Van Campenhout Claude, Nichane Massimo, Antoniou Aline, Pendeville Hélène, Bronchain Odile J, Marine Jean-Christophe, Mazabraud Andre, Voz Marianne L, Bellefroid Eric J
Laboratoire d'Embryologie Moléculaire, Université Libre de Bruxelles, Institut de Biologie et de Médecine Moléculaires (IBMM), rue des Profs. Jeener et Brachet 12, B-6041 Gosselies, Belgium.
Dev Biol. 2006 Jun 1;294(1):203-19. doi: 10.1016/j.ydbio.2006.02.040. Epub 2006 Mar 30.
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.
嗜亲性病毒整合位点1(Evi1)及相关的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。在此,我们表明在非洲爪蟾中,Evi1和MEL1具有部分重叠的受限胚胎表达谱。在前肾中,Evi1和MEL1在远端小管和导管区室中依次表达,在任何前肾形态发生迹象出现之前就能检测到Evi1转录。在斑马鱼胚胎的前肾中,Evi1表达局限于导管的后部,前部具有近端小管的特征。在非洲爪蟾前肾中,视黄酸信号上调Evi1表达,而xWT1的过表达和Notch信号则抑制其表达。从神经胚晚期开始过表达Evi1会特异性抑制近端小管和肾小球前肾标志物的表达。我们表明这种活性需要第一个锌指和CtBP相互作用结构域。一种激素诱导型Evi1-VP16反式显性融合蛋白在神经胚期激活后过表达,会破坏远端小管和导管的形成,并扩大肾小球标志物的表达。尽管这种构建体的过表达在许多胚胎中也会导致近端小管标志物减少,但也观察到了染色扩大和异位的胚胎。总之,这些数据表明Evi1在前肾的近-远模式形成中起作用,并表明它可能通过作为一种依赖CtBP的阻遏物发挥作用。