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Caspase-1 activates gasdermin A in non-mammals

View ORCID ProfileZachary P. Billman, Stephen B. Kovacs, Bo Wei, Kidong Kang, View ORCID ProfileOusmane H. Cissé, Edward A. Miao
doi: https://doi.org/10.1101/2023.09.28.559989
Zachary P. Billman
1Duke University School of Medicine
2University of North Carolina at Chapel Hill
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Stephen B. Kovacs
1Duke University School of Medicine
2University of North Carolina at Chapel Hill
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Bo Wei
1Duke University School of Medicine
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Kidong Kang
1Duke University School of Medicine
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Ousmane H. Cissé
3National Institutes of Health
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Edward A. Miao
1Duke University School of Medicine
2University of North Carolina at Chapel Hill
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  • For correspondence: edward.miao@duke.com
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Abstract

Gasdermins oligomerize to form pores in the cell membrane, causing regulated lytic cell death called pyroptosis. Mammals encode five gasdermins that can trigger pyroptosis: GSDMA, B, C, D, and E. Caspase and granzyme proteases cleave the linker regions of and activate GSDMB, C, D, and E, but no endogenous activation pathways are yet known for GSDMA. Here, we perform a comprehensive evolutionary analysis of the gasdermin family. A gene duplication of GSDMA in the common ancestor of caecilian amphibians, reptiles and birds gave rise to GSDMA-D in mammals. Uniquely in our tree, amphibian, reptile and bird GSDMA group in a separate clade than mammal GSDMA. Remarkably, GSDMA in numerous bird species contain caspase-1 cleavage sites like YVAD or FASD in the linker. We show that GSDMA from birds, amphibians, and reptiles are all cleaved by caspase-1. Thus, GSDMA was originally cleaved by the host-encoded protease caspase-1. In mammals the caspase-1 cleavage site in GSDMA is disrupted; instead, a new protein, GSDMD, is the target of caspase-1. Mammal caspase-1 uses exosite interactions with the GSDMD C-terminal domain to confer the specificity of this interaction, whereas we show that bird caspase-1 uses a stereotypical tetrapeptide sequence to confer specificity for bird GSDMA. Our results reveal an evolutionarily stable association between caspase-1 and the gasdermin family, albeit a shifting one. Caspase-1 repeatedly changes its target gasdermin over evolutionary time at speciation junctures, initially cleaving GSDME in fish, then GSDMA in amphibians/reptiles/birds, and finally GSDMD in mammals.

One Sentence Summary We demonstrate that amphibians, reptiles and birds engage pyroptosis using caspase-1 and GSDMA, filling an evolutionary gap in which caspase-1 cleaves GSDME in fish and GSDMD in mammals.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵¶ Department of Microbiology and Immunology; Chapel Hill, NC, USA;

  • ↵** Critical Care Medicine Department; Bethesda, MD, USA

  • Title changed to remove the word all, we did not test this association in all animals, Text changes to note differences in our phylogeny approach compared to previous strategies highlighted in blue, Figure 3 corrected to show P1

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license.
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Posted November 20, 2023.
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Caspase-1 activates gasdermin A in non-mammals
Zachary P. Billman, Stephen B. Kovacs, Bo Wei, Kidong Kang, Ousmane H. Cissé, Edward A. Miao
bioRxiv 2023.09.28.559989; doi: https://doi.org/10.1101/2023.09.28.559989
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Caspase-1 activates gasdermin A in non-mammals
Zachary P. Billman, Stephen B. Kovacs, Bo Wei, Kidong Kang, Ousmane H. Cissé, Edward A. Miao
bioRxiv 2023.09.28.559989; doi: https://doi.org/10.1101/2023.09.28.559989

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