2011 Fiscal Year Final Research Report
Analyses of mutant mice lacking histone modification factors.
Project/Area Number |
22700451
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Laboratory animal science
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Research Institution | Kanazawa University |
Principal Investigator |
NARUSE Chie 金沢大学, 学際科学実験センター, 助教 (30372486)
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Project Period (FY) |
2010 – 2011
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Keywords | 発生・分化 / 生殖細胞 / マウス / ヒストン修飾 / 遺伝子改変動物 |
Research Abstract |
We generated HP1 gamma mutant mice and found that histone methylation at pericentromeric heterochromatin was reduced in the mutant germ cells at meiosis. Next, we found that HP1 gamma is essential for cell cycle progression of primordial germ cells(PGC). Moreover, we found that histone demethylase regulates expression of Hox genes, and the demethylase-deficient mice died perinatally.
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[Journal Article] HP1γlinks histone methylation marks to meioticsynapsis in mice2011
Author(s)
Takada Y, Naruse C, Costa Y(* equal contribution), Shirakawa T, Tachibana M, Sharif J, Kezuka-Shiotani F, Kakiuchi D, Masumoto H, Shinkai Y, Ohbo K, Peters AH, Turner JM, Asano M and Koseki H
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Journal Title
Development
Volume: 138
Pages: 4207-17
DOI
Peer Reviewed
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[Presentation] β4-galactosyltransferase-5 is a lactosylceramide synthase essential for mouse extra-embryonic development2010
Author(s)
Toshikazu Nishie, Yoko Hikimochi, Kota Zama, Yoshiyasu Fukusumi, Mitutoshi Ito, Haruka Yokoyama, Chie Naruse, Makoto Ito, and Masahide Asano
Organizer
BMB2010
Place of Presentation
Kobe Portisland(Kobe Convention Center, Kobe, Hyogo)
Year and Date
2010-12-10
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