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Identification of the genes causing azoospermia in humans and analysis of protein function and the mechanism of the spermatogenesis

Research Project

Project/Area Number 16390471
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Obstetrics and gynecology
Research InstitutionAsahikawa Medical College

Principal Investigator

ISHIKAWA Mutsuo  Asahikawa Medical College, the medical department, Vicepresident, 医学部, 副学長 (20002131)

Co-Investigator(Kenkyū-buntansha) SENGOKU Kazuo  Asahikawa Medical College, the medical department, Professor, 医学部, 教授 (30163124)
MIYAMOTO Toshinobu  Asahikawa Medical College, the medical department, Assistant Professor, 医学部, 助手 (70360998)
Project Period (FY) 2004 – 2006
Project Status Completed (Fiscal Year 2006)
Budget Amount *help
¥14,100,000 (Direct Cost: ¥14,100,000)
Fiscal Year 2006: ¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 2005: ¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 2004: ¥7,700,000 (Direct Cost: ¥7,700,000)
Keywordsazoospermia / meiosis / SNP / HOP2 / CDK2 / MEISEZ / 原因遺伝子 / HOP / MEI1 / FKBP6 / Mutation
Research Abstract

Recently, homo-mutant mice of the Hop2,Cdk2 and Meisez genes were reported. All of them are infertility. Detail analysis demonstrated that all mice were azoospermia by meiotic arrest. Therefore, we investigated the human HOP2,CDK2 and MEISEZ genes using the DNAs of the azoospermia by meiotic arrest. The patients were European American, Israel and Japanese and total numbers of the patients were 55. All patients and normal persons gave us written informed consent. Mutational analysis was carried out on the all coding regions of the three genes. One SNP could be found on the CDK2 gene and Two SNPS could be detected on the HOP2 gene. However the frequencies were not different between the patient group and normal control group on the both genes. However,11 SNPs could be found on the MEISEZ gene and the frequencies on the two of them were much different between patient group and control group (p<0.05). The present study suggests that the human MEISEZ gene might play critical roles in human spermatogenesis.

Report

(4 results)
  • 2006 Annual Research Report   Final Research Report Summary
  • 2005 Annual Research Report
  • 2004 Annual Research Report
  • Research Products

    (15 results)

All 2006 2005 2004 Other

All Journal Article (15 results)

  • [Journal Article] Is a genetic defect in FKBP6 a common cause of azoospermia?2006

    • Author(s)
      Miyamoto T, Ishikawa M et al.
    • Journal Title

      Cell Mol Biol Lett 11

      Pages: 557-569

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest.2006

    • Author(s)
      Sato H, Miyamoto T, Ishikawa M et al.
    • Journal Title

      J Hum Genet 51

      Pages: 533-540

    • NAID

      10017608347

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Is a genetic defect in FKBP6 a common cause of azoospermia?2006

    • Author(s)
      Miyamoto T, Ishikawa M, et al.
    • Journal Title

      Cell Mol Biol Lett 11

      Pages: 557-569

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Polymorphic alleles of the human MEI1 gene are associated With human azoospermia by meiotic arrest.2006

    • Author(s)
      Sato H, Miyamoto T, Ishikawa M, et al.
    • Journal Title

      J Hum Genet 51

      Pages: 533-540

    • NAID

      10017608347

    • Related Report
      2006 Annual Research Report
  • [Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta2005

    • Author(s)
      Miyamoto T, Ishikawa M et al.
    • Journal Title

      Genetics and Molecular Biology 28・1

      Pages: 44-45

    • NAID

      110004037390

    • Related Report
      2005 Annual Research Report
  • [Journal Article] Regulation of tumor invasion by HOXB13 gene overexpressed in human endometrial cancer2005

    • Author(s)
      Zao Y, Yamashita T, Ishikawa M et al.
    • Journal Title

      Oncol Rep 13・4

      Pages: 721-726

    • Related Report
      2005 Annual Research Report
  • [Journal Article] GATM, the human ortholog of the mouse imprinted Gatm gene, escapes genomic imprinting in placenta.2004

    • Author(s)
      Miyamoto T, Sengoku K, Ishikawa M et al.
    • Journal Title

      Genet and Mol Biol (in press)

    • NAID

      110004037390

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Nuclear Dynamics of Parthenogenesis of Human oocytes : Effect of Oocyte Aging in vitro.2004

    • Author(s)
      Sengoku K, Takuma N, Miyamoto T, Ishikawa M et al.
    • Journal Title

      Gynecol Obstet Invest 58

      Pages: 155-159

    • Related Report
      2004 Annual Research Report
  • [Journal Article] The human transcript induced in spermatogenesis 50.2004

    • Author(s)
      Sasaki Y, Miyamoto T, Sengoku K, Ishikawa M et al.
    • Journal Title

      Reprod Med Biol 3

      Pages: 237-243

    • NAID

      10014259263

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Isolation and Expression analysis of the testis-specific gene, human OPPO1.2004

    • Author(s)
      Miyamoto T, Sengoku K, Ishikawa M et al.
    • Journal Title

      J Assist Reprod Genet 21(4)

      Pages: 129-134

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Integrins are not involved in the process of human sperm-oolemmal fusion.2004

    • Author(s)
      Sengoku K, Takuma N, Miyamoto T, Ishikawa M et al.
    • Journal Title

      Human Reprod 19(3)

      Pages: 639-644

    • NAID

      120003161705

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.

    • Author(s)
      Miyamoto T, Ishikawa M et al.
    • Journal Title

      Turk J Pediatr (in press)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.

    • Author(s)
      Miyamoto T, Ishikawa M et al.
    • Journal Title

      Turk J Pediatr (in press)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2006 Final Research Report Summary
  • [Journal Article] Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract.

    • Author(s)
      Miyamoto T, Ishikawa M, et al.
    • Journal Title

      Turk J Pediatr (in presss)

    • Related Report
      2006 Annual Research Report
  • [Journal Article] Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest

    • Author(s)
      Sato H, Miyamoto T, Ishikawa M et al.
    • Journal Title

      Journal of Human Genetics (in press)

    • NAID

      10017608347

    • Related Report
      2005 Annual Research Report

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Published: 2004-04-01   Modified: 2016-04-21  

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