SIRT1 negatively regulates the mammalian target of rapamycin

Hiyaa Singhee Ghosh, Michael McBurney, Paul D. Robbins

Research output: Contribution to journalArticle

224 Scopus citations

Abstract

The IGF/mTOR pathway, which is modulated by nutrients, growth factors, energy status and cellular stress regulates aging in various organisms. SIRT1 is a NAD+ dependent deacetylase that is known to regulate caloric restriction mediated longevity in model organisms, and has also been linked to the insulin/IGF signaling pathway. Here we investigated the potential regulation of mTOR signaling by SIRT1 in response to nutrients and cellular stress. We demonstrate that SIRT1 deficiency results in elevated mTOR signaling, which is not abolished by stress conditions. The SIRT1 activator resveratrol reduces, whereas SIRT1 inhibitor nicotinamide enhances mTOR activity in a SIRT1 dependent manner. Furthermore, we demonstrate that SIRT1 interacts with TSC2, a component of the mTOR inhibitory-complex upstream to mTORC1, and regulates mTOR signaling in a TSC2 dependent manner. These results demonstrate that SIRT1 negatively regulates mTOR signaling potentially through the TSC1/2 complex.

Original languageEnglish (US)
Article numbere9199
JournalPloS one
Volume5
Issue number2
DOIs
StatePublished - Feb 15 2010
Externally publishedYes

Fingerprint Dive into the research topics of 'SIRT1 negatively regulates the mammalian target of rapamycin'. Together they form a unique fingerprint.

  • Cite this