Literature DB >> 16897709

Yeast as a tool to uncover the cellular targets of drugs.

Christopher M Sturgeon1, Danielle Kemmer, Hilary J Anderson, Michel Roberge.   

Abstract

Knowledge of the spectrum of cellular proteins targeted by experimental therapeutic agents would greatly facilitate drug development. However, identifying the targets of drugs is a daunting challenge. The yeast Saccharomyces cerevisiae is a valuable model organism for human diseases and pathways because it is genetically tractable and shares many functional homolog with humans. In yeast, it is possible to increase or decrease the expression level of essentially every gene and measure changes in drug sensitivity to uncover potential targets. It is also possible to infer mechanism of action from comparing the changes in mRNA expression elicited by drug treatment with those induced by gene deletions or by other drugs. Proteins that bind drugs directly can be identified using yeast protein chips. This review of the use of yeast for discovering targets of drugs discusses the advantages and drawbacks of each approach and how combining methods may reveal targets more efficiently.

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Year:  2006        PMID: 16897709     DOI: 10.1002/biot.200500039

Source DB:  PubMed          Journal:  Biotechnol J        ISSN: 1860-6768            Impact factor:   4.677


  19 in total

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Authors:  Zhun Yan; Nicolas M Berbenetz; Guri Giaever; Corey Nislow
Journal:  Genetics       Date:  2009-03-30       Impact factor: 4.562

Review 2.  Antiprion drugs as chemical tools to uncover mechanisms of prion propagation.

Authors:  Déborah Tribouillard; Fabienne Gug; Hervé Galons; Stéphane Bach; Sven J Saupe; Marc Blondel
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Journal:  Antimicrob Agents Chemother       Date:  2012-03-19       Impact factor: 5.191

4.  Antihyperlipidemic activity of Cassia auriculata flower extract in oleic acid induced hyperlipidemia in Saccharomyces cerevisiae.

Authors:  Vijayakumar Rajendran; Anilkumar Krishnegowda; Vasanthi Nachiappan
Journal:  J Food Sci Technol       Date:  2017-06-06       Impact factor: 2.701

Review 5.  Modern natural products drug discovery and its relevance to biodiversity conservation.

Authors:  David G I Kingston
Journal:  J Nat Prod       Date:  2010-12-07       Impact factor: 4.050

6.  The marine sponge-derived polyketide endoperoxide plakortide F acid mediates its antifungal activity by interfering with calcium homeostasis.

Authors:  Tao Xu; Qin Feng; Melissa R Jacob; Bharathi Avula; Melanie M Mask; Scott R Baerson; Siddharth K Tripathi; Rabab Mohammed; Mark T Hamann; Ikhlas A Khan; Larry A Walker; Alice M Clark; Ameeta K Agarwal
Journal:  Antimicrob Agents Chemother       Date:  2011-02-07       Impact factor: 5.191

7.  Combining chemical genomics screens in yeast to reveal spectrum of effects of chemical inhibition of sphingolipid biosynthesis.

Authors:  Danielle Kemmer; Lianne M McHardy; Shawn Hoon; Delphine Rebérioux; Guri Giaever; Corey Nislow; Calvin D Roskelley; Michel Roberge
Journal:  BMC Microbiol       Date:  2009-01-14       Impact factor: 3.605

8.  A chemical genomic screen in Saccharomyces cerevisiae reveals a role for diphthamidation of translation elongation factor 2 in inhibition of protein synthesis by sordarin.

Authors:  Javier Botet; María Rodríguez-Mateos; Juan P G Ballesta; José Luis Revuelta; Miguel Remacha
Journal:  Antimicrob Agents Chemother       Date:  2008-02-19       Impact factor: 5.191

9.  Role of heme in the antifungal activity of the azaoxoaporphine alkaloid sampangine.

Authors:  Ameeta K Agarwal; Tao Xu; Melissa R Jacob; Qin Feng; Michael C Lorenz; Larry A Walker; Alice M Clark
Journal:  Eukaryot Cell       Date:  2007-12-21

10.  Genetic interactions between a phospholipase A2 and the Rim101 pathway components in S. cerevisiae reveal a role for this pathway in response to changes in membrane composition and shape.

Authors:  M Mattiazzi; A Jambhekar; P Kaferle; J L Derisi; I Krizaj; U Petrovic
Journal:  Mol Genet Genomics       Date:  2010-04-09       Impact factor: 3.291

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