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2014 Fiscal Year Final Research Report

Molecular mechanism for multipotency of stem cells

Planned Research

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Project AreaNeural Diversity and Neocortical Organization
Project/Area Number 22123002
Research Category

Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)

Allocation TypeSingle-year Grants
Review Section Biological Sciences
Research InstitutionKyoto University

Principal Investigator

KAGEYAMA Ryoichiro  京都大学, ウイルス研究所, 教授 (80224369)

Project Period (FY) 2010-04-01 – 2015-03-31
Keywords神経幹細胞 / ヒストンメチル化酵素 / ESET/Setdb1 / 分化決定因子 / Hes1 / 発現振動
Outline of Final Research Achievements

Embryonic neural stem cells give rise to various types of neurons first and glial cells later. Thus, embryonic neural stem cells change their competency during development, but the detailed mechanism is not known. We found that in multipotent neural stem cells, multiple fate determination factors are expressed in an oscillatory manner, and that the expression of the histone methyl transferase ESET, which regulates neuronal and glial gene expression, gradually decreases during development. Because the ESET gene promoter contains multiple binding sites for Hes1, one of the fate determination factors, it was suggested that Hes1 oscillation regulates temporal changes of competency of neural stem cells via ESET expression.

Free Research Field

分子生物学

URL: 

Published: 2016-06-03  

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