The central role of pyruvate metabolism on the epigenetic maturation and transcriptional profile of bovine oocytes

柠檬酸循环 糖酵解 卵母细胞 化学 丙酮酸脱氢酶复合物 新陈代谢 乙酰辅酶A 生物化学 乙酰化 体外成熟 脂质代谢 细胞生物学 生物 胚胎 基因
作者
João Vitor Alcantara da Silva,Jessica Ispada,Ricardo Perecin Nociti,Aldcejam Martins da Fonseca,Camila Bruna de Lima,É. C. dos Santos,Marcos Roberto Chiaratti,Marcella Pécora Milazzotto
出处
期刊:Reproduction [Bioscientifica]
卷期号:167 (4)
标识
DOI:10.1530/rep-23-0181
摘要

In brief Pyruvate metabolism is one of the main metabolic pathways during oocyte maturation. This study demonstrates that pyruvate metabolism also regulates the epigenetic and molecular maturation in bovine oocytes. Abstract Pyruvate, the final product of glycolysis, undergoes conversion into acetyl-CoA within the mitochondria of oocytes, serving as a primary fuel source for the tricarboxylic acid (TCA) cycle. The citrate generated in the TCA cycle can be transported to the cytoplasm and converted back into acetyl-CoA. This acetyl-CoA can either fuel lipid synthesis or act as a substrate for histone acetylation. This study aimed to investigate how pyruvate metabolism influences lysine 9 histone 3 acetylation (H3K9ac) dynamics and RNA transcription in bovine oocytes during in vitro maturation (IVM). Bovine cumulus–oocyte complexes were cultured in vitro for 24 h, considering three experimental groups: Control (IVM medium only), DCA (IVM supplemented with sodium dichloroacetate, a stimulant of pyruvate oxidation into acetyl-CoA), or IA (IVM supplemented with sodium iodoacetate, a glycolysis inhibitor). The results revealed significant alterations in oocyte metabolism in both treatments, promoting the utilization of lipids as an energy source. These changes during IVM affected the dynamics of H3K9ac, subsequently influencing the oocyte's transcriptional activity. In the DCA and IA groups, a total of 148 and 356 differentially expressed genes were identified, respectively, compared to the control group. These findings suggest that modifications in pyruvate metabolism trigger the activation of metabolic pathways, particularly lipid metabolism, changing acetyl-CoA availability and H3K9ac levels, ultimately impacting the mRNA content of in vitro matured bovine oocytes.

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