• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Molecular analysis of Genetic Polymorphisms in Blood and Development of Primers for Genotyping

Research Project

Project/Area Number 09557038
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section展開研究
Research Field Legal medicine
Research InstitutionTottori University

Principal Investigator

YUASA Isao  Department of Legal Medicine, Faculty of Medicine, Tottori University, Assistant Professor, 医学部, 講師 (00093633)

Co-Investigator(Kenkyū-buntansha) IKEBUSHI Jun  Department of Legal Medicine, Faculty of Medicine, Tottori University, Research Associate, 医学部, 助手 (30150361)
UMETSU Kazuo  Department of Forensic Medicine, Yamagata University School of Medicine, Associate Professor, 医学部, 助教授 (10091828)
Project Period (FY) 1997 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥11,900,000 (Direct Cost: ¥11,900,000)
Fiscal Year 1999: ¥1,800,000 (Direct Cost: ¥1,800,000)
Fiscal Year 1998: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1997: ¥8,200,000 (Direct Cost: ¥8,200,000)
KeywordsRed cell antigen types / Serum protein types / Red cell enzyme types / Nucleotide sequences / DNA polymorphisms / Primers / Paternity tests / 塩基配列
Research Abstract

In this projects we have investigated the molecular bases of classical genetic markers in blood to propose simple and rapid genotyping methods. We analyzed (1)ABO, RH and Diego blood group systems as red cell antigens, (2)orosomucoid (alpha-1-acid glycoprotein), group-specific component, inter-alpha-trypsin inhibitor, the R subcomponent of the first component of component, the seventh component of complement, alpha-1-antitrypsin, and the B unit of coagulation factor XIII as serum proteins (3)phosphoglucomutase 1, eaterase D, DNase 1, acetaldehyde dehydrogenase 2, and phosphomannomutase 2 as red cell and other cell enzymes. We also analyzed some null alleles (ORM1ィイD1*ィエD1Q0koln and ITIH1ィイD1*ィエD1Q0iwate), which could cause a false incompatibility between father and child. A nucleotide substitution of de novo mutation, observed in the group-specific component in a German paternity case, was determined. The findings obtained in this study will be useful not only in forensic science but also biological and medical sciences.

Report

(4 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • 1997 Annual Research Report
  • Research Products

    (53 results)

All Other

All Publications (53 results)

