually duplicated before nuclear fusion. At 8-10 hr after electrofusion, each chromosome set was condensing and the nuclear membrane was breaking down. Around 12-14 hr after electrofusion, the two chromosome sets had combined together and had reached the second mitotic metaphase, at this point with 8n sets of chromosomes. Interestingly, we discovered that expression of OCT4, an inner cell mass cells biomarker, is lost by the tetraploid expanded blastocysts, but that CDX2, a trophectoderm cells biomarker, is strongly expressed at this stage. This observation provides evidence clarifying why tetraploid embryos contribute only to trophectoderm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastocyst / cytology
  • Blastocyst / metabolism*
  • CDX2 Transcription Factor
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Chromosomes / metabolism*
  • Embryonic Development / genetics
  • Embryonic Development / physiology*
  • Female
  • Homeodomain Proteins / metabolism
  • Karyotyping
  • Male
  • Mice
  • Octamer Transcription Factor-3 / metabolism
  • Pregnancy
  • Tetraploidy*
  • Transcription Factors / metabolism

Substances

  • CDX2 Transcription Factor
  • Cdx2 protein, mouse
  • Homeodomain Proteins
  • Octamer Transcription Factor-3
  • Pou5f1 protein, mouse
  • Transcription Factors