Protein Expression Landscape of Mouse Embryos during Pre-implantation Development

Yawei Gao(Shanghai First Maternity and Infant Hospital), Xiaoyu Liu(Shanghai First Maternity and Infant Hospital), Bin Tang(East China Normal University), Chong Li(Shanghai First Maternity and Infant Hospital), Zhaohui Kou(National Institute of Biological Sciences, Beijing), Lin Li(National Institute of Biological Sciences, Beijing), Wenqiang Liu(Shanghai First Maternity and Infant Hospital), You Wu(Shanghai First Maternity and Infant Hospital), Xiaochen Kou(Shanghai First Maternity and Infant Hospital), Jingyi Li(Shanghai First Maternity and Infant Hospital), Yanhong Zhao(Shanghai First Maternity and Infant Hospital), Jiqing Yin(Shanghai First Maternity and Infant Hospital), Hong Wang(Shanghai First Maternity and Infant Hospital), She Chen(National Institute of Biological Sciences, Beijing), Lujian Liao(East China Normal University), Shaorong Gao(Shanghai First Maternity and Infant Hospital)
Cell Reports
December 1, 2017
Cited by 222Open Access
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Abstract

Pre-implantation embryo development is an intricate and precisely regulated process orchestrated by maternally inherited proteins and newly synthesized proteins following zygotic genome activation. Although genomic and transcriptomic studies have enriched our understanding of the genetic programs underlying this process, the protein expression landscape remains unexplored. Using quantitative mass spectrometry, we identified nearly 5,000 proteins from 8,000 mouse embryos of each stage (zygote, 2-cell, 4-cell, 8-cell, morula, and blastocyst). We found that protein expression in zygotes, morulas, and blastocysts is distinct from 2- to 8-cell embryos. Analysis of protein phosphorylation identified critical kinases and signal transduction pathways. We highlight key factors and their important roles in embryo development. Combined analysis of transcriptomic and proteomic data reveals coordinated control of RNA degradation, transcription, and translation and identifies previously undefined exon-junction-derived peptides. Our study provides an invaluable resource for further mechanistic studies and suggests core factors regulating pre-implantation embryo development.


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