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

Molecular mechanism for inherited thyroxine-binding globulin excess and isolated growth hormone deficiency

Research Project

Project/Area Number 07671123
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 内分泌・代謝学
Research InstitutionAichi Medical University

Principal Investigator

MORI Yuichi  Aichi Medical University, Associate Professor, 医学部, 助教授 (70230084)

Project Period (FY) 1995 – 1996
Project Status Completed (Fiscal Year 1996)
Budget Amount *help
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1995: ¥1,400,000 (Direct Cost: ¥1,400,000)
KeywordsTBG / isolated GH deficiency / TBG excess / gene amplification / PCR / FISH / TBG-CD / TBG-PD
Research Abstract

1. The gene dosage of TBG was estimated in 7 families with inherited TBG excess (3 Japanese and 4 Caucasian families) and a sporadic Japanese family by using duplex PCR-HPLC method. Amplification of the TBG gene was detected in all 8 families, evaluated in this study, 3 fold in 5 families and 2 fold in 2 inherited families and a boy, considered to be a sporadic case. Serum TBG values were corresponded to TBG gene dosage. Then gene amplification was shown to be a main mechanism for inherited TBG excess.
2. Amplification of the TBG gene was also evaluated in 4 Japanese and one Caucasian families with FISH using chromosomes and a TBG probe. Although, 3 fold amplification, corresponding to the results of PCR-HPLC analysis, was demonstrated in one Japanese and one Caucasian families, other 3 families were shown to be indistinguishable from normal subjects. The size of the amplified unit might be smaller than the detection limit of FISH.
3. In order to clarify the mechanism for the gene amplification, PFLPs were evaluated in 4 Japanese families using genomic DNAs and 12 restriction enzymes. Nevertheless, no RFLP was detected in all subjects, demonstrating that a breakpoint of amplified unit exist outside of 52 kbp covered by 12 enzumes.
4. Gene screening using allele specific amplification was performed in 50 Japanese families manifesting TBG complete or pertial deficiency. A CDJ mutation (a nucleotide deletion in codon 352) was detected in 44 families and a PDJ mutation (a nucleotide replacement in codon 363) in 6 families. Therefore, both mutations were thought to arise in the ansester of Japanese and to expand into offsprings by the founder effect.
5. X chromosome inactivation pattern was analyzed in 10 CDJ and a PDJ families using a PGK-1 gene. Selective inactivation of X chromosome containing a normal TBG gene was detected in 2 famales. Then, a CDJ and a PDJ hemizygote were considered to manifest TBG-CD and to have a TBG value same as PDJ males, respectively.

Report

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

    (30 results)

All Other

All Publications (30 results)

