<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>Sproll, Patrick</dc:creator>
  <dc:creator>Eid, Wassim</dc:creator>
  <dc:creator>Gomes, Camila R.</dc:creator>
  <dc:creator>Mendonca, Berenice B.</dc:creator>
  <dc:creator>Gomes, Nathalia L.</dc:creator>
  <dc:creator>Costa, Elaine M.-F.</dc:creator>
  <dc:creator>Lauber-Biason, Anna</dc:creator>
  <dc:date>2018-09-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Background One of the defining moments of human life occurs early during embryonic  development, when individuals sexually differentiate into either male or female.  Perturbation of this process can lead to disorders/differences of sex development  (DSD). Chromobox protein homolog 2 (CBX2) has two distinct isoforms, CBX2.1 and  CBX2.2: the role of CBX2.1 in DSD has been previously established, yet to date the  function of the smaller isoform CBX2.2 remains unknown. Methods The genomic DNA  of two 46,XY DSD patients was analysed using whole exome sequencing.  Furthermore, protein/DNA interaction studies were performed using DNA adenine  methyltransferase identification (DamID) to identify putative binding partners of CBX2.  Finally, in vitro functional studies were used to elucidate the effect of wild-type and  variant CBX2.2 on selected downstream targets. Results Here, we describe two  patients with features of DSD i.e. atypical external genitalia, perineal hypospadias and  no palpable gonads, each patient carrying a distinct CBX2.2 variant, p.Cys132Arg  (c.394T&gt;C) and p.Cys154fs (c.460delT). We show that both CBX2.2 variants fail to  regulate the expression of genes essential for sexual development, leading to a  severe 46,XY DSD defect, likely because of a defective expression of EMX2 in the  developing gonad. Conclusion Our study indicates a distinct function of the shorter  form of CBX2 and by identifying several of its unique targets, can advance our  understanding of DSD pathogenesis and ultimately DSD diagnosis and management.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307271</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307271/files/bia_ajp.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1002/mgg3.445</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Molecular Genetics &amp; Genomic Medicine. - 2018, vol. 6, no. 5, p. 785–795</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Assembling the jigsaw puzzle: CBX2 isoform 2 and its targets in disorders/differences of sex development</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
