<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>Zanetti, Simone</dc:creator>
  <dc:creator>Grinschgl, Sonja</dc:creator>
  <dc:creator>Meola, Marco</dc:creator>
  <dc:creator>Belfiore, Marco</dc:creator>
  <dc:creator>Rey, Samantha</dc:creator>
  <dc:creator>Bianchi, Pamela</dc:creator>
  <dc:creator>Puoti, Alessandro</dc:creator>
  <dc:date>2012-05-25</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Post-transcriptional control regulates many aspects of germline development in the Caenorhabditis elegans hermaphrodite. This nematode switches from spermatogenesis to oogenesis and is, therefore, capable of self-fertilization. This sperm-oocyte switch requires 3′ UTR-mediated repression of the fem-3 mRNA. Loss of fem-3 repression results in continuous spermatogenesis in hermaphrodites. Although several factors regulating fem-3 have been identified, little is known about the mechanisms that control fem-3. Here, we investigate the steady-state levels of the fem-3 transcript and the expression pattern of its protein product. We show that FEM-3 is exclusively present in germ cells that are committed to spermatogenesis. We found that in fem-3(gf)/+ heterozygotes, mutant fem-3 gain-of-function transcripts are more abundant than their wild-type counterpart. Furthermore, we show that the penetrance of the fem-3(gf) allele correlates with inefficient FBF binding and extended poly(A) tail size of fem-3 mRNAs. Finally, we show that wild-type and gain-of-function mutated fem-3 mRNAs associate equally well with polyribosomes. We propose that the fem-3 mRNA is regulated through stabilization rather than through translatability.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/302550</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/302550/files/puo_sos.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1261/rna.031237.111</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>RNA. - 2012, vol. 18, no. 7, p. 1385-1394</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">fem-3</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Caenorhabditis elegans</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">sex determination</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">germline</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">RNA</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">The sperm-oocyte switch in the C. elegans hermaphrodite is controlled through steady-state levels of the fem-3 mRNA</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
