Linking RNA biology to lncRNAs

被引:145
作者
Goff, Loyal A. [1 ,2 ]
Rinn, John L. [3 ,4 ,5 ]
机构
[1] Johns Hopkins Univ, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Dept Neurosci, Baltimore, MD 21205 USA
[3] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[4] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[5] Broad Inst, Cambridge, MA 02142 USA
关键词
LONG NONCODING RNAS; HUMAN TRANSCRIPTOME; RIBOSOMAL-RNA; XIST RNA; SECONDARY STRUCTURE; FLEXIBLE SCAFFOLD; BINDING PROTEINS; YEAST TELOMERASE; GENE-EXPRESSION; MESSENGER-RNAS;
D O I
10.1101/gr.191122.115
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 regulatory potential of RNA has never ceased to amaze: from RNA catalysis, to RNA-mediated splicing, to RNA-based silencing of an entire chromosome during dosage compensation. More recently, thousands of long noncoding RNA (lncRNA) transcripts have been identified, the majority with unknown function. Thus, it is tempting to think that these lncRNAs represent a cadre of new factors that function through ribonucleic mechanisms. Some evidence points to several lncRNAs with tantalizing physiological contributions and thought-provoking molecular modalities. However, dissecting the RNA biology of lncRNAs has been difficult, and distinguishing the independent contributions of functional RNAs from underlying DNA elements, or the local act of transcription, is challenging. Here, we aim to survey the existing literature and highlight future approaches that will be needed to link the RNA-based biology and mechanisms of lncRNAs in vitro and in vivo.
引用
收藏
页码:1456 / 1465
页数:10
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