The Human Cytomegalovirus Major Immediate-Early Proteins as Antagonists of Intrinsic and Innate Antiviral Host Responses

被引:50
|
作者
Paulus, Christina [1 ]
Nevels, Michael [1 ]
机构
[1] Univ Regensburg, Inst Med Microbiol & Hyg, D-93053 Regensburg, Germany
来源
VIRUSES-BASEL | 2009年 / 1卷 / 03期
关键词
cytomegalovirus; CMV; innate immunity; intrinsic defense; interferon response; nuclear domain 10; apoptosis; immediate-early genes; IE1; IE2; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; LOW-MULTIPLICITY INFECTION; IE2 86-KILODALTON PROTEIN; CELL-CYCLE PROGRESSION; VIRAL GENE-EXPRESSION; NUCLEAR-BODIES; IE86; PROTEIN; FUNCTIONAL INTERACTION; DNA-REPLICATION;
D O I
10.3390/v1030760
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The major immediate-early (IE) gene of human cytomegalovirus (CMV) is believed to have a decisive role in acute infection and its activity is an important indicator of viral reactivation from latency. Although a variety of gene products are expressed from this region, the 72-kDa IE1 and the 86-kDa IE2 nuclear phosphoproteins are the most abundant and important. Both proteins have long been recognized as promiscuous transcriptional regulators. More recently, a critical role of the IE1 and IE2 proteins in counteracting non-adaptive host cell defense mechanisms has been revealed. In this review we will briefly summarize the available literature on IE1- and IE2-dependent mechanisms contributing to CMV evasion from intrinsic and innate immune responses.
引用
收藏
页码:760 / 779
页数:20
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