Abstract

BackgroundGenome-wide sensitivity screens in yeast have been immensely popular following the construction of a collection of deletion mutants of non-essential genes. However, the auxotrophic markers in this collection preclude experiments on minimal growth medium, one of the most informative metabolic environments. Here we present quantitative growth analysis for mutants in all 4,772 non-essential genes from our prototrophic deletion collection across a large set of metabolic conditions.ResultsThe complete collection was grown in environments consisting of one of four possible carbon sources paired with one of seven nitrogen sources, for a total of 28 different well-defined metabolic environments. The relative contributions to mutants' fitness of each carbon and nitrogen source were determined using multivariate statistical methods. The mutant profiling recovered known and novel genes specific to the processing of nutrients and accurately predicted functional relationships, especially for metabolic functions. A benchmark of genome-scale metabolic network modeling is also given to demonstrate the level of agreement between current in silico predictions and hitherto unavailable experimental data.ConclusionsThese data address a fundamental deficiency in our understanding of the model eukaryote Saccharomyces cerevisiae and its response to the most basic of environments. While choice of carbon source has the greatest impact on cell growth, specific effects due to nitrogen source and interactions between the nutrients are frequent. We demonstrate utility in characterizing genes of unknown function and illustrate how these data can be integrated with other whole-genome screens to interpret similarities between seemingly diverse perturbation types.

Highlights

  • Genome-wide sensitivity screens in yeast have been immensely popular following the construction of a collection of deletion mutants of non-essential genes

  • The subsequent refinement of mating-based high-throughput strain construction techniques such as synthetic genetic array (SGA) analysis [2] has further driven the creation of customized yeast deletion arrays

  • The resulting requirement for nutrient supplementation precludes systematic testing of the yeast deletion collection on specific combinations of carbon and nitrogen sources because the auxotrophic nutrient supplements can be used as carbon and nitrogen sources

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Summary

Introduction

Genome-wide sensitivity screens in yeast have been immensely popular following the construction of a collection of deletion mutants of non-essential genes. We present quantitative growth analysis for mutants in all 4,772 non-essential genes from our prototrophic deletion collection across a large set of metabolic conditions. Large scale gene deletion screens have become common in Saccharomyces cerevisiae due to efforts in the yeast community to assemble a near complete collection of non-essential single-mutant strains [1]. Yeast strain collections used in previous high-throughput assays (that is, the deletion collection) are auxotrophic [1], and unable to survive in minimal media unless provided additional nutrients. This requirement reflects the historical use of auxotrophic markers for genetic selection. Previous work has shown that nutrient supplementation can have different physiological consequences from genetic complementation [9] and that auxotrophies can alter the expression of many other genes [10]

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