Long Noncoding RNAs: Molecular Modalities to Organismal Functions

被引:202
作者
Rinn, John L. [1 ]
Chang, Howard Y. [2 ,3 ]
机构
[1] Univ Colorado, Dept Biochem, BioFrontiers Inst, Boulder, CO 80303 USA
[2] Stanford Univ, Ctr Personal Dynam Regulomes, Stanford, CA 94305 USA
[3] Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 89 | 2020年 / 89卷
基金
美国国家卫生研究院;
关键词
long noncoding RNA; lncRNA; RNA-protein interactions; nuclear; localization; RNA structure; massively parallel RNA reporter gene assays; MPRNA; RNA in vivo; RNA grammar; GENOME-WIDE ANALYSIS; X-CHROMOSOME INACTIVATION; XIST RNA; NUCLEAR-LOCALIZATION; PROTEIN INTERACTIONS; GENE-EXPRESSION; TELOMERASE RNA; ENHANCER RNAS; LIVING CELLS; LNCRNA;
D O I
10.1146/annurev-biochem-062917-012708
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
We have known for decades that long noncoding RNAs (lncRNAs) can play essential functions across most forms of life. The maintenance of chromosome length requires an lncRNA (e.g., hTERC) and two lncRNAs in the ribosome that are required for protein synthesis. Thus, lncRNAs can represent powerful RNA machines. More recently, it has become clear that mammalian genomes encode thousands more lncRNAs. Thus, we raise the question: Which, if any, of these lncRNAs could also represent RNA-based machines? Here we synthesize studies that are beginning to address this question by investigating fundamental properties of lncRNA genes, revealing new insights into the RNA structure-function relationship, determining cis- and trans-acting lncRNAs in vivo, and generating new developments in high-throughput screening used to identify functional lncRNAs. Overall, these findings provide a context toward understanding the molecular grammar underlying lncRNA biology.
引用
收藏
页码:283 / 308
页数:26
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