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Ascaroside activity in Caenorhabditis elegans is highly dependent on chemical structure.
Hollister, Kyle A; Conner, Elizabeth S; Zhang, Xinxing; Spell, Mark; Bernard, Gary M; Patel, Pratik; de Carvalho, Ana Carolina G V; Butcher, Rebecca A; Ragains, Justin R.
Afiliación
  • Hollister KA; Department of Chemistry, Louisiana State University, Baton Rouge, 70803, United States.
Bioorg Med Chem ; 21(18): 5754-69, 2013 Sep 15.
Article en En | MEDLINE | ID: mdl-23920482
ABSTRACT
The nematode Caenorhabditis elegans secretes ascarosides, structurally diverse derivatives of the 3,6-dideoxysugar ascarylose, and uses them in chemical communication. At high population densities, specific ascarosides, which are together known as the dauer pheromone, trigger entry into the stress-resistant dauer larval stage. In order to study the structure-activity relationships for the ascarosides, we synthesized a panel of ascarosides and tested them for dauer-inducing activity. This panel includes a number of natural ascarosides that were detected in crude pheromone extract, but as yet have no assigned function, as well as many unnatural ascaroside derivatives. Most of these ascarosides, some of which have significant structural similarity to the natural dauer pheromone components, have very little dauer-inducing activity. Our results provide a primer to ascaroside structure-activity relationships and suggest that slight modifications to ascaroside structure dramatically influence binding to the relevant G protein-coupled receptors that control dauer formation.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feromonas / Glucolípidos / Caenorhabditis elegans Límite: Animals Idioma: En Revista: Bioorg Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Feromonas / Glucolípidos / Caenorhabditis elegans Límite: Animals Idioma: En Revista: Bioorg Med Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos