Saifudeen Zubaida, Diavolitsis Virginia, Stefkova Jana, Dipp Susana, Fan Hao, El-Dahr Samir S
Department of Pediatrics, Section of Pediatric Nephrology, Tulane University Health Sciences Center, New Orleans, Louisiana 70112, USA.
J Biol Chem. 2005 Jun 17;280(24):23094-102. doi: 10.1074/jbc.M414575200. Epub 2005 Apr 1.
p73 is a member of the p53 gene family, which also includes p53 and p63. These proteins share sequence similarity and target genes but also have divergent roles in cancer and development. Unlike p53, transcription of the p73 gene yields multiple full-length (transactivation (TA) domain) and amino terminus-truncated (DeltaN) isoforms. DeltaNp73 acts in a dominant negative fashion to inhibit the actions of TAp73 and p53 on their target genes, promoting cell survival and proliferation and suppressing apoptosis. The balance between TAp73 and its negative regulator, DeltaNp73, may therefore represent an important determinant of developmental cell fate. There is little if anything known regarding the developmental regulation of the p73 gene. In this study, we showed that TAp73 and DeltaNp73 exhibit reciprocal spatiotemporal expression and functions during nephrogenesis. TAp73 was predominantly expressed in the differentiation domain of the renal cortex in an overlapping manner with the vasopressin-sensitive water channel aquaporin-2 (AQP-2). Chromatin immunoprecipitation assays demonstrated that the endogenous AQP-2 promoter was occupied by TAp73 in a developmentally regulated manner. Furthermore TAp73 stimulated AQP-2 promoter-driven reporter expression. TAp73 also activated the bradykinin B2 receptor (B2R) promoter, a developmentally regulated gene involved in regulation of sodium excretion. The transcriptional effects of TAp73 on AQP-2 and B2R were independent of p53. In marked contrast to TAp73, DeltaNp73 isoforms were induced early in development and were preferentially expressed in proliferating nephron precursors. Moreover DeltaNp73 was a potent repressor of B2R gene transcription. We conclude that the p73 gene is developmentally regulated during kidney organogenesis. The spatiotemporal switch from DeltaNp73 to TAp73 may play an important role in the terminal differentiation program of the developing nephron.
p73是p53基因家族的成员之一,该家族还包括p53和p63。这些蛋白质具有序列相似性和靶基因,但在癌症和发育过程中也具有不同的作用。与p53不同,p73基因的转录产生多种全长(反式激活(TA)结构域)和氨基末端截短(DeltaN)的异构体。DeltaNp73以显性负性方式发挥作用,抑制TAp73和p53对其靶基因的作用,促进细胞存活和增殖并抑制细胞凋亡。因此,TAp73与其负调节因子DeltaNp73之间的平衡可能代表发育细胞命运的重要决定因素。关于p73基因的发育调控,所知甚少。在本研究中,我们表明TAp73和DeltaNp73在肾发生过程中表现出相互的时空表达和功能。TAp73主要在肾皮质的分化区域表达,与血管加压素敏感的水通道蛋白-2(AQP-2)重叠。染色质免疫沉淀试验表明,内源性AQP-2启动子以发育调控的方式被TAp73占据。此外,TAp73刺激AQP-2启动子驱动的报告基因表达。TAp73还激活缓激肽B2受体(B2R)启动子,这是一个参与钠排泄调节的发育调控基因。TAp73对AQP-2和B2R的转录作用独立于p53。与TAp73形成鲜明对比的是,DeltaNp73异构体在发育早期被诱导,并优先在增殖的肾单位前体中表达。此外,DeltaNp73是B2R基因转录的有效抑制因子。我们得出结论,p73基因在肾脏器官发生过程中受到发育调控。从DeltaNp73到TAp73的时空转换可能在发育中的肾单位终末分化程序中起重要作用。