<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>Vincenzetti, Lucia</dc:creator>
  <dc:creator>Leoni, Cristina</dc:creator>
  <dc:creator>Chirichella, Michele</dc:creator>
  <dc:creator>Kwee, Ivo</dc:creator>
  <dc:creator>Monticelli, Silvia</dc:creator>
  <dc:date>2019-01-30</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">In mammals, the 5’-methylcytosine (5mC) modification in the genomic DNA contributes to the dynamic control of gene expression. 5mC  erasure is required for the activation of developmental programs and occurs either by passive dilution through DNA replication, or by  enzymatic oxidation of the methyl mark to 5-hydroxymethylcytosine (5hmC), which can persist as such or undergo further oxidation and  enzymatic removal. The relative contribution of each mechanism to epigenetic control in dynamic biological systems still remains a compelling  question. To explore this critical issue, we used primary human T lymphocytes, in which two cellular states can be clearly identified, namely  quiescent naïve T cells, which are slowly or rarely proliferating, and rapidly proliferating activated T cells. We found that active mechanisms of  methylation removal were selectively at work in naïve T cells, while memory T lymphocytes entirely relied on passive, replication-dependent  dilution, suggesting that proliferative capacity influences the choice of the preferential demethylation mechanism. Active processes of  demethylation appear to be critical in quiescent naïve T lymphocytes for the maintenance of regulatory regions poised for rapid responses to  physiological stimuli.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318874</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318874</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318874/files/Vincenzetti_EJI_2019.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/eji.201847967</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318874</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>European Journal of Immunology. - 2019, p. 1-15</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">DNA methylation</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Epigenetics</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">T lymphocytes</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Differentiation</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Activation</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">The contribution of active and passive mechanisms of 5mC and 5hmC removal in human T lymphocytes is differentiation- and activation-dependent</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
