A recap of RNA recapping

被引:40
作者
Trotman, Jackson B. [1 ,2 ,3 ]
Schoenberg, Daniel R. [1 ]
机构
[1] Ohio State Univ, Dept Biol Chem & Pharmacol, Ctr RNA Biol, Columbus, OH 43210 USA
[2] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
capping; cytoplasm; m7G cap; transcriptome complexity; translational control; CAP-BINDING PROTEIN; QUALITY-CONTROL MECHANISM; GLOBIN MESSENGER-RNAS; CAPPING ENZYME BINDS; CRYSTAL-STRUCTURE; POLY(A) TAIL; ERYTHROID TISSUES; DINUCLEOTIDE CAP; TRANSLATION; COMPLEX;
D O I
10.1002/wrna.1504
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The N7-methylguanosine cap is a hallmark of the 5 ' end of eukaryotic mRNAs and is required for gene expression. Loss of the cap was believed to lead irreversibly to decay. However, nearly a decade ago, it was discovered that mammalian cells contain enzymes in the cytoplasm that are capable of restoring caps onto uncapped RNAs. In this review, we summarize recent advances in our understanding of cytoplasmic RNA recapping and discuss the biochemistry of this process and its impact on regulating and diversifying the transcriptome. Although most studies focus on mammalian RNA recapping, we also highlight new observations for recapping in disparate eukaryotic organisms, with the trypanosome recapping system appearing to be a fascinating example of convergent evolution. We conclude with emerging insights into the biological significance of RNA recapping and prospects for the future of this evolving area of study. This article is categorized under: RNA Processing > RNA Editing and Modification Translation > Translation Regulation RNA Processing > Capping and 5 ' End Modifications RNA Turnover and Surveillance > Regulation of RNA Stability
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页数:13
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