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The F-box protein Ppa is a common regulator of core EMT factors Twist Snail Slug and Sip1

机译:F-box蛋白Ppa是核心EMT因子TwistSnailSlug和Sip1的常见调节剂

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摘要

A small group of core transcription factors, including Twist, Snail, Slug, and Sip1, control epithelial–mesenchymal transitions (EMTs) during both embryonic development and tumor metastasis. However, little is known about how these factors are coordinately regulated to mediate the requisite behavioral and fate changes. It was recently shown that a key mechanism for regulating Snail proteins is by modulating their stability. In this paper, we report that the stability of Twist is also regulated by the ubiquitin–proteasome system. We found that the same E3 ubiquitin ligase known to regulate Snail family proteins, Partner of paired (Ppa), also controlled Twist stability and did so in a manner dependent on the Twist WR-rich domain. Surprisingly, Ppa could also target the third core EMT regulatory factor Sip1 for proteasomal degradation. Together, these results indicate that despite the structural diversity of the core transcriptional regulatory factors implicated in EMT, a common mechanism has evolved for controlling their stability and therefore their function.
机译:少数核心转录因子(包括Twist,Snail,Slug和Sip1)在胚胎发育和肿瘤转移过程中控制上皮-间质转化(EMT)。然而,对于如何协调地调节这些因素以调解必要的行为和命运的改变知之甚少。最近显示,调节Snail蛋白的关键机制是调节其稳定性。在本文中,我们报道了Twist的稳定性也受到泛素-蛋白酶体系统的调节。我们发现相同的E3泛素连接酶已知可调控Snail家族蛋白(配对伴侣(Ppa))也可控制Twist稳定性,并以依赖Twist WR丰富结构域的方式进行。出乎意料的是,Ppa还可以将第三核心EMT调节因子Sip1靶向蛋白酶体降解。总之,这些结果表明,尽管涉及EMT的核心转录调控因子在结构上存在多样性,但已经形成了控制其稳定性以及控制其功能的通用机制。

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