Laboratory of Genetics, National Institute on Aging-Intramural Research Program, National Institutes of Health, Baltimore, MD 21224, USA.
J Mol Biol. 2013 Oct 9;425(19):3723-30. doi: 10.1016/j.jmb.2012.11.024. Epub 2012 Nov 23.
Eukaryotic cells transcribe a vast number of noncoding RNA species. Among them, long noncoding RNAs (lncRNAs) have been widely implicated in the regulation of gene transcription. However, examples of posttranscriptional gene regulation by lncRNAs are emerging. Through extended base-pairing, lncRNAs can stabilize or promote the translation of target mRNAs, while partial base-pairing facilitates mRNA decay or inhibits target mRNA translation. In the absence of complementarity, lncRNAs can suppress precursor mRNA splicing and translation by acting as decoys of RNA-binding proteins or microRNAs and can compete for microRNA-mediated inhibition leading to increased expression of the mRNA. Through these regulatory mechanisms, lncRNAs can elicit differentiation, proliferation, and cytoprotective programs, underscoring the rising recognition of lncRNA roles in human disease. In this review, we summarize the mechanisms of posttranscriptional gene regulation by lncRNAs identified until now.
真核细胞转录大量的非编码 RNA 种类。其中,长非编码 RNA(lncRNA)已被广泛牵涉到基因转录的调控中。然而,lncRNA 在后转录水平调控基因的实例正在不断涌现。通过扩展碱基配对,lncRNA 可以稳定或促进靶 mRNA 的翻译,而部分碱基配对则促进 mRNA 的降解或抑制靶 mRNA 的翻译。在没有互补性的情况下,lncRNA 可以通过充当 RNA 结合蛋白或 microRNA 的诱饵,或通过与 microRNA 竞争抑制来抑制前体 mRNA 的剪接和翻译,从而导致 mRNA 表达增加。通过这些调控机制,lncRNA 可以引发分化、增殖和细胞保护程序,突显了人们对 lncRNA 在人类疾病中的作用的认识不断提高。在这篇综述中,我们总结了迄今为止发现的 lncRNA 在后转录水平调控基因的机制。