Functional characterisation guides classification of novel BAP1 germline variants
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 pa...
Saved in:
Main Authors: | , , , , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2021
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/146677 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-146677 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1466772023-03-05T16:48:49Z Functional characterisation guides classification of novel BAP1 germline variants Hong, Jing Han Chong, Siao Ting Lee, Po-Hsien Tan, Jing Heng, Hong Lee Nur Diana Ishak Chan, Sock Hoai Teh, Bin Tean Ngeow, Joanne Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Clinical Genetics Genetics Research 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. Ministry of Health (MOH) National Medical Research Council (NMRC) National Research Foundation (NRF) Published version We would like to thank the patients and research participants for their contribution to the study. This work was supported by the Khoo Postdoctoral Fellowship Award (Duke-NUS-KPFA/2019/0034 to J.H.H), the National Medical Research Council Open Fund—Young Individual Research Grant (MOH-000232 to J.H.H), the National Medical Research Council Open Fund—Individual Research Grant (MOH-000144 to B.T.T), the National Medical Research Council Singapore Translational Research Investigator Award (MOH-000248 to B.T.T.), the NRF-NSFC Joint Research Grant (Data Science) (NRF2016NRF-NSFC001–057 to B.T.T), the LKC Startup Grant (LKC MOE to J.N.), the National Research Foundation Singapore under its Clinical Scientist Award (NMRC/CSA-INV/0017/2017) and administered by the Singapore Ministry of Health’s National Medical Research Council (to J.N.). This work is also partially funded by NCC Research Fund, NCC Cancer Fund, Terry Fox and Lee Foundation supporting funds to J.N. 2021-03-04T08:24:04Z 2021-03-04T08:24:04Z 2020 Journal Article Hong, J. H., Chong, S. T., Lee, P.-H., Tan, J., Heng, H. L., Nur Diana Ishak, . . . Ngeow, J. (2020). Functional characterisation guides classification of novel BAP1 germline variants. npj Genomic Medicine, 5(1), 50-. doi:10.1038/s41525-020-00157-6 2056-7944 0000-0002-2173-9192 0000-0002-9002-350X 0000-0003-1514-1124 0000-0003-1558-3627 https://hdl.handle.net/10356/146677 10.1038/s41525-020-00157-6 33298925 2-s2.0-85096327255 1 5 en MOH-000232 MOH-000144 MOH-000248 NRF2016NRF-NSFC001–057 NMRC/CSA-INV/0017/2017 npj Genomic Medicine © 2020 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing,adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visithttp://creativecommons.org/licenses/by/4.0/. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Science::Medicine Clinical Genetics Genetics Research |
spellingShingle |
Science::Medicine Clinical Genetics Genetics Research Hong, Jing Han Chong, Siao Ting Lee, Po-Hsien Tan, Jing Heng, Hong Lee Nur Diana Ishak Chan, Sock Hoai Teh, Bin Tean Ngeow, Joanne Functional characterisation guides classification of novel BAP1 germline variants |
description |
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. |
author2 |
Lee Kong Chian School of Medicine (LKCMedicine) |
author_facet |
Lee Kong Chian School of Medicine (LKCMedicine) Hong, Jing Han Chong, Siao Ting Lee, Po-Hsien Tan, Jing Heng, Hong Lee Nur Diana Ishak Chan, Sock Hoai Teh, Bin Tean Ngeow, Joanne |
format |
Article |
author |
Hong, Jing Han Chong, Siao Ting Lee, Po-Hsien Tan, Jing Heng, Hong Lee Nur Diana Ishak Chan, Sock Hoai Teh, Bin Tean Ngeow, Joanne |
author_sort |
Hong, Jing Han |
title |
Functional characterisation guides classification of novel BAP1 germline variants |
title_short |
Functional characterisation guides classification of novel BAP1 germline variants |
title_full |
Functional characterisation guides classification of novel BAP1 germline variants |
title_fullStr |
Functional characterisation guides classification of novel BAP1 germline variants |
title_full_unstemmed |
Functional characterisation guides classification of novel BAP1 germline variants |
title_sort |
functional characterisation guides classification of novel bap1 germline variants |
publishDate |
2021 |
url |
https://hdl.handle.net/10356/146677 |
_version_ |
1759858314922950656 |