Oddon Delphine M, Diatloff Eugene, Roberts Stephen K
Department of Biological Sciences, Lancaster Environment Centre, Lancaster University, Lancaster, LA1 4YQ, UK.
Biochim Biophys Acta. 2007 Oct;1768(10):2466-77. doi: 10.1016/j.bbamem.2007.05.022. Epub 2007 Jun 2.
A putative CLC voltage-gated anion channel gene from Aspergillus nidulans (AnCLCA) is characterised. The expression of the AnCLCA cDNA restored the iron-limited growth of the Saccharomyces cerevisiae CLC null mutant strain (gef1) suggesting that AnCLCA functions as a chloride channel. An AnCLCA conditional mutant was created and exhibited a strong and specific growth inhibition in the presence of extracellular copper concentrations >18 microM. This sensitivity was shown to be the result of a hyper-accumulation of copper by the conditional mutant, which generates superoxide to toxic levels inhibiting the growth. Further analysis revealed that copper dependent enzymes were disrupted in the AnCLCA conditional null mutant, specifically, a reduced activity of the copper-zinc superoxide dismutase (CuZn-SOD) and enhanced activity of the cytochrome oxidase (COX). These results suggest that AnCLCA plays a key role in copper homeostasis in A. nidulans and that a malfunction of this chloride channel results in disrupted intracellular copper trafficking.
对来自构巢曲霉的一个假定的CLC电压门控阴离子通道基因(AnCLCA)进行了表征。AnCLCA cDNA的表达恢复了酿酒酵母CLC缺失突变株(gef1)在铁限制条件下的生长,这表明AnCLCA作为氯离子通道发挥作用。构建了一个AnCLCA条件突变体,在细胞外铜浓度>18 microM时表现出强烈且特异性的生长抑制。这种敏感性被证明是条件突变体超积累铜的结果,超积累的铜会产生毒性水平的超氧化物从而抑制生长。进一步分析表明,在AnCLCA条件性缺失突变体中,铜依赖性酶受到破坏,具体而言,铜锌超氧化物歧化酶(CuZn-SOD)的活性降低,而细胞色素氧化酶(COX)的活性增强。这些结果表明,AnCLCA在构巢曲霉的铜稳态中起关键作用,并且该氯离子通道功能异常会导致细胞内铜转运紊乱。