Project/Area Number |
14207022
|
Research Category |
Grant-in-Aid for Scientific Research (A)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Legal medicine
|
Research Institution | University of Fukui (2004-2005) 福井医科大学 (2002-2003) |
Principal Investigator |
MATSUKI Takasumi University of Fukui, Faculty of Medicine, Dept.Forensic Medicine and Human Genetics, Professor, 医学部, 教授 (10126617)
|
Co-Investigator(Kenkyū-buntansha) |
IIDA Reiko University of Fukui, Faculty of Medicine, Dept.Forensic Medicine and Human Genetics, Assist.Prof, 医学部, 助手 (40139788)
TAKATSUKA Hisakazu University of Fukui, Faculty of Medicine, Dept.Forensic Medicine and Human Genetics, Assist.Prof, 医学部, 助手 (40242490)
|
Project Period (FY) |
2002 – 2005
|
Project Status |
Completed (Fiscal Year 2005)
|
Budget Amount *help |
¥41,730,000 (Direct Cost: ¥32,100,000、Indirect Cost: ¥9,630,000)
Fiscal Year 2005: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2004: ¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2003: ¥12,870,000 (Direct Cost: ¥9,900,000、Indirect Cost: ¥2,970,000)
Fiscal Year 2002: ¥20,410,000 (Direct Cost: ¥15,700,000、Indirect Cost: ¥4,710,000)
|
Keywords | DXS10011 / Yfm1 / DYS441 / DYS442 / DYS443 / DYS444 / Mpv17-like protein / mitochondrial DNA / 遺伝子 / 社会医学 / 遺伝子多型 / Y-STR / 年齢依存性マーカー / ミトコンドリアDNA / DYS441〜DYS445 / 陳旧・混合資料 / deoxyribonuclease I / ミトコンドリアDNA定量 / マウス脳 / M-LP(Mpv17-like protein) / DYS445 / DNA多型 / Multiplex PCR |
Research Abstract |
1. Development and application of DNA polymorphic markers We collected 869 chromosome data on our developed marker DXS10011, and found three new mutants. Our developed DNA marker Yfm1 was localized on long arm of Y chromosome as a multi-copy polymorphic marker. New five short tandem repeats markers on Y chromosome (DYS441, DYS442, DYS443, DYS444, DYS445) were found and developed multiplex PCR method. The multiplex PCR method for these STR markers was useful for forensic materials like old samples or mixed samples, and applicable on the distinction of the race from Japanese, white American and African American. 2. Development of age related markers for forensic medicine We found new and functionally unknown gene named as M-LP (Mpv17-like protein) on mouse kidney and spleen by differential display method. The M-LP gene was expressed as age dependent manner, and possibly regulated activities and gene expressions of antioxidant enzymes from experiments of the M-LP gene expressions in COS-7 cells. We developed a new method for the estimation of mitochondrial DNA (mtDNA) amounts on mouse organs. Amounts of mtDNA in bone marrow, spleen and lung were relatively low, and relatively high in heart and skeletal muscles. Amounts of mtDNA, translational products of mtDNA and protein expressions of mtDNA showed gradual increase according to aging in heart, lung, kidney, spleen and skeletal muscles.
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