Inhibition of PKR by RNA and DNA viruses

被引:172
作者
Langland, Jeffrey O.
Cameron, Jason M.
Heck, Michael C.
Jancovich, James K.
Jacobs, Bertram L. [1 ]
机构
[1] Arizona State Univ, Biodesign Inst, Ctr Infect Dis & Vaccinol, Tempe, AZ 85287 USA
[2] Arizona State Univ, Sch Life Sci, Grad Program Mol & Cellular Biol, Tempe, AZ 85287 USA
关键词
PKR; interferon; interferon-resistance; RNA viruses; DNA viruses; innate immune evasion;
D O I
10.1016/j.virusres.2005.10.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Interferons were the first of the anti-viral innate immune modulators to be characterized, initially characterized solely as anti-viral proteins [reviewed in Le Page, C., Genin, R, Baines, M.G., Hiscott, J., 2000. Inteferon activation and innate immunity. Rev. Immunogenet. 2, 374-386]. As we have progressed in our understanding of the interferons they have taken a more central role in our understanding of innate immunity and its interplay with the adaptive immune response. One of the key players in function of interferon is the interferon-inducible enzyme, protein kinase (PKR, activatable by RNA). The key role played by PKR in the innate response to virus infection is emphasized by the large number of viruses, DNA viruses as well as RNA viruses, whose hosts range from insects to humans, that code for PKR inhibitors. In this review we will first describe activation of PKR and then describe the myriad of ways that viruses inhibit function of PKR. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 110
页数:11
相关论文
共 135 条
[11]   The Tat protein of human immunodeficiency virus type 1 is a substrate and inhibitor of the interferon-induced, virally activated protein kinase, PKR [J].
Brand, SR ;
Kobayashi, R ;
Mathews, MB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (13) :8388-8395
[12]   Both carboxy- and amino-terminal domains of the vaccinia virus interferon resistance gene, E3L, are required for pathogenesis in a mouse model [J].
Brandt, TA ;
Jacobs, BL .
JOURNAL OF VIROLOGY, 2001, 75 (02) :850-856
[13]  
Burysek L, 1999, J HUMAN VIROL, V2, P19
[14]   Latently expressed human herpesvirus 8-encoded interferon regulatory factor 2 inhibits double-stranded RNA-activated protein kinase [J].
Burysek, L ;
Pitha, PM .
JOURNAL OF VIROLOGY, 2001, 75 (05) :2345-2352
[15]  
CARROLL K, 1993, J BIOL CHEM, V268, P12837
[16]  
CASSADY KA, 2002, J VIROL, V75, P2345
[17]   RESCUE OF VACCINIA VIRUS LACKING THE E3L GENE BY MUTANTS OF E3L [J].
CHANG, HW ;
URIBE, LH ;
JACOBS, BL .
JOURNAL OF VIROLOGY, 1995, 69 (10) :6605-6608
[18]  
CHANG YF, 1992, J DNA SEQ MAP, V3, P89
[19]   Signals that dictate nuclear, nucleolar, and cytoplasmic shuttling of the γ134.5 protein of herpes simplex virus type 1 [J].
Cheng, GF ;
Brett, ME ;
He, B .
JOURNAL OF VIROLOGY, 2002, 76 (18) :9434-9445
[20]   Biophysical characterization of the complex between double-stranded RNA and the N-terminal domain of the NS1 protein from influenza A virus: Evidence for a novel RNA-binding mode [J].
Chien, CY ;
Xu, YJ ;
Xiao, R ;
Aramini, JM ;
Sahasrabudhe, PV ;
Krug, RM ;
Montelione, GT .
BIOCHEMISTRY, 2004, 43 (07) :1950-1962