Transfer RNA-Derived Small RNAs: Another Layer of Gene Regulation and Novel Targets for Disease Therapeutics

被引:81
作者
Kim, Hak Kyun [1 ]
Yeom, Ji-Hyun [1 ]
Kay, Mark A. [2 ,3 ]
机构
[1] Chung Ang Univ, Dept Life Sci, Seoul 06974, South Korea
[2] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Genet, Stanford, CA 94305 USA
基金
美国国家卫生研究院; 新加坡国家研究基金会;
关键词
SMALL NONCODING RNAS; SPLICING ENDONUCLEASE; TRANSLATIONAL CONTROL; SEQUENCING REVEALS; OXIDATIVE STRESS; FRAGMENTS TRFS; MESSENGER-RNA; RIBOSOMAL-RNA; CYTOCHROME-C; PROTEIN;
D O I
10.1016/j.ymthe.2020.09.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Decades after identification as essential for protein synthesis, transfer RNAs (tRNAs) have been implicated in various cellular processes beyond translation. tRNA-derived small RNAs (tsRNAs), referred to as tRNA-derived fragments (tRFs) or tRNA-derived, stress-induced RNAs (tiRNAs), are produced by cleavage at different sites from mature or pre-tRNAs. They are classified into six major types representing potentially thousands of unique sequences and have been implicated to play a wide variety of regulatory roles in maintaining normal homeostasis, cancer cell viability, tumorigenesis, ribosome biogenesis, chromatin remodeling, translational regulation, intergenerational inheritance, retrotransposon regulation, and viral replication. However, the detailed mechanisms governing these processes remain unknown. Aberrant expression of tsRNAs is found in various human disease conditions, suggesting that a further understanding of the regulatory role of tsRNAs will assist in identifying novel biomarkers, potential therapeutic targets, and gene-regulatory tools. Here, we highlight the classification, biogenesis, and biological role of tsRNAs in regulatory mechanisms of normal and disease states.
引用
收藏
页码:2340 / 2357
页数:18
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