Rac1 Dynamics in the Human Opportunistic Fungal Pathogen Candida albicans

被引:9
|
作者
Vauchelles, Romain [1 ]
Stalder, Daniele [1 ]
Botton, Thomas [1 ]
Arkowitz, Robert A. [1 ]
Bassilana, Martine [1 ]
机构
[1] Univ Nice, CNRS, Fac Sci Parc Valrose, Inst Dev Biol & Canc,UMR 6543, F-06034 Nice, France
来源
PLOS ONE | 2010年 / 5卷 / 10期
关键词
STAT TRANSCRIPTION FACTORS; GTPASE-ACTIVATING PROTEIN; RAS-LIKE GTPASES; RHO-FAMILY; NUCLEAR-LOCALIZATION; MEMBRANE ASSOCIATION; FILAMENTOUS GROWTH; POLYBASIC REGION; EXCHANGE FACTOR; HYPHAL GROWTH;
D O I
10.1371/journal.pone.0015400
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The small Rho G-protein Rac1 is highly conserved from fungi to humans, with approximately 65% overall sequence identity in Candida albicans. As observed with human Rac1, we show that C. albicans Rac1 can accumulate in the nucleus, and fluorescence recovery after photobleaching ( FRAP) together with fluorescence loss in photobleaching ( FLIP) studies indicate that this Rho G-protein undergoes nucleo-cytoplasmic shuttling. Analyses of different chimeras revealed that nuclear accumulation of C. albicans Rac1 requires the NLS-motifs at its carboxyl-terminus, which are blocked by prenylation of the adjacent cysteine residue. Furthermore, we show that C. albicans Rac1 dynamics, both at the plasma membrane and in the nucleus, are dependent on its activation state and in particular that the inactive form accumulates faster in the nucleus. Heterologous expression of human Rac1 in C. albicans also results in nuclear accumulation, yet accumulation is more rapid than that of C. albicans Rac1. Taken together our results indicate that Rac1 nuclear accumulation is an inherent property of this G-protein and suggest that the requirements for its nucleo-cytoplasmic shuttling are conserved from fungi to humans.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Human gut bifidobacteria inhibit the growth of the opportunistic fungal pathogen Candida albicans
    Ricci, Liviana
    Mackie, Joanna
    Donachie, Gillian E.
    Chapuis, Ambre
    Mezerova, Kristyna
    Lenardon, Megan D.
    Brown, Alistair J. P.
    Duncan, Sylvia H.
    Walker, Alan W.
    [J]. FEMS MICROBIOLOGY ECOLOGY, 2022, 98 (10)
  • [2] Messenger RNA transport in the opportunistic fungal pathogen Candida albicans
    McBride, Anne E.
    [J]. CURRENT GENETICS, 2017, 63 (06) : 989 - 995
  • [3] Messenger RNA transport in the opportunistic fungal pathogen Candida albicans
    Anne E. McBride
    [J]. Current Genetics, 2017, 63 : 989 - 995
  • [4] Candida albicans, a major human fungal pathogen
    Joon Kim
    Peter Sudbery
    [J]. The Journal of Microbiology, 2011, 49
  • [5] Candida albicans, a Major Human Fungal Pathogen
    Kim, Joon
    Sudbery, Peter
    [J]. JOURNAL OF MICROBIOLOGY, 2011, 49 (02) : 171 - 177
  • [6] Candida albicans: fundamental research on an opportunistic human pathogen
    Calderone, Richard
    Odds, Frank C.
    Boekhout, Teun
    [J]. FEMS YEAST RESEARCH, 2009, 9 (07) : 971 - 972
  • [7] The role of manganese in morphogenesis and pathogenesis of the opportunistic fungal pathogen Candida albicans
    Wildeman, Asia S. S.
    Patel, Naisargi K. K.
    Cormack, Brendan p P.
    Culotta, Valeria C. C.
    [J]. PLOS PATHOGENS, 2023, 19 (06)
  • [8] Is Candida albicans an opportunistic oncogenic pathogen?
    Sultan, Ahmed S.
    Theofilou, Vasileios Ionas
    Alfaifi, Areej
    Montelongo-Jauregui, Daniel
    Jabra-Rizk, Mary-Ann
    [J]. PLOS PATHOGENS, 2022, 18 (04)
  • [9] Genetics of Candida albicans, a diploid human fungal pathogen
    Noble, Suzanne M.
    Johnson, Alexander D.
    [J]. ANNUAL REVIEW OF GENETICS, 2007, 41 : 193 - 211
  • [10] Genomic Plasticity of the Human Fungal Pathogen Candida albicans
    Selmecki, Anna
    Forche, Anja
    Berman, Judith
    [J]. EUKARYOTIC CELL, 2010, 9 (07) : 991 - 1008