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Comparative analysis of human and mouse expression data illuminates tissue-specific evolutionary patterns of miRNAs

机译:人类和小鼠表达数据的比较分析阐明了miRNA的组织特异性进化模式

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摘要

MicroRNAs (miRNAs) constitute an important class of gene regulators. While models have been proposed to explain their appearance and expansion, the validation of these models has been difficult due to the lack of comparative studies. Here, we analyze miRNA evolutionary patterns in two mammals, human and mouse, in relation to the age of miRNA families. In this comparative framework, we confirm some predictions of previously advanced models of miRNA evolution, e.g. that miRNAs arise more frequently de novo than by duplication, or that the number of protein-coding gene targeted by miRNAs decreases with evolutionary time. We also corroborate that miRNAs display an increase in expression level with evolutionary time, however we show that this relation is largely tissue-dependent, and especially low in embryonic or nervous tissues. We identify a bias of tag-sequencing techniques regarding the assessment of breadth of expression, leading us, contrary to predictions, to find more tissue-specific expression of older miRNAs. Together, our results refine the models used so far to depict the evolution of miRNA genes. They underline the role of tissue-specific selective forces on the evolution of miRNAs, as well as the potential co-evolution patterns between miRNAs and the protein-coding genes they target.
机译:微小RNA(miRNA)构成了一类重要的基因调节剂。虽然已经提出了模型来解释它们的出现和扩展,但是由于缺乏比较研究,很难对这些模型进行验证。在这里,我们分析了与miRNA家族的年龄有关的两种哺乳动物(人和小鼠)中的miRNA进化模式。在此比较框架中,我们确认了miRNA进化的先前高级模型的一些预测,例如miRNA从头开始出现的频率要高于通过复制产生的频率,或者miRNA靶向的蛋白质编码基因的数量随进化时间而减少。我们还证实了miRNA在进化水平上显示出表达水平的增加,但是我们证明这种关系在很大程度上取决于组织,尤其是在胚胎或神经组织中较低。我们发现在表达广度评估方面标签测序技术存在偏见,这导致我们发现与预期相反的事实是,发现更多的特定miRNA的组织特异性表达。总之,我们的结果完善了迄今为止用于描述miRNA基因进化的模型。他们强调了组织特异性选择力对miRNA进化的作用,以及miRNA与它们靶向的蛋白质编码基因之间潜在的共同进化模式。

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