P300 Regulates Histone Crotonylation and Preimplantation Embryo Development

Author:

Sun Qing-Yuan1ORCID,Gao Di2,Li Chao3,Liu Shao Yuan4,Lin Xiao Ting3,Tan Yong Peng3,Gao Fu Min3,Yi Li Tao3,Zhang Jian V5,Ma Jun Yu3,Meng Tie-Gang1ORCID,Yeung William Shu Biu6,Liu Kui7ORCID,Ou Xiang Hong3,Su Ruibao3

Affiliation:

1. Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou

2. the University of Hong Kong Shenzhen Hospital

3. Guangdong Second Provincial General Hospital

4. Guangxi University

5. Shenzhen Institutes of Advanced Technology

6. The University of Hong Kong

7. University of Hong Kong

Abstract

Abstract Histone lysine crotonylation, an evolutionarily conserved modification differing from acetylation, exerts pivotal control over diverse biological processes. Among these are gene transcriptional regulation, spermatogenesis, and cell cycle processes. However, the dynamic changes and functions of histone crotonylation in preimplantation embryonic development in mammals remain unclear. Here, we showed that the transcription coactivator P300 functioned as a writer of histone crotonylation during embryonic development. Depletion of P300 resulted in significant developmental defects and dysregulation of the transcriptome of embryos. Importantly, we demonstrated that P300 catalyzes the crotonylation of histone, directly stimulating transcription and regulating gene expression, thereby ensuring successful progression of embryo development up to the blastocyst stage. Moreover, the modification of histone H3 lysine 18 crotonylation (H3K18cr) was primarily localized to active promoter regions. This modification served as a distinctive epigenetic indicator of crucial transcriptional regulators, facilitating the activation of gene transcription. Together, our results propose a model wherein P300-mediated histone crotonylation plays a crucial role in regulating the fate of embryonic development.

Publisher

Research Square Platform LLC

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