<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>Durmaz, Esra</dc:creator>
  <dc:creator>Rajpurohit, Subhash</dc:creator>
  <dc:creator>Betancourt, Nicolas</dc:creator>
  <dc:creator>Fabian, Daniel K.</dc:creator>
  <dc:creator>Kapun, Martin</dc:creator>
  <dc:creator>Schmidt, Paul</dc:creator>
  <dc:creator>Flatt, Thomas</dc:creator>
  <dc:date>2019</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">A fundamental aim of adaptation genomics is to identify polymorphisms that underpin  variation in fitness traits. In Drosophila melanogaster, latitudinal life‐history clines exist  on multiple continents and make an excellent system for dissecting the genetics of  adaptation. We have previously identified numerous clinal single‐nucleotide  polymorphism in insulin/insulin‐like growth factor signaling (IIS), a pathway known  from mutant studies to affect life history. However, the effects of natural variants in this  pathway remain poorly understood. Here we investigate how two clinal alternative  alleles at foxo, a transcriptional effector of IIS, affect fitness components (viability,  size, starvation resistance, fat content). We assessed this polymorphism from the  North American cline by reconstituting outbred populations, fixed for either the low‐ or  high‐latitude allele, from inbred DGRP lines. Because diet and temperature modulate  IIS, we phenotyped alleles across two temperatures (18°C, 25°C) and two diets  differing in sugar source and content. Consistent with clinal expectations, the high‐ latitude allele conferred larger body size and reduced wing loading. Alleles also  differed in starvation resistance and expression of insulin‐like receptor, a  transcriptional target of FOXO. Allelic reaction norms were mostly parallel, with few  GxE interactions. Together, our results suggest that variation in IIS makes a major  contribution to clinal life‐history adaptation.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307966</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307966/files/fla_cpi.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307966/files/fla_cpi_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/evo.13759</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Evolution. - 2019, vol. 73, no. 9, p. 1774–1792</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">A clinal polymorphism in the insulin signaling transcription factor foxo contributes to life-history adaptation in Drosophila*</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
