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Pathophysiology and novel drug development targeting deafness-associated potassium channel KCNQ4

Research Project

Project/Area Number 19K18802
Research Category

Grant-in-Aid for Early-Career Scientists

Allocation TypeMulti-year Fund
Review Section Basic Section 56050:Otorhinolaryngology-related
Research InstitutionShinshu University

Principal Investigator

Timothy Day  信州大学, 医学部, 研究員 (00838667)

Project Period (FY) 2019-04-01 – 2021-03-31
Project Status Completed (Fiscal Year 2020)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2020: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2019: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
Keywords難聴 / 遺伝子 / モデルマウス / KCNQ4 / inner ear / hair cell / model mice / hearing loss / deafness / potassium channel
Outline of Research at the Start

1 Reproduction of KCNQ4 c.211delC 2 Construction of a functional detection system using a fluorescent plate reader 3 Drug discovery candidate selection 4 Generation and characterization of c.211delC knock-in mouse 5 Trial of treatment with candidate drugs for knock-in mice

Outline of Final Research Achievements

We have completed experimental testing for data in the project titled “Pathophysiology and novel drug development targeting deafness- associated potassium channel KCNQ4”. Using the KCNQ4 c.211delC knock-in mouse we collected all auditory brain stem response (ABR), and otoacoustic radiation (DPOAE). The KCNQ4 c.211delC mice had significant hearing loss compared to wild-type control and heterozygous control mice. Hearing loss began shortly after birth, and the mice were deaf by 2 months old. DPOAE results indicate loss of outer hair cells (OHC). Inner ear cellular composition was examined by confocal microscopy to visualize loss of OHC. The project is currently in manuscript preparation for publication in a peer reviewed journal.

Academic Significance and Societal Importance of the Research Achievements

本研究では、常染色体優性遺伝形式をとる日本人難聴患者に比較的高頻度に認められるKCNQ4遺伝子変異を導入したモデルマウスを確立するとともに、その聴力を経時的に測定し、また、病理組織の観察を行った。得られた情報は将来的な治療法(遺伝子治療等)を確立するための基盤として有用であると期待される。

Report

(3 results)
  • 2020 Annual Research Report   Final Research Report ( PDF )
  • 2019 Research-status Report
  • Research Products

    (5 results)

All 2020 2019

All Journal Article (2 results) (of which Int'l Joint Research: 1 results,  Peer Reviewed: 2 results,  Open Access: 2 results) Presentation (3 results)

  • [Journal Article] Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss.2020

    • Author(s)
      Miyajima H, Moteki H, Day T, Nishio SY, et al
    • Journal Title

      Sci Rep.

      Volume: 10 Issue: 1 Pages: 7056-7056

    • DOI

      10.1038/s41598-020-63690-5

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.2020

    • Author(s)
      Oka SI, Day TF, Nishio SY, Moteki H, Miyagawa M, et al
    • Journal Title

      Genes

      Volume: 11 Issue: 3 Pages: 273-273

    • DOI

      10.3390/genes11030273

    • Related Report
      2019 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] Identification of Hearing-Loss Associated Mutations in MYO6 and IN Vitro Functional Analysis.2020

    • Author(s)
      Day T.F. Oka S,Kitajiri S, Moteki H, Nishio S, Usami SI
    • Organizer
      43th ANNUAL MidWinter Meeting
    • Related Report
      2019 Research-status Report
  • [Presentation] Molecular investigations of deafness-related genes ACTG1 and MYO6 in vitro2019

    • Author(s)
      Day Timothy, 岡晋一郎、宮嶋宏樹、北尻真一郎、西尾信哉、宇佐美真一
    • Organizer
      第64回日本聴覚医学会
    • Related Report
      2019 Research-status Report
  • [Presentation] ACTG1変異による難聴症例の臨床像と変位型γアクチンの細胞内局在2019

    • Author(s)
      宮嶋宏樹、茂木英明、Timothy Day, 西尾信哉、北尻真一郎、宇佐美真一
    • Organizer
      第64回 日本人類遺伝学会
    • Related Report
      2019 Research-status Report

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Published: 2019-04-18   Modified: 2022-01-27  

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