Proteomic analysis of male 4C germ cell proteins involved in mouse meiosis
Male meiosis is a specialized type of cell division that gives rise to sperm. Errors in this process can result in the generation of aneuploid gametes, which are associated with birth defects and infertility in humans. Until now, there has been a lack of a large-scale identification of proteins invo...
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Published in: | Proteomics (Weinheim) Vol. 11; no. 2; pp. 298 - 308 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
Wiley-VCH Verlag
01-01-2011
WILEY-VCH Verlag WILEY‐VCH Verlag Wiley-VCH Wiley Subscription Services, Inc |
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Online Access: | Get full text |
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Summary: | Male meiosis is a specialized type of cell division that gives rise to sperm. Errors in this process can result in the generation of aneuploid gametes, which are associated with birth defects and infertility in humans. Until now, there has been a lack of a large-scale identification of proteins involved in male meiosis in mammals. In this study, we report the high-confidence identification of 3625 proteins in mouse male germ cells with 4C DNA content undergoing meiosis I. Of these, 397 were found to be testis specific. Bioinformatics analysis of the proteome led to the identification of 28 proteins known to be essential for male meiosis in mice. We also found 172 proteins that had yeast orthologs known to be essential for meiosis. Chromosome distribution analysis of the proteome showed underrepresentation of the identified proteins on the X chromosome, which may be due to meiotic sex chromosome inactivation. Characterization of the proteome of 4C germ cells from mouse testis provides an inventory of proteins, which is useful for understanding meiosis and the mechanisms of male infertility. |
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Bibliography: | http://dx.doi.org/10.1002/pmic.200900726 973 program - No. 2011CB944304 istex:6A74F684E079C7EBF01480A33A3B72288317B203 ark:/67375/WNG-NFJP9J8P-P ArticleID:PMIC200900726 Chinese Natural Science Funds - No. 30630030 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 1615-9853 1615-9861 1615-9861 |
DOI: | 10.1002/pmic.200900726 |