<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>Jadhav, Shyamalagauri</dc:creator>
  <dc:creator>Russo, Sarah</dc:creator>
  <dc:creator>Cottier, Stéphanie</dc:creator>
  <dc:creator>Schneiter, Roger</dc:creator>
  <dc:creator>Cowart, Ashley</dc:creator>
  <dc:creator>Greenberg, Miriam L.</dc:creator>
  <dc:date>2016-10-14</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Bipolar disorder (BD), which is characterized by depression and mania, affects 1–2%  of the world population. Current treatments are effective in only 40–60% of cases and  cause severe side effects. Valproate (VPA) is one of the most widely used drugs for  the treatment of BD, but the therapeutic mechanism of action of this drug is not  understood. This knowledge gap has hampered the development of effective  treatments. To identify candidate pathways affected by VPA, we performed a genome-  wide expression analysis in yeast cells grown in the presence or absence of the drug.  VPA caused up-regulation of FEN1 and SUR4, encoding fatty acid elongases that  catalyze the synthesis of very long chain fatty acids (C24 to C26) required for  ceramide synthesis. Interestingly, fen1Δ and sur4Δ mutants exhibited VPA sensitivity.  In agreement with increased fatty acid elongase gene expression, VPA increased  levels of phytoceramide, especially those containing C24–C26 fatty acids. Consistent  with an increase in ceramide, VPA decreased the expression of amino acid  transporters, increased the expression of ER chaperones, and activated the unfolded  protein response element (UPRE), suggesting that VPA induces the UPR pathway.  These effects were rescued by supplementation of inositol and similarly observed in  inositol-starved ino1Δ cells. Starvation of ino1Δ cells increased expression of FEN1  and SUR4, increased ceramide levels, decreased expression of nutrient transporters,  and induced the UPR. These findings suggest that VPA-mediated inositol depletion  induces the UPR by increasing the de novo synthesis of ceramide.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/305215</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305215/files/sch_vai_sm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/305215/files/Journal_of_Biological_Chemistry_2016.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M116.752634</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Journal of Biological Chemistry. - 2016, vol. 291, no. 42, p. 22253–22261</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Valproate induces the unfolded protein response by increasing ceramide levels</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
