Zheng Xinde, Wang Yanming, Wang Yue
Institute of Molecular and Cell Biology, Singapore, Singapore.
EMBO J. 2004 Apr 21;23(8):1845-56. doi: 10.1038/sj.emboj.7600195. Epub 2004 Apr 8.
The human fungal pathogen Candida albicans switches from yeast to hyphal growth when exposed to serum or phagocytosed. However, the importance of this morphological switch for virulence remains highly controversial due to the lack of a mutant that affects hyphal morphogenesis only. Although many genes specifically expressed in hyphal cells have been identified and shown to encode virulence factors, none is required for hyphal morphogenesis. Here we report the first hypha-specific gene identified, HGC1, which is essential for hyphal morphogenesis. Deletion of HGC1 abolished hyphal growth in all laboratory conditions tested and in the kidneys of systemically infected mice with markedly reduced virulence. HGC1 expression is co-regulated with other virulence genes such as HWP1 by the cAMP/protein kinase A signaling pathway and transcriptional repressor Tup1/Nrg1. Hgc1 is a G1 cyclin-related protein and co-precipitated with the cyclin-dependent kinase (Cdk) CaCdc28. It has recently emerged that cyclin/Cdk complexes promote other forms of polarized cell growth such as tumor cell migration and neurite outgrowth. C. albicans seems to have adapted a conserved strategy to control specifically hyphal morphogenesis.
人类真菌病原体白色念珠菌在接触血清或被吞噬时会从酵母形态转变为菌丝形态。然而,由于缺乏仅影响菌丝形态发生的突变体,这种形态转变对毒力的重要性仍存在高度争议。尽管已经鉴定出许多在菌丝细胞中特异性表达的基因,并表明它们编码毒力因子,但没有一个基因是菌丝形态发生所必需的。在此,我们报告了第一个被鉴定出的菌丝特异性基因HGC1,它对菌丝形态发生至关重要。在所有测试的实验室条件下以及在全身感染小鼠的肾脏中,HGC1的缺失都消除了菌丝生长,毒力显著降低。HGC1的表达与其他毒力基因如HWP1通过cAMP/蛋白激酶A信号通路和转录抑制因子Tup1/Nrg1共同调控。Hgc1是一种与G1细胞周期蛋白相关的蛋白,并与细胞周期蛋白依赖性激酶(Cdk)CaCdc28共沉淀。最近发现,细胞周期蛋白/Cdk复合物促进其他形式的极化细胞生长,如肿瘤细胞迁移和神经突生长。白色念珠菌似乎采用了一种保守策略来特异性地控制菌丝形态发生。