Sir2 Blocks Extreme Life-Span Extension

Abstract : Sir2 is a conserved deacetylase that modulates life span in yeast, worms, and flies and stress response in mammals. In yeast, Sir2 is required for maintaining replicative life span, and increasing Sir2 dosage can delay replicative aging. We address the role of Sir2 in regulating chronological life span in yeast. Lack of Sir2 along with calorie restriction and/or mutations in the yeast AKT homolog, Sch9, or Ras pathways causes a dramatic chronological life-span extension. Inactivation of Sir2 causes uptake and catabolism of ethanol and upregulation of many stress-resistance and sporulation genes. These changes while suffi- cient to extend chronological life span in wild-type yeast require severe calorie restriction or additional mutations to extend life span of sir2 D mutants. Our results demonstrate that effects of SIR2on chrono- logical life span are opposite to replicatve life span and suggest that the relevant activities of Sir2-like deacetylases may also be complex in higher eu- karyotes.
Type de document :
Article dans une revue
Cell, Elsevier, 2005, 123, pp.655-667. 〈10.1016/j.cell.2005.08.042〉
Liste complète des métadonnées

https://hal-ens-lyon.archives-ouvertes.fr/ensl-00705803
Contributeur : Agnès Ganivet <>
Soumis le : vendredi 8 juin 2012 - 12:03:51
Dernière modification le : dimanche 17 décembre 2017 - 07:04:03

Lien texte intégral

Identifiants

Collections

Citation

Paola Fabrizio, Cristina Gattazzo, Kristen Battistella, Min Wei, Chao Cheng, et al.. Sir2 Blocks Extreme Life-Span Extension. Cell, Elsevier, 2005, 123, pp.655-667. 〈10.1016/j.cell.2005.08.042〉. 〈ensl-00705803〉

Partager

Métriques

Consultations de la notice

61