TMEM106A inhibits enveloped virus release from cell surface

被引:3
|
作者
Mao, Dexin [1 ,2 ]
Yan, Feixiang [1 ,2 ]
Zhang, Xiaolin [1 ]
Gao, Guangxia [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Biophys, CAS Key Lab Infect & Immun, 15 Datun Rd, Beijing 100101, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; FRONTOTEMPORAL DEMENTIA; RISK-FACTOR; HIV-1; INFECTION; PROTEIN; TETHERIN; LOCALIZATION; EXPRESSION; TYPE-1; OLIGOMERIZATION;
D O I
10.1016/j.isci.2022.103843
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enveloped viruses pose constant threat to hosts from ocean to land. Virion particle release from cell surface is a critical step in the viral life cycle for most enveloped viruses, making it a common antiviral target for the host defense system. Here we report that host factor TMEM106A inhibits the release of enveloped viruses from the cell surface. TMEM106A is a type II transmembrane protein localized on the plasma membrane and can be incorporated into HIV-1 virion particles. Through intermolecular interactions of its C-terminal domains on virion particle and plasma membrane, TMEM106A traps virion particles to the cell surface. HIV-1 Env interacts with TMEM106A to interfere with the intermolecular interactions and partially suppresses its antiviral activity. TMEM106A orthologs from various species displayed potent antiviral activity against multiple enveloped viruses. These results suggest that TMEM106A is an evolutionarily conserved antiviral factor that inhibits the release of enveloped viruses from the cell surface.
引用
收藏
页数:25
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