2015 Fiscal Year Final Research Report
Analyses on mammalian-specific genomic function
Project/Area Number |
23221010
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Research Category |
Grant-in-Aid for Scientific Research (S)
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Allocation Type | Single-year Grants |
Research Field |
Genome biology
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Research Institution | Tokyo Medical and Dental University |
Principal Investigator |
ISHINO Fumitoshi 東京医科歯科大学, 難治疾患研究所, 教授 (60159754)
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Co-Investigator(Kenkyū-buntansha) |
KANEKO Tomoko (ISHINO Tomoko) 東海大学, 健康科学部, 教授 (20221757)
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Co-Investigator(Renkei-kenkyūsha) |
KOHDA Takashi 東京医科歯科大学, 難治疾患研究所, 准教授 (60211893)
ONO Ryuichi 東京医科歯科大学, 難治疾患研究所, 助教 (10401358)
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Project Period (FY) |
2011-04-01 – 2016-03-31
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Keywords | レトロトランスポゾン / 獲得遺伝子 / 哺乳類 / 胎盤 / 脳機能進化 / ゲノムインプリンティング / リプログラミング / 能動的脱メチル化 |
Outline of Final Research Achievements |
To elucidate "mammalian-specific epigenetic functions", we addressed two issues. From a viewpoint of mammalian-specific genetics, we analyzed biological functions of LTR retrotransposon-derived genes and demonstrated that Sirh7/Ldoc1 plays an essential role in differentiation and maturation of all types of placental cells, thereby contributing to the regulation of gestation and parturition in mice and also that Sirh11/Zcchc16 plays an important role in cognitive function, such as attention, impulsivity and space memory via regulation of noradrenaline levels in prefrontal cortex. From a viewpoint of mammalian-specific epigenetic, we demonstrated that active DNA demethylation mechanism plays an important role in imprinting memory erasure in primordial germ cells.
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Free Research Field |
分子生物学、分子発生学、エピジェネティクス
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