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The Characteristics of Y Chromosome in Japanese

Research Project

Project/Area Number 07407064
Research Category

Grant-in-Aid for Scientific Research (A)

Allocation TypeSingle-year Grants
Section一般
Research Field Human genetics
Research InstitutionThe University of Tokyshima (1997)
The University of Tokyo (1995-1996)

Principal Investigator

NAKAHORI Yutaka  The University of Tokushima, School of Medicine Department of Public Health, Professor, 医学部, 教授 (10172389)

Co-Investigator(Kenkyū-buntansha) TODA Tatsushi  The Institute of Medical Science, The University of Tokyo, Department of Genome, 医科学研究所, 助教授 (30262025)
Project Period (FY) 1995 – 1997
Project Status Completed (Fiscal Year 1997)
Budget Amount *help
¥18,500,000 (Direct Cost: ¥18,500,000)
Fiscal Year 1997: ¥4,300,000 (Direct Cost: ¥4,300,000)
Fiscal Year 1996: ¥6,200,000 (Direct Cost: ¥6,200,000)
Fiscal Year 1995: ¥8,000,000 (Direct Cost: ¥8,000,000)
KeywordsY-chromosome / Japanese / DNA polymorphism / ハプロタイプ / SRY遺伝子
Research Abstract

The Y chromosome is a single haploid entity passed only from father to son, and thus it represents the paternal lineage in human males. DNA markers located in non-recombining part of the Y chromosome are especially useful for tracing the paternal lineage in evolutionary studies. However, progress in this field has been slow because it has been difficult to find suitable markers. We have been studying the Y chromosome structure and reported some polymorphisms found in Japanese. Here, we report the PCR-based techniques for 3 DNA polymorphisms in SRY,DXYS5Y and DXYS241 loci on the Y chromosome. Using these techniques as well as YAP polymorphism, we have analyzed the Y chromosome of Japanese males and constructed a genealogical tree of the Y chromosome. The Japanese Y chromosomes were classified into 4 groups (i.c., haplotypes) based on the allele combintion in the 4 loci. Population study of these hapotypes in the Korean, Caucasian, Negroid and Okinawan samples illustrated the characteristics of the Y chromosome in Japanese and indicated the origin of the Japanese males.

Report

(4 results)
  • 1997 Annual Research Report   Final Research Report Summary
  • 1996 Annual Research Report
  • 1995 Annual Research Report
  • Research Products

    (40 results)

All Other

All Publications (40 results)

  • [Publications] Kotbearouo, E.S.: "A novel (CA) n polymorphism on 6p21, 1-21, 2." Jpn.J.Human Genetics. 41. 423-425 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ito.T.: "Sex reworosal in a Child with Duplication of Sex Reversing focus ovthe Short Arm of the X Chromosome (Xp)" J.of Pediatric Endocrimalogy Metabolism (JPEM). 9. 429-433 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Miyake, M.: "YAC and cosmid contigs emecompassing the Fukuyama Dype congenital muscular dyotrophy (ECMD) candidete region on 9q31" Genomics. 40. 284-293 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotliasosa, E.S.: "Novel Marker DXYS 241 on the human Y chromosame shows four enolutionary ecent ofter diuergence of human and chempony" Human Biology.

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Yoshida, A.: "Dicentric YChromesome inan Azoopermic Male." Mol.Hum.Reproduction. 3. 709-712 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Yoshida, A.: "An Apoospermic Male with An Unbalance Autosome-Y Translocation." Jpn.J.Human Genetics. 42. 451-455 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Toda, T.: "Congenital Mascular Dystrophies" Elsevier, 440 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotlearoua, E.S.: "ISFH Hakone on DNA polymorpbisms" TOYOSHOTEN, (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotliarova, E.S., Toda, T., Matsushita, I., Nakagome, Y., Nakahori, Y.: "A novel (CA) n polymorphism on 6p21.1-21.2" Jpn J Hum.Genet.41. 423-425 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Ito, T., Kaino, Y., Hirai, H., Kida, K., Nakahori, Y., Nakagome, Y.: "ex reversal in a child with duplication of sex reversing locus on the short arm of the x chromosome (Xp)" J.of Pediatric Endocrinology Metabolism (JPEM). 9. 429-433 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Miyake, M., Nakahori, Y., Matsushita, I., Kobayashi, K,Mizuno, K., Hirai, M., Kanazawa, I., Nakagome, Y., Tokunaga, Toda, T.: "YAC and cosmid contigs emcompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31" Genomics. 40. 284-293 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotliarova, E.S., Toda, T., Takenaka, O., Matsushita, I., Hida, A., Shinka, T., Goto, J., Tokunaga, K., Nakagome, Y., Nakahori, Y.: "Novel Marker DXYS241 on the human Y chromosome shows four evolutionary event after divergence of human and chimpanzee" Hum.Biol.(in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Yoshida, A., Nakahori, Y., Kuroki, Y., Motoyama, M., Araki, Y., Miura, K., Shirai, M.: "Dicentric Y Chromosome in an Azoospermic Male." Mol.Hum.Reproduction. 3. 709-712 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Yoshida, A., Nakahori, Y., Kuroki, Y., Miura, K., Shirai, M.: "An azoospermic male with an unbalanced autosomal-Y translocation" Jpn.J.Hum.Genet. 42. 451-455 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Toda, T., Miyake, M., Nakahori, Y., Segawa, M., Nomura, Y., Nonaka, I., Ikegawa, S., Kondo, E., Saito, K., Fukuyama, Y., Yoshioka, M., Shimizu, T., Kanazawa, I., Nakamura, Y., Nakagome, Y.: Toward the identification of the Fukuyama type congenital muscular dystrophy (FCMD) gene. in Fukuyama, Y., Osawa, M., Saito, Keds : Congenital Muscular Dystrophies.Elsevier, Tokyo, 301-308 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotliarova, E.S., Matsusshita, I., Shinka, T., Hida, A., Toda, T., Tokunaga, K., Nakagome, Y., Nakahori, Y.: Novel polymorphic CA repeat on the Yp11 with non-random allele distribution on sex chromosomes is a useful marker for forensic analysis. ISFH Hakone symposium on DNA polymorphisms. TOYOSHOTEN, 108-112 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1997 Final Research Report Summary
  • [Publications] Kotliaroua,E.S.: "A novel (CA)n polymorphism on 6p21,1-21,2." Jpn.J.Human Genetics. 41. 423-425 (1996)

