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比较分析人和鼠的表达数据揭示了 miRNA 在组织特异性进化中的模式。

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

机构信息

Department of Ecology and Evolution, Biophore, University of Lausanne, Switzerland.

出版信息

Nucleic Acids Res. 2012 Jul;40(13):5890-900. doi: 10.1093/nar/gks279. Epub 2012 Mar 28.

Abstract

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.

摘要

微小 RNA(miRNAs)是一类重要的基因调控因子。虽然已经提出了一些模型来解释它们的出现和扩展,但由于缺乏比较研究,这些模型的验证一直很困难。在这里,我们分析了两种哺乳动物,人类和小鼠中的 miRNA 进化模式与 miRNA 家族的年龄之间的关系。在这个比较框架中,我们证实了一些先前提出的 miRNA 进化模型的预测,例如 miRNA 更多地是从头产生而不是通过复制产生,或者 miRNA 靶向的蛋白质编码基因数量随进化时间减少。我们还证实了 miRNA 的表达水平随进化时间增加,但我们表明这种关系在很大程度上依赖于组织,尤其是在胚胎或神经组织中较低。我们发现了标签测序技术在评估表达广度方面存在偏差,这导致我们与预测相反,发现较老的 miRNA 具有更多的组织特异性表达。总之,我们的结果细化了迄今为止用于描述 miRNA 基因进化的模型。它们强调了组织特异性选择压力对 miRNA 进化的作用,以及 miRNA 与其靶向的蛋白质编码基因之间的潜在共同进化模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/436f/3401464/5660b18fada4/gks279f1.jpg

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