Abstract
Genetic interactions help map biological processes and their functional relationships. A genetic interaction is defined as a deviation from the expected phenotype when combining multiple genetic mutations. In Saccharomyces cerevisiae, most genetic interactions are measured under a single phenotype - growth rate in standard laboratory conditions. Recently genetic interactions have been collected under different phenotypic readouts and experimental conditions. How different are these networks and what can we learn from their differences? We conducted a systematic analysis of quantitative genetic interaction networks in yeast performed under different experimental conditions. We find that networks obtained using different phenotypic readouts, in different conditions and from different laboratories overlap less than expected and provide significant unique information. To exploit this information, we develop a novel method to combine individual genetic interaction data sets and show that the resulting network improves gene function prediction performance, demonstrating that individual networks provide complementary information. Our results support the notion that using diverse phenotypic readouts and experimental conditions will substantially increase the amount of gene function information produced by genetic interaction screens.
Highlights
A genetic interaction is defined as an unexpected phenotype for a combination of mutations given each mutation’s individual effect [1]
How different are these networks and what can we learn from their differences? We analyzed quantitative genetic interaction networks mapped in yeast under different experimental conditions and phenotypic readouts and found that they provide significant unique information
As a measure of complementarity, we asked if combining networks mapped under different experimental conditions could improve gene function prediction
Summary
A genetic interaction is defined as an unexpected phenotype for a combination of mutations given each mutation’s individual effect [1]. Genetic interactions provide valuable information about gene function and are useful to study the organization of biological processes in the cell [2]. Experimental techniques are available to map genetic interactions at a large scale, in particular in Saccharomyces cerevisiae [3]. A genetic interaction is obtained in an experiment using a particular phenotypic readout and set of experimental conditions in a given species. A single, easy to observe phenotype, such as cell growth, is used to measure genetic interactions on a large scale [3]. We ask how much more genetic interaction and gene function information is gained by mapping genetic interactions using different phenotypic readouts and experimental conditions
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