Cullin-4 regulates Wingless and JNK signaling-mediated cell death in the Drosophila eye

Meghana Tare1, Ankita Sarkar1, Shimpi Bedi1

  • 1Department of Biology, University of Dayton, Dayton, OH, USA.

Cell Death & Disease
|December 30, 2016
PubMed

Insights

Cullin-4 (cul-4) normally promotes cell survival in developing Drosophila eyes. Loss of cul-4 triggers cell death via Wingless (Wg) and JNK signaling pathways, revealing its role in restricting these signals.

Area of Science:

  • Developmental Biology
  • Cell Biology
  • Genetics

Background:

  • Cell proliferation and death are vital for organism growth and tissue homeostasis.
  • The developing Drosophila eye is a model for studying growth and cell survival regulation.
  • Molecular mechanisms controlling these processes are not fully understood.

Purpose of the Study:

  • Investigate the role of cullin-4 (cul-4) in Drosophila eye development.
  • Determine how cul-4 influences cell survival and death pathways.
  • Elucidate the molecular mechanisms by which cul-4 regulates cell fate.

Main Methods:

  • Gain-of-function screen to identify genes affecting eye development.
  • Genetic characterization of cul-4 loss-of-function mutants.
  • Analysis of cell survival using twin-spot assays.
  • Assessment of caspase activation and signaling pathway involvement (Wg, JNK).

Main Results:

  • Loss of cul-4 function leads to reduced eye size and failure of cul-4 mutant clones to survive.
  • Cul-4 deficient cells undergo apoptosis due to caspase activation.
  • Aberrant Wingless (Wg) and c-Jun-amino-terminal-(NH2)-Kinase (JNK) signaling are induced in cul-4 mutant clones.
  • Modulating Wg and JNK signaling impacts cul-4 mutant phenotypes.

Conclusions:

  • Cul-4 is essential for cell survival in the developing Drosophila eye.
  • Cul-4 restricts Wingless (Wg) signaling and downregulates JNK signaling-mediated cell death.
  • This study reveals a novel role for cul-4 in promoting cell survival during early eye development.