Intrinsic apoptosis is evolutionarily divergent among metazoans

Author:

Krasovec Gabriel1ORCID,Horkan Helen R2,Quéinnec Éric1,Chambon Jean-Philippe3

Affiliation:

1. ISYEB - UMR 7205, Institut de Systématique, Evolution et Biodiversité, Sorbonne Université, CNRS, MNHN , Paris , France

2. Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway , Galway , Ireland

3. Centre de Recherche en Biologie cellulaire de Montpellier (CRBM), Université de Montpellier, CNRS , Montpellier , France

Abstract

Abstract Apoptosis is regulated cell death that depends on caspases. A specific initiator caspase is involved upstream of each apoptotic signaling pathway. Characterized in nematode, fly, and mammals, intrinsic apoptosis is considered to be ancestral, conserved among animals, and depends on shared initiators: caspase-9, Apaf-1 and Bcl-2. However, the biochemical role of mitochondria, the pivotal function of cytochrome c and the modality of caspase activation remain highly heterogeneous and hide profound molecular divergence among apoptotic pathways in animals. Uncovering the phylogenetic history of apoptotic actors, especially caspases, is crucial to shed light on the evolutionary history of intrinsic apoptosis. Here, we demonstrate with phylogenetic analyses that caspase-9, the fundamental key of intrinsic apoptosis, is deuterostome-specific, while caspase-2 is ancestral to bilaterians. Our analysis of Bcl-2 and Apaf-1 confirms heterogeneity in functional organization of apoptotic pathways in animals. Our results support emergence of distinct intrinsic apoptotic pathways during metazoan evolution.

Funder

French Ministry of Education, Research and Innovation

Fondation ARC pour la recherche sur le cancer

Science Foundation Ireland Centre for Research Training in Genomics Data Science

Publisher

Oxford University Press (OUP)

Subject

Genetics,Ecology, Evolution, Behavior and Systematics

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