SIRT1 undergoes alternative splicing in a novel auto-regulatory loop with p53 | Research - Institut Pasteur

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Innate immune response to Mycobacterium tuberculosis Beijing and other genotypes

Aggressive behavior during social interaction in mice is controlled by the modulation of tyrosine hydroxylase expression in the prefrontal cortex

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Published in PloS one - 21 Oct 2010

Lynch CJ, Shah ZH, Allison SJ, Ahmed SU, Ford J, Warnock LJ, Li H, Serrano M, Milner J

Link to Pubmed [PMID] – 20975832

PLoS ONE 2010;5(10):e13502

The NAD-dependent deacetylase SIRT1 is a nutrient-sensitive coordinator of stress-tolerance, multiple homeostatic processes and healthspan, while p53 is a stress-responsive transcription factor and our paramount tumour suppressor. Thus, SIRT1-mediated inhibition of p53 has been identified as a key node in the common biology of cancer, metabolism, development and ageing. However, precisely how SIRT1 integrates such diverse processes remains to be elucidated.

Published on: 21 Oct 2010