Transcriptional Regulation of Antiviral Interferon-Stimulated Genes

被引:144
|
作者
Wang, Wenshi [1 ,2 ]
Xu, Lei [1 ,2 ]
Su, Junhong [3 ]
Peppelenbosch, Maikel P. [1 ,2 ]
Pan, Qiuwei [1 ,2 ]
机构
[1] Erasmus MC, Univ Med Ctr, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[2] Postgrad Sch Mol Med, Rotterdam, Netherlands
[3] Kunming Univ Sci & Technol, Med Fac, Kunming, Peoples R China
关键词
ACTIVATED PROTEIN-KINASE; TUMOR-NECROSIS-FACTOR; HISTONE DEACETYLASE ACTIVITY; RANDOMIZED PHASE 2B; CHRONIC HEPATITIS-B; SERINE PHOSPHORYLATION; TYROSINE-PHOSPHATASE; PHOSPHATIDYLINOSITOL; 3-KINASE; SIGNAL-TRANSDUCTION; IKK-EPSILON;
D O I
10.1016/j.tim.2017.01.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interferon-stimulated genes (ISGs) are a group of gene products that coordinately combat pathogen invasions, in particular viral infections. Transcription of ISGs occurs rapidly upon pathogen invasion, and this is classically provoked via activation of the Janus kinase/signal transducer and activator of transcription (JAK-STAT) pathway, mainly by interferons (IFNs). However, a plethora of recent studies have reported a variety of non-canonical mechanisms regulating ISG transcription. These new studies are extremely important for understanding the quantitative and temporal differences in ISG transcription under specific circumstances. Because these canonical and non-canonical regulatory mechanisms are essential for defining the nature of host defense and associated detrimental proinflammatory effects, we comprehensively review the state of this rapidly evolving field and the clinical implications of recently acquired knowledge in this respect.
引用
收藏
页码:574 / 585
页数:12
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