Publication date: 26 December 2017
Source:Cell Reports, Volume 21, Issue 13
Author(s): Yawei Gao, Xiaoyu Liu, Bin Tang, Chong Li, Zhaohui Kou, Lin Li, Wenqiang Liu, You Wu, Xiaochen Kou, Jingyi Li, Yanhong Zhao, Jiqing Yin, Hong Wang, She Chen, Lujian Liao, Shaorong Gao
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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Proteomic analysis of pre-implantation embryos has not been explored for the minimal amount of material available. Gao et al. used a quantitative mass spectrometry strategy to elucidate the dynamic changes of the embryo proteome from the zygote to the blastocyst stage, which provides direct insight into the molecular details governing embryonic development.http://ift.tt/2E20Plg
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