2012 Fiscal Year Final Research Report
Functional analysis of DNA damage response of transcription factor FOXO1 in lifespan regulation
Project/Area Number |
22688029
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Research Category |
Grant-in-Aid for Young Scientists (A)
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Allocation Type | Single-year Grants |
Research Field |
Applied molecular and cellular biology
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Research Institution | University of Tsukuba |
Principal Investigator |
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Project Period (FY) |
2010 – 2012
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Keywords | 老化 / 転写因子 / 紫外線 / DNA損傷修復 |
Research Abstract |
Transcription factor FOXO1 is known to be involved in lifespan extension and anti-aging; however, the molecular mechanism remains unclear. In this study, we found that FOXO1 contributes to tlanslesion DNA synthesis, which serves as the DNA damage response against ultra violet (UV) irradiation. Furthermore, genetic analysis using C. elegans showed that FOXO1/DAF-16 plays a crucial role in UV resistance during larval development. Our finding will help to elucidate the anti-aging mechanism of FOXO1.
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[Journal Article] Asymmetric arginine dimethylation determines life span in C. elegans by regulating forkhead transcription factor DAF-162011
Author(s)
Takahashi Y, Daitoku H, Hirota K, Tamiya H, Yokoyama A, Kako K, Nagashima Y, Nakamura A, Shimada, T, Watanabe S, Yamagata K, Yasuda K, Ishii N, Fukamizu A
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Journal Title
Cell Metab
Volume: 13
Pages: 505-516
DOI
Peer Reviewed
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