2009 Fiscal Year Final Research Report
An evolution of mammalian viviparity by retrotransposon
Project/Area Number |
20770002
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Genetics/Genome dynamics
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Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
ONO Ryuichi Tokyo Medical and Dental University, 難治疾患研究所, 助教 (10401358)
|
Project Period (FY) |
2008 – 2009
|
Keywords | レトロトランスポゾン / 胎盤 |
Research Abstract |
I have previously identified Peg10 as a novel imprinted gene. Moreover, I have confirmed that Peg10 is a retrotransposon-derived gene and have an essential function for placental development. In this grant, to reveal the mechanism of Peg10 function in placenta, I have established Peg10 KO TS (Trophoblast Stem) cell lines from Peg10 KO mice. By comparing the gene expression between Peg10 KO TS cell lines and wild type TS cell lines, I could succeed in the isolation of Peg10 down regulated genes. These genes must be important for the evolution of mammalian viviparity.
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