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Allelic variation of the human ABO secretor locus (FUT2) in the world wide populations

Research Project

Project/Area Number 14570399
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Legal medicine
Research InstitutionKURUME UNIVERSITY

Principal Investigator

TEYE Kwesi (2003)  Kurume University, Forensic Medicine, Assistant professor, 医学部, 助手 (80352128)

木村 博司 (2002)  久留米大学, 医学部, 教授 (20112039)

Co-Investigator(Kenkyū-buntansha) OKAMURA Torahiko  Kurume University, Forensic Medicine, Assistant professor, 医学部, 助手 (60343688)
SOEJIMA Mikiko  Kurume University, Forensic Medicine, Assistant professor, 医学部, 助手 (80279140)
KODA Yoshiro  Kurume University, Forensic Medicine, Professor, 医学部, 教授 (90231307)
KWESI Teye  久留米大学, 医学部, 助手 (80352128)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2003: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 2002: ¥2,700,000 (Direct Cost: ¥2,700,000)
KeywordsFUT2 / secretor / SNPs / New Guinea / Sri Lanka / variation / null allele / タミル / シンハラ / Papua New Guinea / Irianese
Research Abstract

We analyzed allelic variation of the FUT2 in New Guinean and Sri Lanka populations. Coding exon of FUT2 was sequenced about Irianese (90), Admixed Irianese (101), Papua New Guineans (32) in New Guinea and Sinhalese (54), Tamil (58) individuals in Sri Lanka. Whereas the total frequency of nonfunctional alleles at the FUT2 in many populations so far examined is around 0.5, only one individual was heterozygous for a nonfunctional allele in Irianese and a frequency of nonfunctional alleles was 0.1-0.2 in Admixed Irianese. New Guinean populations had unique functional alleles (Se^<375>, which was detected only in Africa, and Se^<400>) with high frequencies. F_<st> values indicates large genetic differentiation between New Guinean populations and other neighboring populations. These results reflects the early human migration from Africa to New Guinea and long isolation from neighboring populations. Total frequency of nonfunctional alleles was 0.38 for Sinhalese and 0.53 for Tamil populations … More and major nonfunctional alleles were different, while allelic polymorphisms of both populations were similar to that of Bangladeshi. No Asian specific null allele se^<385> was encountered while Se278, which was identified in Iraniase population, was encountered in both populations. These results suggest that genetic backgrounds of these two populations were not identical and that no or less contribution from Asian populations. We also analyzed STR located 3.8 kb downstream of the FUT2 (FUT2/01) in 300 individuals from three major races. FUT2/01 locus showed high microvariation in both African and Caucasian populations, whereas it exhibited a simple repeat structure in a Japanese population. Complex allele structures, regular grouping of structural sequences and characteristic distributions in the FUT2/01 locus demonstrated significant race differences. In addition, the African population shared a part of haplotypes with both Caucasian and Japanese populations. The results support the out-of-Africa hypothesis of modern human origins. Less

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report
  • Research Products

    (48 results)

All Other

All Publications (48 results)

