Goudela Sophia, Reichard Utz, Amillis Sotiris, Diallinas George
Faculty of Biology, Department of Botany, University of Athens, Panepistimioupolis, Athens 15781, Greece.
Fungal Genet Biol. 2008 Apr;45(4):459-72. doi: 10.1016/j.fgb.2007.08.001. Epub 2007 Aug 10.
Three genes encoding putative purine transporters have been identified in silico in the genome of Aspergillus fumigatus by their very close similarity of their translation products to well-studied homologues in A. nidulans. Two of these transporters, called AfUapC and AfAzgA, were found responsible for bulk uptake of purines and studied in detail herein. Genetic knock-out analysis, regulation of transcription, direct purine uptake assays and heterologous expression in A. nidulans have unequivocally shown that AfUapC and AfAzgA are high-affinity, high-capacity, purine/H(+) symporters, the first being specific for xanthine, uric acid and oxypurinol, whereas the second for adenine, hypoxanthine, guanine and purine. The expression of these transporters is primarily controlled at the level of transcription. Transcription of both genes is purine-inducible, albeit with different efficiencies, whereas AfuapC is also ammonium-repressible. We characterised in detail the kinetics of the AfUapC and AfAzgA transporters, both in A. fumigatus and in A. nidulans, using a plethora of possible purine substrates. This analysis led us to propose kinetic models describing the molecular interactions of AfUapC and AfAzgA with purines. These models are discussed comparatively with analogous models from other purine transporters from fungi, bacteria and humans, and within the frame of a systematic development of novel purine-related antifungals.
通过在烟曲霉基因组中进行电子鉴定,发现了三个编码推定嘌呤转运蛋白的基因,其翻译产物与构巢曲霉中经过充分研究的同源物具有高度相似性。其中两个转运蛋白,即AfUapC和AfAzgA,被发现负责嘌呤的大量摄取,并在本文中进行了详细研究。基因敲除分析、转录调控、直接嘌呤摄取测定以及在构巢曲霉中的异源表达均明确表明,AfUapC和AfAzgA是高亲和力、高容量的嘌呤/H(+)同向转运蛋白,前者对黄嘌呤、尿酸和氧嘌呤醇具有特异性,而后者对腺嘌呤、次黄嘌呤、鸟嘌呤和嘌呤具有特异性。这些转运蛋白的表达主要在转录水平受到控制。两个基因的转录均受嘌呤诱导,尽管效率不同,而AfuapC也受铵抑制。我们使用大量可能的嘌呤底物,详细表征了烟曲霉和构巢曲霉中AfUapC和AfAzgA转运蛋白的动力学。该分析使我们提出了描述AfUapC和AfAzgA与嘌呤分子相互作用的动力学模型。这些模型与来自真菌、细菌和人类的其他嘌呤转运蛋白的类似模型进行了比较讨论,并在新型嘌呤相关抗真菌剂的系统开发框架内进行了讨论。