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Candida Infection Biology – fungal armoury, battlefields ... - FINSysB

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Poster number: 03<br />

The transcription factor Sko1 represses the yeast-tohypha<br />

transition and mediates the oxidative stress<br />

response in <strong>Candida</strong> albicans.<br />

Inês Correia, Elvira Román, David M. Arana, Daniel Prieto, Verónica<br />

Urrialde, César Nombela, Rebeca Alonso-Monge and Jesús Pla. §<br />

Departamento de Microbiología II. Facultad de Farmacia. Universidad Complutense de<br />

Madrid. Plaza de Ramón y Cajal s/n. E-28040 MADRID. SPAIN<br />

Cells adapt to external changes by triggering transcriptional responses. These<br />

responses are complex and are mediated by different transcription factors. Mutants<br />

lacking the transcription factor Sko1 were generated in <strong>Candida</strong> albicans and its<br />

roles on the physiology of this opportunistic pathogen are reported. Genome-wide<br />

transcriptional analysis revealed that Sko1 acts as a transcriptional repressor of<br />

genes involved in pathogenesis and hyphal formation. The sko1 mutant displayed<br />

an increased expression of the hyphal related genes ECE1 and HWP1 but showed<br />

no drastic alterations in the mouse model of systemic infection. Deletion of SKO1<br />

rendered mutants derepressed in the yeast-to-hypha transition. Moreover, Sko1<br />

was shown to be involved in the response to oxidative stress and sko1 mutants<br />

increased the sensitivity of hog1 mutants to the myelomonocytic cell line HL-60.<br />

Alterations in the phosphorylation pattern of MAP kinase mutants in response to<br />

oxidative challenge were also observed. Genome-wide transcriptional analysis after<br />

hydrogen peroxide treatment revealed that sko1 mutants were able to generate an<br />

adaptive response similar to wild type strains, although important differences were<br />

detected in the magnitude of such transcriptional response. Collectively, these<br />

results implicate Sko1 as a key mediator of the oxidative stress response and<br />

morphological transition in C. albicans.<br />

116

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