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Massively parallel variant characterization identifies NUDT15 alleles associated with thiopurine toxicity

Suiter, Chase C. (author)
St Jude Children´s Research Hospital, Memphis
Moriyama, Takaya (author)
St Jude Children´s Research Hospital, Memphis
Matreyek, Kenneth A. (author)
University of Washington, Seattle
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Yang, Wentao (author)
St Jude Children´s Research Hospital, Memphis
Scaletti, Emma Rose (author)
Stockholm University,Lunds universitet,Stockholms universitet,Institutionen för biokemi och biofysik,Lund University, Sweden,Strukturell biokemi,Forskargrupper vid Lunds universitet,Structural Biochemistry,Lund University Research Groups
Nishii, Rina (author)
St Jude Children´s Research Hospital, Memphis
Yang, Wenjian (author)
St Jude Children´s Research Hospital, Memphis
Hoshitsuki, Keito (author)
St Jude Children´s Research Hospital, Memphis
Singh, Minu (author)
Postgraduate Institute of Medical Education and Research
Trehan, Amita (author)
Postgraduate Institute of Medical Education and Research
Parish, Chris (author)
St Jude Children´s Research Hospital, Memphis
Smith, Colton (author)
St Jude Children´s Research Hospital, Memphis
Li, Lie (author)
St Jude Children´s Research Hospital, Memphis
Bhojwani, Deepa (author)
Children's Hospital Los Angeles
Yuen, Liz Y. P. (author)
Hong Kong Children's Hospital
Li, Chi-kong (author)
Chinese University of Hong Kong
Li, Chak-ho (author)
Tuen Mun Hospital
Yang, Yung-li (author)
National Taiwan University Hospital
Walker, Gareth J. (author)
University of Exeter
Goodhand, James R. (author)
Royal Devon & Exeter Hospital,University of Exeter
Kennedy, Nicholas A. (author)
University of Exeter,Royal Devon & Exeter Hospital
Klussmann, Federico Antillon (author)
Francisco Marroquín University
Bhatia, Smita (author)
University of Alabama
Relling, Mary V. (author)
St Jude Children´s Research Hospital, Memphis
Kato, Motohiro (author)
National Center for Child Health and Development
Hori, Hiroki (author)
Mie University
Bhatia, Prateek (author)
Postgraduate Institute of Medical Education and Research
Ahmad, Tariq (author)
University of Exeter,Royal Devon & Exeter Hospital
Yeoh, Allen E. J. (author)
National University of Singapore
Stenmark, Pål (author)
Stockholm University,Lunds universitet,Stockholms universitet,Institutionen för biokemi och biofysik,Lund University, Sweden,Strukturell biokemi,Forskargrupper vid Lunds universitet,Structural Biochemistry,Lund University Research Groups
Fowler, Douglas M. (author)
Canadian Institute for Advanced Research (CIFAR),University of Washington, Seattle
Yang, Jun J. (author)
St Jude Children´s Research Hospital, Memphis
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 (creator_code:org_t)
2020-02-24
2020
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424 .- 1091-6490. ; 117:10, s. 5394-5401
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • As a prototype of genomics-guided precision medicine, individualized thiopurine dosing based on pharmacogenetics is a highly effective way to mitigate hematopoietic toxicity of this class of drugs. Recently, NUDT15 deficiency was identified as a genetic cause of thiopurine toxicity, and NUDT15-informed preemptive dose reduction was quickly adopted in clinical settings. To exhaustively identify pharmacogenetic variants in this gene, we developed massively parallel NUDT15 function assays to determine the variants' effect on protein abundance and thiopurine cytotoxicity. Of the 3,097 possible missense variants, we characterized the abundance of 2,922 variants and found 54 hotspot residues at which variants resulted in complete loss of protein stability. Analyzing 2,935 variants in the thiopurine cytotoxicity-based assay, we identified 17 additional residues where variants altered NUDT15 activity without affecting protein stability. We identified structural elements key to NUDT15 stability and/or catalytical activity with single amino acid resolution. Functional effects for NUDT15 variants accurately predicted toxicity risk alleles in patients treated with thiopurines with far superior sensitivity and specificity compared to bioinformatic prediction algorithms. In conclusion, our massively parallel variant function assays identified 1,152 deleterious NUDT15 variants, providing a comprehensive reference of variant function and vastly improving the ability to implement pharmacogenetics-guided thiopurine treatment individualization.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Keyword

thiopurines
NUDT15
pharmacogenetics
massively parallel variant function assay

Publication and Content Type

ref (subject category)
art (subject category)

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