The AAA-ATPase Ter94 regulates wing size in Drosophila by suppressing the Hippo pathway

Commun Biol. 2024 May 6;7(1):533. doi: 10.1038/s42003-024-06246-x.

Abstract

Insect wing development is a fascinating and intricate process that involves the regulation of wing size through cell proliferation and apoptosis. In this study, we find that Ter94, an AAA-ATPase, is essential for proper wing size dependently on its ATPase activity. Loss of Ter94 enables the suppression of Hippo target genes. When Ter94 is depleted, it results in reduced wing size and increased apoptosis, which can be rescued by inhibiting the Hippo pathway. Biochemical experiments reveal that Ter94 reciprocally binds to Mer, a critical upstream component of the Hippo pathway, and disrupts its interaction with Ex and Kib. This disruption prevents the formation of the Ex-Mer-Kib complex, ultimately leading to the inactivation of the Hippo pathway and promoting proper wing development. Finally, we show that hVCP, the human homolog of Ter94, is able to substitute for Ter94 in modulating Drosophila wing size, underscoring their functional conservation. In conclusion, Ter94 plays a positive role in regulating wing size by interfering with the Ex-Mer-Kib complex, which results in the suppression of the Hippo pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism
  • Animals
  • Apoptosis
  • Drosophila / genetics
  • Drosophila / growth & development
  • Drosophila / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / growth & development
  • Drosophila melanogaster* / metabolism
  • Gene Expression Regulation, Developmental
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Membrane Proteins*
  • Neurofibromin 2 / genetics
  • Neurofibromin 2 / metabolism
  • Protein Serine-Threonine Kinases* / genetics
  • Protein Serine-Threonine Kinases* / metabolism
  • Signal Transduction*
  • Tumor Suppressor Proteins*
  • Wings, Animal* / growth & development
  • Wings, Animal* / metabolism

Substances

  • Drosophila Proteins
  • Protein Serine-Threonine Kinases
  • hpo protein, Drosophila
  • Intracellular Signaling Peptides and Proteins
  • ex protein, Drosophila
  • merlin, Drosophila
  • Neurofibromin 2
  • kibra protein, Drosophila
  • Adenosine Triphosphatases
  • Membrane Proteins
  • Tumor Suppressor Proteins