Ma Yerong, Zhang Yingyi, Yang Weijie, Tong Xiaomei, Liu Siya, Zhou Yan, Qiu Mengjia, Jiang Huifang, Hu Zhanhong, Ren Peipei, Rong Yan, Lai Mengru, Jin Jiamin, Huang Fei, Ouyang Liujian, Zhou Feng, Fan Heng-Yu, Zhang Yin-Li, Zhang Songying
Assisted Reproduction Unit, Department of Obstetrics and Gynecology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Zhejiang Key Laboratory of Precise Protection and Promotion of Fertility, Zhejiang Provincial Clinical Research Center for Reproductive Health and Disease, Hangzhou, 310016, P. R. China.
MOE Key Laboratory of Biosystems Homeostasis and Protection and Zhejiang Provincial Key Laboratory for Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, Zhejiang, 310058, P. R. China.
Adv Sci (Weinh). 2025 Aug;12(31):e14367. doi: 10.1002/advs.202414367. Epub 2025 Jun 5.
Metabolic processes and epigenetic reprogramming are intricately interconnected; however, their mechanistic interplay remains unclear. This study elucidates the role of ATP-citrate lyase (ACLY), an essential enzyme in acetyl-CoA production that uniquely localizes to the nucleus in oocytes and early embryos. Maternal Acly deletion in oocytes preserves fertility due to the compensatory upregulation of Acetyl-CoA Synthetase 2 (ACSS2), whereas zygotic Acly knockout causes developmental arrest at the pre-blastocyst stage without ACSS2 induction. Mechanistically, nuclear ACLY recruits and interacts with histone acetyltransferases, specifically E1A binding protein p300 (P300) and histone acetyltransferase 1 (HAT1), supplying acetyl-CoA for histone acetylation to activate transcription, which is essential for embryogenesis. Clinically, enhanced ACLY nuclear localization correlates with superior quality of human embryos. Functionally, AKT-mediated phosphorylation (Thr447/Ser451/Ser455) drives the nuclear translocation of ACLY and facilitates its interaction with HAT1 and P300. Inhibition of ACLY or its phosphorylation disrupts the promoting effects of AKT activators, such as insulin-like growth factor-1 (IGF-1), on blastocyst formation. These findings suggest that ACLY is a metabolic hub that bridges signaling and epigenetic remodeling, ensuring acetyl-CoA availability for chromatin modifications, and offering insights into the metabolic determinants of embryo viability and potential therapeutic targets for infertility.
代谢过程与表观遗传重编程紧密相连;然而,它们之间的机制相互作用仍不清楚。本研究阐明了ATP-柠檬酸裂解酶(ACLY)的作用,ACLY是乙酰辅酶A生成过程中的一种关键酶,在卵母细胞和早期胚胎中特异地定位于细胞核。卵母细胞中母体Acly的缺失由于乙酰辅酶A合成酶2(ACSS2)的代偿性上调而保留了生育能力,而合子Acly基因敲除导致在囊胚前期发育停滞,且没有ACSS2的诱导。从机制上讲,核内ACLY招募组蛋白乙酰转移酶并与之相互作用,特别是E1A结合蛋白p300(P300)和组蛋白乙酰转移酶1(HAT1),为组蛋白乙酰化提供乙酰辅酶A以激活转录,这对胚胎发育至关重要。临床上,ACLY核定位增强与人类胚胎的优质相关。在功能上,AKT介导的磷酸化(Thr447/Ser451/Ser455)驱动ACLY的核转位,并促进其与HAT1和P300的相互作用。抑制ACLY或其磷酸化会破坏AKT激活剂(如胰岛素样生长因子-1(IGF-1))对囊胚形成的促进作用。这些发现表明,ACLY是一个连接信号传导和表观遗传重塑的代谢枢纽,确保有可用于染色质修饰的乙酰辅酶A,并为胚胎活力的代谢决定因素及不孕症的潜在治疗靶点提供了见解。