Proapoptotic RHG genes and mitochondria play a key non-apoptotic role in remodelling the<i>Drosophila</i>sensory system

<jats:title>Abstract</jats:title><jats:p>Caspases are best known for their role in programmed cell death but have also been found to be important in several non-apoptotic phenomena such as cell fate specification, cell migration and terminal differentiation. The dynamics of such sub-lethal caspase events and the molecular mechanisms regulating them are still largely unknown. As more tools for visualizing and manipulating caspase activation<jats:italic>in vivo</jats:italic>become available, greater insights into this biology are being made. Using a new and sensitive<jats:italic>in vivo</jats:italic>effector caspase probe, called SR4VH, we demonstrate that effector caspases are activated in pruning sensory neurons earlier than previously thought and that the level of caspase activation in these neurons is consistently lower than in neurons undergoing cell death. We reveal that Grim and Reaper, two of the four pro-apoptotic RHG proteins, are required for sensory neuron pruning and that disrupting the dynamics of the mitochondrial network prevents effector caspase activation in both pruning and dying sensory neurons. Overall, our findings demonstrate that a sublethal deployment of the ‘apoptotic machinery’ is critical for remodelling dendrites and also reveal a direct link between mitochondria and sensory neuron cell death<jats:italic>in vivo</jats:italic>.</jats:p>