Maeng Shinae, Ko Young-Joon, Kim Gyu-Bum, Jung Kwang-Woo, Floyd Anna, Heitman Joseph, Bahn Yong-Sun
Department of Biotechnology, Center for Fungal Pathogenesis, Yonsei University, 134 Shinchon-dong, Seodaemun-gu, 120-749 Seoul, Republic of Korea.
Eukaryot Cell. 2010 Mar;9(3):360-78. doi: 10.1128/EC.00309-09. Epub 2010 Jan 22.
The cyclic AMP (cAMP) pathway plays a central role in the growth, differentiation, and virulence of pathogenic fungi, including Cryptococcus neoformans. Three upstream signaling regulators of adenylyl cyclase (Cac1), Ras, Aca1, and Gpa1, have been demonstrated to control the cAMP pathway in C. neoformans, but their functional relationship remains elusive. We performed a genome-wide transcriptome analysis with a DNA microarray using the ras1Delta, gpa1Delta, cac1Delta, aca1Delta, and pka1Delta pka2Delta mutants. The aca1Delta, gpa1Delta, cac1Delta, and pka1Delta pka2Delta mutants displayed similar transcriptome patterns, whereas the ras1Delta mutant exhibited transcriptome patterns distinct from those of the wild type and the cAMP mutants. Interestingly, a number of environmental stress response genes are modulated differentially in the ras1Delta and cAMP mutants. In fact, the Ras signaling pathway was found to be involved in osmotic and genotoxic stress responses and the maintenance of cell wall integrity via the Cdc24-dependent signaling pathway. Notably, the Ras and cAMP mutants exhibited hypersensitivity to a polyene drug, amphotericin B, without showing effects on ergosterol biosynthesis, which suggested a novel method of antifungal combination therapy. Among the cAMP-dependent gene products that we characterized, two small heat shock proteins, Hsp12 and Hsp122, were found to be involved in the polyene antifungal drug susceptibility of C. neoformans.
环磷酸腺苷(cAMP)信号通路在包括新生隐球菌在内的致病真菌的生长、分化和毒力方面发挥着核心作用。已证实腺苷酸环化酶(Cac1)、Ras、Aca1和Gpa1这三种上游信号调节因子可控制新生隐球菌中的cAMP信号通路,但其功能关系仍不清楚。我们使用DNA微阵列对ras1Delta、gpa1Delta、cac1Delta、aca1Delta和pka1Delta pka2Delta突变体进行了全基因组转录组分析。aca1Delta、gpa1Delta、cac1Delta和pka1Delta pka2Delta突变体表现出相似的转录组模式,而ras1Delta突变体表现出与野生型和cAMP突变体不同的转录组模式。有趣的是,许多环境应激反应基因在ras1Delta和cAMP突变体中受到不同的调节。事实上,发现Ras信号通路通过依赖Cdc24的信号通路参与渗透和基因毒性应激反应以及细胞壁完整性的维持。值得注意的是,Ras和cAMP突变体对多烯药物两性霉素B表现出超敏反应,而对麦角固醇生物合成没有影响,这提示了一种新的抗真菌联合治疗方法。在我们鉴定的cAMP依赖性基因产物中,发现两种小热休克蛋白Hsp12和Hsp122参与了新生隐球菌对多烯抗真菌药物的敏感性。