Effects of oocyte growth on development and histone modification during preimplantation in mouse parthenogenetic embryos.

IF 3.1 2区 生物学 Q2 REPRODUCTIVE BIOLOGY
Wataru Yamazaki, Misako Higashiya, Yuriko Fujii, Megumi Yano, Takanori Oikawa, Shinsuke Seki
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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; 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, Zscan4d, 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.

卵母细胞生长对小鼠孤雌胚胎着床前发育和组蛋白修饰的影响。
孤雌生殖胚胎有两组来自完全发育的卵母细胞的基因组(fg/fg),在小鼠胚胎期9.5天时具有胚胎致死性。在生长阶段,卵母细胞经历表观遗传修饰,包括DNA甲基化和组蛋白修饰。先前的一项研究表明,来自未生长的卵母细胞(ng/ng)的孤雌胚胎在8细胞阶段被捕获。然而,生长期卵母细胞基因组(gr/gr)对孤雌生殖胚胎发育动力学和组蛋白修饰的影响尚未完全阐明。在这里,我们研究了胚胎着床前小鼠单性生殖胚胎中全局组蛋白修饰的发展和动态。在ng/ng胚胎中观察到双细胞期严重的发育停滞。gr/gr胚胎的发育能力随供体卵母细胞直径的增大而逐渐提高。在gr/gr和fg/fg胚胎中,H3K4/9me3的组蛋白修饰水平从两细胞期的早期到晚期显著降低,但在ng/ng胚胎中保持不变。我们还研究了全球合子从头转录活性;Ng / Ng胚胎在1细胞期和2细胞期表现出与fg/fg胚胎相当的活性。然而,合子基因组激活相关基因Zscan4d的转录水平在ng/ng胚胎的两细胞后期显著降低。本研究描述了ng/ng和gr/gr胚胎着床前早期的全局组蛋白修饰特征,表明在孤雌生殖胚胎着床前,早期生长阶段的卵母细胞基因组导致发育不全和组蛋白修饰被破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biology of Reproduction
Biology of Reproduction 生物-生殖生物学
CiteScore
6.30
自引率
5.60%
发文量
214
审稿时长
1 months
期刊介绍: Biology of Reproduction (BOR) is the official journal of the Society for the Study of Reproduction and publishes original research on a broad range of topics in the field of reproductive biology, as well as reviews on topics of current importance or controversy. BOR is consistently one of the most highly cited journals publishing original research in the field of reproductive biology.
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