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               <dc:title>Regulation of FAS exon definition and apoptosis by the ewing sarcoma protein</dc:title>
               <dc:creator>Paronetto, Maria Paola</dc:creator>
               <dc:creator>Bernardis, Isabella</dc:creator>
               <dc:creator>Volpe, Elisabetta</dc:creator>
               <dc:creator>Bechara, Elias</dc:creator>
               <dc:creator>Sebestyén, Endre</dc:creator>
               <dc:creator>Eyras Jiménez, Eduardo</dc:creator>
               <dc:creator>Valcárcel, J. (Juan)</dc:creator>
               <dc:subject>Proteïnes</dc:subject>
               <dc:subject>Antígens CD</dc:subject>
               <dc:subject>RNA</dc:subject>
               <dc:description>The Ewing sarcoma protein EWS is an RNA and DNA binding protein implicated in transcription, pre-mRNA splicing, and DNA damage response. Using CLIP-seq, we identified EWS RNA binding sites in exonic regions near 5′ splice sites. A prominent target was exon 6 of the FAS/CD95 receptor, which is alternatively spliced to generate isoforms with opposing activities in programmed cell death. Depletion and overexpression experiments showed that EWS promotes exon 6 inclusion and consequently the synthesis of the proapoptotic FAS/CD95 isoform, whereas an EWS-FLI1 fusion protein characteristic of Ewing sarcomas shows decreased activity. Biochemical analyses revealed that EWS binding promotes the recruitment of U1snRNP and U2AF65 to the splice sites flanking exon 6 and therefore exon definition. Consistent with a role for EWS in the regulation of programmed cell death, cells depleted of EWS show decreased sensitivity to FAS-induced apoptosis, and elevated EWS expression enhances apoptosis in EWS-haploinsufficient Ewing sarcoma cells.</dc:description>
               <dc:description>M.P.P. was supported by a fellowship from the HFSP. This project was supported by Fundación Botín, Fundación Sandra Ibarra (FSI2013), the European Union Sixth Framework Programme under grant agreement Nr. LSHG-CT-2005-518238-V (EURASNET), the Spanish Ministry of Economy and Competitiveness (grant no. CSD2009-00080, Consolider RNAREG/BFU2011-29583 / BIO2011-23920), and AIRC (Grant MFAG 11658). We also acknowledge support of the Spanish Ministry of Economy and Competitiveness, “Centro de Excelencia Severo Ochoa 2013-2017” (SEV-2012-0208)</dc:description>
               <dc:date>2015-06-04T06:56:36Z</dc:date>
               <dc:date>2015-06-04T06:56:36Z</dc:date>
               <dc:date>2014</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Cell Reports. 2014; 7: 1211-1226</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/EC/FP6/518238</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/3PN/CSD2009-00080</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/3PN/BFU2011-29583</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/ES/3PN/BIO2011-23920</dc:relation>
               <dc:rights>© 2014, Elsevier. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 International http://creativecommons.org/licenses/by-nc-nd/3.0/ http://dx.doi.org/10.1016/j.celrep.2014.03.077</dc:rights>
               <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Elsevier</dc:publisher>
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