<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>Marques, Filipe</dc:creator>
  <dc:creator>Saro, Gabriella</dc:creator>
  <dc:creator>Lia, Andrei-Stefan</dc:creator>
  <dc:creator>Poole, Richard J.</dc:creator>
  <dc:creator>Falquet, Laurent</dc:creator>
  <dc:creator>Glauser, Dominique A.</dc:creator>
  <dc:date>2019-12-31</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Understanding how the nervous system bridges sensation and behavior requires the  elucidation of complex neural and molecular networks. Forward genetic approaches,  such as screens conducted in C. elegans, have successfully identified genes required  to process natural sensory stimuli. However, functional redundancy within the  underlying neural circuits, which are often organized with multiple parallel neural  pathways, limits our ability to identify ‘neural pathway-specific genes’, i.e. genes that  are essential for the function of some, but not all of these redundant neural pathways.  To overcome this limitation, we developed a ‘forward optogenetics’ screening strategy  in which natural stimuli are initially replaced by the selective optogenetic activation of  a specific neural pathway. We used this strategy to address the function of the  polymodal FLP nociceptors mediating avoidance of noxious thermal and mechanical  stimuli. According to our expectations, we identified both mutations in ‘general’  avoidance genes that broadly impact avoidance responses to a variety of natural  noxious stimuli (unc-4, unc-83, and eat-4) and mutations that produce a narrower  impact, more restricted to the FLP pathway (syd-2, unc-14 and unc-68). Through a  detailed follow-up analysis, we further showed that the Ryanodine receptor UNC-68  acts cell-autonomously in FLP to adjust heat-evoked calcium signals and aversive  behaviors. As a whole, our work (i) reveals the importance of properly regulated ER  calcium release for FLP function, (ii) provides new entry points for new nociception  research and (iii) demonstrates the utility of our forward optogenetic strategy, which  can easily be transposed to analyze other neural pathways.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309111</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309111/files/fal_plog_19.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1008509</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>PLOS Genetics. - 2019, vol. 15, no. 12, p. e1008509</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Identification of avoidance genes through neural pathway-specific forward optogenetics</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
