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Pervasive regulation of Drosophila Notch target genes by GY-box- Brd-box- and K-box-class microRNAs

机译:果蝇Notch靶基因的GY框Brd框和K框类microRNA的普遍调节。

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摘要

Although hundreds of distinct animal microRNAs (miRNAs) are known, the specific biological functions of only a handful are understood at present. Here, we demonstrate that three different families of Drosophila miRNAs directly regulate two large families of Notch target genes, including basic helix–loop–helix (bHLH) repressor and Bearded family genes. These miRNAs regulate Notch target gene activity via GY-box (GUCUUCC), Brd-box (AGCUUUA), and K-box (cUGUGAUa) motifs. These are conserved sites in target 3′-untranslated regions (3′-UTRs) that are complementary to the 5′-ends of miRNAs, or “seed” regions. Collectively, these motifs represent >40 miRNA-binding sites in Notch target genes, and we show all three classes of motif to be necessary and sufficient for miRNA-mediated regulation in vivo. Importantly, many of the validated miRNA-binding sites have limited pairing to miRNAs outside of the “box:seed” region. Consistent with this, we find that seed-related miRNAs that are otherwise quite divergent can regulate the same target sequences. Finally, we demonstrate that ectopic expression of several Notch-regulating miRNAs induces mutant phenotypes that are characteristic of Notch pathway loss of function, including loss of wing margin, thickened wing veins, increased bristle density, and tufted bristles. Collectively, these data establish insights into miRNA target recognition and demonstrate that the Notch signaling pathway is a major target of miRNA-mediated regulation in Drosophila.
机译:尽管已知数百种不同的动物microRNA(miRNA),但目前仅了解少数几种特定的生物学功能。在这里,我们证明了果蝇miRNA的三个不同家族直接调节Notch靶基因的两个大家族,包括基本螺旋-环-螺旋(bHLH)阻遏物和Bearded家族基因。这些miRNA通过GY-box(GUCUUCC),Brd-box(AGCUUUA)和K-box(cUGUGAUa)​​基序调节Notch靶基因的活性。这些是靶标3'非翻译区(3'-UTR)中的保守位点,与miRNA或“种子”区的5'端互补。这些基序共同代表Notch靶基因中的40多个miRNA结合位点,并且我们显示所有这三类基序对于miRNA介导的体内调节都是必要和充分的。重要的是,许多经过验证的miRNA结合位点与“ box:seed”区域之外的miRNA的配对受到限制。与此相符,我们发现原本相当不同的种子相关miRNA可以调节相同的靶序列。最后,我们证明了几种Notch调节miRNA的异位表达诱导了Notch通路功能丧失的特征性突变表型,包括机翼边缘缺失,机翼静脉增厚,刷毛密度增加和簇状刷毛。总体而言,这些数据建立了对miRNA靶标识别的见识,并证明Notch信号通路是果蝇中miRNA介导的调控的主要靶标。

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