  • [Publications] Watanabe, G.: "Amplified product length, polymorphism, (APLP) : a novel strategy for genotyping the ABO blood group"Human Genetics. 99. 34-37 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yuasa, I.: "Human orosomucoid polymorphism : molecular basis of the three common ORM1 alleles, ORM1^*F1, ORM1^*F2, and ORM1^*S"Human Genetics. 99. 397-398 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakayashiki, N.: "ITIH1^*Q0 imate, a null allele of inter alpha-trypsin inhibitor H1 caused by deletion/frameshift mutation"Japanese Journal of Human Genetics. 42. 363-368 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Yuasa, I.: "Simple and rapid determination of the acetaldehyde dehydrogenase (ALDH2) genotypes by nonradioactive single-strand conformation polymorphism analysis"Electrophoresis. 18. 1940-1941 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Weidinger, S.: "Detection of a de novo mutation in the GC system by DNA sequence analysis"Progress in Forensic Haemogenetics. 7. 240-242 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakamura, H.: "Molecular analysis of human orosomucoid gene : ORM1^*Q0 Koln responsible for the incompatibility in a German paternity case"International Journal of Legal Medicine. (印刷中).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] G.Watanabe, K.Umetsu, I.Yuasa, T.Suzuki: "Amplified product length polymorphism (APLP) : a novel strategy for genotyping the ABO blood group"Human Genetics. 99(1). 34-37 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.M.Sebetan, S.Oshida, I.Yuasa: "Genetic polymorphisms of orosomucoid ORM1 and ORM2 in Egyptians, Sudanese, and Qataris : occurrence of two new alleles"Human Biology. 69(1). 121-129 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.Yuasa, K.Umetsu, U.Vogt, H.Nakamura, E.Nanba, N.Tamaki, Y.Irizawa: "Human orosomucoid polymorphism : molecular basis of the three common ORM1 alleles, ORM1ィイD1*ィエD1F1, ORMィイD1*ィエD1F2, and ORM1ィイD1*ィエD1S"Human Genetics. 99(3). 393-398 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Y.Murawaki, H.Sugisaki, I.Yuasa, H.Kawasaki: "Serum carbohydrate deficient transferrin in patients with nonalcoholic liver disease and with hepatocellular carcinoma"Clinica Chimica Acta. 259(1-2). 97-108 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] T.Yasuda, H.Takeshita, R.Iida, I.Yuasa, K.Kishi: "Population studies of human deoxyribonuclease I polymorphism"Human Heredity. 47(3). 121-124 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] N.Nakayashiki, M.Ding, K.Umetsu, I.Yuasa, T.Suzuki, Y.Aoki: "ITIH1ィイD1*ィエD1Q0ィイD2iwateィエD2, a null allele of inter-alpha-trypsin inhibitor H1 caused by deletion/frameshift mutation"Japanese Journal of Human Genetics. 42(2). 363-368 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] G.Watanabe, K.Umetsu, I.Yuasa, U.Vogt, T.Suzuki: "Nucleotide substitution in the 5'flanking region of D1S80 locus"Forensic Science International. 89(1-2). 75-80 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] R.Iida, T.Yasuda, M.Aoyama, E.Tsubota, M.Kobayashi, I.Yuasa, T.Matsuki, K.Kishi: "The fifth allele of the human deoxyribonuclease I (DNase I) polymorphism"Electrophoresis. 18(11). 1936-1939 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.Yuasa, K.Umetsu, M.Nakagawa, J.Ikebuchi, T.Inoue, Y.Irizawa: "Simple and rapid determination of the acetaldehyde dehydrogenase (ALDH2) genotypes by nonradioactive single-strand conformation polymorphism analysis"Electrophoresis. 18(11). 1940-1941 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Y.Tomie, Y.Horie, F.Tajima, S.Kitaoka, E.Nanba, I.Yuasa, H.Kawasaki: "Mutation in the exon 10 (R173W) of the hydroxymethylbilane synthase gene in two unrelated Japanese families with acute intermittent porphyria"Research Communications in Molecular Pathology and Pharmacology. 99(1). 5-15 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] T.Aoshima, K.Umetsu, I.Yuasa, G.Watanabe, T.Suzuki: "Simultaneous genotyping of alcohol dehydrogenase 2 (ADH2) and aldehyde dehydrogenase (ALDH2) loci by amplified product length polymorphism (APLP) analysis"Electrophoresis. 19(5). 659-660 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] G.Watanabe, K.Umetsu, I.Yuasa, T.Suzuki: "Simultaneous determinations of STR polymorphism and a new nucleotide substitution in its flanking region at the CD4 locus"Journal of Forensic Sciences. 43(4). 733-737 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Akaba, T.Kimura, A.Sasaki, S.Tanabe, T.Ikegami, M.Hashimoto, H.Umeda, H.Yoshida, K.Umetsu, H.Chiba, I.Yuasa, K.Hayasaka: "Neonatal hyperbillirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene : a common missense mutation among Japanese, Korean and Chinese"Biochemistry and Molecular Biology International. 46(1). 21-26 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] S.Ichisaka, K.Ohno, I.Yuasa, E.Nanba, H.Sakuraba, Y.Suzuki: "Increased expression of beta-hexosaminidase alpha chain in cultured skin fibroblasts from patients with carbohydrate-deficient glycoprotein syndrome type I"Brain and Development. 20(5). 302-306 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Ago, I.Yuasa, O.Tsuganezawa: "Transferrin polymorphism in the Nansei Islands : Description of a new variant TF Dama and clines of allele frequencies in Japanese populations"Anthropological Science. 106(3). 