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Cooperative target mRNA destabilization and translation inhibition by miR-58 microRNA family in C. elegans

机译:秀丽隐杆线虫中miR-58 microRNA家族的合作目标mRNA失稳和翻译抑制

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摘要

In animals, microRNAs frequently form families with related sequences. The functional relevance of miRNA families and the relative contribution of family members to target repression have remained, however, largely unexplored. Here, we used the Caenorhabditis elegans miR-58 miRNA family, composed primarily of the four highly abundant members miR-58.1, miR-80, miR-81, and miR-82, as a model to investigate the redundancy of miRNA family members and their impact on target expression in an in vivo setting. We found that miR-58 family members repress largely overlapping sets of targets in a predominantly additive fashion. Progressive deletions of miR-58 family members lead to cumulative up-regulation of target protein and RNA levels. Phenotypic defects could only be observed in the family quadruple mutant, which also showed the strongest change in target protein levels. Interestingly, although the seed sequences of miR-80 and miR-58.1 differ in a single nucleotide, predicted canonical miR-80 targets were efficiently up-regulated in the mir-58.1 single mutant, indicating functional redundancy of distinct members of this miRNA family. At the aggregate level, target binding leads mainly to mRNA degradation, although we also observed some degree of translational inhibition, particularly in the single miR-58 family mutants. These results provide a framework for understanding how miRNA family members interact to regulate target mRNAs.
机译:在动物中,microRNA经常与相关序列形成家族。 miRNA家族的功能相关性和家族成员对靶向抑制的相对贡献仍未得到充分探索。在这里,我们使用秀丽隐杆线虫miR-58 miRNA家族(主要由四个高度丰富的成员miR-58.1,miR-80,miR-81和miR-82组成)作为模型来研究miRNA家族成员的冗余和它们在体内对靶标表达的影响。我们发现miR-58家族成员主要以累加方式抑制大部分重叠的靶标。 miR-58家族成员的逐渐缺失导致靶蛋白和RNA水平的累积上调。表型缺陷只能在家族四倍体突变体中观察到,该突变体还显示出目标蛋白质水平的最强变化。有趣的是,尽管miR-80和miR-58.1的种子序列在单个核苷酸上有所不同,但在mir-58.1单个突变体中有效预测了预定的规范性miR-80靶标,表明该miRNA家族不同成员的功能冗余。在总体水平上,目标结合主要导致mRNA降解,尽管我们也观察到了一定程度的翻译抑制,尤其是在单个miR-58家族突变体中。这些结果为理解miRNA家族成员如何相互作用以调节靶标mRNA提供了框架。

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