<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>Fabian, Daniel K.</dc:creator>
  <dc:creator>Garschall, Kathrin</dc:creator>
  <dc:creator>Klepsatel, Peter</dc:creator>
  <dc:creator>Santos-Matos, Gonçalo</dc:creator>
  <dc:creator>Sucena, Élio</dc:creator>
  <dc:creator>Kapun, Martin</dc:creator>
  <dc:creator>Lemaitre, Bruno</dc:creator>
  <dc:creator>Schlötterer, Christian</dc:creator>
  <dc:creator>Arking, Robert</dc:creator>
  <dc:creator>Flatt, Thomas</dc:creator>
  <dc:date>2018-11-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Much has been learned about the genetics of aging from studies in model organisms,  but still little is known about naturally occurring alleles that contribute to variation in  longevity. For example, analysis of mutants and transgenes has identified insulin  signaling as a major regulator of longevity, yet whether standing variation in this  pathway underlies microevolutionary changes in lifespan and correlated fitness traits  remains largely unclear. Here, we have analyzed the genomes of a set of Drosophila  melanogaster lines that have been maintained under direct selection for postponed  reproduction and indirect selection for longevity, relative to unselected control lines, for  over 35 years. We identified many candidate loci shaped by selection for longevity  and late‐life fertility, but – contrary to expectation – we did not find overrepresentation  of canonical longevity genes. Instead, we found an enrichment of immunity genes,  particularly in the Toll pathway, suggesting that evolutionary changes in immune  function might underpin – in part – the evolution of late‐life fertility and longevity. To  test whether this genomic signature is causative, we performed functional  experiments. In contrast to control flies, long‐lived flies tended to downregulate the  expression of antimicrobial peptides upon infection with age yet survived fungal,  bacterial, and viral infections significantly better, consistent with alleviated  immunosenescence. To examine whether genes of the Toll pathway directly affect  longevity, we employed conditional knockdown using in vivo RNAi. In adults, RNAi  against the Toll receptor extended lifespan, whereas silencing the pathway antagonist  cactus‐–causing immune hyperactivation – dramatically shortened lifespan. Together,  our results suggest that genetic changes in the age‐dependent regulation of immune  homeostasis might contribute to the evolution of longer life.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307288</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307288/files/fla_eli.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/evl3.89</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Evolution Letters. - 2018, vol. 2, no. 6, p. 567–579</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Aging</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Drosophila</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">evolve</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">immunity</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">longevity</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">resequence</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Evolution of longevity improves immunity in Drosophila</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