209-219 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Ago, I.Yuasa, O.Tsuganezawa: "Distribution of group-specific component/vitamin D-binding protein alleles in Southwestern Japan and geographical clines of allele frequencies in Japanese populations"Anthropological Science. 106(4). 385-395 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.Kondo, K.Mizugishi, Y.Yoneda, T.Hashimoto, K.Kuwajima, I.Yuasa, K.Shigemoto, Y.Kuroda: "Missense mutations in phosphomannomutase 2 gene in two Japanese families with carbohydrate-deficient glycoprotein syndrome type 1"Clinical Genetics. 55(1). 50-54 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] H.Zhang, T.Yamamoto, E.Nanba, Y.Kitamura, T.Terada, S.Akaboshi, I.Yuasa, K.Ohtani, S.Nakamoto, K.Takeshita: "Novel TSC2 mutation in a patient with pulmonary tuberous sclerosis : lack of loss of heterozygosity in a lung cyst"American Journal of Medical Genetics. 82(59. 368-370 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] M.Nakagawa, I.Yuasa, K.Umetsu, Y.Irizawa: "A new single-nucleotide polymorphism in the seventh components of complement (C7) gene"Journal of Human Genetics. 44(4). 272-273 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Mizugishi, K.Yamanaka, K.Kuwajima, I.Yuasa, K.Shigemoto, I.Kondo: "Missense mutations in the phosphomannomutase 2 gene of two Japanese siblings with carbohydrate-deficient glycoprotein syndrome type I"Brain and Development. 21(3). 223-228 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Yoshikawa, K.Umetsu, H,Shinzawa, I.Yuasa, K.Maruyama, T.Ohkura, K.Yamashita, T.Suzuki: "Determination of carbohydrate-deficient transferrin separated by lectin affinity chromatography for detecting chronic alcohol abuse"FEBS Letter. 458(2). 112-116 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] G.Watanabe, K.Umetsu, I.Yuasa, T.Suzuki: "Improved haplotype analysis of human myelin basic protein (MBP) STR loci"Human Biology. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] G.Watanabe, K.Umetsu, I.Yuasa, T.Suzuki: "DXS10011 : a hypervariable tetranucleotide STR polymorphism on the X chromosome"International Journal of Legal Medicine. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] E.Naito, K.Umetsu, I.Yuasa, K.Dewa, H.Sumi, H.Yamanouchi: "A novel dimorphism in the human SRY gene : usefulness in human migration study"International Journal of Legal Medicine. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] H.Nakamura, I.Yuasa, K.Umetsu, J.Henke, L.Henke, E.Nanba: "Molecular analysis of human orosomucoid gene : ORM1ィイD1*ィエD1Q0ィイD2kolnィエD2 responsible for the incompatibility in a German paternity case"International Journal of Legal Medicine. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] H.Nishimukai, Y.Fukumori, T.Okiura, I.Yuasa: "Genotyping of the ABO blood group system by PCR-based methods. Advances in Research on DNA Polymorphism (ISFH Hakone Symposium Program on Committee, ed.)"TOYOSHOTEN, Tokyo. 369-373 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.Yuasa, K.Umetsu, N.Tamaki, Y.Irizawa: "Molecular basis of orosomucoid-1 polymorphism. Advances in Research on DNA Polymorphism (ISFH Hakone Symposium Program on Committee, ed.)"TOYOSHOTEN, Tokyo. 387-391 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] S.Weidinger, I.Yuasa, M.Schroder, A.G.Gathof: "Detection of a de novo mutation in the GC system by DNA sequence analysis. Progress in Forensic Haemogenetics (B. Olaisen, B. Brinkmann, and P. J. Lincoln, ed.), vol.7"ELSEVIER, Netherland. 240-242 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Ago, O.Tsuganezawa, I.Yuasa: "TF polymorphism in the southwestern part of Japan and geographical clines of TF allele frequencies in Japanese populations. 6th Indo-Pacific Congress on Legal Medicine and Forensic Sciences (Y.Tatsuno, ed.)"917-920 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] H.Nakamura, I.Yuasa, K.Umetsu, J.Henke: "Molecular basis of a hybrid allele ORM2ィイD1*ィエD1L7 and a silent allele ORM1ィイD1*ィエD1Q0. 6th Indo-Pacific Congress on Legal Medicine and Forensic Sciences (Y.Tatsuno, ed.)"929-932 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Umetsu, G.Watanabe, I.Yuasa, K.Ago, N.Nakayashiki, A.Miyoshi, S.Kashimura: "Haplotype distribution of four Y-chromosome STR loci in the East Asian populations. Progress in Forensic Haemogenetics (G. F. Sensabaugh, B. Brinkmann, and P. J. Lincoln, ed.), vol.8"(in press), ELSEVIER, Netherland.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] K.Ago, I.Yuasa, K.Umetsu, O.Tsuganezawa: "Inter-alpha-trypsin inhibitor polymorphism in Southwestern Japan : Geographical clines allele frequencies in Japanese populations. Progress in Forensic Haemogenetics (G. F. Sensabaugh, B. Brinkmann, and P. J. Lincoln, ed.), vol.8"(in press), ELSEVIER, Netherland.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] I.Yuasa, K.Umetsu, E.Naito, A.Miyoshi, K.Ago, Y.Irizawa: "Distribution of a C-to-T polymorphism in the sex-determining region Y (SRY) gene. Progress in Forensic Haemogenetics (G. F. Sensabaugh, B. Brinkmann, and P. J. Lincoln, ed.), vol.8"(in press), ELSEVIER, Netherland.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] Nakagawa M: "A new single-nucleottde polymorphism in the seventh component of complement(C7)gene"Journal of Human Genetics. 44・4. 272-273 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Watanabe G: "Improved naplotype analysis of humcm myelin basic prptein (MBP)STR Coci"Human Biology. (印刷中).

