Musmeci Giulia, Franchi Fernanda Fagali, Mossa Francesca, Luciano Alberto Maria, Lodde Valentina, Franciosi Federica
Reproductive and Developmental Biology Laboratory, Department of Veterinary Medicine and Animal Sciences, University of Milan, Lodi, LO, Italy.
Department of Veterinary Medicine, University of Sassari, Sassari, SS, Italy.
Results Probl Cell Differ. 2025;75:165-188. doi: 10.1007/978-3-031-91459-1_6.
Histone acetylation is an epigenetic modification responsible for changes in chromatin architecture, accessibility, and ultimately gene expression. At the onset of a new life, when the fully differentiated parental genomes fuse together to generate a new totipotent cell, the gametes' epigenetic program must be erased, and new ones are progressively installed. Together with other epigenetic modifications, histone acetylation participates in the early events of embryogenesis, undergoing dynamic changes that involve several amino acid residues on different histone proteins. By analyzing studies that followed these changes during the preimplantation development in different mammals, we identified critical windows of acetylation/deacetylation in relation to the oocyte-to-zygote transition, the activation of the embryonic genome, and the specification of cell lineages, all crucial events for early embryo development, the establishment of pluripotent embryonic tissue, and ultimately of a multicellular organism.Finally, this survey points out the possibility that while contributing to the necessary plasticity of the embryonic stem cells, the reversibility of histone acetylation/deacetylation patterns renders this mechanism prone to be hijacked by environmental conditions, such as maternal diet or pollutants, leading to the alterations of epigenetic marks that can be potentially transmitted to the daughter cells and up to adulthood.
组蛋白乙酰化是一种表观遗传修饰,负责染色质结构、可及性以及最终基因表达的变化。在新生命开始时,当完全分化的亲代基因组融合在一起产生一个新的全能细胞时,配子的表观遗传程序必须被清除,并逐步建立新的程序。与其他表观遗传修饰一起,组蛋白乙酰化参与胚胎发生的早期事件,经历涉及不同组蛋白上几个氨基酸残基的动态变化。通过分析追踪不同哺乳动物着床前发育过程中这些变化的研究,我们确定了与卵母细胞到合子转变、胚胎基因组激活以及细胞谱系特化相关的关键乙酰化/去乙酰化窗口,这些都是早期胚胎发育、多能胚胎组织建立以及最终多细胞生物体形成的关键事件。最后,这项调查指出,虽然组蛋白乙酰化/去乙酰化模式的可逆性有助于胚胎干细胞的必要可塑性,但这种机制可能容易被环境条件(如母体饮食或污染物)劫持,导致表观遗传标记的改变,这些改变可能会传递给子细胞并直至成年。