2017 Fiscal Year Final Research Report
In vitro reconstitution of the initiation process of transcription-coupled nucleotide-excision repair
Project/Area Number |
26291005
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Molecular biology
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Research Institution | Nagoya University (2015-2017) Nagasaki University (2014) |
Principal Investigator |
OGI Tomoo 名古屋大学, 環境医学研究所, 教授 (80508317)
|
Co-Investigator(Kenkyū-buntansha) |
真下 知士 大阪大学, 医学系研究科, 准教授 (80397554)
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Project Period (FY) |
2014-04-01 – 2018-03-31
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Keywords | DNA修復 / 転写と共役したヌクレオチド除去修復 |
Outline of Final Research Achievements |
Transcription-coupled nucleotide-excision repair (TC-NER) is one of the versatile DNA repair process that removes major UV-induced DNA lesions from actively transcribed genes. To investigate the initiation process of TC-NER reaction, we focused on a molecular mechanism that involves DNA-damage induced ubiquitination of RNA polymerase IIo (RNA pol IIo). The process is dependent on a recently identified TC-NER factor, UVSSA. To determine the ubiquitination sites, we performed in vitro ubiquitination assay as well as SILAC-based High-Resolution Accurate Mass (HRAM) spectrometry. From the studies, we identified UVSSA-dependent ubiquitination sites required for the efficient TC-NER activity.
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Free Research Field |
DNA修復学、分子生物学
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