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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.
Abstract:
In all multicellular organisms, the fundamental processes of cell proliferation and cell death are crucial for growth regulation during organogenesis. Strict regulation of cell death is important to maintain tissue homeostasis by affecting processes like regulation of cell number, and elimination of unwanted/unfit cells. The developing Drosophila eye is a versatile model to study patterning and growth, where complex signaling pathways regulate growth and cell survival. However, the molecular mechanisms underlying regulation of these processes is not fully understood. In a gain-of-function screen, we found that misexpression of cullin-4 (cul-4), an ubiquitin ligase, can rescue reduced eye mutant phenotypes. Previously, cul-4 has been shown to regulate chromatin remodeling, cell cycle and cell division. Genetic characterization of cul-4 in the developing eye revealed that loss-of-function of cul-4 exhibits a reduced eye phenotype. Analysis of twin-spots showed that in comparison with their wild-type counterparts, the cul-4 loss-of-function clones fail to survive. Here we show that cul-4 clones are eliminated by induction of cell death due to activation of caspases. Aberrant activation of signaling pathways is known to trigger cell death in the developing eye. We found that Wingless (Wg) and c-Jun-amino-terminal-(NH2)-Kinase (JNK) signaling are ectopically induced in cul-4 mutant clones, and these signals co-localize with the dying cells. Modulating levels of Wg and JNK signaling by using agonists and antagonists of these pathways demonstrated that activation of Wg and JNK signaling enhances cul-4 mutant phenotype, whereas downregulation of Wg and JNK signaling rescues the cul-4 mutant phenotypes of reduced eye. Here we present evidences to demonstrate that cul-4 is involved in restricting Wg signaling and downregulation of JNK signaling-mediated cell death during early eye development. Overall, our studies provide insights into a novel role of cul-4 in promoting cell survival in the developing Drosophila eye.
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.
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