  • [Publications] Akemi Inagaki: "Gene screening of thyroxine-binding globulin deficiency in Japanese : only two mutaions account for TBG deficiencies in the Japanese." J Clin Endocrinol Metab. 81. 580-585 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Hideki Okamoto: "Molecular analysis of a female manifesting complete thyroxine-binding globulin deficiency (TBG-CD) : selective X-chromosome inactivation responsible for the difference between" J Clin Endocrinol Metab. 81. 2204-2208 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Refetoff Samuel: "Thyroxine-binding globulin : Organization of the gene and variants." Hormone Research. 45. 128-138 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yuichi Mori: "Gene amplification as a cause for inherited thyroxine-binding globulin excess in Japanese families" J Clin Endocrinol Metab. 80. 3758-3762 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yuichi Mori: "Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization." Human Genetics. 96. 481-482 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Katsuyoshi Tojo: "Familial thyroxine-binding globulin deficiency associated with hyperthyroidism" Internal Med. 34. 413-417 (1995)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] 岡博: "Annual Review内分泌、代謝 1996" 中外医学社, 275 (1996)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] 赤沼安夫: "『内分泌・代謝疾患-state of arts』の概要" 医歯薬出版(in press), (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Akemi Inagaki et al.: "Gene screening of thyroxine-binding globulin deficiency in Japanese : only two mutations account for TBG deficiencies in the Japanese." J Clin Endocrinol Metab. 81. 580-585 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Hideki Okamoto et al.: "Molecular analysis of a female manifesting complete thyroxine-binding globulin deficiency (TBG-CD) : selective X-chromosome inactivation responsible for the difference between phenotype an genotype in TBG-deficient females." J Clin Endocrinol Metab. 81. 2204-2208 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Refetoff Samuel et al.: "Thyroxine-binding globulin : Organization of the gene and variants." Hormone Research. 45. 128-138 (1996)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yuichi Mori et al.: "Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2by fluorescence in situ hybridization." Human Genetics. 96. 481-482 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yuichi Mori et al.: "Gene amplification as a cause for inherited thyroxine-binding globulin excess in Japanese families" J Clin Endocrinol Metab. 80. 3758-3762 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Katsuyoshi Tojo et al.: "Familial thyroxine-binding globulin deficiency associated with hyperthyroidism" Internal Med. 34. 413-417 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yuichi Mori et al.: "Abnormalities in serum TBG (in Japanese)" Current Therapy. 13. 128-132 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Yoshitaka Miura et al.: "Molecular analysis of TBG deficiencies (in Japanese)" Modern Physician. 15. 791-794 (1995)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1996 Final Research Report Summary
  • [Publications] Akemi Inagaki: "Gene screening of thyoxine-binding globulin deficiency in Japanese : only two mutations account for TBG deficiencies in the Japanese." J Clin Endocrinol Metab. 81. 580-585 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Hideki Okamoto: "Molecular analysis of a female manifesting complete thyroxine-binding globulin deficiency (TBG-CD): selective X-chromosome inactivation responsible for the difference between" J Clin Endocrinol Merab. 81. 2204-2208 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Refetoff Samuel: "Thyroxine-binding globulin : Organization of the gene and variants." Hormone Research. 45. 128-138 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Yuichi Mori: "Gene amplification as a cause for inherited thyroxine-binding globulin excess in Japanese families." J Clin Endocrinol Metab. 80. 3758-3762 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] Yuichi Mori: "Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization." Human Genetics. 96. 481-482 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] Katsuyoshi Tojo: "Familial thyroxine-binding globulin deficiency associated with hyperthyroidism" Internal Med. 34. 413-417 (1995)

    • Related Report
      1996 Annual Research Report
  • [Publications] 岡博: "Annual Review内分泌、代謝1996" 中外医学社, 275 (1996)

    • Related Report
      1996 Annual Research Report
  • [Publications] Yuichi Mori: "Gene amplification as a cause for inherited thyroxine-binding globulin excess in Japanese families." J Clin Endocrinol Metab. 80. 3758-3762 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Yuichi Mori: "Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization." Hum Genet. 96. 481-482 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Katsuyoshi Tojo: "Familial thyroxine-binding globulin deficiency associated with hyperthyroidisn." Intern Med. 34. 413-417 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] Akemi Inagaki: "Gene screening of thyroxine-binding globulin deficiencies in Japanese: only two mutations account for TBG deficiencies in the Japanese." J Clin Endocrinol Metab. 81. 580-585 (1996)

    • Related Report
      1995 Annual Research Report
  • [Publications] Hideki Okamoto: "Molecular analysis of a female manifesting complete thyroxine-binding globulin deficiency (TBG-CD): selective X-chromosome inactivation responsible for the difference between" J Clin Endocrinol Metab. (in press).

    • Related Report
      1995 Annual Research Report
  • [Publications] 森 祐一: "TBG異常値" カレントテラピー. 13. 128-132 (1995)

    • Related Report
      1995 Annual Research Report
  • [Publications] 岡 博: "Annual Review内分泌、代謝 1996" 中外医学社, 275 (1996)

    • Related Report
      1995 Annual Research Report

URL: 

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

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi