Cervera A M, Gozalbo D, McCreath K J, Gow N A, Martínez J P, Casanova M
Departamento de Microbiología y Ecología, Facultad de Farmacia, Universitat de València, Burjasot, Spain.
Mol Microbiol. 1998 Oct;30(1):67-81. doi: 10.1046/j.1365-2958.1998.01039.x.
Immunoscreening of a Candida albicans cDNA library with a monoclonal antibody (mAb 4C12) recognizing an epitope present in high-molecular-weight mannoprotein (HMWM) components specific for the mycelial cell walls (a 180 kDa component and a poly-dispersed 260 kDa species) resulted in the isolation of the gene CaCYC3 encoding for cytochrome c haem lyase (CCHL). The CaCYC3 gene was transcribed preferentially in mycelial cells in which two mRNA transcripts of 0.8 and 1 kb were found. The nucleotide and the deduced amino acid sequences of this gene displayed 45% homology and 46% identity, respectively, to the Saccharomyces cerevisiae CYC3 gene and shared common features with other reported genes encoding for CCHL. The CaCYC3 gene restored the respiratory activity when transformed in a S. cerevisiae cyc3- mutant strain. A C. albicans CYC3 null mutant was constructed after sequential disruption using the hisG::URA3::hisG ('ura-blaster') cassette. Null mutant cells were unable to use lactate as a sole carbon source and had a reduced ability to form germ tubes. Western immunoblotting analysis of subcellular fractions from wild-type and null mutant strains demonstrated the presence of two gene products, a 33kDa mitochondrial protein and a 40 kDa cell wall-associated moiety reacting with antibodies against CCHL, in both yeast cells and germ tubes. mAb 4C12 still reacted with the CaCYC3 null mutant (by immunofluorescence and immunoblotting) but showed an altered pattern of immunoreactivity against cell wall HMWM species, indicating a relationship between these moieties and the CaCYC3 gene products. The results suggest that the CaCYC3 gene encodes two proteins, one targeted to the mitochondria and the other to the cell wall.
用一种单克隆抗体(mAb 4C12)对白色念珠菌cDNA文库进行免疫筛选,该抗体识别存在于菌丝细胞壁特异性高分子量甘露糖蛋白(HMWM)成分中的一个表位(一种180 kDa成分和一种多分散的260 kDa物质),结果分离出编码细胞色素c血红素裂解酶(CCHL)的CaCYC3基因。CaCYC3基因在菌丝细胞中优先转录,在其中发现了0.8和1 kb的两种mRNA转录本。该基因的核苷酸序列和推导的氨基酸序列与酿酒酵母CYC3基因分别具有45%的同源性和46%的同一性,并与其他报道的编码CCHL的基因具有共同特征。当转入酿酒酵母cyc3-突变株时,CaCYC3基因恢复了呼吸活性。使用hisG::URA3::hisG(“ura-爆破盒”)盒进行连续破坏后构建了白色念珠菌CYC3缺失突变体。缺失突变体细胞不能将乳酸作为唯一碳源利用,形成芽管的能力降低。对野生型和缺失突变体菌株亚细胞组分的Western免疫印迹分析表明,在酵母细胞和芽管中均存在两种基因产物,一种33 kDa的线粒体蛋白和一种与抗CCHL抗体反应的40 kDa细胞壁相关部分。mAb 4C12仍与CaCYC3缺失突变体反应(通过免疫荧光和免疫印迹),但对细胞壁HMWM物质的免疫反应模式发生了改变,表明这些部分与CaCYC3基因产物之间存在关系。结果表明,CaCYC3基因编码两种蛋白质,一种靶向线粒体,另一种靶向细胞壁。