Zhang Yang, Yang Li, Chen Ling-Ling
State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai, China.
Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Int J Biochem Cell Biol. 2014 Sep;54:338-49. doi: 10.1016/j.biocel.2013.10.009. Epub 2013 Oct 26.
While most long noncoding RNAs (lncRNAs) appear indistinguishable from mRNAs, having 5' cap structures and 3' poly(A) tails, recent work has revealed new formats. Rather than taking advantage of the canonical cleavage and polyadenylation for their 3' end maturation, such lncRNAs are processed and stablized by a number of other mechanisms, including the RNase P cleavage to generate a mature 3' end, or capped by snoRNP complexes at both ends, or by forming circular structures. Importantly, such lncRNAs have also been implicated in gene expression regulation in mammalian cells. Here, we highlight recent progress in our understanding of the biogenesis and function of lncRNAs without a poly(A) tail. This paper is part of a directed issue entitled: The Non-coding RNA Revolution.
虽然大多数长链非编码RNA(lncRNA)看起来与mRNA难以区分,具有5'帽结构和3' poly(A)尾,但最近的研究揭示了新的形式。这类lncRNA并非利用经典的切割和聚腺苷酸化来实现其3'端成熟,而是通过多种其他机制进行加工和稳定,包括通过核糖核酸酶P切割产生成熟的3'端,或两端被snoRNP复合物加帽,或形成环状结构。重要的是,这类lncRNA也参与了哺乳动物细胞中的基因表达调控。在这里,我们重点介绍了我们对无poly(A)尾lncRNA的生物发生和功能的理解的最新进展。本文是名为:非编码RNA革命的定向专题的一部分。