Inukai Tatsuya, Nagi Minoru, Morita Akihiro, Tanabe Koichi, Aoyama Toshihiro, Miyazaki Yoshitsugu, Bard Martin, Nakayama Hironobu
Faculty of Pharmaceutical Sciences, Suzuka University of Medical Science, Japan; Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Japan; Division of Pathology, Immunology and Microbiology, Graduate School of Medicine, The University of Tokyo, Japan.
Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Japan.
Biochim Biophys Acta. 2015 Feb;1851(2):141-51. doi: 10.1016/j.bbalip.2014.11.002. Epub 2014 Nov 11.
Sterol uptake in the pathogenic fungus, Candida glabrata, occurs via the sterol transporter, CgAus1p. Azole inhibition of sterol biosynthesis can under certain circumstances be reversed by adding exogenously sterol. Here we demonstrate that the CgTIR3 (CAGL0C03872g) gene product is also required for sterol uptake, since Cgtir3Δ strains fail to take up sterol both aerobically and under hypoxic conditions. Western analysis using an HA-tagged TIR3 strain showed that CgTir3p localizes to the cell wall, and its expression is induced by serum. Semi-quantitative reverse transcriptase-PCR also showed that two transcription regulatory genes, CgUPC2A and CgUPC2B, control CgTIR3 as well as CgAUS1 gene expression. Interestingly, complementation studies using Cgtir3Δ showed that ScDAN1, a mannoprotein required for sterol uptake in Saccharomyces cerevisiae, could not complement the C. glabrata TIR3 function. Furthermore, sterol analyses, in which both the CgAUS1 and CgTIR3 genes were constitutively expressed, resulted in aerobic sterol uptake although the amount of uptake was considerably less than that of cells cultured aerobically with serum. These results suggest that additional factors other than CgAUS1 and CgTIR3 are required for sterol uptake in C. glabrata.
致病性真菌光滑念珠菌中的甾醇摄取是通过甾醇转运蛋白CgAus1p进行的。在某些情况下,通过外源添加甾醇可以逆转唑类对甾醇生物合成的抑制作用。在此我们证明,CgTIR3(CAGL0C03872g)基因产物对于甾醇摄取也是必需的,因为Cgtir3Δ菌株在需氧和缺氧条件下均无法摄取甾醇。使用带有HA标签的TIR3菌株进行的蛋白质免疫印迹分析表明,CgTir3p定位于细胞壁,并且其表达受血清诱导。半定量逆转录聚合酶链反应还表明,两个转录调控基因CgUPC2A和CgUPC2B控制CgTIR3以及CgAUS1基因的表达。有趣的是,使用Cgtir3Δ进行的互补研究表明,酿酒酵母中甾醇摄取所需的甘露糖蛋白ScDAN1不能互补光滑念珠菌的TIR3功能。此外,对同时组成型表达CgAUS1和CgTIR3基因的菌株进行甾醇分析,结果显示在需氧条件下有甾醇摄取,尽管摄取量远低于在血清中需氧培养的细胞。这些结果表明,光滑念珠菌摄取甾醇除了需要CgAUS1和CgTIR3之外,还需要其他因素。