Role of sirtuins in lifespan regulation is linked to methylation of nicotinamide

  • Kathrin Schmeisser
  • , Johannes Mansfeld
  • , Doreen Kuhlow
  • , Sandra Weimer
  • , Steffen Priebe
  • , Ines Heiland
  • , Marc Birringer
  • , Marco Groth
  • , Alexandra Segref
  • , Yariv Kanfi
  • , Nathan L. Price
  • , Sebastian Schmeisser
  • , Stefan Schuster
  • , Andreas F.H. Pfeiffer
  • , Reinhard Guthke
  • , Matthias Platzer
  • , Thorsten Hoppe
  • , Haim Y. Cohen
  • , Kim Zarse
  • , David A. Sinclair
  • Michael Ristow

Research output: Contribution to journalArticlepeer-review

199 Scopus citations

Abstract

Sirtuins, a family of histone deacetylases, have a fiercely debated role in regulating lifespan. In contrast with recent observations, here we find that overexpression of sir-2.1, the ortholog of mammalian SirT1, does extend Caenorhabditis elegans lifespan. Sirtuins mandatorily convert NAD + into nicotinamide (NAM). We here find that NAM and its metabolite, 1-methylnicotinamide (MNA), extend C. elegans lifespan, even in the absence of sir-2.1. We identify a previously unknown C. elegans nicotinamide-N- methyltransferase, encoded by a gene now named anmt-1, to generate MNA from NAM. Disruption and overexpression of anmt-1 have opposing effects on lifespan independent of sirtuins, with loss of anmt-1 fully inhibiting sir-2.1-mediated lifespan extension. MNA serves as a substrate for a newly identified aldehyde oxidase, GAD-3, to generate hydrogen peroxide, which acts as a mitohormetic reactive oxygen species signal to promote C. elegans longevity. Taken together, sirtuin-mediated lifespan extension depends on methylation of NAM, providing an unexpected mechanistic role for sirtuins beyond histone deacetylation.

Original languageEnglish
Pages (from-to)693-700
Number of pages8
JournalNature Chemical Biology
Volume9
Issue number11
DOIs
StatePublished - Nov 2013
Externally publishedYes

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