Vicentefranqueira Rocío, Amich Jorge, Marín Laura, Sánchez Clara Inés, Leal Fernando, Calera José Antonio
Instituto de Biología Funcional y Genómica (IBFG-CSIC), Departamento de Microbiología y Genética, Universidad de Salamanca, 37007 Salamanca, Spain.
Manchester Fungal Infection Group (MFIG), Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9NT, UK.
Genes (Basel). 2018 Jun 26;9(7):318. doi: 10.3390/genes9070318.
One of the most important features that enables to grow within a susceptible individual and to cause disease is its ability to obtain Zn ions from the extremely zinc-limited environment provided by host tissues. Zinc uptake from this source in relies on ZIP transporters encoded by the , and genes. The expression of these genes is tightly regulated by the ZafA transcription factor that regulates zinc homeostasis and is essential for virulence. We combined the use of microarrays, Electrophoretic Mobility Shift Assays (EMSA) analyses, DNase I footprinting assays and in silico tools to better understand the regulation of the homeostatic and adaptive response of to zinc starvation. We found that under zinc-limiting conditions, ZafA functions mainly as a transcriptional activator through binding to a zinc response sequence located in the regulatory regions of its target genes, although it could also function as a repressor of a limited number of genes. In addition to genes involved in the homeostatic response to zinc deficiency, ZafA also influenced, either directly or indirectly, the expression of many other genes. It is remarkable that the expression of many genes involved in iron uptake and ergosterol biosynthesis is strongly reduced under zinc starvation, even though only the expression of some of these genes appeared to be influenced directly or indirectly by ZafA. In addition, it appears to exist in a zinc/iron cross-homeostatic network to allow the adaptation of the fungus to grow in media containing unbalanced Zn:Fe ratios. The adaptive response to oxidative stress typically linked to zinc starvation was also mediated by ZafA, as was the strong induction of genes involved in gliotoxin biosynthesis and self-protection against endogenous gliotoxin. This study has expanded our knowledge about the regulatory and metabolic changes displayed by in response to zinc starvation and has helped us to pinpoint new ZafA target genes that could be important for fungal pathogens to survive and grow within host tissues and, hence, for virulence.
能够在易感个体内生长并引发疾病的最重要特征之一,是其从宿主组织提供的极度锌限制环境中获取锌离子的能力。在[具体物种名称]中,从该来源摄取锌依赖于由[具体基因名称]、[具体基因名称]和[具体基因名称]基因编码的ZIP转运蛋白。这些基因的表达受到ZafA转录因子的严格调控,该转录因子调节锌稳态,对[具体物种名称]的毒力至关重要。我们结合使用微阵列、电泳迁移率变动分析(EMSA)、DNase I足迹分析和计算机工具,以更好地了解[具体物种名称]对锌饥饿的稳态和适应性反应的调控。我们发现,在锌限制条件下,ZafA主要通过与位于其靶基因调控区域的锌反应序列结合而作为转录激活因子发挥作用,尽管它也可能作为少数基因的阻遏物发挥作用。除了参与对锌缺乏的稳态反应的基因外,ZafA还直接或间接地影响许多其他基因的表达。值得注意的是,尽管只有其中一些基因的表达似乎直接或间接受ZafA影响,但在锌饥饿条件下,许多参与铁摄取和麦角固醇生物合成的基因的表达会大幅降低。此外,似乎在[具体物种名称]中存在一个锌/铁交叉稳态网络,以使真菌能够适应在锌:铁比例不平衡的培养基中生长。对通常与锌饥饿相关的氧化应激的适应性反应也由ZafA介导,参与gliotoxin生物合成和对内源性gliotoxin自我保护的基因的强烈诱导也是如此。这项研究扩展了我们对[具体物种名称]在应对锌饥饿时所表现出的调控和代谢变化的认识,并帮助我们确定了新的ZafA靶基因,这些基因可能对真菌病原体在宿主组织内存活和生长以及因此对毒力很重要。