mRNA capping: biological functions and applications

被引:592
作者
Ramanathan, Anand [1 ,2 ]
Robb, G. Brett [1 ]
Chan, Siu-Hong [1 ]
机构
[1] New England Biolabs Inc, 240 Cty Rd, Ipswich, MA 01938 USA
[2] Agios Pharmaceut, 88 Sidney St, Cambridge, MA 02139 USA
关键词
CAP-BINDING COMPLEX; VESICULAR STOMATITIS-VIRUS; RECEPTOR RIG-I; 25-KDA THIAMINE TRIPHOSPHATASE; QUALITY-CONTROL MECHANISM; CARBOXY-TERMINAL DOMAIN; CENTRAL-NERVOUS-SYSTEM; IFIT FAMILY-MEMBERS; BLUETONGUE VIRUS; STRUCTURAL BASIS;
D O I
10.1093/nar/gkw551
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
The 5' m7G cap is an evolutionarily conserved modification of eukaryotic mRNA. Decades of research have established that the m7G cap serves as a unique molecular module that recruits cellular proteins and mediates cap-related biological functions such as pre-mRNA processing, nuclear export and cap-dependent protein synthesis. Only recently has the role of the cap 2'O methylation as an identifier of self RNA in the innate immune system against foreign RNA has become clear. The discovery of the cytoplasmic capping machinery suggests a novel level of control network. These new findings underscore the importance of a proper cap structure in the synthesis of functional messenger RNA. In this review, we will summarize the current knowledge of the biological roles of mRNA caps in eukaryotic cells. We will also discuss different means that viruses and their host cells use to cap their RNA and the application of these capping machineries to synthesize functional mRNA. Novel applications of RNA capping enzymes in the discovery of new RNA species and sequencing the microbiome transcriptome will also be discussed. We will end with a summary of novel findings in RNA capping and the questions these findings pose.
引用
收藏
页码:7511 / 7526
页数:16
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