Continuing analysis of microRNA origins: Formation from transposable element insertions and noncoding RNA mutations.

Mobile genetic elements Pub Date : 2013-11-01 Epub Date: 2014-01-10 DOI:10.4161/mge.27755
Justin T Roberts, Elvera A Cooper, Connor J Favreau, Jacob S Howell, Lee G Lane, James E Mills, Derrick C Newman, Tabitha J Perry, Meaghan E Russell, Brittany M Wallace, Glen M Borchert
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引用次数: 29

Abstract

MicroRNAs (miRs) are small noncoding RNAs that typically act as regulators of gene expression by base pairing with the 3' UTR of messenger RNAs (mRNAs) and either repressing their translation or initiating degradation. As of this writing over 24,500 distinct miRs have been identified, but the functions of the vast majority of these remain undescribed. This paper represents a summary of our in depth analysis of the genomic origins of miR loci, detailing the formation of 1,213 of the 7,321 recently identified miRs and thereby bringing the total number of miR loci with defined molecular origin to 3,605. Interestingly, our analyses also identify evidence for a second, novel mechanism of miR locus generation through describing the formation of 273 miR loci from mutations to other forms of noncoding RNAs. Importantly, several independent investigations of the genomic origins of miR loci have now supported the hypothesis that miR hairpins are formed by the adjacent genomic insertion of two complementary transposable elements (TEs) into opposing strands. While our results agree that subsequent transcription over such TE interfaces leads to the formation of the majority of functional miR loci, we now also find evidence suggesting that a subset of miR loci were actually formed by an alternative mechanism-point mutations in other structurally complex, noncoding RNAs (e.g., tRNAs and snoRNAs).

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microRNA起源的持续分析:转座元件插入和非编码RNA突变的形成。
MicroRNAs (miRs)是一种小的非编码rna,通常通过与信使rna (mrna)的3' UTR碱基配对,抑制其翻译或启动降解,从而作为基因表达的调节剂。在撰写本文时,已经确定了超过24,500种不同的mir,但其中绝大多数的功能仍未被描述。本文总结了我们对miR位点基因组起源的深入分析,详细介绍了最近鉴定的7,321个miR中的1,213个的形成,从而使具有确定分子起源的miR位点总数达到3,605个。有趣的是,我们的分析还通过描述从突变到其他形式的非编码rna的273个miR位点的形成,确定了miR位点产生的第二种新机制的证据。重要的是,对miR位点基因组起源的几项独立研究现在支持了miR发夹是由相邻的基因组插入两个互补的转座因子(te)到相反的链中形成的假设。虽然我们的研究结果一致认为,在这些TE界面上的后续转录会导致大多数功能性miR位点的形成,但我们现在也发现证据表明,miR位点的一个子集实际上是由其他结构复杂的非编码rna(例如trna和snorna)中的点突变形成的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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