Leberer E, Harcus D, Broadbent I D, Clark K L, Dignard D, Ziegelbauer K, Schmidt A, Gow N A, Brown A J, Thomas D Y
Biotechnology Research Institute, National Research Council of Canada, Montreal, Canada.
Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13217-22. doi: 10.1073/pnas.93.23.13217.
The CST20 gene of Candida albicans was cloned by functional complementation of a deletion of the STE20 gene in Saccharomyces cerevisiae. CST20 encodes a homolog of the Ste20p/p65PAK family of protein kinases. Colonies of C. albicans cells deleted for CST20 revealed defects in the lateral formation of mycelia on synthetic solid "Spider" media. However, hyphal development was not impaired in some other media. A similar phenotype was caused by deletion of HST7, encoding a functional homolog of the S. cerevisiae Ste7p protein kinase. Overexpression of HST7 partially complemented the deletion of CST20. Cells deleted for CST20 were less virulent in a mouse model for systemic candidiasis. Our results suggest that more than one signaling pathway can trigger hyphal development in C. albicans, one of which has a protein kinase cascade that is analogous to the mating response pathway in S. cerevisiae and might have become adapted to the control of mycelial formation in asexual C. albicans.
通过对酿酒酵母中STE20基因缺失进行功能互补,克隆了白色念珠菌的CST20基因。CST20编码Ste20p/p65PAK蛋白激酶家族的一个同源物。缺失CST20的白色念珠菌细胞菌落显示,在合成固体“蜘蛛”培养基上菌丝体的侧向形成存在缺陷。然而,在其他一些培养基中,菌丝发育并未受损。缺失编码酿酒酵母Ste7p蛋白激酶功能同源物的HST7也会导致类似的表型。HST7的过表达部分弥补了CST20的缺失。在系统性念珠菌病小鼠模型中,缺失CST20的细胞毒力较低。我们的结果表明,不止一条信号通路可以触发白色念珠菌的菌丝发育,其中一条具有与酿酒酵母交配反应通路类似的蛋白激酶级联反应,可能已适应于控制无性白色念珠菌的菌丝体形成。