Literature DB >> 18416308

Chemical-genetic approaches for exploring the mode of action of natural products.

Andres Lopez1, Ainslie B Parsons, Corey Nislow, Guri Giaever, Charles Boone.   

Abstract

Determining the mode of action of bioactive compounds, including natural products, is a central problem in chemical biology. Because many genes are conserved from the yeast Saccharomyces cerevisiae to humans and a number of powerful genomics tools and methodologies have been developed for this model system, yeast is making a major contribution to the field of chemical genetics. The set of barcoded yeast deletion mutants, including the set of approximately 5000 viable haploid and homozygous diploid deletion mutants and the complete set of approximately 6000 heterozygous deletion mutants, containing the set of approximately 1000 essential genes, are proving highly informative for identifying chemical-genetic interactions and deciphering compound mode of action. Gene deletions that render cells hypersensitive to a specific drug identify pathways that buffer the cell against the toxic effects of the drug and thereby provide clues about both gene and compound function. Moreover, compounds that show similar chemical-genetic profiles often perturb similar target pathways. Gene dosage can be exploited to discover connections between compounds and their targets. For example, haploinsufficiency profiling of an antifungal compound, in which the set of approximately 6000 heterozygous diploid deletion mutants are scored for hypersensitivity to a compound, may identify the target directly. Creating deletion mutant collections in other fungal species, including the major human fungal pathogen Candida albicans, will expand our chemical genomics tool set, allowing us to screen for antifungal lead drugs directly. The yeast deletion mutant collection is also being exploited to map large-scale genetic interaction data obtained from genome-wide synthetic lethal screens and the integration of this data with chemical genetic data should provide a powerful system for linking compounds to their target pathway. Extensive application of chemical genetics in yeast has the potential to develop a small molecule inhibitor for the majority of all approximately 6000 yeast genes.

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Year:  2008        PMID: 18416308     DOI: 10.1007/978-3-7643-8595-8_5

Source DB:  PubMed          Journal:  Prog Drug Res        ISSN: 0071-786X


  17 in total

1.  Introduction to focus issue: genetic interactions.

Authors:  Daniel Segrè; Christopher J Marx
Journal:  Chaos       Date:  2010-06       Impact factor: 3.642

Review 2.  Functional profiling of human fungal pathogen genomes.

Authors:  Alexi I Goranov; Hiten D Madhani
Journal:  Cold Spring Harb Perspect Med       Date:  2014-11-06       Impact factor: 6.915

3.  Functional profiling in Streptococcus mutans: construction and examination of a genomic collection of gene deletion mutants.

Authors:  R G Quivey; E J Grayhack; R C Faustoferri; C J Hubbard; J D Baldeck; A S Wolf; M E MacGilvray; P L Rosalen; K Scott-Anne; B Santiago; S Gopal; J Payne; R E Marquis
Journal:  Mol Oral Microbiol       Date:  2015-06-19       Impact factor: 3.563

4.  Confirmation of the cellular targets of benomyl and rapamycin using next-generation sequencing of resistant mutants in S. cerevisiae.

Authors:  Dustin A Wride; Nader Pourmand; Walter M Bray; Jacob J Kosarchuk; Sean C Nisam; Tiffani K Quan; Ray F Berkeley; Sol Katzman; Grant A Hartzog; Carlos E Dobkin; R Scott Lokey
Journal:  Mol Biosyst       Date:  2014-12

Review 5.  Antifungal drug discovery: the process and outcomes.

Authors:  Richard Calderone; Nuo Sun; Francoise Gay-Andrieu; William Groutas; Pathum Weerawarna; Sridhar Prasad; Deepu Alex; Dongmei Li
Journal:  Future Microbiol       Date:  2014       Impact factor: 3.165

6.  A chemical genetic screen for modulators of asymmetrical 2,2'-dimeric naphthoquinones cytotoxicity in yeast.

Authors:  Ashkan Emadi; Ashley E Ross; Kathleen M Cowan; Yolanda M Fortenberry; Milena Vuica-Ross
Journal:  PLoS One       Date:  2010-05-26       Impact factor: 3.240

7.  Reverse genetics in Candida albicans predicts ARF cycling is essential for drug resistance and virulence.

Authors:  Elias Epp; Ghyslaine Vanier; Doreen Harcus; Anna Y Lee; Gregor Jansen; Michael Hallett; Don C Sheppard; David Y Thomas; Carol A Munro; Alaka Mullick; Malcolm Whiteway
Journal:  PLoS Pathog       Date:  2010-02-05       Impact factor: 6.823

8.  Identification and characterization of a small molecule inhibitor of formin-mediated actin assembly.

Authors:  Syed A Rizvi; Erin M Neidt; Jiayue Cui; Zach Feiger; Colleen T Skau; Margaret L Gardel; Sergey A Kozmin; David R Kovar
Journal:  Chem Biol       Date:  2009-11-25

Review 9.  Combination chemical genetics.

Authors:  Joseph Lehár; Brent R Stockwell; Guri Giaever; Corey Nislow
Journal:  Nat Chem Biol       Date:  2008-11       Impact factor: 15.040

10.  Chemical-genetic profile analysis in yeast suggests that a previously uncharacterized open reading frame, YBR261C, affects protein synthesis.

Authors:  Md Alamgir; Veronika Eroukova; Matthew Jessulat; Jianhua Xu; Ashkan Golshani
Journal:  BMC Genomics       Date:  2008-12-03       Impact factor: 3.969

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