Literature DB >> 15893935

Studying phospholipid metabolism using yeast systematic and chemical genetics.

Gregory D Fairn1, Christopher R McMaster.   

Abstract

Most phospholipid metabolic pathways in the budding yeast Saccharomyces cerevisiae are analogous to their mammalian counterparts. The biological tractability of yeast provides for an opportunity to rapidly determine functions of specific lipids or lipid metabolic pathways using both classical and chemical-genetic techniques. The recent generation of the yeast genome deletion collection revealed that approximately 75% of yeast genes are not essential for life. Coupling analysis of the yeast deletion collection with automation using high-throughput robotics enables yeast genetic screens to be more thorough and bypasses the requirement for library screens to identify genes of interest. Two high-throughput yeast genetic methods are described, systematic synthetic lethality and chemical genetics. Systematic synthetic lethality is based on the principle that inactivation of two genes separately has minimal effects on cell growth whereas inactivation of both genes simultaneously results in growth defects due to their shared requirement in a particular cellular process. Chemical genetics is the analysis of bioactive compounds to determine processes that regulate susceptibility to the compound under study, and provides powerful data regarding precise targets and mechanism of action that regulate action of the compound.

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Year:  2005        PMID: 15893935     DOI: 10.1016/j.ymeth.2004.11.005

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  5 in total

1.  Alteration of plasma membrane organization by an anticancer lysophosphatidylcholine analogue induces intracellular acidification and internalization of plasma membrane transporters in yeast.

Authors:  Ola Czyz; Teshager Bitew; Alvaro Cuesta-Marbán; Christopher R McMaster; Faustino Mollinedo; Vanina Zaremberg
Journal:  J Biol Chem       Date:  2013-01-23       Impact factor: 5.157

2.  The oxysterol binding protein Kes1p regulates Golgi apparatus phosphatidylinositol-4-phosphate function.

Authors:  Gregory D Fairn; Amy J Curwin; Christopher J Stefan; Christopher R McMaster
Journal:  Proc Natl Acad Sci U S A       Date:  2007-09-19       Impact factor: 11.205

3.  Phospholipid transfer protein Sec14 is required for trafficking from endosomes and regulates distinct trans-Golgi export pathways.

Authors:  Amy J Curwin; Gregory D Fairn; Christopher R McMaster
Journal:  J Biol Chem       Date:  2009-01-06       Impact factor: 5.157

4.  Localization of lipid raft proteins to the plasma membrane is a major function of the phospholipid transfer protein Sec14.

Authors:  Amy J Curwin; Marissa A Leblanc; Gregory D Fairn; Christopher R McMaster
Journal:  PLoS One       Date:  2013-01-30       Impact factor: 3.240

Review 5.  How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases.

Authors:  Katherine A Strynatka; Michelle C Gurrola-Gal; Jason N Berman; Christopher R McMaster
Journal:  Genetics       Date:  2018-03       Impact factor: 4.562

  5 in total

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