Post-transcriptional regulation of gene expression in innate immunity

被引:292
作者
Carpenter, Susan [1 ]
Ricci, Emiliano P. [2 ]
Mercier, Blandine C. [2 ]
Moore, Melissa J. [2 ]
Fitzgerald, Katherine A. [1 ,3 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Med, Div Infect Dis & Immunol,Program Innate Immun, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Howard Hughes Med Inst, Worcester, MA 01605 USA
[3] Norwegian Univ Sci & Technol, Dept Canc Res & Mol Med, Ctr Mol Inflammat Res, N-7491 Trondheim, Norway
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; MESSENGER-RNA TRANSLATION; SPLICE VARIANT; NONCODING RNA; TNF-ALPHA; TRANSCRIPTIONAL REGULATION; DEPENDENT TRANSLATION; GAMMA-INTERFERON; TEMPORAL-ORDER; CUTTING EDGE;
D O I
10.1038/nri3682
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate immune responses combat infectious microorganisms by inducing inflammatory responses, antimicrobial pathways and adaptive immunity. Multiple genes within each of these functional categories are coordinately and temporally regulated in response to distinct external stimuli. The substantial potential of these responses to drive pathological inflammation and tissue damage highlights the need for rigorous control of these responses. Although transcriptional control of inflammatory gene expression has been studied extensively, the importance of post-transcriptional regulation of these processes is less well defined. In this Review, we discuss the regulatory mechanisms that occur at the level of mRNA splicing, mRNA polyadenylation, mRNA stability and protein translation, and that have instrumental roles in controlling both the magnitude and duration of the inflammatory response.
引用
收藏
页码:361 / 376
页数:16
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