2020 Fiscal Year Final Research Report
Studies on mitochondrial long noncoding RNA
Project/Area Number |
18K06935
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Review Section |
Basic Section 48040:Medical biochemistry-related
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Research Institution | Fukushima Medical University |
Principal Investigator |
Homma Yoshimi 福島県立医科大学, 医学部, 教授 (60192324)
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Project Period (FY) |
2018-04-01 – 2021-03-31
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Keywords | ミトコンドリア / RNA |
Outline of Final Research Achievements |
Mitochondrial were purified from hepatocytes of normal C57BL/6 mice and their metabolic disease models (C57BL/6-ob, C57BL/6-db, C57BL/6-NASH), and ncRNA present in the fractions was comprehensively analyzed by RNA-seq method, and the results were registered in the GEO database. The breakdown of RNA was 92.5% for mRNA (including fragments) and 3.2% for lncRNA. There were 330 unidentified RNAs. Preliminary results obtained by the Fish method showed the presence of malat1 and lncRNA in the nucleus and mitochondrial matrix were. Human HEK293 cells were also used to identify lncRNAs contained in the respiratory chain II complex and beta-oxidation complex.
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Free Research Field |
生体機能分子医化学
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Academic Significance and Societal Importance of the Research Achievements |
最近、RNAの細胞内の動きや新しい機能について新しい発見が相次いでいる。核内遺伝子の調節に関与するRNAの報告は膨大に存在するが、ミトコンドリアに関する記述は全く無く、データベースも存在しない。今回、マウスモデルの肝ミトコンドリアに含まれるRNA情報を網羅的に解析し、データベースに登録したことで、将来、この分野の研究におおきく貢献できる。また、RNAを用いてミトコンドリア機能を回復させることも現実的と考えられ、代謝疾患の新しい治療法の開拓に道を拓く可能性を包含する。
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