Caspase cleavesDrosophilaBubR1to modulate spindle assembly checkpoint function and lifespan of the organism

Abstract

Caspases cleave over 1500 substrates in the human proteome in both lethal and non‐lethal scenarios. However, reports of the physiological consequences of substrate cleavage are limited. Additionally, the manner in which caspase cleaves only a subset of substrates in the non‐lethal scenario remains to be elucidated. BubR1, a spindle assembly checkpoint component, is a caspase substrate in humans, the physiological function of which remains unclear. Here, we found that caspases, especially Drice, cleaveDrosophilaBubR1 between the N‐terminal KEN box motif and C‐terminal kinase domain. By using proximity labelling, we found that Drice, but not Dcp‐1, is in proximity to BubR1, suggesting that protein proximity facilitates substrate preference. The cleaved fragments displayed altered subcellular localization and protein–protein interactions. Flies that harboured cleavage‐resistant BubR1 showed longer duration of BubR1 localization to the kinetochore upon colchicine treatment. Furthermore, these flies showed extended lifespan. Thus, we propose that the caspase‐mediated cleavage of BubR1 limits spindle assembly checkpoint and organismal lifespan. Our results highlight the importance of the individual analysis of substratesin vivoto determine the biological significance of caspase‐dependent non‐lethal cellular processes.