Two Rac paralogs regulate polarized growth in the human fungal pathogen Cryptococcus neoformans

被引:20
作者
Ballou, Elizabeth Ripley [1 ,2 ]
Selvig, Kyla [1 ,2 ]
Narloch, Jessica L. [1 ]
Nichols, Connie B. [1 ]
Alspaugh, J. Andrew [1 ,2 ]
机构
[1] Duke Univ, Sch Med, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
关键词
Cryptococcus neoformans; Rac GTPase; Paralogs; Polarization; Hyphal growth; ROS; GTP-BINDING-PROTEIN; BUD-SITE SELECTION; CELL POLARITY; BASIDIOMYCETOUS YEAST; PENICILLIUM-MARNEFFEI; HOMOLOG FUNCTIONS; HIGH-TEMPERATURE; STRESS-RESPONSE; HYPHAL GROWTH; NADPH OXIDASE;
D O I
10.1016/j.fgb.2013.05.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A genome wide analysis of the human fungal pathogen Cryptococcus neoformans var. grubii has revealed a number of duplications of highly conserved genes involved in morphogenesis. Previously, we reported that duplicate Cdc42 paralogs provide C neoformans with niche-specific responses to environmental stresses: Cdc42 is required for thermotolerance, while Cdc420 supports the formation of titan cells. The related Rho-GTPase Rac1 has been shown in C neoformans var. neoformans to play a major role in filamentation and to share Cdc42/Cdc420 binding partners. Here we report the characterization of a second Rac paralog in C neoformans, Rac2, and describe its overlapping function with the previously described CnRac, Rac1. Further, we demonstrate that the Rac paralogs play a primary role in polarized growth via the organization of reactive oxygen species and play only a minor role in the organization of actin. Finally, we provide preliminary evidence that pharmacological inhibitors of Rac activity and actin stability have synergistic activity. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:58 / 75
页数:18
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