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Novel regulation and functional interaction of polycistronic miRNAs

机译:多顺反子miRNA的新型调控和功能相互作用。

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The importance of microRNAs in gene expression and disease is well recognized. However, what is less appreciated is that almost half of miRNA genes are organized in polycistronic clusters and are therefore coexpressed. The mir-11-998 cluster consists of two miRNAs, miR-11 and miR-998. Here, we describe a novel layer of regulation that links the processing and expression of miR-998 to the presence of the mir-11 gene. We show that the presence of miR-11 in the pri-miRNA is required for processing by Drosha, and deletion of mir-11 prevents the expression of mi R-998. Replacing mir-11 with an unrelated mi RNA rescued miR-998 expression in vivo and in vitro, as did expressing miR-998 from a shorter, more canonical miRNA scaffold. The embedded regulation of miR-998 is functionally important because unchecked miR-998 expression in the absence of miR-11 resulted in pleiotropic developmental defects. This novel regulation of expression of miRNAs within a cluster is not limited to the mir-11-998 cluster and, thus, likely reflects the more general cis-regulation of expression of individual miRNAs. Collectively, our results uncover a novel layer of regulation within miRNA clusters that tempers the functions of the individual miRNAs. Unlinking their expression has the potential to change the expression of multiple miRNA targets and shift a biological response.
机译:众所周知,microRNA在基因表达和疾病中的重要性。然而,人们很少意识到的是,近一半的miRNA基因组织在多顺反子簇中,因此是共表达的。 mir-11-998簇包含两个miRNA,即miR-11和miR-998。在这里,我们描述了一个新的调控层,它将miR-998的加工和表达与mir-11基因的存在联系起来。我们显示pri-miRNA中miR-11的存在是Drosha处理所必需的,而mir-11的缺失则阻止了mi R-998的表达。用不相关的mi RNA替代mir-11可以在体内和体外挽救miR-998的表达,就像从较短,规范的miRNA支架中表达miR-998一样。 miR-998的嵌入式调控在功能上很重要,因为在没有miR-11的情况下未经检查的miR-998表达会导致多效性发育缺陷。簇内miRNA表达的这种新颖调节不仅限于mir-11-998簇,因此,可能反映了单个miRNA表达的更一般的顺式调节。总的来说,我们的结果揭示了miRNA簇内新的调控层,可调节单个miRNA的功能。解除它们的表达链接可能会改变多个miRNA靶标的表达并改变生物学反应。

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