Kim Kyu-Han, Cho Eun-Gyung, Yu Seok Jong, Kang Hyojin, Kim Yoon-Jin, Kim Sang Hoon, Lee Tae Ryong
Bioscience Research Division, R&D Unit, AmorePacific Corporation, Yongin-si, Gyeonggi-do 446-729, Republic of Koreaf.
National Institute of Supercomputing and Networking, Korea Institute of Science and Technology Information, Daejeon 305-806, Republic of Korea.
Nucleic Acids Res. 2015 Sep 3;43(15):7462-79. doi: 10.1093/nar/gkv735. Epub 2015 Jul 21.
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.
ΔNp63对于角质形成细胞的增殖和分化均是必需的,但其在这些细胞分化中的作用却知之甚少。相应基因TP63在其内含子中含有MIR944序列。然而,miR - 944的生物合成机制及其功能尚不清楚。我们发现miR - 944在角质形成细胞中高度表达,其方式与ΔNp63 mRNA一致,但在各种条件下miR - 944表达的调控与ΔNp63并不对应。生物信息学分析和功能研究表明MIR944有其自身的启动子。我们在此证明MIR944是ΔNp63的一个靶标。启动子分析显示,ΔNp63的结合显著增强了MIR944启动子的活性,在角质形成细胞分化过程中,AP - 2的支持作用维持了这种活性。我们的结果表明,miR - 944的生物合成依赖于ΔNp63蛋白,尽管它是由不依赖于ΔNp63 mRNA的转录本产生的。我们还证明,miR - 944通过抑制ERK信号传导和上调p53表达来诱导角蛋白1和角蛋白10的表达。我们的研究结果表明,miR - 944作为一种内含子miRNA和ΔNp63的直接靶标,有助于ΔNp63在诱导表皮分化中的功能。