首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Differential Role of Snail1 and Snail2 Zinc Fingers in E-cadherin Repression and Epithelial to Mesenchymal Transition
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Differential Role of Snail1 and Snail2 Zinc Fingers in E-cadherin Repression and Epithelial to Mesenchymal Transition

机译:Snail1和Snail2锌指在E-钙粘蛋白抑制和上皮向间质转化中的差异作用

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摘要

Snail1 (Snail) and Snail2 (Slug) are transcription factors that share a similar DNA binding structure of four and five C2H2 zinc finger motifs (ZF), respectively. Both factors bind specifically to a subset of E-box motifs (E2-box: CAGGTG/CACCTG) in target promoters like the E-cadherin promoter and are key mediators of epithelial-to-mesenchymal transition (EMT). However, there are differences in the biological actions, in binding affinities to E-cadherin promoter, and in the target genes of Snail1 and Snail2, although the molecular bases are presently unknown. In particular, the role of each Snail1 and Snail2 ZF in the binding to E-boxes and in EMT induction has not been previously explored. We have approached this question by modeling Snail1 and Snail2 protein-DNA interactions and through mutational and functional assays of different ZFs. Results show that Snail1 efficient repression and binding to human and mouse E-cadherin promoter as well as EMT-inducing ability require intact ZF1 and ZF2, while for Snail2, either ZF3 or ZF4 is essential for those functions. Furthermore, the differential distribution of E2-boxes in mouse and human E-cadherin promoters also contributes to the differential Snail factor activity. These data indicate a non-equivalent role of Snail1 and Snail2 ZFs in gene repression, contributing to the elucidation of the molecular differences between these important EMT regulators.
机译:Snail1(Snail)和Snail2(Slug)是分别具有四个和五个C2H2锌指基序(ZF)的相似DNA结合结构的转录因子。两种因子都特异性结合靶启动子(如E-钙粘蛋白启动子)中的E-box模体子集(E2-box:CAGGTG / CACCTG),并且是上皮到间质转化(EMT)的关键介体。但是,尽管目前尚不知道分子基础,但在生物学作用,与E-钙粘蛋白启动子的结合亲和力以及Snail1和Snail2的靶基因方面存在差异。特别是,以前尚未探讨过每个Snail1和Snail2 ZF在与E-box结合以及在EMT诱导中的作用。我们通过对Snail1和Snail2蛋白质-DNA相互作用进行建模并通过不同ZF的突变和功能分析来解决这个问题。结果表明,Snail1的有效抑制和与人和小鼠E-钙粘蛋白启动子的结合以及EMT诱导能力需要完整的ZF1和ZF2,而对于Snail2,ZF3或ZF4对于这些功能必不可少。此外,小鼠和人E-钙粘蛋白启动子中E2-盒的差异分布也有助于差异化的Snail因子活性。这些数据表明Snail1和Snail2 ZF在基因阻遏中的作用不相同,有助于阐明这些重要的EMT调节剂之间的分子差异。

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