<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Hannich, J. Thomas</dc:creator>
  <dc:creator>Mellal, Denia</dc:creator>
  <dc:creator>Feng, Suihan</dc:creator>
  <dc:creator>Zumbuehl, Andreas</dc:creator>
  <dc:creator>Riezman, Howard</dc:creator>
  <dc:date>2017-05-03</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Sphingolipids are bio-active metabolites that show structural diversity among  eukaryotes. They are essential for growth of all eukaryotic cells but when produced in  an uncontrolled manner can lead to cell death and pathologies including auto-immune  reactions, cancer, diabetes and neurodegeneration. Caenorhabditis elegans is an  important genetic model organism both to find new drug-targets against parasitic  nematodes and to study the conserved roles of sphingolipids in animals like their  essential functions in very basic cellular processes ranging from maintenance of cell  polarity and mitochondrial repair to growth and survival. C. elegans produces sphingoid  bases which are structurally distinct from those of other animals as both iso- and  anteiso-branched species have been reported. Using metabolic labeling we show that  most worm sphingoid bases are iso-branched. We have synthesized the nematode- specific C17 iso-branched sphinganine and its 1-deoxy analogue and could show that  both the iso-branch and the 1-hydroxyl group are essential to form functional  nematode sphingolipids which are needed to maintain intestinal function. The organism  specificity was examined by complementation experiments in Saccharomyces  cerevisiae yeast cells lacking sphingoid base synthesis. We found that iso-branched  sphingoid base did not support growth of mutant cells and was toxic to wild type yeast.  1-Deoxy sphingolipids have been linked to the hereditary disease HSAN1A and other  metabolic disorders including diabetes. We found that in C. elegans the 1-deoxy  analogue cannot rescue the intestinal phenotype caused by sphingoid base depletion.  In fact, in wild-type animals with normal sphingoid base biosynthesis, exogenous 1- deoxy analogue had a disruptive effect on apical cytoskeletal organization of intestinal  cells indicating that atypical bases can interfere with normal sphingolipid function.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305385</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305385/files/zum_scf.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305385/files/zum_scf_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1039/C6SC04831E</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Chemical Science. - 2017, vol. 8, no. 5, p. 3676–3686</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Structure and conserved function of iso-branched sphingoid bases from the nematode Caenorhabditis elegans</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
