Epigenetic regulation of mouse preimplantation embryo development

被引:44
作者
Fu, Xudong [1 ,2 ,3 ]
Zhang, Chunxia [1 ,2 ,3 ]
Zhang, Yi [1 ,2 ,3 ,4 ,5 ]
机构
[1] Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Dept Pediat, Div Hematol Oncol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[5] Harvard Stem Cell Inst, Boston, MA 02115 USA
关键词
ZYGOTIC GENOME ACTIVATION; CELL NUCLEAR TRANSFER; LINEAGE SPECIFICATION; CHROMATIN ARCHITECTURE; GENE-EXPRESSION; KEY ACTIVATOR; FATE; PLURIPOTENCY; H3K4ME3; TROPHECTODERM;
D O I
10.1016/j.gde.2020.05.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
After fertilization, mouse embryos go through preimplantation development to give rise to blastocyst. Two key molecular events, zygotic genome activation (ZGA) and the first cell lineage specification, are essential for the process. Recent advances in low-input epigenomics profiling techniques allow the analysis of these events at a molecular level, which revealed a critical role of epigenetic and chromatin reprogramming in ZGA and the first cell lineage specification. Additionally, the establishment of an in vitro embryonic stem cell (ESC) to two-cell embryo-like conversion system have also contributed to the molecular understanding of preimplantation development. In this review, we summarize recent advances in epigenetic regulation of mouse preimplantation development, point out the remaining questions, and propose strategies to tackle these questions.
引用
收藏
页码:13 / 20
页数:8
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