| Project/Area Number |
14360170
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Applied animal science
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| Research Institution | TOKYO UNIVERSITY OF AGRICULTURE |
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Principal Investigator |
KONO Tomohiro TOKYO UNIVERSITY OF AGRICULTURE, DEPARTMENT OF BIOSCIENCE, PROFESSOR, 応用生物科学部, 教授 (80153485)
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| Co-Investigator(Kenkyū-buntansha) |
MIYANO Takashi KOBE UNIVERSITY, DEPARTMENT OF AGRICULTURE, PROFESSOR, 農学部, 教授 (80200195)
HATADA Izuho GUNMA UNIVERSITY, GENE RESEARCH CENTER, ASSOCIATE PROFESSOR, 遺伝子実験施設, 助教授 (50212147)
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| Project Period (FY) |
2002 – 2003
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| Project Status |
Completed (Fiscal Year 2003)
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| Budget Amount *help |
¥15,000,000 (Direct Cost: ¥15,000,000)
Fiscal Year 2003: ¥6,500,000 (Direct Cost: ¥6,500,000)
Fiscal Year 2002: ¥8,500,000 (Direct Cost: ¥8,500,000)
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| Keywords | Oocytes / Nuclear transfer / Genomic imprinting / In vitro culture / Development / 体外培養 |
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| Research Abstract |
In this study we evaluated epigenetic modification during oocyte growth in mice and pig in relation to in vitro production of oocytes. The results obtained were summarized as follows. 1)Production system for competent oocytes commencing from day 12.5 fetal ovaries has been developed in vitro. The fetal ovary with mesonephroi was cultured in vitro for 8 days, and followed by 10 days culture after removal of mesonephroi. Developed follicles were dissected and collected from the ovaries, and then the follicles were further cultured for 11 days. Finally, oocytes developed over 60μm in diameter were obtained. 2)To evaluate epigenetic status, methylation status of the differentially methylated region of Igf2r, Zac1 and H19 genes were analyzed in the in vitro produced oocytes. The results showed that oocytes acquired appropriate epigenetic modification during their growth period in vitro. Nuclear transfer study revealed that the genome derived from in vitro produced oocytes was competent to support normal development. 3)In pig, significantly small oocytes, which were collected from adult ovary, were applied for in vitro culture and the full size oocytes were successfully obtained. 4)Molecular analysis for parental imprinting, we detected that 27 of imprinted genes are epigenetically modified in the female germ line. Together, the present study show that genomic imprinting in female germ line plays definitive role for supporting normal development.
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