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Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication

BACKGROUND: Nasopharyngeal carcinoma (NPC) exhibits significant familial aggregation; however, its susceptibility genes are largely unknown. Thus, this study aimed to identify germline mutations that might contribute to the risk of familial NPC, and explore their biological functions. METHODS: Whole...

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Autores principales: Xiao, Ruo-Wen, Wang, Fang, Wang, Tong-Min, Zhang, Jiang-Bo, Wu, Zi-Yi, Deng, Chang-Mi, Liao, Ying, Zhou, Ting, Yang, Da-Wei, Dong, Si-Qi, Xue, Wen-Qiong, He, Yong-Qiao, Zheng, Xiao-Hui, Li, Xi-Zhao, Zhang, Pei-Fen, Zhang, Shao-Dan, Hu, Ye-Zhu, Liu, Yu-Ying, Xia, Yun-Fei, Gao, Song, Mu, Jian-Bing, Feng, Lin, Jia, Wei-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486052/
https://www.ncbi.nlm.nih.gov/pubmed/36116213
http://dx.doi.org/10.1016/j.ebiom.2022.104267
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author Xiao, Ruo-Wen
Wang, Fang
Wang, Tong-Min
Zhang, Jiang-Bo
Wu, Zi-Yi
Deng, Chang-Mi
Liao, Ying
Zhou, Ting
Yang, Da-Wei
Dong, Si-Qi
Xue, Wen-Qiong
He, Yong-Qiao
Zheng, Xiao-Hui
Li, Xi-Zhao
Zhang, Pei-Fen
Zhang, Shao-Dan
Hu, Ye-Zhu
Liu, Yu-Ying
Xia, Yun-Fei
Gao, Song
Mu, Jian-Bing
Feng, Lin
Jia, Wei-Hua
author_facet Xiao, Ruo-Wen
Wang, Fang
Wang, Tong-Min
Zhang, Jiang-Bo
Wu, Zi-Yi
Deng, Chang-Mi
Liao, Ying
Zhou, Ting
Yang, Da-Wei
Dong, Si-Qi
Xue, Wen-Qiong
He, Yong-Qiao
Zheng, Xiao-Hui
Li, Xi-Zhao
Zhang, Pei-Fen
Zhang, Shao-Dan
Hu, Ye-Zhu
Liu, Yu-Ying
Xia, Yun-Fei
Gao, Song
Mu, Jian-Bing
Feng, Lin
Jia, Wei-Hua
author_sort Xiao, Ruo-Wen
collection PubMed
description BACKGROUND: Nasopharyngeal carcinoma (NPC) exhibits significant familial aggregation; however, its susceptibility genes are largely unknown. Thus, this study aimed to identify germline mutations that might contribute to the risk of familial NPC, and explore their biological functions. METHODS: Whole-exome sequencing was performed in 13 NPC pedigrees with multiple cases. Mutations co-segregated with disease status were further validated in a cohort composed of 563 probands from independent families, 2,953 sporadic cases, and 3,175 healthy controls. Experimental studies were used to explore the functions of susceptibility genes and their disease-related mutations. FINDINGS: The three rare missense mutations in POLN (DNA polymerase nu) gene, P577L, R303Q, and F545C, were associated with familial NPC risk (5/576 [0·87%] in cases vs. 2/3374 [0·059%] in healthy controls with an adjusted OR of 44·84 [95% CI:3·91-514·34, p = 2·25 × 10(−3)]). POLN was involved in Epstein-Barr virus (EBV) lytic replication in NPC cells in vitro. POLN promoted viral DNA replication, immediate-early and late lytic gene expression, and progeny viral particle production, ultimately affecting the proliferation of host cells. The three mutations were located in two pivotal functional domains and were predicted to alter the protein stability of POLN in silico. Further assays demonstrated that POLN carrying any of the three mutations displayed reduced protein stability and decreased expression levels, thereby impairing its ability to promote complete EBV lytic replication and facilitate cell survival. INTERPRETATION: We identified a susceptibility gene POLN for familial NPC and elucidated its function. FUNDING: This study was funded by the National Key Research and Development Program of China (2021YFC2500400); the National Key Research and Development Program of China (2020YFC1316902); the Basic and Applied Basic Research Foundation of Guangdong Province, China (2021B1515420007); the National Natural Science Foundation of China (81973131); the National Natural Science Foundation of China (82003520); the National Natural Science Foundation of China (81903395).
