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Intrinsic apoptosis is evolutionarily divergent among metazoans.
Krasovec, Gabriel; Horkan, Helen R; Quéinnec, Éric; Chambon, Jean-Philippe.
Afiliação
  • Krasovec G; ISYEB - UMR 7205, Institut de Systématique, Evolution et Biodiversité, Sorbonne Université, CNRS, MNHN, Paris, France.
  • Horkan HR; Centre for Chromosome Biology, School of Biological and Chemical Sciences, University of Galway, Galway, Ireland.
  • Quéinnec É; ISYEB - UMR 7205, Institut de Systématique, Evolution et Biodiversité, Sorbonne Université, CNRS, MNHN, Paris, France.
  • Chambon JP; Centre de Recherche en Biologie cellulaire de Montpellier (CRBM), Université de Montpellier, CNRS, Montpellier, France.
Evol Lett ; 8(2): 267-282, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38525035
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article