Veses Verónica, Casanova Manuel, Murgui Amelia, Domínguez Angel, Gow Neil A R, Martínez José P
Departamento de Microbiología y Ecologí, Facultad de Farmacia, Universitat de València, 46100-Burjasot, Valencia, Spain.
Eukaryot Cell. 2005 Jun;4(6):1088-101. doi: 10.1128/EC.4.6.1088-1101.2005.
Immunoscreening of a Candida albicans expression library resulted in the isolation of a novel gene encoding a 32.9-kDa polypeptide (288 amino acids), with 27.7% homology to the product of Saccharomyces cerevisiae YGR106c, a putative vacuolar protein. Heterozygous mutants in this gene displayed an altered budding growth pattern, characterized by the formation of chains of buds, decreasingly in size towards the apex, without separation of the daughter buds. Consequently, this gene was designated ABG1. A conditional mutant for ABG1 with the remaining allele under the control of the MET3 promoter did not grow in the presence of methionine and cysteine, demonstrating that ABG1 was essential for viability. Western analysis revealed the presence of a major 32.9-kDa band, mainly in a particulate fraction (P40) enriched in vacuoles, and tagging with green fluorescent protein confirmed that Abg1p localized to the vacuole. Vacuole inheritance has been linked to the regulation of branching frequency in C. albicans. Under repressing conditions, the conditional mutant had an increased frequency of branching under hyphal inducing conditions and an altered sensitivity to substances that interfered with cell wall assembly. Repression of ABG1 in the conditional mutant strain caused disturbance of normal size and number of vacuoles both in yeast and mycelial cells and also in the asymmetric vacuole inheritance associated with the characteristic pattern of germ tubes and branching in C. albicans. These observations indicate that ABG1 plays a key role in vacuole biogenesis, cytokinesis, and hyphal branching.
对白念珠菌表达文库进行免疫筛选,分离出一个编码32.9 kDa多肽(288个氨基酸)的新基因,该基因与酿酒酵母YGR106c(一种假定的液泡蛋白)的产物具有27.7%的同源性。该基因的杂合突变体表现出出芽生长模式改变,其特征是形成芽链,芽的大小朝着顶端逐渐减小,子芽不分离。因此,该基因被命名为ABG1。ABG1的一个条件突变体,其剩余等位基因受MET3启动子控制,在蛋氨酸和半胱氨酸存在的情况下无法生长,这表明ABG1对生存力至关重要。蛋白质免疫印迹分析显示存在一条主要的32.9 kDa条带,主要存在于富含液泡的颗粒组分(P40)中,用绿色荧光蛋白标记证实Abg1p定位于液泡。液泡遗传与白念珠菌分支频率的调节有关。在抑制条件下,该条件突变体在菌丝诱导条件下分支频率增加,对干扰细胞壁组装的物质敏感性改变。在条件突变菌株中抑制ABG1会导致酵母细胞和菌丝体细胞中液泡的正常大小和数量受到干扰,也会导致与白念珠菌芽管和分支特征模式相关的不对称液泡遗传受到干扰。这些观察结果表明,ABG1在液泡生物发生、胞质分裂和菌丝分支中起关键作用。