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Functional characterisation guides classification of novel BAP1 germline variants.


ABSTRACT: We have identified six patients harbouring distinct germline BAP1 mutations. In this study, we functionally characterise known BAP1 pathogenic and likely benign germline variants out of these six patients to aid in the evaluation and classification of unknown BAP1 germline variants. We found that pathogenic germline variants tend to encode truncated proteins, show diminished expression of epithelial-mesenchymal transition (EMT) markers, are localised in the cytosol and have reduced deubiquitinase capabilities. We show that these functional assays are useful for BAP1 variant curation and may be added in the American College of Medical Genetics and Genomics (ACMG) criteria for BAP1 variant classification. This will allow clinicians to distinguish between BAP1 pathogenic and likely benign variants reliably and may aid to quickly benchmark newly identified BAP1 germline variants. Classification of novel BAP1 germline variants allows clinicians to inform predisposed patients and relevant family members regarding potential cancer risks, with appropriate clinical interventions implemented if required.

SUBMITTER: Hong JH 

PROVIDER: S-EPMC7678838 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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Functional characterisation guides classification of novel <i>BAP1</i> germline variants.

Hong Jing Han JH   Chong Siao Ting ST   Lee Po-Hsien PH   Tan Jing J   Heng Hong Lee HL   Ishak Nur Diana Binte NDB   Chan Sock Hoai SH   Teh Bin Tean BT   Ngeow Joanne J  

NPJ genomic medicine 20201119


We have identified six patients harbouring distinct germline <i>BAP1</i> mutations. In this study, we functionally characterise known <i>BAP1</i> pathogenic and likely benign germline variants out of these six patients to aid in the evaluation and classification of unknown <i>BAP1</i> germline variants. We found that pathogenic germline variants tend to encode truncated proteins, show diminished expression of epithelial-mesenchymal transition (EMT) markers, are localised in the cytosol and have  ...[more]

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