Joint effects of genes underlying a temperature specialization tradeoff in yeast

• Published in: PLoS genetics Vol. 17; no. 9; p. e1009793
• Main Authors: AlZaben, Faisal, Chuong, Julie N., Abrams, Melanie B., Brem, Rachel B.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 14.09.2021; Public Library of Science (PLoS)
• Subjects: Adaptation; Adaptation (Biology); Alleles; Biology and Life Sciences; Biomass; Efficiency; Epistasis; Epistasis, Genetic; Evolution; Evolution, Molecular; Evolutionary genetics; Genes; Genes, Fungal; Genetic aspects; Genetic engineering; Genetic research; Genotype & phenotype; Heat tolerance (Biology); High temperature; Molecular evolution; Natural history; Phenotypes; Research and Analysis Methods; Saccharomyces - genetics; Saccharomyces cerevisiae; Saccharomyces cerevisiae - genetics; Sibling species; Species Specificity; Temperature; Temperature tolerance; Thermotolerance - genetics; Yeast; Yeast fungi; United States
• ISSN: 1553-7404; 1553-7390; 1553-7404
• DOI: 10.1371/journal.pgen.1009793

A central goal of evolutionary genetics is to understand, at the molecular level, how organisms adapt to their environments. For a given trait, the answer often involves the acquisition of variants at unlinked sites across the genome. Genomic methods have achieved landmark successes in pinpointing these adaptive loci. To figure out how a suite of adaptive alleles work together, and to what extent they can reconstitute the phenotype of interest, requires their transfer into an exogenous background. We studied the joint effect of adaptive, gain-of-function thermotolerance alleles at eight unlinked genes from Saccharomyces cerevisiae , when introduced into a thermosensitive sister species, S . paradoxus . Although the loci damped each other’s beneficial impact (that is, they were subject to negative epistasis), most boosted high-temperature growth alone and in combination, and none was deleterious. The complete set of eight genes was sufficient to confer ~15% of the S . cerevisiae thermotolerance phenotype in the S . paradoxus background. The same loci also contributed to a heretofore unknown advantage in cold growth by S . paradoxus . Together, our data establish temperature resistance in yeasts as a model case of a genetically complex evolutionary tradeoff, which can be partly reconstituted from the sequential assembly of unlinked underlying loci.