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Analysis of G-protein coupled receptors as candidate genes for autism

Research Project

Project/Area Number 12670773
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Pediatrics
Research InstitutionJichi Medical School

Principal Investigator

YAMAGATA Takanori  Jichi Medical School, Pediatrics, Assistant Professor, 医学部, 講師 (00239857)

Co-Investigator(Kenkyū-buntansha) NAKAMURA Miki  Jichi Medical School, Pediatrics, Assistant, 医学部, 助手 (20296114)
SUWA Kiyotaka  Jichi Medical School, Pediatrics, Assistant, 医学部, 助手 (30285796)
野崎 靖之  自治医科大学, 医学部, 助手 (90281295)
Project Period (FY) 2000 – 2001
Project Status Completed (Fiscal Year 2001)
Budget Amount *help
¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 2001: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2000: ¥1,700,000 (Direct Cost: ¥1,700,000)
Keywordsautism / mutation analysis / secretin / secretin receptor / GRPR / G-protein coupled receptor / Hereditary Multiple Exostosis / EXT1 / GRPR / ノックアウトマウス
Research Abstract

1) We analyzed secretin gene, secretin receptor (SCRC) gene and gastrin releasing peptide receptor (GRPR) gene for mutation on autism patients.
In secretin gene analysis, we found mutations in promoter region that decrease the gene expression, and missense mutations in 5 of 104 patients. However, they were not confirmed as a gene for autism because they were found in control. And there was no secretin gene mutation on the patients of secretin treatment responder.
No pathogenic mutation was detected in SCRC and GRPR genes.
2) Secretin and SCRC gene knockout mice were developed.
For secretin gene knockout mice, all of four exons of secretin gene were replaced with β-galactosidase and neomycine gene. The knockout mice were delivered. For SCRC gene knockout mice, exon 1 was replaced with β-galactosidase and neomycine gene. The knockout mice were established and the absence of SCRC gene expression in knockout homo mice were confirmed by RT-PCR.
We are planing to analyze these knockout mice pathologically and biochemically, additon to the behavior analysis.

Report

(3 results)
  • 2001 Annual Research Report   Final Research Report Summary
  • 2000 Annual Research Report
  • Research Products

    (6 results)

All Other

All Publications (6 results)

  • [Publications] LiH, Yamagata T, Mon M, Momoi MY: "Association of autism in two patients with hereditary multiple exostoses that is caused by the novel deletion mutations of EXT1"Journal of Human Genetics. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Yamagata T, Aradhya S, Mori M, Inoue K, Momoi MY, Nelson DL: "The Human Secretin gene : Fine Structure in 11p15.5 and Sequence Variation in Patients with Autism"Genomics. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Li H, Yamagata T, Mori M, Momoi MY: "Association of autism in two patients with hereditary multiple exostoses that is caused by the novel deletion mutations of EXT1"Journal of Human Genetics. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Yamagata T, Aradhya S, Mori M, Inoue K, Momoi MY, Nelson DL: "The Human Secretin gene : Fine Structure in 11p15.5 and Sequence Variation in Patients with Autism"Genomics. (in press). (2002)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2001 Final Research Report Summary
  • [Publications] Li H, Yamagata T, Mori M, Momoi M: "Association of autism in two patients with hereditary multiple exostoses that is caused by the novel deletion mutations of EXT1"Journal of Human Genetics. (印刷中). (2002)

    • Related Report
      2001 Annual Research Report
  • [Publications] Yamagata T, Swaroop Aradhya, Mori M, Inoue K, Momoi MY, David L.Nelson: "The Human Secretin gene : Fine Structure in 11p15.5 and Sequence Variation in Patients with Autism"Genomics. (印刷中). (2002)

    • Related Report
      2001 Annual Research Report

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Published: 2000-04-01   Modified: 2016-04-21  

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