Generating genomic platforms to study Candida albicans pathogenesis
Mélanie LegrandiD, Sophie Bachellier‐BassiiD, Keunsook K. LeeiD, Yogesh ChaudhariiD, Hélène Tournu, Laurence Arbogast, Hélène BoyeriD, Murielle Chauvel, Vitor CabraliD, Corinne MaufraisiD, Audrey Nesseir, Irena Maslanka, Emmanuelle PermaliD, Tristan RossignoliD, Louise A. WalkeriD, Ute Zeidler, Sadri ZnaidiiD, Floris SchoetersiD, Charlotte Majgier, Renaud A Julien, Laurence MaiD, Magali Tichit, Christiane BouchieriD, Patrick Van DijckiD, Carol A. MunroiD, Christophe d’EnfertiD
Abstract
The advent of the genomic era has made elucidating gene function at large scale a pressing challenge. ORFeome collections, whereby almost all ORFs of a given species are cloned and can be subsequently leveraged in multiple functional genomic approaches, represent valuable resources towards this endeavor. Here we provide novel, genome-scale tools for the study of Candida albicans, a commensal yeast that is also responsible for frequent superficial and disseminated infections in humans. We have generated an ORFeome collection composed of 5,102 ORFs cloned in a Gateway donor vector, representing 83% of the currently annotated coding sequences of C. albicans. Sequencing data of the cloned ORFs are available in the CandidaOrfDB database at http://candidaorfeome.eu. We also engineered 49 expression vectors with a choice of promoters, tags, and selection markers and demonstrated their applicability to the study of target ORFs transferred from the C. albicans ORFeome. In addition, the use of the ORFeome in the detection of protein-protein interaction was demonstrated. Mating-compatible strains as well as Gateway-compatible two-hybrid vectors were engineered, validated and used in a proof of concept experiment. These unique and valuable resources should greatly facilitate future functional studies in C. albicans and the elucidation of mechanisms that underlie its pathogenicity.
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