Sasso Emanuele, Vitale Monica, Monteleone Francesca, Boffo Francesca Ludovica, Santoriello Margherita, Sarnataro Daniela, Garbi Corrado, Sabatella Mariangela, Crifò Bianca, Paolella Luca Alfredo, Minopoli Giuseppina, Winum Jean-Yves, Zambrano Nicola
Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Napoli, Italy ; CEINGE Biotecnologie Avanzate, Via Gaetano Salvatore 486, 80145 Napoli, Italy ; Associazione Culturale DiSciMuS RFC, 80026 Casoria, Italy.
Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università di Napoli Federico II, 80131 Napoli, Italy ; CEINGE Biotecnologie Avanzate, Via Gaetano Salvatore 486, 80145 Napoli, Italy.
Biomed Res Int. 2015;2015:674920. doi: 10.1155/2015/674920. Epub 2015 Feb 22.
Carbonic anhydrase IX (CA IX) is a surrogate marker of hypoxia, involved in survival and pH regulation in hypoxic cells. We have recently characterized its interactome, describing a set of proteins interacting with CA IX, mainly in hypoxic cells, including several members of the nucleocytoplasmic shuttling apparatuses. Accordingly, we described complex subcellular localization for this enzyme in human cells, as well as the redistribution of a carbonic anhydrase IX pool to nucleoli during hypoxia. Starting from this evidence, we analyzed the possible contribution of carbonic anhydrase IX to transcription of the 45 S rDNA genes, a process occurring in nucleoli. We highlighted the binding of carbonic anhydrase IX to nucleolar chromatin, which is regulated by oxygen levels. In fact, CA IX was found on 45 S rDNA gene promoters in normoxic cells and less represented on these sites, in hypoxic cells and in cells subjected to acetazolamide-induced acidosis. Both conditions were associated with increased representation of carbonic anhydrase IX/exportin-1 complexes in nucleoli. 45 S rRNA transcript levels were accordingly downrepresented. Inhibition of nuclear export by leptomycin B suggests a model in which exportin-1 acts as a decoy, in hypoxic cells, preventing carbonic anhydrase IX association with 45 S rDNA gene promoters.
碳酸酐酶IX(CA IX)是缺氧的替代标志物,参与缺氧细胞的存活和pH调节。我们最近对其相互作用组进行了表征,描述了一组与CA IX相互作用的蛋白质,主要存在于缺氧细胞中,包括核质穿梭装置的几个成员。因此,我们描述了该酶在人类细胞中的复杂亚细胞定位,以及缺氧期间碳酸酐酶IX池向核仁的重新分布。基于这一证据,我们分析了碳酸酐酶IX对45 S rDNA基因转录的可能贡献,这一过程发生在核仁中。我们强调了碳酸酐酶IX与核仁染色质的结合,其受氧水平调节。事实上,在常氧细胞中,CA IX存在于45 S rDNA基因启动子上,而在缺氧细胞和乙酰唑胺诱导酸中毒的细胞中,这些位点上的CA IX较少。这两种情况都与核仁中碳酸酐酶IX/输出蛋白-1复合物的增加有关。相应地,45 S rRNA转录水平降低。雷帕霉素B对核输出的抑制表明了一种模型,即在缺氧细胞中,输出蛋白-1充当诱饵,阻止碳酸酐酶IX与45 S rDNA基因启动子结合。