    • Related Report
      1997 Annual Research Report
  • [Publications] Ito,T.: "Sex Reversal in a Child with Duplication of Sex Reversing Locus on the Short Arm of the X Chromosome (Xp)" J.of Pediatric Endocrinology Metabolism (JPEM). 9. 429-433 (1996)

    • Related Report
      1997 Annual Research Report
  • [Publications] Miyake,M.: "YAC and cosmid contigs emcompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9g31" Genomics. 40. 284-293 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Kotliaroua,E.S.: "Novel Marker DXYS241 on the human Y chromosome shows four evolutionary event after divergence of human and chimpanzee" Human Biology.

    • Related Report
      1997 Annual Research Report
  • [Publications] Yoshida,A.: "Dicentric Y Chromosome in an Azoospermic Male." Mol.Hum.Reproduction. 3. 709-712 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yoshida,A.: "An Azoospermic Male With An Unbalanced Autosome-Y Translocation." Jpn.J.Human Genetics. 42. 451-455 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Toda,T.: "Congenital Mascular Dystrophies" Elsevier, 440 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Kotliaroua,E.S.: "ISFH Hakone on DNA polymorphisms" TOYOSHOTEN, (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yanagisawa,H.,Nakahori,Y.et al.: "A unique origin and multistep process for genetation of expanded DRPLA triplet repeats" Hum.Mol.Genet.5. 373-379 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Shimmoto,M.,Nakahori,Y.et al.: "A human protective protein gene partially overlaps the gene encoding phospholipid trasfer protein on the complementary strand of DNA" Biochem.Biphys.Res.Comm.220. 802-806 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Lin,S.J.,Nakahori,Y.et al.: "Long Y-associated(GATA)n alleles were observed in a few ethic groups in Asia" Jpn.J.Hum.Genet.41. 243-246 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Nakahori,Y.,Kuroki,Y.et al.: "The Y chromosome region essetial for spermatogenesis" Hormone Res.46. 20-23 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Toda,T.,Nakahori,Y.et al.: "Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy(FCMD)candidate region to<100Kb" Amer.J.Hum.Genet.59. 1313-1320 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Jobling,M.A.,Nakahori,Y.et al.: "Recent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males" Hum.Mol.Genet.5. 1767-1775 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] 中堀豊: "性の決定とその異常疾患:分子医科学シリーズ" メジカルビュー社, 97-129 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] 中堀豊: "蛋白質・核酸・酵素 Y染色体-構造,機能,進化-" 共立出版, 2306-2314 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Nakahori,Y: "The incidence of the fragile X syndrome in Japanese.(Commentary)." Brain & Development. 17. 322-322 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Iwamoto.T.,Nakahori,Y.: "Pericentric inversion with a minute deletion of the Y chromosome." Clin.Genet.48. 272-274 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Okada.T.,Nakahori,Y.: "46,XY female karyotype containing SRY." Clin.Pediatr.Endocrinol. 4. 103-107 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Ogata.T.,Nakahori,Y.: "Chromosomal Iocalization fo a Y-specific growth gene(s)." J.Med.Genet.32. 572-575 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Muroya.K.,Nakahori,Y.: "Refinement of the locus for X-linled recessive chondrodysplasia punctata by genotype-phenotype correlations." Hum.Genet.95. 577-580 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Shiojima,I.,Nakahori,Y.: "Assignment of Cardiac-specific homeobox gene CSX to human chromosome 5q34." Genomics. 27. 204-206 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] 中堀豊: "遺伝性疾患の遺伝子診断 眼科学体系10A目の発生と遺伝" 中山書店, 97-106 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] 中堀豊: "(翻訳)遺伝病 病態で学ぶ免疫遺伝学" 丸善(in press), (1996)

    • Related Report
      1995 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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