Literature DB >> 20876089

Proteome of mouse oocytes at different developmental stages.

Shufang Wang1, Zhaohui Kou, Zhiyi Jing, Yu Zhang, Xinzheng Guo, Mengqiu Dong, Ian Wilmut, Shaorong Gao.   

Abstract

The mammalian oocyte possesses powerful reprogramming factors, which can reprogram terminally differentiated germ cells (sperm) or somatic cells within a few cell cycles. Although it has been suggested that use of oocyte-derived transcripts may enhance the generation of induced pluripotent stem cells, the reprogramming factors in oocytes are undetermined, and even the identified proteins composition of oocytes is very limited. In the present study, 7,000 mouse oocytes at different developmental stages, including the germinal vesicle stage, the metaphase II (MII) stage, and the fertilized oocytes (zygotes), were collected. We successfully identified 2,781 proteins present in germinal vesicle oocytes, 2,973 proteins in MII oocytes, and 2,082 proteins in zygotes through semiquantitative MS analysis. Furthermore, the results of the bioinformatics analysis indicated that different protein compositions are correlated with oocyte characteristics at different developmental stages. For example, specific transcription factors and chromatin remodeling factors are more abundant in MII oocytes, which may be crucial for the epigenetic reprogramming of sperm or somatic nuclei. These results provided important knowledge to better understand the molecular mechanisms in early development and may improve the generation of induced pluripotent stem cells.

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Year:  2010        PMID: 20876089      PMCID: PMC2955136          DOI: 10.1073/pnas.1013185107

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  52 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-12       Impact factor: 11.205

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7.  Essential role of STAT3 for embryonic stem cell pluripotency.

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  93 in total

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5.  Integrated Analysis of Quantitative Proteome and Transcriptional Profiles Reveals the Dynamic Function of Maternally Expressed Proteins After Parthenogenetic Activation of Buffalo Oocyte.

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6.  Germ-Cell-Specific Inflammasome Component NLRP14 Negatively Regulates Cytosolic Nucleic Acid Sensing to Promote Fertilization.

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8.  Systems genetics implicates cytoskeletal genes in oocyte control of cloned embryo quality.

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9.  The E3 ubiquitin ligase RNF114 and TAB1 degradation are required for maternal-to-zygotic transition.

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Review 10.  Cell signaling and transcription factors regulating cell fate during formation of the mouse blastocyst.

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