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Human genetical studies on native minority groups (Kouzan-Zoku) in Taiwan

Research Project

Project/Area Number 02041095
Research Category

Grant-in-Aid for international Scientific Research

Allocation TypeSingle-year Grants
SectionField Research
Research InstitutionNational Institute of Genetics

Principal Investigator

HORAI Satoshi  National Institute of Genetics, 総合遺伝研究系, 助教授 (40126157)

Co-Investigator(Kenkyū-buntansha) 潘 以宏  台湾大学, 医学院・微生物学, 教授
SAITOU Naruya  National Institute of Genetics, 集団遺伝研究系, 助教授 (30192587)
ISHIDA Takafumi  The University of Tokyo, 理学部, 助手 (20184533)
PAN I-Hung  National University of Taiwan
Project Period (FY) 1991 – 1992
Project Status Completed (Fiscal Year 1991)
Budget Amount *help
¥4,000,000 (Direct Cost: ¥4,000,000)
Fiscal Year 1991: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1990: ¥2,000,000 (Direct Cost: ¥2,000,000)
KeywordsHuman Genetics / Population Genetics / Taiwan aborigines / Blood Groups / Mitochondrial DNA / HTLV-I / Miltenberger
Research Abstract

This study was conducted in 1990 and 1991. Taiwan aborigines are classified into nine tribes based on the cultural and linguistic differences. The objectives of the present study were threefold ; (1) to describe the genetic characteristics of each tribe by using various genetic markers, (2) to clarify the genetic relationship of these Taiwan aborigines by comparing them with other human populations, and (3) to preserve the precious samples thorough immortalized lymphocyte cell lines.
We obtained blood samples from five Southern Taiwan tribes and from Yami tribe, who lives in Orchid lsland from the field survey of 1990. We conducted the field survey in 1991 to collect blood samples from the remaining three populations (Tayal, Tsuo, and Sayshat). Sample size exceeded the minimum requirement (40 individuals) for all the populatiofis surveyed. The results of our preliminary analyses are as follows.
(1) A total of ten blood groups were examined. The blood group study was a collaboration with … More Japanese Red Cross Central Blood Center. The most significant finding was the high prevalence of Miltenberger-positive individuals ; 90% for Ami (highest in the world) and 50% for Yami. Genetic distance analysis was also conducted and a large difference among the nine Taiwan aboriginal tribes were observed. This suggests that these aboriginal populations have been genetically isolated until recently.
(2) Existence of antibody for HTLV-I was examined, and only one individual of Tayal tribe was positive. Selected blood samples were EB-transformed and now we have more than 100 immortalized lymphocyte cell lines.
(3) Asian-specific 9-base pair deletion was examined for mitochondrial DNA. The frequency of this type varied substantially ; the lowest was 3% for Tayal and the highest was 46% for Yami and Tsuo. The average frequency (28%) is the highest among the East Asian populations examined so far. D-loop region of mitochondrial DNA were sequenced for selected samples, and aphylogenetic tree was constructed. The tree suggests that Taiwan aborigines have a characteristic of Southern Mongoloid. Less

Report

(3 results)
  • 1991 Annual Research Report   Final Research Report Summary
  • 1990 Annual Research Report
  • Research Products

    (23 results)

All Other

All Publications (23 results)

  • [Publications] K.Hayasaka et al.: "Heteroplasmy and polymorphisms in the major nonーcoding region of mitochondrial DNA in Japanese monkeys:Association with tandemly repeated sequences" Mol.Biol.Evol.8(4). 399-415 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] M.Hasegawa et al.: "Time of the deepest root for polymorphisms in human mitochondrial DNA." J.Mol.Evol.32. 37-42 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Horai et al.: "Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNA" Phil.Trans.R.Soc.Lond.B.333. 409-417 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] Y.Goto et al.: "A new mtDNA mutation associated with mitochondrial myopathy,encephalopathy,lactic acidosis and strokeーlike episodes(MELAS)." Biochimica et Biophysica Acta.1097. 238-240 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Miyabayashi et al.: "A new type of mitochondrial DNA deletion in patients with encephalomyopathy." J.Inher.Metab.Dis.14. 805-812 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] Y.NakagawaーHattori et al.: "Is Parkinson's disease a mitochondrialdisorder?" J.Neurol.Sci.107. 29-33 (1992)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Horai: "New aspects of the genetics of molecular evolution" M.Kimura and N.Takahata eds.Japan Sci.Soc.Press,Tokyo/SpringerーVerlag,Berlin., 135-152 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S.Horai: "New era of bioenergetics." Y.Mukohata.eds.Academic Press,Tokyo., 273-299 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Horai et al.: "Phylogenetic affiliation of ancient and contemporary human inferred from mitochondrial DNA." Phyl. Trans. Roy. Soc. London B. 333. 409-417 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] K. Hayasaka et al.: "Heteroplasmy and polymorphisms in the major noncoding region of mitochondrial DNA in Japanese monkeys : Association with tandemly repeated sequences." Mol. Biol. Evol.8. 399-415 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] M. Hasegawa et al.: "Time of the deepest root for polymorphisms in human mitochondrial DNA." J. Mol. Evol.32. 37-42 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] Y. Goto et al.: Biochimica et Biophysica Acta. 1097. 238-240 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Miyabayashi et al.: "A new type of mitochondrial DNA deletion in patients with encephalomyopathy." J. Inher. Metab. Dis.14. 805-812 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Horai: Japan Sci. Soc. Press, Tokyo. New aspects of the genetics of molecular evolution, 135-152 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] S. Horai: Academic Press, Tokyo. New era of bioenergetics, 273-299 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1991 Final Research Report Summary
  • [Publications] M.Hasegawa et al.: "Mitochondrial DNA evolution in primates:Transition rate has been extremely low in lemur." J.Mol.Evol.31. 113-121 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] S.Horai et al.: "Intraspecific nucleotide sequence differences in the major noncoding region of human mitochodrial DNA." Am.J.Hum.Genet.46. 828-842 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Y.Goto et al.: "Chronic progressive external ophthalmoplegia:A correlative study of mitochondrial DNA deletions and their phenotypic exression in muscle biopsies." J.Neurol.Sci.100. 63-69 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] M.Hasegawa et al.: "Time of the deepest root for polymorphisms in human mitochondrial DNA." J.Mol.Evol.32. 37-42 (1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] M.Yoneda et al.: "A common mitochondrial DNA mutation in the tーRNA^<Lys> of patients with myoclonus epilepsy associated with raggedーred fibers." Biochem.Int.21ー5. 789-796 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Y.Goto et al.: "A mutation in the tRNA^<Leu(UUR)> gene associated with the MELAS subgroup of mitochondrial encephalopathies." Nature.348. 651-653 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] S.Horai: "M.Kimura and N.Takahata eds.Japan Sci.Soc.Press,Tokyo/SpringerーVerlag,Berlin." New aspects of the genetics of molecular evolution., 322 (1991)

    • Related Report
      1990 Annual Research Report
  • [Publications] S.Horai et al.: "Royal Sciety,London." Biomolecular Palaeontology,Philosophical Transations of Royal Society,B.,

    • Related Report
      1990 Annual Research Report

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Published: 1990-04-01   Modified: 2016-04-21  

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