{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Guo Y"],"funding":["Ministry of Science and Technology of the People's Republic of China","National Natural Science Foundation of China","Natural Science Research of Jiangsu Higher Education Institutions of China","National Key Research and Development Program of China"],"pagination":["100882"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11728983"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["24(1)"],"pubmed_abstract":["Once ovulated, the oocyte has to be fertilized in a short time window or it will undergo post-ovulation aging (POA), whose underlying mechanisms are still not elucidated. Here, we optimized single-cell proteomics methods and performed single-cell transcriptomic, proteomic, and phosphoproteomic analysis of fresh, POA, and melatonin-treated POA oocytes. POA oocytes showed downregulation of most differentially expressed proteins, with little correlation with mRNA expression, and the protein changes can be rescued by melatonin treatment. MG132 treatment rescued the decreased fertilization and polyspermy rates and upregulated fragmentation and parthenogenesis rates of POA oocytes. MG132-treated oocytes displayed health status at proteome, phosphoproteome, and fertilization ability similar to fr"],"journal":["Molecular & cellular proteomics : MCP"],"pubmed_title":["Single-Cell Multi-Omics Analysis of In Vitro Post-Ovulatory-Aged Oocytes Revealed Aging-Dependent Protein Degradation."],"pmcid":["PMC11728983"],"funding_grant_id":["22KJB310011","2021YFC2700200","82371606","82371623","32071133","32300716","82221005"],"pubmed_authors":["Guo Y","Wang B","Guo X","Zhang H","Yan T","Han X","Zhu H","Liu X","Li Y","Gao M","Qi Y","Situ C","Wang Y"],"additional_accession":[]},"is_claimable":false,"name":"Single-Cell Multi-Omics Analysis of In Vitro Post-Ovulatory-Aged Oocytes Revealed Aging-Dependent Protein Degradation.","description":"Once ovulated, the oocyte has to be fertilized in a short time window or it will undergo post-ovulation aging (POA), whose underlying mechanisms are still not elucidated. Here, we optimized single-cell proteomics methods and performed single-cell transcriptomic, proteomic, and phosphoproteomic analysis of fresh, POA, and melatonin-treated POA oocytes. POA oocytes showed downregulation of most differentially expressed proteins, with little correlation with mRNA expression, and the protein changes can be rescued by melatonin treatment. MG132 treatment rescued the decreased fertilization and polyspermy rates and upregulated fragmentation and parthenogenesis rates of POA oocytes. MG132-treated oocytes displayed health status at proteome, phosphoproteome, and fertilization ability similar to fr","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jan","modification":"2026-06-01T07:54:50.114Z","creation":"2025-04-07T05:28:00.415Z"},"accession":"S-EPMC11728983","cross_references":{"pubmed":["39571909"],"doi":["10.1016/j.mcpro.2024.100882"]}}