Resurrection of an ancient inflammatory locus reveals switch to caspase-1 specificity on a caspase-4 scaffold

J Biol Chem. 2022 Jun;298(6):101931. doi: 10.1016/j.jbc.2022.101931. Epub 2022 Apr 12.

Abstract

Pyroptosis is a mechanism of inflammatory cell death mediated by the activation of the prolytic protein gasdermin D by caspase-1, caspase-4, and caspase-5 in human, and caspase-1 and caspase-11 in mouse. In addition, caspase-1 amplifies inflammation by proteolytic activation of cytokine interleukin-1β (IL-1β). Modern mammals of the order Carnivora lack the caspase-1 catalytic domain but express an unusual version of caspase-4 that can activate both gasdermin D and IL-1β. Seeking to understand the evolutionary origin of this caspase, we utilized the large amount of data available in public databases to perform ancestral sequence reconstruction of an inflammatory caspase of a Carnivora ancestor. We expressed the catalytic domain of this putative ancestor in Escherichia coli, purified it, and compared its substrate specificity on synthetic and protein substrates to extant caspases. We demonstrated that it activates gasdermin D but has reduced ability to activate IL-1β. Our reconstruction suggests that caspase-1 was lost in a Carnivora ancestor, perhaps upon a selective pressure for which the generation of biologically active IL-1β by caspase-1 was detrimental. We speculate that later, a Carnivora encountered selective pressures that required the production of IL-1β, and caspase-4 subsequently gained this activity. This hypothesis would explain why extant Carnivora possess an inflammatory caspase with caspase-1 catalytic function placed on a caspase-4 scaffold.

Keywords: caspase; cell death; inflammation; interleukin 1; protein evolution.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Carnivora / genetics
  • Carnivora / metabolism
  • Caspase 1 / genetics
  • Caspase 1 / metabolism
  • Caspases* / genetics
  • Caspases* / metabolism
  • Escherichia coli / genetics
  • Inflammation / genetics
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Phosphate-Binding Proteins / genetics
  • Phosphate-Binding Proteins / metabolism
  • Pyroptosis / physiology
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Selection, Genetic

Substances

  • Interleukin-1beta
  • Phosphate-Binding Proteins
  • Recombinant Proteins
  • Caspases
  • Caspase 1