Affiliation:
1. Department of Histology and Embryology, School of Pre-Clinical Medicine, Guangxi Medical University , Nanning, Guangxi 530021, P. R. China
2. Central Laboratory, School of Pre-Clinical Medicine, Guangxi Medical University , Nanning, Guangxi 530021, P. R. China
Abstract
Abstract
Background
Maternal proteins have important roles during early embryonic development. However, our understanding of maternal proteins is still very limited. The integrated analysis of mouse uniparental (parthenogenetic) and biparental (fertilized) embryos at the protein level creates a protein expression landscape that can be used to explore preimplantation mouse development.
Results
Using label-free quantitative mass spectrometry (MS) analysis, we report on the maternal proteome of mouse parthenogenetic embryos at pronucleus, 2-cell, 4-cell, 8-cell, morula, and blastocyst stages and highlight dynamic changes in protein expression. In addition, comparison of proteomic profiles of parthenogenotes and fertilized embryos highlights the different fates of maternal proteins. Enrichment analysis uncovered a set of maternal proteins that are strongly correlated with the subcortical maternal complex, and we report that in parthenogenotes, some of these maternal proteins escape the fate of protein degradation. Moreover, we identified a new maternal factor-Fbxw24, and highlight its importance in early embryonic development. We report that Fbxw24 interacts with Ddb1-Cul4b and may regulate maternal protein degradation in mouse.
Conclusions
Our study provides an invaluable resource for mechanistic analysis of maternal proteins and highlights the role of the novel maternal factor Fbw24 in regulating maternal protein degradation during preimplantation embryo development.
Funder
China Postdoctoral Science Foundation
Natural Science Foundation of Guangxi Province
Guangxi First-Class Discipline Project for Basic Medicine Sciences
Publisher
Oxford University Press (OUP)
Subject
Computer Science Applications,Health Informatics
Cited by
3 articles.
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