  • [Publications] Pang H, Soejima M, Koda Y, Kimura H.: "A novel tetrameric short tandem repeat located in the 3'flanking region of the human ABO-Secretor gene (FUT2) and association between FUT2 and FUT2/01"Hum Biol.. (In press). (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Ishida T, Tachida H, Wang B, Pang H, Soejima M, Soemantri A, Kimura H: "DNA sequence variation of the human ABO-secretor locus (FUT2)in New Guinean populations : possible early human migration from Africa."Hum Genet.. 113. 534-541 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Tachida H, Soejima M, Takenaka O, Kimura H.: "Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene."Ann Hum Genet.. 68. 110-119 (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Quaye I, Koda Y, Soejima M, Pang H, Tsuneoka M, Amoah AG, Adjei A, Kimura H.: "A novel I247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahatolobinemia."Hum Genet.. 114. 499-502 (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Tsuneoka M, Arima N, Koda Y, Nakamura Y, Ueta Y, Shirouzu K, Kimura H: "Increase expression of a Myc target gene Mina53 in human colon cancer."Am J Pathol.. 164. 205-216 (2004)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Quaye I, Koda Y, Soejima M, Tsuneoka M, Pang H, Ekem I, Amoah A, Adjei A, Kimura H.: "A-61C and C-101G Hp gene promoter polymorphisms are, respectively associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana."Clin Genet.. 64. 439-443 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Tsuneoka M, Umata T, Kimura H, Koda Y, Nakajima M, Kosai K, Takahashi T, Takahashi Y, Yamamoto A.: "c-Myc induces autophagy in rat 3Yl fibroblast cells."Cell Struct Funct.. 28. 195-204 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Seto Y, Takeichi S, Kimura H.: "Fatal subarachnoid hemorrhage complicating actinomycotic meningitis."Forensic Sci Int.. 134. 169-171 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Amano S, Yamagishi S, Koda Y, Tsuneoka M, Soejima M, Okamoto T, Inagaki Y, Yamada K, Kimura H.: "Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy."Med Hypotheses.. 60. 550-551 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Pang H, Koda Y, Yamagishi SI, Amano S, Inagaki Y, Okamoto T, Yamada K, Kimura H.: "N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications."Diabetic Med.. 20. 419-420 (2003)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yamagishi S, Amano S, Inagaki Y, Okamoto T, Koda Y. Soejima M, Kimura H.: "Pigment epithelium-derived factor Met72Thr polymorphism in patients with diabetic icroangiopathy."Int J Clin Pharmacol Res.. 22. 67-71 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Yamagishi S, Amano S, Okamoto T, Inagaki Y, Yamada K, Kimura H.: "Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients."Diabetologia.. 45. 1039-1040 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Pang H, Koda Y, Soejima M, Kimura H.: "Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamino-phospate mutase (AGM1)."Ann Hum Genet.. 66. 139-144 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Tsuneoa M, Koda Y, Soejima M, Teye K, Kimura H.: "A novel myc target gene, mina53, that is involved in cell proliferation."J Biol Chem.. 277. 35450-35459 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Wang B, Pang H, Koda Y, Soejima M, Kimura H.: "Polymorphisms of eight STR loci in Chinese and African (Xhosa) populations."Forensic Sci Int.. 125. 279-280 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Tsuneoka M, Yasumoto K, Higashitani T, Sagawa K, Kimura H.: "Hetorozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman."Br J Haematol.. 117. 220-225 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nakayama K, Fukamachi S, Kimura H, Koda Y, Soemantri A, Ishida T.: "Distinctive distribution of AIM1 polymorphism among major human populations with different skin color."J Hum Genet.. 47. 92-94 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Sato H, Maeda Y, Kimura H.: "Three-base deletion and one-base insertion of the alpha(1,4)galactosyltransfeerase gene responsible for the phenotype."Transfusion. 42. 48-51 (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Pang H, Soejima M, Koda Y, Kimura H.: "A novel tetrameric short tandem repeat located in the 3' flanking region of the human ABO-Secretor gene (FUT2) and association between FUT2 and FUT2/01 loci."Hum Biol.. (in press). (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Tachida H, Soejima M, Takenaka O, Kimura H.: "Population differences sequence in DNA variation and linkage disequilibrium at the PON1 gene."Ann Hum Genet.. 68. 110-119 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Quaye IK, Koda Y, Soejima M, Pang H, Tsuneoka M, Amoah AG, Adjei A, Kimura H.: "A novel 1247T missense mutation in the haptoglobin 2 beta-chain decreases the expression of the protein and is associated with ahaptoglobinemia."Hum Genet.. 114. 499-502 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Tsuneoka M, Arima N, Koda Y, Nakamura Y, Ueta Y, Shirouzu K, Kimura H.: "Increased expression of a Myc target gene Mina53 in human colon cancer."Am J Pathol.. 164. 205-216 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Teye K, Quaye I, Koda Y, Soejima M, Tsuneoka M, Pang H, Ekem I, Amoah A, Adjei A, Kimura H.: "A-61C and C-101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana."Clin Genet.. 64. 439-443 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Ishida T, Tachida H, Wang B, Pang H, Soejima M, Soemantri A, Kimura H.: "DNA sequence variation of the human ABO-secretor locus (FUT2) in New Guineanpopulations : possible early human migration from Africa."Hum Genet.. 113. 534-541 (2004)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Tsuneoka M, Umata T, Kimura H, Koda Y, Nakajima M, Kosai K, Takahashi T, Takahashi Y, Yamamoto A.: "c-Myc induces autophagy in rat 3Y1 fibroblast cells. Cell"Struct Funct.. 28. 195-204 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Seto Y, Takeichi 5, Kimura H.: "Fatal subarachnoid hemorrhage Complicating actinomycotic meningitis."Forensic Sci Int.. 134. 169-171 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Amano S, Yamagishi S, Koda Y, Tsuneoka M, Soejima M, Okamoto T, Inagaki Y, Yamada K, Kimura H.: "Polymorphisms of sorbitol dehydrogenase (SDH) gene and susceptibility to diabetic retinopathy."Med Hypotheses.. 60. 550-551 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Pang H, Koda Y, Yamagishi SI, Amano S, Inagaki Y, Okamoto T, Yamada K, Kimura H.: "N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications."Diabetic Med.. 20. 419-420 (2003)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Yamagishi S, Amano S, Inagaki Y, Okamoto T, Koda Y, Soejima M, Kimura H.: "Pigment epithelium-derived factor Met72Thr polymorphism in patients with diabetic icroangiopathy."Int J Clin Pharmacol Res.. 22. 67-71 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Yamagishi S, Amano S, Okamoto T, Inagaki Y, Yamada K, Kimura H.: "Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients."Diabetologia.. 45. 1039-1040 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Pang H, Koda Y, Soejima M, Kimura H.: "Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)."Ann Hum Genet.. 66. 139-144 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Tsuneoka M, Koda Y, Soejima M, Teye K, Kimura H.: "A novel myc target gene, mina53, that is involved in cell proliferation."J Biol Chem.. 277. 35450-35459 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Wang B, Pang H, Koda Y, Soejima M, Kimura H.: "Polymorphisms of eight STR loci in Chinese and African (Xhosa)populations."Forensic Sci Int.. 125. 279-280 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Tsuneoka M, Yasumoto K, Higashitani T, Sagawa K, Kimura H.: "Heterozygosity for two novel null alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman."Br J Haematol.. 117. 220-225 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Nakayama K, Fukamachi S, Kimura H, Koda Y, Soemantri A, Ishida T.: "Distinctive distribution of AIM1 polymorphism among major human populations with different skin color."J Hum Genet.. 47. 92-94 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y, Soejima M, Sato H, Maeda Y, Kimura H.: "Three-base deletion and one-base 'insertion of the alpha( 1,4)galactosyltransferase gene responsible for the p phenotype."Transfusion.. 42. 48-51 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2003 Final Research Report Summary
  • [Publications] Koda Y et al.: "DNA sequence variation of the human ABO-secretor locus (FUT2) in New Guinean populations : possible early human migration from Africa."Human Genetics. 113. 534-541 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Teye K et al.: "A-61C and C-101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana."Clinical Genetics. 64. 439-443 (2003)

