<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>Ardissone, Silvia</dc:creator>
  <dc:creator>Redder, Peter</dc:creator>
  <dc:creator>Russo, Giancarlo</dc:creator>
  <dc:creator>Frandi, Antonio</dc:creator>
  <dc:creator>Fumeaux, Coralie</dc:creator>
  <dc:creator>Patrignani, Andrea</dc:creator>
  <dc:creator>Schlapbach, Ralph</dc:creator>
  <dc:creator>Falquet, Laurent</dc:creator>
  <dc:creator>Viollier, Patrick H.</dc:creator>
  <dc:date>2016-12-20</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Heritable DNA methylation imprints are ubiquitous and underlie genetic variability from  bacteria to humans. In microbial genomes, DNA methylation has been implicated in  gene transcription, DNA replication and repair, nucleoid segregation, transposition and  virulence of pathogenic strains. Despite the importance of local (hypo)methylation at  specific loci, how and when these patterns are established during the cell cycle  remains poorly characterized. Taking advantage of the small genomes and the  synchronizability of α-proteobacteria, we discovered that conserved determinants of  the cell cycle transcriptional circuitry establish specific hypomethylation patterns in the  cell cycle model system Caulobacter crescentus. We used genome-wide methyl-N6- adenine (m6A-) analyses by restriction-enzyme-cleavage sequencing (REC-Seq) and  single-molecule real-time (SMRT) sequencing to show that MucR, a transcriptional  regulator that represses virulence and cell cycle genes in S-phase but no longer in  G1-phase, occludes 5'-GANTC-3' sequence motifs that are methylated by the DNA  adenine methyltransferase CcrM. Constitutive expression of CcrM or heterologous  methylases in at least two different α-proteobacteria homogenizes m6A patterns even  when MucR is present and affects promoter activity. Environmental stress (phosphate  limitation) can override and reconfigure local hypomethylation patterns imposed by the  cell cycle circuitry that dictate when and where local hypomethylation is instated.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309101</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309101/files/fal_plog_16.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1006499</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>PLOS Genetics. - 2016, vol. 12, no. 12, p. e1006499</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Cell cycle constraints and environmental control of local DNA hypomethylation in α-proteobacteria</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
