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Functional analyses of SMPDL3A as a candidate gene of congenital radioulnar synostosis

Research Project

Project/Area Number 19K09572
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Review Section Basic Section 56020:Orthopedics-related
Research InstitutionShinshu University

Principal Investigator

Nakamura Yukio  信州大学, 医学部, 特任教授 (00549488)

Project Period (FY) 2019-04-01 – 2023-03-31
Project Status Completed (Fiscal Year 2022)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2022: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2021: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2020: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Keywords遺伝子 / 骨格発生 / 形態形成
Outline of Research at the Start

本事業ではsmpdl3a遺伝子改変動物を作製し、表現型の確認と主要なシグナル伝達を明らかにする。また細胞実験を用いて上記現象を確認しsmpdl3a遺伝子の詳細な役割を明らかにする。最終的にはsmpdl3a遺伝子が先天性橈尺骨癒合症の病態に関与する分子メカニズムを明らかにする。

Outline of Final Research Achievements

In this study, SMPDL3A was identified using whole exome suquencing as candidate genes of congenital radioulnar synostosis (CRUS). Amino acid similarities of SMPDL3A were approximately 54% across humans and zebrafish, which is quite high. In situ hybridization analyses revealed that the strong expression was detected in the craniofacial and pectoral fin regions of zebrafish embryos and larvae. Also, the genetically-modified zebrafish showed that SMPDL3A regulates BMP signaling during skeletogenesis. Furthermore, SMPDL3A containing potentially the disease-causing mutations, had reduced activity of BMP or Wnt signaling.

Academic Significance and Societal Importance of the Research Achievements

全エクソン解析により先天性橈尺骨癒合症の候補遺伝子としてSMPDL3Aを同定した。。
本研究では骨格形態・形成過程におけるSMPDL3A遺伝子の分子メカニズムを明らかにすることにより、先天性橈尺骨癒合症の病態に迫る。骨格形態・形成過程におけるSMPDL3A遺伝子の分子メカニズムを世界に先駆けて実証しており、ヒトの正常な骨格発生・分化の理解のみならず、骨系統疾患の病態に繋がると期待できる。

Report

(5 results)
  • 2022 Annual Research Report   Final Research Report ( PDF )
  • 2021 Research-status Report
  • 2020 Research-status Report
  • 2019 Research-status Report

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Published: 2019-04-18   Modified: 2024-01-30  

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