Abstract

Teresa O'Meara works in the field of functional genomics of Candida albicans, with a focus on host-pathogen interactions. In this mSphere of Influence article, she reflects on how papers entitled "Systematic Screens of a Candida albicans Homozygous Deletion Library Decouple Morphogenetic Switching and Pathogenicity" by S. M. Noble, S. French, L. A. Kohn, V. Chen, and A. D. Johnson (Nat Genet 42:590-598, 2010, https://doi.org/10.1038/ng.605) and "Exploring Quantitative Yeast Phenomics with Single-Cell Analysis of DNA Damage Foci" by E. B. Styles et al. (Cell Syst 3:264-277.e10, 2016, https://doi.org/10.1016/j.cels.2016.08.008) impacted her research and thinking through pioneering functional genomic screens. These articles show the power of combining defined mutant libraries with screens for interesting phenotypes to understand new biology.

Highlights

  • Functional genomic screens bring together the best of both experimental genetic worlds

  • In “Systematic Screens of a Candida albicans Homozygous Deletion Library Decouple Morphogenetic Switching and Pathogenicity,” the authors built the first large-scale homozygous mutant collection for Candida albicans, covering 674 open reading frames, or approximately 11% of the genome

  • The authors screened this collection for three phenotypes: growth in defined medium at 37°C, morphogenesis upon incubation in a filamentation-inducing cue, and virulence during systemic infection in a mouse model of candidiasis

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Summary

Introduction

Functional genomic screens bring together the best of both experimental genetic worlds. Functional genomic screening approaches have proved to be a powerful way to discover gene function, including in the human fungal pathogen Candida albicans, where many of the predicted proteins have no annotated function. The papers “Systematic Screens of a Candida albicans Homozygous Deletion Library Decouple Morphogenetic Switching and Pathogenicity” (1) and “Exploring Quantitative Yeast Phenomics with Single-Cell Analysis of DNA Damage Foci” (2) show the power of functional genomic screens for understanding new biology.

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