2012 Fiscal Year Final Research Report
Molecular mechanism of transcriptional regulation forDNA repair genes: Identification of partner proteins for CXXC5, a novel MLH1 transcriptional factor
Project/Area Number |
22591495
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Digestive surgery
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Research Institution | Toho University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
KANNO Shin-ichiro 東北大学, 加齢医学研究所, 講師 (10400417)
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Project Period (FY) |
2010 – 2012
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Keywords | 小腸大腸肛門外科学 |
Research Abstract |
In this study, CXXC5, DNA-binding protein recognizing the FP3CAT site of MLH1 promoter, was identified as an activator of MLH1 transcription. Co-immunoprecipitation and LC/MS/MS analysis revealed that CXXC5 and SYF2, previously screened as an FP3 site-binding protein, share common interacting protein HNRNPH1 and may co-operatively trans-activate MLH1. In hypoxia, all three protein levels were down-regulated and endogenous over-expression of them partially rescued MLH1 down-regulation. Hypoxic down-regulationof MLH1 may be mediated by CXXC5, SYF2, and HNRNPH1.
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[Journal Article] Down-regulation of MutS homolog 3 by hypoxia in human colorectal cancer2012
Author(s)
Li J, Koike J, Kugoh H, Arita M, Ohhira T, Kikuchi Y, Funahashi K, Takamatsu K, Boland CR, Koi M, Hemmi H
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Journal Title
Biochim Biophys Acta
Volume: 1823
Pages: 889-99
DOI
Peer Reviewed
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[Presentation] ヒト尿細管上皮細胞におけるブドウ糖,ヒト血清アルブミンによる ACE2 発現の変化2010
Author(s)
青木敏行,水入苑生,有田通恒,逸見仁道,大谷隆俊,鈴木康紀,服部吉成,田中仁英,大橋靖,酒井謙,相川厚
Organizer
第53回日本腎臓学会総会
Place of Presentation
神戸
Year and Date
2010-06-16