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ΔNp63 intronic miR-944 is implicated in the ΔNp63-mediated induction of epidermal differentiation

机译:ΔNp63内含子miR-944与ΔNp63介导的表皮分化诱导有关

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摘要

ΔNp63 is required for both the proliferation and differentiation of keratinocytes, but its role in the differentiation of these cells is poorly understood. The corresponding gene, TP63, harbors the MIR944 sequence within its intron. However, the mechanism of biogenesis and the function of miR-944 are unknown. We found that miR-944 is highly expressed in keratinocytes, in a manner that is concordant with that of ΔNp63 mRNA, but the regulation of miR-944 expression under various conditions did not correspond with that of ΔNp63. Bioinformatics analysis and functional studies demonstrated that MIR944 has its own promoter. We demonstrate here that MIR944 is a target of ΔNp63. Promoter analysis revealed that the activity of the MIR944 promoter was markedly enhanced by the binding of ΔNp63, which was maintained by the supportive action of AP-2 during keratinocyte differentiation. Our results indicated that miR-944 biogenesis is dependent on ΔNp63 protein, even though it is generated from ΔNp63 mRNA-independent transcripts. We also demonstrated that miR-944 induces keratin 1 and keratin 10 expression by inhibiting ERK signaling and upregulating p53 expression. Our findings suggested that miR-944, as an intronic miRNA and a direct target of ΔNp63, contributes to the function of ΔNp63 in the induction of epidermal differentiation.
机译:ΔNp63对于角质形成细胞的增殖和分化都是必需的,但人们对它在这些细胞分化中的作用了解甚少。相应的基因TP63在其内含子中带有MIR944序列。但是,生物发生的机制和miR-944的功能尚不清楚。我们发现miR-944在角质形成细胞中以与ΔNp63mRNA一致的方式高表达,但在各种条件下miR-944表达的调节与ΔNp63的表达并不对应。生物信息学分析和功能研究表明,MIR944具有自己的启动子。我们在这里证明MIR944是ΔNp63的目标。启动子分析显示,通过ΔNp63的结合,MIR944启动子的活性显着增强,而ΔNp63的结合在角质形成细胞分化过程中通过AP-2的支持作用得以维持。我们的结果表明,miR-944生物发生依赖于ΔNp63蛋白,即使它是由不依赖于ΔNp63mRNA的转录本产生的。我们还证明了miR-944通过抑制ERK信号传导并上调p53表达来诱导角蛋白1和角蛋白10的表达。我们的发现表明,作为内含子miRNA和ΔNp63的直接靶标的miR-944有助于ΔNp63在诱导表皮分化中的功能。

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