CircRNAs: a regulator of cellular stress

被引:196
作者
Fischer, Joseph W. [1 ,2 ]
Leung, Anthony K. L. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, 615 North Wolfe St,W8041, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD USA
关键词
Circular RNA; stress; circRNA biogenesis; circRNA degradation; environment; circularization; back-splicing; RNA stability; CIRCULAR RNA EXPRESSION; MESSENGER-RNA; PROFILING REVEALS; CANCER-DIAGNOSIS; SRY TRANSCRIPT; OVARIAN-CANCER; NONCODING RNA; GROWTH-FACTOR; MOUSE TESTIS; GENE SRY;
D O I
10.1080/10409238.2016.1276882
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Circular RNAs (CircRNAs) were first identified as a viroid and later found to also be an endogenous RNA splicing product in eukaryotes. In recent years, a series of RNA-sequencing analyses from a diverse range of eukaryotes have shed new light on these eukaryotic circRNAs, revealing dynamic expression patterns in various developmental stages and physiological conditions. In this review, we focus on circRNAs implicated in stress response pathways and explore potential mechanisms underlying their regulation. To date, circRNAs have been shown to act as scaffolds in the assembly of protein complexes, sequester proteins from native subcellular localization, activate transcription of parental genes, inhibit RNA-protein interactions, and function as regulators of microRNA activity. Although the mechanism modulating circRNA levels during stress remains unclear, circRNAs are shown to be regulated during biogenesis, degradation, and exportation. As circRNAs do not have 5 and 3 ends, there are no entry points for exoribonucleases to initiate degradation. Such inherent stability makes this class of RNA a strong candidate to maintain homeostasis in the face of environmental challenges.
引用
收藏
页码:220 / 233
页数:14
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