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Parallel functional annotation of cancer-associated missense mutations in histone methyltransferases.
Canning, Ashley J; Viggiano, Susan; Fernandez-Zapico, Martin E; Cosgrove, Michael S.
Afiliação
  • Canning AJ; Department of Biochemistry and Molecular Biology, State University of New York (SUNY) Upstate Medical University, 4261 Weiskotten Hall, Syracuse, NY, 13210, USA.
  • Viggiano S; Department of Biochemistry and Molecular Biology, State University of New York (SUNY) Upstate Medical University, 4261 Weiskotten Hall, Syracuse, NY, 13210, USA.
  • Fernandez-Zapico ME; Schulze Center for Novel Therapeutics, Division of Oncology Research, Mayo Clinic, Rochester, MN, USA.
  • Cosgrove MS; Department of Biochemistry and Molecular Biology, State University of New York (SUNY) Upstate Medical University, 4261 Weiskotten Hall, Syracuse, NY, 13210, USA. cosgrovm@upstate.edu.
Sci Rep ; 12(1): 18487, 2022 11 02.
Article em En | MEDLINE | ID: mdl-36323913
Using exome sequencing for biomarker discovery and precision medicine requires connecting nucleotide-level variation with functional changes in encoded proteins. However, for functionally annotating the thousands of cancer-associated missense mutations, or variants of uncertain significance (VUS), purifying variant proteins for biochemical and functional analysis is cost-prohibitive and inefficient. We describe parallel functional annotation (PFA) of large numbers of VUS using small cultures and crude extracts in 96-well plates. Using members of a histone methyltransferase family, we demonstrate high-throughput structural and functional annotation of cancer-associated mutations. By combining functional annotation of paralogs, we discovered two phylogenetic and clustering parameters that improve the accuracy of sequence-based functional predictions to over 90%. Our results demonstrate the value of PFA for defining oncogenic/tumor suppressor functions of histone methyltransferases as well as enhancing the accuracy of sequence-based algorithms in predicting the effects of cancer-associated mutations.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto / Neoplasias Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Sci Rep Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Reino Unido