<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>Boldajipour, Bijan</dc:creator>
  <dc:creator>Doitsidou, Maria</dc:creator>
  <dc:creator>Tarbashevich, Katsiaryna</dc:creator>
  <dc:creator>Laguri, Cedric</dc:creator>
  <dc:creator>Yu, Shuizi Rachel</dc:creator>
  <dc:creator>Ries, Jonas</dc:creator>
  <dc:creator>Dumstrei, Karin</dc:creator>
  <dc:creator>Thelen, Sylvia</dc:creator>
  <dc:creator>Dörries, Julia</dc:creator>
  <dc:creator>Messerschmidt, Esther-Maria</dc:creator>
  <dc:creator>Thelen, Marcus</dc:creator>
  <dc:creator>Schwille, Petra</dc:creator>
  <dc:creator>Brand, Michael</dc:creator>
  <dc:creator>Lortat-Jacob, Hugues</dc:creator>
  <dc:creator>Raz, Erez</dc:creator>
  <dc:date>2011-06-21</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The active migration of primordial germ cells (PGCs) from their site of specification  towards their target is a valuable model for investigating directed cell migration within the  complex environment of the developing embryo. In several vertebrates, PGC migration is  guided by Cxcl12, a member of the chemokine superfamily. Interestingly, two distinct  Cxcl12 paralogs are expressed in zebrafish embryos and contribute to the  chemotattractive landscape. Although this offers versatility in the use of chemokine  signals, it also requires a mechanism through which migrating cells prioritize the relevant  cues that they encounter. Here, we show that PGCs respond preferentially to one of the  paralogs and define the molecular basis for this biased behavior. We find that a single  amino acid exchange switches the relative affinity of the Cxcl12 ligands for one of the  duplicated Cxcr4 receptors, thereby determining the functional specialization of each  chemokine that elicits a distinct function in a distinct process. This scenario represents an  example of protein subfunctionalization – the specialization of two gene copies to perform  complementary functions following gene duplication – which in this case is based on  receptor-ligand interaction. Such specialization increases the complexity and flexibility of  chemokine signaling in controlling concurrent developmental processes.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318805</dc:identifier>
  <dc:identifier>https://susi.usi.ch/global/documents/318805</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318805/files/boldajipour_development_2011.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1242/dev.068379</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318805</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>Rights reserved</dc:rights>
  <dc:source>Development. - 2011, vol. 138, no. 14, p. 2909-2914</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Cxcr4</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Cell migration</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Chemokine</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Evolution</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Germ cell</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Zebrafish</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Cxcl12 evolution – subfunctionalization of a ligand through altered interaction with the chemokine receptor</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
