ACLY的核定位通过募集P300和HAT1促进组蛋白乙酰化和转录来保护早期胚胎发育。

IF 14.3 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Yerong Ma, Yingyi Zhang, Weijie Yang, Xiaomei Tong, Siya Liu, Yan Zhou, Mengjia Qiu, Huifang Jiang, Zhanhong Hu, Peipei Ren, Yan Rong, Mengru Lai, Jiamin Jin, Fei Huang, Liujian Ouyang, Feng Zhou, Heng-Yu Fan, Yin-Li Zhang, Songying Zhang
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引用次数: 0

摘要

代谢过程和表观遗传重编程错综复杂地相互关联;然而,它们的相互作用机制尚不清楚。这项研究阐明了atp -柠檬酸裂解酶(ACLY)的作用,ACLY是一种在乙酰辅酶a生产中必不可少的酶,它独特地定位于卵母细胞和早期胚胎的细胞核。由于乙酰辅酶a合成酶2 (ACSS2)的代偿性上调,母代卵母细胞中的Acly缺失保留了生育能力,而在没有ACSS2诱导的情况下,合子细胞中的Acly敲除会导致囊胚前阶段的发育停滞。从机制上讲,核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,这是胚胎发生所必需的。临床上,ACLY核定位的增强与人类胚胎质量的提高有关。功能上,akt介导的磷酸化(Thr447/Ser451/Ser455)驱动ACLY的核易位,并促进其与HAT1和P300的相互作用。抑制ACLY或其磷酸化可破坏AKT激活因子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是连接信号和表观遗传重塑的代谢枢纽,确保乙酰辅酶a可用于染色质修饰,并为胚胎活力的代谢决定因素和不孕症的潜在治疗靶点提供见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Nuclear Localization of ACLY Guards Early Embryo Development Through Recruiting P300 and HAT1 to Promote Histone Acetylation and Transcription.

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.

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来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
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