2010 Fiscal Year Final Research Report
Roles of an RNA-binding protein MBNL1 in polyglutamine diseases
Project/Area Number |
21790854
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Neurology
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Research Institution | The Institute of Physical and Chemical Research |
Principal Investigator |
KINO Yoshihiro The Institute of Physical and Chemical Research, 構造神経病理研究チーム, 研究員 (80415140)
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Project Period (FY) |
2009 – 2010
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Keywords | RNA結合タンパク質 / 神経変性疾患 / MBNL1 / CAGリピート / 筋強直性ジストロフィー / 選択的スプライシング / ポリグルタミン |
Research Abstract |
In CAG repeat expansion diseases including Huntington's disease, mutant proteins with an expanded polyglutamine tract are thought to have toxic effects in the cells. It is also possible that expanded CAG repeat RNA has toxicity in these diseases. MBNL1 is an RNA-binding protein that interacts with expanded CAG repeat RNA and can be involved in the RNA metabolisms of diseases caused by CAG/CTG repeat expansion. This study identified the effects of MBNL1 on the metabolisms of mutant RNA associated with repeat expansion diseases.
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[Journal Article] Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein.2010
Author(s)
Bauer PO, Goswami A, Wong HK, Okuno M, Kurosawa M, Yamada M, Miyazaki H, Matsumoto G, Kino Y, Nagai Y, Nukina N.
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Journal Title
Nature Biotechnologyz 28
Pages: 256-263
Peer Reviewed
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