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Updated: Aug 20, 2026

In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening
Published on: October 6, 2022
The apical caspase dronc governs programmed and unprogrammed cell death in Drosophila
Su Kit Chew1, Fatih Akdemir, Po Chen
1Department of Cell Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Abstract:
Among the seven caspases encoded in the fly genome, only dronc contains a caspase recruitment domain. To assess the function of this gene in development, we produced a null mutation in dronc. Animals lacking zygotic dronc are defective for programmed cell death (PCD) and arrest as early pupae. These mutants present a range of defects, including extensive hyperplasia of hematopoietic tissues, supernumerary neuronal cells, and head involution failure. dronc genetically interacts with the Ced4/Apaf1 counterpart, Dark, and adult structures lacking dronc are disrupted for fine patterning. Furthermore, in diverse models of metabolic injury, dronc- cells are completely insensitive to induction of cell killing. These findings establish dronc as an essential regulator of cell number in development and illustrate broad requirements for this apical caspase in adaptive responses during stress-induced apoptosis.
Insights
The fly caspase dronc (death-related ced-3 N-terminal caspase) is essential for programmed cell death (PCD). Loss of dronc causes developmental defects and impairs cellular responses to metabolic injury.
Area of Science:
- Developmental Biology
- Cell Death Pathways
- Apoptosis Research
Background:
- The fly genome encodes seven caspases, but only dronc possesses a caspase recruitment domain.
- Understanding the role of caspases is crucial for cell death research.
Purpose of the Study:
- To investigate the developmental function of the fly caspase dronc.
- To determine dronc's role in programmed cell death and stress responses.
Main Methods:
- Generation of a null mutation in the dronc gene.
- Analysis of developmental defects in dronc mutant animals.
- Genetic interaction studies with Dark (Drosophila Apaf-1-related killer).
Main Results:
- Zygotic dronc mutants exhibit defective programmed cell death and arrest as early pupae.
- Mutants show hyperplasia in hematopoietic tissues and supernumerary neurons.
- dronc null mutants are insensitive to stress-induced cell killing.
Conclusions:
- dronc is an essential regulator of cell number during fly development.
- This apical caspase plays broad roles in adaptive responses to apoptosis during metabolic stress.
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