    • Related Report
      2003 Annual Research Report
  • [Publications] Koda Y et al.: "Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene."Annnals of Human Genetics. (in press). (2004)

    • Related Report
      2003 Annual Research Report
  • [Publications] H.Pang: "N-acetylglucosamine-phosphate mutase genotype and diabetic microvascular complications"Diabetic Med. (in press).

    • Related Report
      2002 Annual Research Report
  • [Publications] S.Yamagishi: "PEDF Met72Thr polymorphism in patients with diabetic microangiopathy"Int.J.Clin.Pharm.Res. (in press).

    • Related Report
      2002 Annual Research Report
  • [Publications] M.Tsuneoka: "A novel Myc target gene, mina53, that is involed in cell proliferation"J.Biol.Chem. 277. 35450-35459 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] H.Pang: "Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)"Ann.Hum.Genet. 66. 139-144 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Y.Koda: "Haptoglobin genotype and diabetic microangiopathies in Japanese diabetic patients"Diabetologia. 45. 1039-1040 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] B.Wang: "Polymorphisms of eight STR loci in Chinese and African (Xhosa) populations"Forensic Sci.Int. 125. 279-280 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Y.Koda: "Three-base deletion and one-base insertion of the α(1,4)galactosyltransferase gene responsible for the p phenotype"Transfusion. 42. 48-51 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] Y.Koda: "Heterozygosity for two novel alleles of the KEL gene causes the Kell-null phenotype in a Japanese woman"Br.J.Haematol. 117. 220-225 (2002)

    • Related Report
      2002 Annual Research Report
  • [Publications] K.Nakayama: "Distinctive distribution of AIM1 polymorphism among major human populations with different skin color"J.Hum.Genet. 47. 92-94 (2002)

    • Related Report
      2002 Annual Research Report

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Published: 2002-04-01   Modified: 2016-04-21  

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