| Literature DB >> 33068521 |
Ling Li1, Shuai Zhu1, Wenjie Shu2, Yueshuai Guo1, Yusheng Guan3, Juan Zeng1, Haichao Wang1, Longsen Han1, Jiaqi Zhang1, Xiaohui Liu4, Chunling Li1, Xiaojing Hou1, Min Gao4, Juan Ge1, Chao Ren2, Hao Zhang5, Tim Schedl6, Xuejiang Guo7, Minjian Chen8, Qiang Wang9.
Abstract
Well-balanced and timed metabolism is essential for making a high-quality egg. However, the metabolic framework that supports oocyte development remains poorly understood. Here, we obtained the temporal metabolome profiles of mouse oocytes during in vivo maturation by isolating large number of cells at key stages. In parallel, quantitative proteomic analyses were conducted to bolster the metabolomic data, synergistically depicting the global metabolic patterns in oocytes. In particular, we discovered the metabolic features during meiotic maturation, such as the fall in polyunsaturated fatty acids (PUFAs) level and the active serine-glycine-one-carbon (SGOC) pathway. Using functional approaches, we further identified the key targets mediating the action of PUFA arachidonic acid (ARA) on meiotic maturation and demonstrated the control of epigenetic marks in maturing oocytes by SGOC network. Our data serve as a broad resource on the dynamics occurring in metabolome and proteome during oocyte maturation.Entities:
Keywords: embryo; epigenetics; metabolism; oocyte; proteomics
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Year: 2020 PMID: 33068521 PMCID: PMC8034554 DOI: 10.1016/j.molcel.2020.09.022
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970