Dissecting morphogenetic apoptosis through a genetic screen in Drosophila

Audrey Barbaste1, Sonia Schott1, Corinne Benassayag1,2

  • 1Laboratoire de Biologie Cellulaire et Moléculaire des Mécanismes du Contrôle de la Prolifération (LBCMCP), Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, UPS, Toulouse, France.

Life Science Alliance
|July 26, 2023
PubMed

Insights

This study identifies genes involved in morphogenetic apoptosis, focusing on how cell death influences tissue development. It reveals new insights into the non-autonomous roles of apoptosis in shaping tissues during development.

Area of Science:

  • Cell Biology
  • Developmental Biology
  • Genetics

Background:

  • Apoptosis is crucial for development and disease, but its non-autonomous signaling remains poorly understood.
  • Previous research focused on cell-autonomous apoptosis, neglecting signals from dying cells and their impact on surroundings.
  • The morphogenetic apoptosis pathway, governing tissue shaping via cell death, requires further investigation.

Purpose of the Study:

  • To identify novel genes regulating the non-autonomous aspects of apoptosis during morphogenesis.
  • To investigate the role of apoptosis in tissue development using a genetic screen.
  • To understand the signals involved in the morphogenetic apoptosis pathway.

Main Methods:

  • Conducted an unbiased RNAi-based genetic screen in the *Drosophila* leg model system.
  • Screened approximately 1,400 candidate genes.
  • Utilized adult joint morphology, morphogenetic fold formation, and apoptotic patterns as key readouts.

Main Results:

  • Identified 41 genes potentially involved in morphogenetic apoptosis.
  • Discovered genes regulating the apoptotic process itself.
  • Found genes associated with the formation, extrusion, and elimination of apoptotic bodies.
  • Identified genes contributing to morphogenesis downstream of apoptosis.

Conclusions:

  • The study elucidates key components of the morphogenetic apoptosis pathway.
  • Identified genes offer new targets for understanding how apoptosis shapes tissues during development.
  • This research expands knowledge of non-autonomous apoptosis signaling in developmental contexts.