Lactate regulates major zygotic genome activation by H3K18 lactylation in mammals

• Published in: National science review Vol. 11; no. 2; p. nwad295
• Main Authors: Li, Jingyu, Hou, Weibo, Zhao, Qi, Han, Wei, Cui, Hongdi, Xiao, Songling, Zhu, Ling, Qu, Jiadan, Liu, Xiaoyu, Cong, Weitao, Shen, Jingling, Zhao, Yuzheng, Gao, Shaorong, Huang, Guoning, Kong, Qingran
• Format: Journal Article
• Language: English
• Published: China Oxford University Press 01.02.2024
• Subjects: mammalian preimplantation development; epigenetic remodeling; histone lactylation; lactate; zygotic genome activation
• ISSN: 2095-5138; 2053-714X
• DOI: 10.1093/nsr/nwad295

Lactate is present at a high level in the microenvironment of mammalian preimplantation embryos and . However, its role in preimplantation development is unclear. Here, we report that lactate is highly enriched in the nuclei of early embryos when major zygotic genome activation (ZGA) occurs in humans and mice. The inhibition of its production and uptake results in developmental arrest at the 2-cell stage, major ZGA failure, and loss of lactate-derived H3K18lac, which could be rescued by the addition of Lac-CoA and recapitulated by overexpression of H3K18R mutation. By profiling the landscape of H3K18lac during mouse preimplantation development, we show that H3K18lac is enriched on the promoter regions of most major ZGA genes and correlates with their expressions. In humans, H3K18lac is also enriched in ZGA markers and temporally concomitant with their expressions. Taken together, we profile the landscapes of H3K18lac in mouse and human preimplantation embryos, and demonstrate the important role for H3K18lac in major ZGA, showing that a conserved metabolic mechanism underlies preimplantation development of mammalian embryos.