The Multiple Functions of TRBP, at the Hub of Cell Responses to Viruses, Stress, and Cancer

被引:78
作者
Daniels, Sylvanne M. [1 ,2 ]
Gatignol, Anne [1 ,2 ,3 ]
机构
[1] McGill Univ, Lady Davis Inst Med Res, Montreal, PQ, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] McGill Univ, Div Expt Med, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
RNA-BINDING-PROTEIN; DOUBLE-STRANDED-RNA; SMALL INTERFERING RNAS; HIV-1 TAR RNA; TERMINAL REPEAT EXPRESSION; DEPENDENT KINASE PKR; RISC-LOADING COMPLEX; HUMAN DICER; IN-VIVO; MICRORNA BIOGENESIS;
D O I
10.1128/MMBR.00012-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The TAR RNA binding protein (TRBP) has emerged as a key player in many cellular processes. First identified as a cellular protein that facilitates the replication of human immunodeficiency virus, TRBP has since been shown to inhibit the activation of protein kinase R (PKR), a protein involved in innate immune responses and the cellular response to stress. It also binds to the PKR activator PACT and regulates its function. TRBP also contributes to RNA interference as an integral part of the minimal RNA-induced silencing complex with Dicer and Argonaute proteins. Due to its multiple functions in the cell, TRBP is involved in oncogenesis when its sequence is mutated or its expression is deregulated. The depletion or overexpression of TRBP results in malignancy, suggesting that the balance of TRBP expression is key to normal cellular function. These studies show that TRBP is multifunctional and mediates cross talk between different pathways. Its activities at the molecular level impact the cellular function from normal development to cancer and the response to infections.
引用
收藏
页码:652 / 666
页数:15
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