Evidence map›Paper›PMID 36914622›Full record

ArticleCell discovery2023

Dynamics of histone acetylation during human early embryogenesis.

Keliang Wu, Dongdong Fan, Han Zhao, Zhenbo Liu, Zhenzhen Hou, Wenrong Tao, Guanling Yu, Shenli Yuan, Xiaoxiao Zhu, Mengyao Kang and 4 more

Open access · goldFull text read
In one paragraph

Article in Cell discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
10.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 66 citations in OpenAlex.

  1. The Landscape and Regulation of Histone Crotonylation in Mammalian Gametes and Early Embryos.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Review
  3. The multi-omics regulatory landscape of human early embryogenesis.Cellular and molecular life sciences : CMLS · 2026
    Review
  4. Article
  5. Article
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  8. Review
  9. Article
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  11. Exit from totipotency in mammals: an epigenetic perspective.Frontiers in cell and developmental biology · 2026
    Review
  12. Epigenetic remodeling during early embryonic development.Frontiers in cell and developmental biology · 2026
    Review
  13. Histone Modifications in Mammalian Early Embryos.Advances in experimental medicine and biology · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Keliang Wu *Center for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China.ORCID http://orcid.org/0000-0001-9552-6096
Dongdong Fan *University of Chinese Academy of Sciences, Beijing, China.
Han ZhaoCenter for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China.
Zhenbo LiuCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, China.
Zhenzhen HouCenter for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China.
Wenrong TaoCenter for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China.
Guanling YuCenter for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China.
Shenli YuanUniversity of Chinese Academy of Sciences, Beijing, China.
Xiaoxiao ZhuUniversity of Chinese Academy of Sciences, Beijing, China.
Mengyao KangUniversity of Chinese Academy of Sciences, Beijing, China.
Yong TianUniversity of Chinese Academy of Sciences, Beijing, China. ytian@ibp.ac.cn.ORCID http://orcid.org/0000-0002-8790-1148
Zi-Jiang ChenCenter for Reproductive Medicine, National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Key laboratory of Reproductive Endocrinology for Ministry of Education, Shandong University, Jinan, Shandong, China. chenzijiang@hotmail.com.ORCID http://orcid.org/0000-0001-6637-6631
Jiang LiuUniversity of Chinese Academy of Sciences, Beijing, China. liuj@big.ac.cn.ORCID http://orcid.org/0000-0002-5687-5047
Lei GaoCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, China. gaol@big.ac.cn.
Chinese Academy of Sciences · CNShandong University · CNInstitute of Biophysics · CNKunming Institute of Zoology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It remains poorly understood about the regulation of gene and transposon transcription during human early embryogenesis. Here, we report that broad H3K27ac domains are genome-widely distributed in human 2-cell and 4-cell embryos and transit into typical peaks in the 8-cell embryos. The broad H3K27ac domains in early embryos before zygotic genome activation (ZGA) are also observed in mouse. It suggests that broad H3K27ac domains play conserved functions before ZGA in mammals. Intriguingly, a large portion of broad H3K27ac domains overlap with broad H3K4me3 domains. Further investigation reveals that histone deacetylases are required for the removal or transition of broad H3K27ac domains and ZGA. After ZGA, the number of typical H3K27ac peaks is dynamic, which is associated with the stage-specific gene expression. Furthermore, P300 is important for the establishment of H3K27ac peaks and the expression of associated genes in early embryos after ZGA. Our data also indicate that H3K27ac marks active transposons in early embryos. Interestingly, H3K27ac and H3K18ac signals rather than H3K9ac signals are enriched at ERVK elements in mouse embryos after ZGA. It suggests that different types of histone acetylations exert distinct roles in the activation of transposons. In summary, H3K27ac modification undergoes extensive reprogramming during early embryo development in mammals, which is associated with the expression of genes and transposons.

Identifiers

PMID36914622
PMCPMC10011383
OpenAlexW4324129977

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.