To further understand the role that homologous recombination pathways play in genome maintenance and DNA damage resistance in Candida albicans, we have examined the phenotypes of two genes proposed to be involved in homologous recombination based on their homology to the Saccharomyces cerevisiae genes. In Saccharomyces Gefitinib cerevisiae, two members of the SNF2 family of chromatin remodelers, RAD54 and RDH54 act in the repair of double strand DNA breaks through homologous recombination [14–16]. In vitro data suggest that Rad54 and Rdh54 act at stages of recombination involving strand www.selleckchem.com/products/tpx-0005.html displacement and D-loop formation [17]. RAD54 and RDH54 belong to the RAD52

epistasis group, which contains genes required for repair of double strand breaks generated through spontaneous events or exogenous damage. In humans, two RAD54 homologues, hRAD54 and RAD54B are present, and mutation of these is associated with tumor formation [18–20]. Despite similar in vitro activities of the Rad54 and Rdh54 selleck chemicals llc proteins, the Saccharomyces

cerevisiae mutants have different phenotypes with respect to mitotic and meiotic recombination [16] and DNA damage [14]. The work presented here on Candida albicans RAD54 and RDH54 examines the role these genes play in DNA damage sensitivity and in FLC susceptibility in Candida albicans. We found that Candida albicans RAD54 is required for normal cell growth and in its absence cells had an aberrant cell cycle, misdivide the nucleus, and appeared 3-oxoacyl-(acyl-carrier-protein) reductase to have a DNA damage checkpoint arrest. In contrast, we found no DNA damage sensitivity or alteration of the cell cycle in rdh54Δ/rdh54Δ mutants. We did not observe a changed growth response to FLC, but merely observed slower growth

of the rad54Δ/rad54Δ strain with or without FLC. Interestingly, Candida albicans RAD54 and RDH54 appeared to have some functional overlap as we were unable to construct the double mutant rad54Δ/rad54Δ rdh54Δ/rdh54Δ. Results Identification of Candida albicans homologues of Saccharomyces cerevisiae RAD54 and RDH54 To identify putative homologues of Saccharomyces cerevisiae RAD54 and RDH54, the protein sequence from each ORF was used for BLAST analysis. For each protein, putative homologues encoded in the Candida albicans genome were identified. For Rad54, a BLAST score of 1.6e-245 and 69% amino acid identity over the region of highest homology was obtained. BLAST analysis of Rdh54 identified a homologue with a score of 2.6e-128 and with 45% amino acid identity. The genes identified in the BLAST searches correspond to ORF 19.5004 and 19.5367, respectively in the Candida Genome Database maintained at Stanford University (http://​www.​candidagenome.​org).