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Young intragenic miRNAs are less coexpressed with host genes than old ones: implications of miRNA–host gene coevolution

机译:年轻的内源性miRNA与宿主基因的共表达要比旧基因少:miRNA-宿主基因协同进化的意义

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摘要

MicroRNAs (miRNAs) have emerged as key regulators of gene expression. Intragenic miRNAs account for ∼50% of mammalian miRNAs. Classic studies reported that they are usually coexpressed with host genes. Here, using genome-wide miRNA and gene expression profiles from five sample sets, we show that evolutionarily conserved (‘old’) intragenic miRNAs tend to be coexpressed with host genes, but non-conserved (‘young’) ones rarely do so. This result is robust: in all sample sets, the coexpression rate of young miRNAs is significantly lower than that of conserved ones even after controlling for abundance. As a result, although young miRNAs dominate in human genome, the majority of intragenic miRNAs that show coexpression with host genes are phylogenetically old ones. For younger miRNAs, extrapolation of their expression profiles from those of their host genes should be treated with caution. We propose a model to explain this phenomenon in which the majority of young miRNAs are unlikely to be coexpressed with host genes; however, for some fraction of young miRNAs coexpression with their host genes, initially imbued by chromatin level effects, is advantageous and these are the ones likely to embed into the system and evolve ever higher levels of coexpression, possibly by evolving piggybacking mechanisms.
机译:微小RNA(miRNA)已经成为基因表达的关键调节因子。基因内miRNA约占哺乳动物miRNA的50%。经典研究报告说,它们通常与宿主基因共表达。在这里,使用来自五个样本集的全基因组miRNA和基因表达谱,我们显示出进化保守的(“旧”)基因内miRNA倾向于与宿主基因共表达,但非保守的(“年轻”)基因很少。该结果是可靠的:在所有样品集中,即使控制了丰度,年轻miRNA的共表达率也显着低于保守miRNA的共表达率。结果,尽管年轻的miRNA在人类基因组中占主导地位,但大多数与宿主基因共表达的基因内miRNA都是系统发育较老的。对于年轻的miRNA,应谨慎对待从其宿主基因的表达谱推断其表达谱。我们提出了一个模型来解释这种现象,其中大多数年轻的miRNA不太可能与宿主基因共表达。但是,对于某些年轻的miRNA与宿主基因的共表达,最初受到染色质水平的影响,是有利的,并且可能嵌入系统并发展出更高水平的共表达,可能是通过piggy带机制的发展。

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