Functional analyses of PATE4 in sperm maturation using genetically modified mice
Project/Area Number |
25890013
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Research Category |
Grant-in-Aid for Research Activity Start-up
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Allocation Type | Single-year Grants |
Research Field |
Laboratory animal science
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Research Institution | Osaka University |
Principal Investigator |
NODA Taichi 大阪大学, 微生物病研究所, 特任研究員(常勤) (50712551)
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Project Period (FY) |
2013-08-30 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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Keywords | 精嚢腺 / 副生殖腺 / 精子成熟 / 精巣上体 / 遺伝子改変マウス |
Outline of Final Research Achievements |
In general, cauda epididymal sperm are used for in vitro fertilization. However, in vivo, seminal vesicle secretions (SVSs) are attached to epididymal sperm when those sperm are ejaculated. To reveal the function of SVSs in vivo, male mice removed the seminal vesicle were made. Those males led to the decrease in male reproductive performance, suggesting the importance of the seminal vesicle in male fertility. Next, the function of an SVS called PATE4 (prostate and testis expression 4) was analyzed using genetically modified mice. Pate4 KO mice were created with a gene targeting method and then WT females cohabited with Pate4 KO males barely delivered newborns, indicating that Pate4 KO males tended towards subfertility. The cause of the phenotype in the Pate4 KO male will be analyzed in detail.
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Report
(3 results)
Research Products
(11 results)
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[Journal Article] Feasibility for a large scale mouse mutagenesis by injecting CRISPR/Cas plasmid into zygotes2014
Author(s)
Mashiko D, Young SA, Muto M, Kato H, Nozawa K, Ogawa M, Noda T, Kim YJ, Satouh Y, Fujihara Y, Ikawa M.
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Journal Title
Development, Growth & Differentiation
Volume: 56
Issue: 1
Pages: 122-129
DOI
Related Report
Peer Reviewed
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