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Progressive lengthening of 3′ untranslated regions of mRNAs by alternative polyadenylation during mouse embryonic development

机译:在小鼠胚胎发育过程中通过交替的多腺苷酸化作用逐步延长mRNA的3非翻译区

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摘要

The 3′ untranslated regions (3′ UTRs) of mRNAs contain cis-acting elements for posttranscriptional regulation of gene expression. Here, we report that mouse genes tend to express mRNAs with longer 3′ UTRs as embryonic development progresses. This global regulation is controlled by alternative polyadenylation and coordinates with initiation of organogenesis and aspects of embryonic development, including morphogenesis, differentiation, and proliferation. Using myogenesis of C2C12 myoblast cells as a model, we recapitulated this process in vitro and found that 3′ UTR lengthening is likely caused by weakening of mRNA polyadenylation activity. Because alternative 3′ UTR sequences are typically longer and have higher AU content than constitutive ones, our results suggest that lengthening of 3′ UTR can significantly augment posttranscriptional control of gene expression during embryonic development, such as microRNA-mediated regulation.
机译:mRNA的3'非翻译区(3'UTR)包含顺式作用元件,用于基因表达的转录后调控。在这里,我们报道随着胚胎发育的进展,小鼠基因倾向于表达具有较长3'UTR的mRNA。这种全球性调控是由交替的聚腺苷酸化控制的,并与器官发生的开始和胚胎发育的各个方面(包括形态发生,分化和增殖)相协调。以C2C12成肌细胞的成肌为模型,我们在体外总结了这一过程,发现3'UTR延长很可能是由mRNA多聚腺苷酸化活性的减弱引起的。因为替代性3'UTR序列通常比组成性序列更长,并且具有更高的AU含量,所以我们的结果表明,延长3'UTR可以显着增强胚胎发育过程中基因表达的转录后控制,例如microRNA介导的调控。

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