Resetting histone modifications during human parental-to-zygotic transition

Author:

Xia Weikun1ORCID,Xu Jiawei2ORCID,Yu Guang1ORCID,Yao Guidong2ORCID,Xu Kai1,Ma Xueshan2ORCID,Zhang Nan2ORCID,Liu Bofeng1,Li Tong2,Lin Zili1,Chen Xia3,Li Lijia1,Wang Qiujun1,Shi Dayuan2,Shi Senlin2ORCID,Zhang Yile2,Song Wenyan2ORCID,Jin Haixia2ORCID,Hu Linli2,Bu Zhiqin2,Wang Yang2,Na Jie3ORCID,Xie Wei1ORCID,Sun Ying-Pu2ORCID

Affiliation:

1. Center for Stem Cell Biology and Regenerative Medicine, MOE Key Laboratory of Bioinformatics, THU-PKU Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing 100084, China.

2. Center for Reproductive Medicine, Henan Key Laboratory of Reproduction and Genetics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, China.

3. Center for Stem Cell Biology and Regenerative Medicine, School of Medicine, Tsinghua University, Beijing 100084, China.

Abstract

Epigenetics of human embryonic development Substantial epigenetic reprogramming occurs in mammalian early development. Xia et al. investigated the reprogramming dynamics of three key histone modifications in human early embryonic development. The reprogramming in humans is highly species-specific and different than that in mice. A globally permissive chromatin state connects parental and zygotic epigenomes during maternal-to-zygotic transition. Inner-cell mass-specific, but not trophectoderm-specific, genes are asymmetrically patterned by a histone mark during early lineage segregation. Science , this issue p. 353

Funder

National Natural Science Foundation of China

National Basic Research Program of China

National Key R&D Program

HHMI International Research Scholar

THU-PKU Center for Life Sciences

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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