Borchert Glen M, Holton Nathaniel W, Williams Jonathan D, Hernan William L, Bishop Ian P, Dembosky Joel A, Elste James E, Gregoire Nathaniel S, Kim Jee-Ah, Koehler Wesley W, Lengerich Joe C, Medema Arianna A, Nguyen Marilyn A, Ower Geoffrey D, Rarick Michelle A, Strong Brooke N, Tardi Nicholas J, Tasker Nathan M, Wozniak Darren J, Gatto Craig, Larson Erik D
School of Biological Sciences; Illinois State University; Normal, IL USA.
Mob Genet Elements. 2011 May;1(1):8-17. doi: 10.4161/mge.1.1.15766.
MicroRNAs (miRs) are small non-coding RNAs that generally function as negative regulators of target messenger RNAs (mRNAs) at the posttranscriptional level. MiRs bind to the 3'UTR of target mRNAs through complementary base pairing, resulting in target mRNA cleavage or translation repression. To date, over 15,000 distinct miRs have been identified in organisms ranging from viruses to man and interest in miR research continues to intensify. Of note, the most enlightening aspect of miR function-the mRNAs they target-continues to be elusive. Descriptions of the molecular origins of independent miR molecules currently support the hypothesis that miR hairpin generation is based on the adjacent insertion of two related transposable elements (TEs) at one genomic locus. Thus transcription across such TE interfaces establishes many, if not the majority of functional miRs. The implications of these findings are substantial for understanding how TEs confer increased genomic fitness, describing miR transcriptional regulations and making accurate miR target predictions. In this work, we have performed a comprehensive analysis of the genomic events responsible for the formation of all currently annotated miR loci. We find that the connection between miRs and transposable elements is more significant than previously appreciated, and more broadly, supports an important role for repetitive elements in miR origin, expression and regulatory network formation. Further, we demonstrate the utility of these findings in miR target prediction. Our results greatly expand the existing repertoire of defined miR origins, detailing the formation of 2,392 of 15,176 currently recognized miR genomic loci and supporting a mobile genetic element model for the genomic establishment of functional miRs.
微小RNA(miRs)是一类小的非编码RNA,通常在转录后水平作为靶信使RNA(mRNAs)的负调控因子发挥作用。miRs通过互补碱基配对与靶mRNAs的3'非翻译区(3'UTR)结合,导致靶mRNA切割或翻译抑制。迄今为止,在从病毒到人类的各种生物体中已鉴定出超过15,000种不同的miRs,并且对miR研究的兴趣持续增强。值得注意的是,miR功能中最具启发性的方面——它们所靶向的mRNAs——仍然难以捉摸。目前对独立miR分子分子起源的描述支持这样一种假说,即miR发夹结构的产生是基于两个相关转座元件(TEs)在一个基因组位点的相邻插入。因此,跨越此类TE界面的转录建立了许多(如果不是大多数)功能性miRs。这些发现对于理解TEs如何赋予基因组更高的适应性、描述miR转录调控以及进行准确的miR靶标预测具有重要意义。在这项工作中,我们对负责所有当前注释的miR基因座形成的基因组事件进行了全面分析。我们发现miRs与转座元件之间的联系比以前认识到的更为显著,更广泛地说,支持了重复元件在miR起源、表达和调控网络形成中的重要作用。此外,我们证明了这些发现在miR靶标预测中的实用性。我们的结果极大地扩展了已定义的miR起源的现有库,详细描述了15,176个当前公认的miR基因组位点中的2,392个的形成,并支持了功能性miRs基因组建立的移动遗传元件模型。