Literature DB >> 29401383

Metabolomic "Dark Matter" Dependent on Peroxisomal β-Oxidation in Caenorhabditis elegans.

Alexander B Artyukhin1, Ying K Zhang1, Allison E Akagi2, Oishika Panda1, Paul W Sternberg2, Frank C Schroeder1.   

Abstract

Peroxisomal β-oxidation (pβo) is a highly conserved fat metabolism pathway involved in the biosynthesis of diverse signaling molecules in animals and plants. In Caenorhabditis elegans, pβo is required for the biosynthesis of the ascarosides, signaling molecules that control development, lifespan, and behavior in this model organism. Via comparative mass spectrometric analysis of pβo mutants and wildtype, we show that pβo in C. elegans and the satellite model P. pacificus contributes to life stage-specific biosynthesis of several hundred previously unknown metabolites. The pβo-dependent portion of the metabolome is unexpectedly diverse, e.g., intersecting with nucleoside and neurotransmitter metabolism. Cell type-specific restoration of pβo in pβo-defective mutants further revealed that pβo-dependent submetabolomes differ between tissues. These results suggest that interactions of fat, nucleoside, and other primary metabolism pathways can generate structural diversity reminiscent of that arising from combinatorial strategies in microbial natural product biosynthesis.

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Year:  2018        PMID: 29401383      PMCID: PMC5890438          DOI: 10.1021/jacs.7b11811

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  58 in total

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Authors:  Lilin Zhao; Xinxing Zhang; Yanan Wei; Jiao Zhou; Wei Zhang; Peijun Qin; Satya Chinta; Xiangbo Kong; Yunpeng Liu; Haiying Yu; Songnian Hu; Zhen Zou; Rebecca A Butcher; Jianghua Sun
Journal:  Nat Commun       Date:  2016-08-01       Impact factor: 14.919

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  21 in total

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2.  Deep Interrogation of Metabolism Using a Pathway-Targeted Click-Chemistry Approach.

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3.  An Untargeted Approach for Revealing Electrophilic Metabolites.

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5.  A Large Family of Enzymes Responsible for the Modular Architecture of Nematode Pheromones.

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6.  Natural variation in C. elegans arsenic toxicity is explained by differences in branched chain amino acid metabolism.

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7.  Combinatorial Assembly of Modular Glucosides via Carboxylesterases Regulates C. elegans Starvation Survival.

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8.  Photoaffinity probes for nematode pheromone receptor identification.

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Review 9.  Quo Vadis Caenorhabditis elegans Metabolomics-A Review of Current Methods and Applications to Explore Metabolism in the Nematode.

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10.  Nematode Signaling Molecules Are Extensively Metabolized by Animals, Plants, and Microorganisms.

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