    • Related Report
      1999 Annual Research Report
  • [Publications] Kondo I: "Missense mutations in phosphomannomutase 2 goue in two Japanese famuilies with carlo by drele dficiount glycopreke syndome"Clinical Genetics. 55・1. 50-54 (1999)

    • Related Report
      1999 Annual Research Report
  • [Publications] Watanabe G: "DXSIOOII; a lyper vavioffe tetra nucbtide STR polymorphism on the Xtbrcmosome"International Journal of Legal Meicine. (印刷中).

    • Related Report
      1999 Annual Research Report
  • [Publications] Nakamura H: "Mole culor analysis of Iwman orosoinucoid gene ORMA*00 responsible for ** incompatibility in a heman petcnitycans"International Journal of Legal Meicine. (印刷中).

    • Related Report
      1999 Annual Research Report
  • [Publications] Yuasa I: "Distribution of a C-to-T polymorphism in the sex determininy segion Y (SRY)gene"progress in Forensic Haematogenetics. (印刷中).

    • Related Report
      1999 Annual Research Report
  • [Publications] Neidinger S: "Detection of a de novo mutation in the Gc system by DNA sepuence analysis" Progress in Forensic Genetics. 7. 240-242 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Aoshima T: "Simultareous genotyping of clcoholadhytro gonase 2 (ADH2) and aldeleyle dehyduogsnase 2 (ACDH2) loci by amplitied product leugthpolyHorphism (APCP)analasis" Elecpophoresis. 19・5. 659-660 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] 中村博明: "オロソムコイド変異型の遺伝子解析-ORM2座の対立遺伝子について" DNA多型. 6. 36-39 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Yasuda,T: "Population studies of Human deoxyribonuclease I polymorphism" Human Heredity. 47・3. 121-124 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Nakayashiki N: "ITIHI^*QOiwale a null allele of inter-alpha-typsin inhibitor H1 caused by deletion 1 frameshift mutation" Japanese Journal of Human Genetics. 42・2. 363-368 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] 湯浅 勲: "Diego血液型システムのDI1とDI2の遺伝子タイピング" DNA多型. 5. 254-257 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yuasa,I: "Simple and rapid determination of the acetaldehyde dehydrogenase (ALDH2) genotypes by nonradioactive single-strand conformation polymorphism analysis" Electrophoresis. 18・11. 1940-1941 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Iida,R: "The fifth allele of the human deoxyribonuclease I (DNase I)polymorphism" Electrophoresis. 18・11. 1936-1940 (1997)

    • Related Report
      1997 Annual Research Report

URL: 

Published: 1997-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi