Altered apoptosis/autophagy and epigenetic modifications cause the impaired postimplantation octaploid embryonic development in mice

Cell Cycle. 2017 Jan 2;16(1):82-90. doi: 10.1080/15384101.2016.1252884. Epub 2016 Nov 10.

Abstract

Polyploids are pervasive in plants and have large impacts on crop breeding, but natural polyploids are rare in animals. Mouse diploid embryos can be induced to become tetraploid by blastomere fusion at the 2-cell stage and tetraploid embryos can develop to the blastocyst stage in vitro. However, there is little information regarding mouse octaploid embryonic development and precise mechanisms contributing to octaploid embryonic developmental limitations are unknown. To investigate the genetic and epigenetic mechanisms underlying octaploid embryonic development, we generated mouse octaploid embryos and evaluated the in vitro/in vivo developmental potential. Here we show that octaploid embryos can develop to the blastocyst stage in vitro, but all fetus impaired immediately after implantation. Our results indicate that cell lineage specification of octaploid embryo was disorganized. Furthermore, these octaploid embryos showed increased apoptosis as well as alterations in epigenetic modifications when compared with diploid embryos. Thus, our cumulative data provide cues for why mouse octaploid embryonic development is limited and its failed postimplantation development.

Keywords: apoptosis; embryo development; epigenetics; octaploid.

MeSH terms

  • Animals
  • Apoptosis / genetics*
  • Autophagy / genetics*
  • Biomarkers / metabolism
  • Blastocyst / cytology
  • Blastocyst / metabolism
  • Cell Lineage / genetics
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Embryonic Development / genetics*
  • Epigenesis, Genetic*
  • Female
  • Mice, Inbred ICR
  • Models, Biological
  • Polyploidy*

Substances

  • Biomarkers