鼻咽癌
溶解循环
生物
爱泼斯坦-巴尔病毒
基因
遗传学
突变
病毒
病毒复制
病毒学
医学
内科学
放射治疗
作者
Ruowen Xiao,Fang Wang,Tong‐Min Wang,Jiangbo Zhang,Ziyi Wu,Changmi Deng,Ying Liao,Ting Zhou,Dawei Yang,Siqi Dong,Wen‐Qiong Xue,Yong‐Qiao He,Xiao‐Hui Zheng,Xi‐Zhao Li,Peifen Zhang,Shaodan Zhang,Ye‐Zhu Hu,Yuying Liu,Yunfei Xia,Song Gao
出处
期刊:EBioMedicine
[Elsevier BV]
日期:2022-09-15
卷期号:84: 104267-104267
被引量:14
标识
DOI:10.1016/j.ebiom.2022.104267
摘要
BackgroundNasopharyngeal 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.MethodsWhole-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.FindingsThe 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.InterpretationWe identified a susceptibility gene POLN for familial NPC and elucidated its function.FundingThis 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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