Cañero Dolores Cordoba, Roncero M Isabel G
Departamento de Genetica, Universidad de Cordoba, Campus de Rabanales, Edif. Gregor Mendel, E-14071 Cordoba, Spain.
Microbiology (Reading). 2008 May;154(Pt 5):1474-1481. doi: 10.1099/mic.0.2007/015388-0.
CLC-type voltage-gated chloride channels are a family of proteins which mediate chloride transport across the plasma and intracellular membranes. A clc1 gene from the vascular wilt fungus Fusarium oxysporum was characterized and disrupted. The predicted Clc1 protein contained highly conserved transmembrane and CBS domains of this protein family and showed significant identities to the Saccharomyces cerevisiae GEF1 and the Cryptococcus neoformans CLC-A chloride channels. Inactivation of clc1 caused a deficiency in laccase activity which was more severe than that found in any of the structural laccase mutants previously described. The addition of copper sulphate to the growth medium resulted in total recovery of extracellular laccase activity in Deltaclc1 mutants, although it did not activate transcription of any laccase genes. The pleiotropic phenotype displayed by the Fusarium chloride channel-deficient mutants included a significant delay in the development of disease on tomato plants, with a higher sensitivity to oxidative stress compounds as well as a significant decrease in laccase activity, thus suggesting a possible connection between virulence and the two processes. Nevertheless, we cannot rule out that additional phenotypes present in the Deltaclc1 mutants could play an essential role in the full virulence of Fusarium.
CLC型电压门控氯离子通道是一类介导氯离子跨质膜和内膜转运的蛋白质家族。对来自枯萎病真菌尖孢镰刀菌的clc1基因进行了表征和破坏。预测的Clc1蛋白包含该蛋白家族高度保守的跨膜和CBS结构域,并且与酿酒酵母GEF1和新型隐球菌CLC-A氯离子通道具有显著的同源性。clc1的失活导致漆酶活性缺陷,该缺陷比先前描述的任何结构漆酶突变体都更严重。向生长培养基中添加硫酸铜可使Deltaclc1突变体的细胞外漆酶活性完全恢复,尽管它没有激活任何漆酶基因的转录。尖孢镰刀菌氯离子通道缺陷型突变体表现出的多效性表型包括番茄植株上疾病发展的显著延迟,对氧化应激化合物的更高敏感性以及漆酶活性的显著降低,因此表明毒力与这两个过程之间可能存在联系。然而,我们不能排除Deltaclc1突变体中存在的其他表型可能在尖孢镰刀菌的完全毒力中起重要作用。