Your browser doesn't support javascript.
loading
Modular metabolite assembly in Caenorhabditis elegans depends on carboxylesterases and formation of lysosome-related organelles.
Le, Henry H; Wrobel, Chester Jj; Cohen, Sarah M; Yu, Jingfang; Park, Heenam; Helf, Maximilian J; Curtis, Brian J; Kruempel, Joseph C; Rodrigues, Pedro Reis; Hu, Patrick J; Sternberg, Paul W; Schroeder, Frank C.
Affiliation
  • Le HH; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Wrobel CJ; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Cohen SM; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
  • Yu J; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Park H; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
  • Helf MJ; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Curtis BJ; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Kruempel JC; Department of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, United States.
  • Rodrigues PR; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
  • Hu PJ; Departments of Medicine and Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, United States.
  • Sternberg PW; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, United States.
  • Schroeder FC; Boyce Thompson Institute and Department of Chemistry and Chemical Biology, Cornell University, Ithaca, United States.
Elife ; 92020 10 16.
Article de En | MEDLINE | ID: mdl-33063667
ABSTRACT
Signaling molecules derived from attachment of diverse metabolic building blocks to ascarosides play a central role in the life history of C. elegans and other nematodes; however, many aspects of their biogenesis remain unclear. Using comparative metabolomics, we show that a pathway mediating formation of intestinal lysosome-related organelles (LROs) is required for biosynthesis of most modular ascarosides as well as previously undescribed modular glucosides. Similar to modular ascarosides, the modular glucosides are derived from highly selective assembly of moieties from nucleoside, amino acid, neurotransmitter, and lipid metabolism, suggesting that modular glucosides, like the ascarosides, may serve signaling functions. We further show that carboxylesterases that localize to intestinal organelles are required for the assembly of both modular ascarosides and glucosides via ester and amide linkages. Further exploration of LRO function and carboxylesterase homologs in C. elegans and other animals may reveal additional new compound families and signaling paradigms.
Sujet(s)
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Carboxylic ester hydrolases / Caenorhabditis elegans / Lysosomes Limites: Animals Langue: En Journal: Elife Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Carboxylic ester hydrolases / Caenorhabditis elegans / Lysosomes Limites: Animals Langue: En Journal: Elife Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique