2010 Fiscal Year Final Research Report
Analyses of the mechanism that maintains cell fates in an acetylated histone-dependent manner
Project/Area Number |
21770247
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Developmental biology
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Research Institution | The Institute of Physical and Chemical Research |
Principal Investigator |
SHIBATA Yukimasa The Institute of Physical and Chemical Research, 細胞運命研究チーム, 研究員 (80314053)
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Project Period (FY) |
2009 – 2010
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Keywords | クロマチン / アセチル化ヒストン / 運命の維持 / C. elegans |
Research Abstract |
The requirement of histone acetylation in the maintenance of cell fates had not been clear. However, recently, I showed that C. elegans acetylate histone binding protein, BET-1, is required for the maintenance of cell fates. In this research project, I found that BET-1 functions through developmental determinants. In addition, their expressions appear to be regulated by histone variant, H2A.z, and histone demethylase, UTX-1.
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