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刘鑫

Supervisor of Doctorate Candidates
Supervisor of Master's Candidates
Name (Simplified Chinese):刘鑫
Name (Pinyin):Liu Xin
Professional Title:副研究员(自然科学)
Business Address:第四综合楼E615
E-Mail:
Alma Mater:西北农林科技大学
Teacher College:College of Animal Sciences & Technology / College of Veterinary Medicine
School/Department:动物科学技术学院、动物医学院
Discipline:Animal Genetic Breeding and Reproduction    
Other Contact Information:

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Paper Publications
Coordination of zygotic genome activation entry and exit by H3K4me3 and H3K27me3 in porcine early embryos
Release time:2022-07-24    Hits:

Impact Factor:9.438

DOI number:10.1101/gr.276207.121

Journal:Genome Research (B刊)

Abstract:Histone modifications are critical epigenetic indicators of chromatin state associated with gene expression. Although the reprogramming patterns of H3K4me3 and H3K27me3 have been elucidated in mouse and human preimplantation embryos, the relationship between these marks and zygotic genome activation (ZGA) remains poorly understood. By ultra-low-input native chromatin immunoprecipitation and sequencing, we profiled global H3K4me3 and H3K27me3 in porcine oocytes and in vitro fertilized (IVF) embryos. We found that promoters of ZGA genes occupied sharp H3K4me3 peaks in oocytes, and these peaks became broader after fertilization, and reshaped into sharp again during ZGA. By simultaneous depletion of H3K4me3 demethylase KDM5B and KDM5C, we determined that broad H3K4me3 domain maintenance impaired ZGA gene expression, suggesting its function to prevent premature ZGA entry. By contrast, broad H3K27me3 domains underwent global removal upon fertilization, followed by a re-establishment for H3K4me3/H3K27me3 bivalency in morulae. We also found that bivalent marks were deposited at promoters of ZGA genes, and inhibiting this deposition was correlated with the activation of ZGA genes. It suggests that promoter bivalency contributes to ZGA exit in porcine embryos. Moreover, we demonstrated that aberrant reprogramming of H3K4me3 and H3K27me3 triggered ZGA dysregulation in somatic cell nuclear transfer (SCNT) embryos, whereas H3K27me3-mediated imprinting did not exist in porcine IVF and SCNT embryos. Our findings highlight two previously unknown epigenetic reprogramming modes coordinated with ZGA in porcine preimplantation embryos. Finally, the similarities observed between porcine and human histone modification dynamics suggest that the porcine embryo may also be a useful model for human embryo research.

Co-author:Zhang JJ,Yu LT,Zhou K,Wang SK,Li ZK,Fan ZG,Wang TT,Hu TT,Hu RF,Liu ZT,Wu LH,Zhang X,Zhao SH,

First Author:Bu GW#,Zhu W#,Liu X#

Indexed by:Journal paper

Correspondence Author:Miao YL*

Volume:Online

Page Number:1-39

Translation or Not:no

Date of Publication:2022-07-22

Included Journals:SCI

Links to published journals:https://genome.cshlp.org/content/early/2022/07/22/gr.276207.121