Defining the Yeast Resistome through in vitro Evolution and Whole Genome Sequencing

Author:

Ottilie SabineORCID,Luth Madeline R.ORCID,Hellemann Erich,Goldgof Gregory M.,Vigil Eddy,Kumar Prianka,Cheung Andrea L.,Song Miranda,Godinez-Macias Karla P.,Carolino Krypton,Yang Jennifer,Lopez Gisel,Abraham Matthew,Tarsio Maureen,LeBlanc Emmanuelle,Whitesell Luke,Schenken Jake,Gunawan Felicia,Patel Reysha,Smith Joshua,Love Melissa S.,Williams Roy M.,McNamara Case W.,Gerwick William H.,Ideker Trey,Suzuki Yo,Wirth Dyann F.,Lukens Amanda K.,Kane Patricia M.,Cowen Leah E.,Durrant Jacob D.,Winzeler Elizabeth A.ORCID

Abstract

SummaryIn vitro evolution and whole genome analysis were used to comprehensively identify the genetic determinants of chemical resistance in the model microbe, Saccharomyces cerevisiae. Analysis of 355 curated, laboratory-evolved clones, resistant to 80 different compounds, demonstrates differences in the types of mutations that are identified in selected versus neutral evolution and reveals numerous new, compound-target interactions. Through enrichment analysis we further identify a set of 137 genes strongly associated with or conferring drug resistance as indicated by CRISPR-Cas9 engineering. The set of 25 most frequently mutated genes was enriched for transcription factors and for almost 25 percent of the compounds, resistance was mediated by one of 100 independently derived, gain-of-function, single nucleotide variants found in 170-amino-acid domains in two Zn2C6 transcription factors, YRR1 and YRM1 (p < 1x 10 −100). This remarkable enrichment for transcription factors as drug resistance genes may explain why it is challenging to develop effective antifungal killing agents and highlights their important role in evolution.

Publisher

Cold Spring Harbor Laboratory

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