RT Journal Article SR Electronic T1 Heterologous expression of human pro-inflammatory Caspase-1 in Saccharomyces cerevisiae and comparison to pro-apoptotic Caspase-8 JF bioRxiv FD Cold Spring Harbor Laboratory SP 2021.02.07.430150 DO 10.1101/2021.02.07.430150 A1 Marta Valenti A1 María Molina A1 Víctor J Cid YR 2021 UL http://biorxiv.org/content/early/2021/02/08/2021.02.07.430150.abstract AB Caspases are a family of cysteine proteases that play an essential role in inflammation, apoptosis, cell death, and development. Here we delve into the effects caused by heterologous expression of human Caspase-1 in the yeast Saccharomyces cerevisiae and compare them to those of Caspase-8. Overexpression of both caspases in the heterologous model led to their activation, and caused mitochondrial depolarization, ROS production, damage to different organelles, and cell death. All these effects were dependent on their protease activity, and Caspase-8 was more aggressive than Caspase-1. Growth arrest could be at least partially explained by dysfunction of the actin cytoskeleton as a consequence of the processing of the yeast Bni1 formin, which we identify here as a likely direct substrate of both caspases. Through the modulation of the GAL1 promoter by using different galactose:glucose ratios in the culture medium, we have established a scenario in which Caspase-1 is sufficiently expressed to become activated while yeast growth is not impaired. Finally, we used the yeast model to explore the role of death-fold domains (DD) of both caspases in their activity. Peculiarly, the DDs of either caspase showed an opposite involvement in its intrinsic activity, as the deletion of the caspase activation and recruitment domain (CARD) of Caspase-1 enhanced its activity, while the deletion of the death effector domain (DED) of Caspase-8 diminished it. We propose the yeast model as a useful and manageable tool to explore Caspase-1 structure-function relationships, the impact of mutations or the activity of putative inhibitors or regulators.Competing Interest StatementThe authors have declared no competing interest.AbbreviationsDDdeath-fold domain;CARDcaspase recruitment and activation domain;CASP1, DEDdeath effector domain;PCDprogrammed cell death;SMOCsupra-molecular organizing center; Caspase-1;CASP8Caspase-8;ROSreactive oxygen species;PIpropidium iodideRd123rhodamine 123;DHEdihydroethidium;TGNtrans-Golgi network;ERendoplasmic reticulum;WGDwhole genome deletion;SDsynthetic dextrose;SGsynthetic galactose;SRsynthetic raffinose;ODoptical density;SDSsodium dodecyl sulfate;PMSFphenylmethylsulfonyl fluoride;SDS-PAGEsodium dodecyl sulfate polyacrylamide gel electrophoresis;TCAtrichloroacetic acid;DICdifferential interference contrast;YPDyeast peptone dextrose;PBSphosphate buffered saline