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Proc Natl Acad Sci U S A


Title:Acyl-CoA oxidase complexes control the chemical message produced by Caenorhabditis elegans
Author(s):Zhang X; Feng L; Chinta S; Singh P; Wang Y; Nunnery JK; Butcher RA;
Address:"Department of Chemistry, University of Florida, Gainesville, FL 32611. Department of Chemistry, University of Florida, Gainesville, FL 32611 butcher@chem.ufl.edu"
Journal Title:Proc Natl Acad Sci U S A
Year:2015
Volume:20150316
Issue:13
Page Number:3955 - 3960
DOI: 10.1073/pnas.1423951112
ISSN/ISBN:1091-6490 (Electronic) 0027-8424 (Print) 0027-8424 (Linking)
Abstract:"Caenorhabditis elegans uses ascaroside pheromones to induce development of the stress-resistant dauer larval stage and to coordinate various behaviors. Peroxisomal beta-oxidation cycles are required for the biosynthesis of the fatty acid-derived side chains of the ascarosides. Here we show that three acyl-CoA oxidases, which catalyze the first step in these beta-oxidation cycles, form different protein homo- and heterodimers with distinct substrate preferences. Mutations in the acyl-CoA oxidase genes acox-1, -2, and -3 led to specific defects in ascaroside production. When the acyl-CoA oxidases were expressed alone or in pairs and purified, the resulting acyl-CoA oxidase homo- and heterodimers displayed different side-chain length preferences in an in vitro activity assay. Specifically, an ACOX-1 homodimer controls the production of ascarosides with side chains with nine or fewer carbons, an ACOX-1/ACOX-3 heterodimer controls the production of those with side chains with seven or fewer carbons, and an ACOX-2 homodimer controls the production of those with omega-side chains with less than five carbons. Our results support a biosynthetic model in which beta-oxidation enzymes act directly on the CoA-thioesters of ascaroside biosynthetic precursors. Furthermore, we identify environmental conditions, including high temperature and low food availability, that induce the expression of acox-2 and/or acox-3 and lead to corresponding changes in ascaroside production. Thus, our work uncovers an important mechanism by which C. elegans increases the production of the most potent dauer pheromones, those with the shortest side chains, under specific environmental conditions"
Keywords:"Acyl-CoA Oxidase/*metabolism Animals Caenorhabditis elegans/*enzymology Catalysis Chromatography, Liquid Mutation Oxygen/metabolism Pheromones/*metabolism Polymerase Chain Reaction Protein Multimerization Substrate Specificity Tandem Mass Spectrometry Tem;"
Notes:"MedlineZhang, Xinxing Feng, Likui Chinta, Satya Singh, Prashant Wang, Yuting Nunnery, Joshawna K Butcher, Rebecca A eng K99 GM087533/GM/NIGMS NIH HHS/ P40 OD010440/OD/NIH HHS/ R00 GM087533/GM/NIGMS NIH HHS/ GM87533/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2015/03/17 Proc Natl Acad Sci U S A. 2015 Mar 31; 112(13):3955-60. doi: 10.1073/pnas.1423951112. Epub 2015 Mar 16"

 
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Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
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