PDZD8 Is a Novel Gag-Interacting Factor That Promotes Retroviral Infection

被引:29
作者
Henning, Matthew S. [1 ]
Morham, Scott G. [2 ]
Goff, Stephen P. [3 ]
Naghavi, Mojgan H. [1 ]
机构
[1] Natl Univ Ireland Univ Coll Dublin, Ctr Res Infect Dis, Sch Med & Med Sci, Dublin 4, Ireland
[2] Myriad Pharmaceut Inc, Salt Lake City, UT 84108 USA
[3] Columbia Univ, Howard Hughes Med Inst, Dept Biochem & Mol Biophys, New York, NY 10032 USA
基金
爱尔兰科学基金会;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; STABLE MICROTUBULE FORMATION; REVERSE TRANSCRIPTION; HIV-1; REPLICATION; CULTURED-CELLS; LIFE-CYCLE; T-CELLS; PROTEIN; DOMAINS; ESTABLISHMENT;
D O I
10.1128/JVI.00843-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In a yeast two-hybrid screen for cellular factors that could interact with human immunodeficiency virus type 1 (HIV-1) Gag protein, we identified PDZD8 and confirmed the interaction by coimmunoprecipitation (co-IP). PDZD8 overexpression promoted the initiation of reverse transcription and increased infection by pseudotyped retroviruses independent of the route of viral entry, while transient knockdown of endogenous levels decreased HIV-1 infection. A mutant of PDZD8 lacking a predicted coiled-coil domain in its Gag-interacting region failed to bind Gag and promote HIV-1 infection, identifying the domain of PDZD8 required for mediating these effects. As such, we identify PDZD8 as a novel positive mediator of retroviral infection.
引用
收藏
页码:8990 / 8995
页数:6
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