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Evi1 is specifically expressed in the distal tubule and duct of the Xenopus pronephros and plays a role in its formation.

机译:Evi1在非洲爪蟾的远端小管和导管中特异性表达,并在其形成中起作用。

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摘要

The ecotropic viral integration site 1 (Evi1) and related MEL1 (MDS1/Evi1-like gene 1) genes are zinc finger oncogenic transcription factors involved in myeloid leukaemia. Here, we show that in Xenopus, Evi1 and MEL1 have partially overlapping restricted embryonic expression profiles. Within the pronephros, Evi1 and MEL1 are sequentially expressed within the distal tubule and duct compartments, Evi1 transcription being detected prior to any sign of pronephric morphogenesis. In the pronephros of zebrafish embryos, Evi1 expression is restricted to the posterior portion of the duct, the anterior portion having characteristics of proximal tubules. In the Xenopus pronephros, Evi1 expression is upregulated by retinoid signaling and repressed by overexpression of xWT1 and by Notch signaling. Overexpression of Evi1 from late neurula stage specifically inhibits the expression of proximal tubule and glomus pronephric markers. We show that the first zinc finger and CtBP interaction domains are required for this activity. Overexpression of a hormone-inducible Evi1-VP16 antimorphic fusion with activation at neurula stage disrupts distal tubule and duct formation and expands the expression of glomus markers. Although overexpression of this construct also causes in many embryos a reduction of proximal tubule markers, embryos with expanded and ectopic staining have been also observed. Together, these data indicate that Evi1 plays a role in the proximo-distal patterning of the pronephros and suggest that it may do so by functioning as a CtBP dependent repressor.
机译:亲热病毒整合位点1(Evi1)和相关的MEL1(MDS1 / Evi1样基因1)基因是参与髓系白血病的锌指致癌转录因子。在这里,我们显示在非洲爪蟾中,Evi1和MEL1具有部分重叠的限制性胚胎表达谱。在前肾中,Evi1和MEL1在远端肾小管和导管室中顺序表达,在任何前肾形态发生的迹象之前先检测到Evi1转录。在斑马鱼胚胎的前翅中,Evi1表达仅限于导管的后部,其前部具有近端小管的特征。在非洲爪蟾中,Evi1表达被类维生素A信号上调,被xWT1的过表达和Notch信号抑制。从神经末期开始,Evi1的过度表达会特异性抑制近端小管和肾小球前肾标志物的表达。我们显示此活动需要第一个锌指和CtBP相互作用域。荷尔蒙诱导型Evi1-VP16抗形态融合蛋白在神经元阶段被激活而过度表达,破坏了远端小管和导管的形成,并扩展了球蛋白标记物的表达。尽管这种构建体的过表达也导致许多胚胎中近端肾小管标志物的减少,但是也观察到了具有扩大的和异位染色的胚胎。总之,这些数据表明Evi1在前肾的近端-远端构型中起作用,并暗示它可以通过充当CtBP依赖性阻遏物来发挥作用。

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