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spelling pubmed-94860522022-09-21 Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication Xiao, Ruo-Wen Wang, Fang Wang, Tong-Min Zhang, Jiang-Bo Wu, Zi-Yi Deng, Chang-Mi Liao, Ying Zhou, Ting Yang, Da-Wei Dong, Si-Qi Xue, Wen-Qiong He, Yong-Qiao Zheng, Xiao-Hui Li, Xi-Zhao Zhang, Pei-Fen Zhang, Shao-Dan Hu, Ye-Zhu Liu, Yu-Ying Xia, Yun-Fei Gao, Song Mu, Jian-Bing Feng, Lin Jia, Wei-Hua eBioMedicine Articles BACKGROUND: Nasopharyngeal carcinoma (NPC) exhibits significant familial aggregation; however, its susceptibility genes are largely unknown. Thus, this study aimed to identify germline mutations that might contribute to the risk of familial NPC, and explore their biological functions. METHODS: Whole-exome sequencing was performed in 13 NPC pedigrees with multiple cases. Mutations co-segregated with disease status were further validated in a cohort composed of 563 probands from independent families, 2,953 sporadic cases, and 3,175 healthy controls. Experimental studies were used to explore the functions of susceptibility genes and their disease-related mutations. FINDINGS: The three rare missense mutations in POLN (DNA polymerase nu) gene, P577L, R303Q, and F545C, were associated with familial NPC risk (5/576 [0·87%] in cases vs. 2/3374 [0·059%] in healthy controls with an adjusted OR of 44·84 [95% CI:3·91-514·34, p = 2·25 × 10(−3)]). POLN was involved in Epstein-Barr virus (EBV) lytic replication in NPC cells in vitro. POLN promoted viral DNA replication, immediate-early and late lytic gene expression, and progeny viral particle production, ultimately affecting the proliferation of host cells. The three mutations were located in two pivotal functional domains and were predicted to alter the protein stability of POLN in silico. Further assays demonstrated that POLN carrying any of the three mutations displayed reduced protein stability and decreased expression levels, thereby impairing its ability to promote complete EBV lytic replication and facilitate cell survival. INTERPRETATION: We identified a susceptibility gene POLN for familial NPC and elucidated its function. FUNDING: This study was funded by the National Key Research and Development Program of China (2021YFC2500400); the National Key Research and Development Program of China (2020YFC1316902); the Basic and Applied Basic Research Foundation of Guangdong Province, China (2021B1515420007); the National Natural Science Foundation of China (81973131); the National Natural Science Foundation of China (82003520); the National Natural Science Foundation of China (81903395). Elsevier 2022-09-15 /pmc/articles/PMC9486052/ /pubmed/36116213 http://dx.doi.org/10.1016/j.ebiom.2022.104267 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Xiao, Ruo-Wen
Wang, Fang
Wang, Tong-Min
Zhang, Jiang-Bo
Wu, Zi-Yi
Deng, Chang-Mi
Liao, Ying
Zhou, Ting
Yang, Da-Wei
Dong, Si-Qi
Xue, Wen-Qiong
He, Yong-Qiao
Zheng, Xiao-Hui
Li, Xi-Zhao
Zhang, Pei-Fen
Zhang, Shao-Dan
Hu, Ye-Zhu
Liu, Yu-Ying
Xia, Yun-Fei
Gao, Song
Mu, Jian-Bing
Feng, Lin
Jia, Wei-Hua
Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title_full Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title_fullStr Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title_full_unstemmed Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title_short Rare POLN mutations confer risk for familial nasopharyngeal carcinoma through weakened Epstein-Barr virus lytic replication
title_sort rare poln mutations confer risk for familial nasopharyngeal carcinoma through weakened epstein-barr virus lytic replication
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486052/
https://www.ncbi.nlm.nih.gov/pubmed/36116213
http://dx.doi.org/10.1016/j.ebiom.2022.104267
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