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Isolation and Characterization of Mouse Antral Oocytes Based on Nucleolar Chromatin Organization
Published on: January 7, 2016
Effects of oocyte growth on development and histone modification during preimplantation in mouse parthenogenetic
Wataru Yamazaki1,2, Misako Higashiya1, Yuriko Fujii1
1Animal Research Division, Bioscience Education and Research Support Center, Akita University, Akita, Japan.
Abstract:
Parthenogenetic embryos have two sets of genomes derived from fully grown oocytes (fg/fg) and are embryonically lethal by embryonic day 9.5 in mice. During growth phase, oocytes undergo epigenetic modifications, including DNA methylation and histone modification. A previous study demonstrated that parthenogenetic embryos derived from nongrowing oocytes (ng/ng) were arrested at the eight-cell stage. However, effects of growing-stage oocyte genomes (gr/gr) on dynamics of development and histone modifications in parthenogenetic embryos have not been fully elucidated. Here, we investigated the development and dynamics of global histone modifications during preimplantation in mouse parthenogenetic embryos derived from ng and gr oocytes. Severe developmental arrest at the two-cell stage was observed in ng/ng embryos. Developmental competence in gr/gr embryos gradually improved depending on donor oocyte diameter. Global histone modification levels of H3K4/9me3 were significantly decreased from early to late two-cell stages in gr/gr and fg/fg embryos, but were maintained in ng/ng embryos. We also investigated the global zygotic de novo transcriptional activity, and ng/ng embryos at the one- and two-cell stages showed comparable activity to that of fg/fg embryos. However, the transcript level of zygotic genome activation-related gene, zinc finger and SCAN domain containing 4 or Zscan4d (previously known as EG545913), was significantly low in ng/ng embryos at the late two-cell stage. This study describes the characteristics of global histone modifications during early preimplantation in ng/ng and gr/gr embryos, suggesting that oocyte genomes during early growth phase lead to developmental incompetence and disrupted histone modifications during preimplantation in parthenogenetic embryos.

