TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

AUTHORS

  • Caubit Xavier
  • Gubellini Paolo
  • Andrieux Joris
  • Roubertoux Pierre L.
  • Metwaly Mehdi
  • Jacq Bernard
  • Fatmi Ahmed
  • Had-Aissouni Laurence
  • Kwan Kenneth Y.
  • Salin Pascal
  • Carlier Michèle
  • Liedén Agne
  • Rudd Eva
  • Shinawi Marwan
  • Vincent-Delorme Catherine
  • Cuisset Jean-Marie
  • Lemaitre Marie-Pierre
  • Abderrehamane Fatimetou
  • Duban Benedicte
  • Lemaître Jean-François
  • Woolf Adrian S.
  • Bockenhauer Detlef
  • Severac Dany
  • Dubois Emeric
  • Zhu Ying
  • Sestan Nenad
  • Garratt Alistair N.
  • Goff Lydia Kerkerian-Le
  • Fasano Laurent

keywords

  • Neurodevelopmental disorders
  • Gene regulation
  • Neuroscience
  • Neurogenesis

Document type

Journal articles

ABSTRACT

TSHZ3, which encodes a zinc-finger transcription factor, was recently positioned as a hub gene in a module of the genes with the highest expression in the developing human neocortex, but its functions remained unknown. Here we identify TSHZ3 as the critical region for a syndrome associated with heterozygous deletions at 19q12-q13.11, which includes autism spectrum disorder (ASD). In Tshz3-null mice, differentially expressed genes include layer-specific markers of cerebral cortical projection neurons (CPNs), and the human orthologs of these genes are strongly associated with ASD. Furthermore, mice heterozygous for Tshz3 show functional changes at synapses established by CPNs and exhibit core ASD-like behavioral abnormalities. These findings highlight essential roles for Tshz3 in CPN development and function, whose alterations can account for ASD in the newly defined TSHZ3 deletion syndrome.

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