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Accelerating functional gene discovery in osteoarthritis

Author

Listed:
  • Natalie C. Butterfield

    (Imperial College London)

  • Katherine F. Curry

    (Imperial College London)

  • Julia Steinberg

    (Helmholtz Zentrum München – German Research Center for Environmental Health
    Wellcome Trust Sanger Institute
    Cancer Council NSW)

  • Hannah Dewhurst

    (Imperial College London)

  • Davide Komla-Ebri

    (Imperial College London)

  • Naila S. Mannan

    (Imperial College London)

  • Anne-Tounsia Adoum

    (Imperial College London)

  • Victoria D. Leitch

    (Imperial College London)

  • John G. Logan

    (Imperial College London)

  • Julian A. Waung

    (Imperial College London)

  • Elena Ghirardello

    (Imperial College London)

  • Lorraine Southam

    (Helmholtz Zentrum München – German Research Center for Environmental Health
    Wellcome Trust Sanger Institute)

  • Scott E. Youlten

    (University of New South Wales Medicine)

  • J. Mark Wilkinson

    (University of Sheffield
    University of Sheffield)

  • Elizabeth A. McAninch

    (Rush University Medical Center)

  • Valerie E. Vancollie

    (Wellcome Trust Sanger Institute)

  • Fiona Kussy

    (Wellcome Trust Sanger Institute)

  • Jacqueline K. White

    (Wellcome Trust Sanger Institute
    The Jackson Laboratory)

  • Christopher J. Lelliott

    (Wellcome Trust Sanger Institute)

  • David J. Adams

    (Wellcome Trust Sanger Institute)

  • Richard Jacques

    (University of Sheffield)

  • Antonio C. Bianco

    (University of Chicago)

  • Alan Boyde

    (Queen Mary University of London, Mile End Road)

  • Eleftheria Zeggini

    (Helmholtz Zentrum München – German Research Center for Environmental Health
    Wellcome Trust Sanger Institute)

  • Peter I. Croucher

    (University of New South Wales Medicine)

  • Graham R. Williams

    (Imperial College London)

  • J. H. Duncan Bassett

    (Imperial College London)

Abstract

Osteoarthritis causes debilitating pain and disability, resulting in a considerable socioeconomic burden, yet no drugs are available that prevent disease onset or progression. Here, we develop, validate and use rapid-throughput imaging techniques to identify abnormal joint phenotypes in randomly selected mutant mice generated by the International Knockout Mouse Consortium. We identify 14 genes with functional involvement in osteoarthritis pathogenesis, including the homeobox gene Pitx1, and functionally characterize 6 candidate human osteoarthritis genes in mouse models. We demonstrate sensitivity of the methods by identifying age-related degenerative joint damage in wild-type mice. Finally, we phenotype previously generated mutant mice with an osteoarthritis-associated polymorphism in the Dio2 gene by CRISPR/Cas9 genome editing and demonstrate a protective role in disease onset with public health implications. We hope this expanding resource of mutant mice will accelerate functional gene discovery in osteoarthritis and offer drug discovery opportunities for this common, incapacitating chronic disease.

Suggested Citation

  • Natalie C. Butterfield & Katherine F. Curry & Julia Steinberg & Hannah Dewhurst & Davide Komla-Ebri & Naila S. Mannan & Anne-Tounsia Adoum & Victoria D. Leitch & John G. Logan & Julian A. Waung & Elen, 2021. "Accelerating functional gene discovery in osteoarthritis," Nature Communications, Nature, vol. 12(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-020-20761-5
    DOI: 10.1038/s41467-020-20761-5
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