<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>Fritsch, Cornelia</dc:creator>
  <dc:creator>Bernardo-Garcia, F. Javier</dc:creator>
  <dc:creator>Humberg, Tim-Henning</dc:creator>
  <dc:creator>Mishra, Abhishek Kumar</dc:creator>
  <dc:creator>Miellet, Sara</dc:creator>
  <dc:creator>Almeida, Silvia</dc:creator>
  <dc:creator>Frochaux, Michael V.</dc:creator>
  <dc:creator>Deplancke, Bart</dc:creator>
  <dc:creator>Huber, Armin</dc:creator>
  <dc:creator>Sprecher, Simon G.</dc:creator>
  <dc:date>2019-07-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Development of eye tissue is initiated by a conserved set of transcription factors  termed retinal determination network (RDN). In the fruit fly Drosophila melanogaster,  the zinc-finger transcription factor Glass acts directly downstream of the RDN to  control identity of photoreceptor as well as non-photoreceptor cells. Tight control of  spatial and temporal gene expression is a critical feature during development, cell-fate  determination as well as maintenance of differentiated tissues. The molecular  mechanisms that control expression of glass, however, remain largely unknown. We  here identify complex regulatory mechanisms controlling expression of the glass  locus. All information to recapitulate glass expression are contained in a compact 5.2  kb cis-acting genomic element by combining different cell-type specific and general  enhancers with repressor elements. Moreover, the immature RNA of the locus  contains an alternative small open reading frame (smORF) upstream of the actual  glass translation start, resulting in a small peptide instead of the three possible Glass  protein isoforms. CRISPR/Cas9-based mutagenesis shows that the smORF is not  required for the formation of functioning photoreceptors, but is able to attenuate  effects of glass misexpression. Furthermore, editing the genome to generate glass loci  eliminating either one or two isoforms shows that only one of the three proteins is  critical for formation of functioning photoreceptors, while removing the two other  isoforms did not cause defects in developmental or photoreceptor function. Our  results show that eye development and function is largely unaffected by targeted  manipulations of critical features of the glass transcript, suggesting a strong selection  pressure to allow the formation of a functioning eye.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308097</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308097/files/spr_mrg.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pgen.1008269</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. 7, p. e1008269</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Multilevel regulation of the glass locus during Drosophila eye development</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
