首页> 外文期刊>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:蜗牛的差异1和Snail2锌手指在E-cadherin镇压和上皮细胞间充质过渡中

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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(蜗牛)和蜗牛2(SLUG)是分别具有四种和5个C2H2锌手指基序(ZF)的类似DNA结合结构的转录因子。两种因素特异性地结合到e-cadherin启动子等目标启动子中的E-Box基序(E2-BOX:CAGGTG / Cacctg)的子集,并且是上皮 - 间充质转换的关键介质(EMT)。然而,生物学作用的差异是对e-cadherin启动子的结合亲和力,并且在蜗牛1和Snail2的靶基因中,尽管分子碱目前未知。特别是,预先探讨了每个SNAI1和SNAIL2 ZF在与电子箱的结合和EMT感应中的作用。我们通过建模Snail1和Snail2蛋白DNA相互作用以及通过不同ZFS的突变和功能测定来实现这个问题。结果表明,蜗牛1有效抑制和与人和小鼠E-CADHERIN启动子的结合以及EMT诱导能力需要完整的ZF1和ZF2,而对于蜗牛2,ZF3或ZF4对于这些功能至关重要。此外,小鼠和人E-Cadherin启动子中E2箱的差异分布也有助于差异蜗牛因子活性。这些数据表明Snail1和Snail2 ZFS在基因抑制中的不等同作用,有助于阐明这些重要的EMT调节因子之间的分子差异。

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