Discovering Modes of Action for Therapeutic Compounds Using a Genome-Wide Screen of Yeast Heterozygotes

• Published in: Cell Vol. 116; no. 1; pp. 121 - 137
• Main Authors: Lum, Pek Yee, Armour, Christopher D., Stepaniants, Sergey B., Cavet, Guy, Wolf, Maria K., Butler, J.Scott, Hinshaw, Jerald C., Garnier, Philippe, Prestwich, Glenn D., Leonardson, Amy, Garrett-Engele, Philip, Rush, Christopher M., Bard, Martin, Schimmack, Greg, Phillips, John W., Roberts, Christopher J., Shoemaker, Daniel D.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 09.01.2004
• Subjects: Drug Evaluation, Preclinical - methods; exosomes; Fluorouracil - pharmacology; Gene Expression Profiling - methods; Genome, Fungal; Heterozygote; Intramolecular Transferases - drug effects; Intramolecular Transferases - metabolism; molsidomine; Molsidomine - pharmacology; Predictive Value of Tests; Reproducibility of Results; RNA, Ribosomal - drug effects; RNA, Ribosomal - metabolism; Saccharomyces cerevisiae; Saccharomyces cerevisiae - drug effects; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae - metabolism; sterols
• ISSN: 0092-8674; 1097-4172
• DOI: 10.1016/S0092-8674(03)01035-3

Modern medicine faces the challenge of developing safer and more effective therapies to treat human diseases. Many drugs currently in use were discovered without knowledge of their underlying molecular mechanisms. Understanding their biological targets and modes of action will be essential to design improved second-generation compounds. Here, we describe the use of a genome-wide pool of tagged heterozygotes to assess the cellular effects of 78 compounds in Saccharomyces cerevisiae. Specifically, lanosterol synthase in the sterol biosynthetic pathway was identified as a target of the antianginal drug molsidomine, which may explain its cholesterol-lowering effects. Further, the rRNA processing exosome was identified as a potential target of the cell growth inhibitor 5-fluorouracil. This genome-wide screen validated previously characterized targets or helped identify potentially new modes of action for over half of the compounds tested, providing proof of this principle for analyzing the modes of action of clinically relevant compounds.