In the past granting period, we have identified genes and pathways that determine the life span ofyeast mother cells, including SIR2 and SSD1. Importantly, we showed that Sir2p is an NAD-dependent deacetylase, and, as such, mediates the extension in life span due to calorie restriction (CR) in yeast. The C. elegans SIR2 ortholog was also shown to determine life span in that organism. This conservation prompted us to begin a study of the effects of the mammalian SIR2 ortholog, Sirtl, in mice. In particular, we showed that Sirtl is required for at least one phenotype of mammalian CR- the increase in activity induced by this dietary regimen. In the next period, we propose to study the role of Sirtl in life extension induced by CR using several genetically altered mice strains. These include Sirtl knockout (KO) mice, Sirtl transgenic mice, and Sirtl tissue-specific KO mice. We will also examine the effect of CR on Sirtl functional activity and other mammalian physiological parameters. Finally, we will explore the roles of two othermammalian SIR2 homologs, SirtS and Sirt4, which are both mitochondrial proteins. In sum, these studies will shed light on the functions of these Sir2 proteins in mammalian physiology and, in particular, on their role in CR. The roles of specific tissues in CR will also be addressed. The importance of these studies for human health may be large. Understanding the molecular underpinnings of CR and its relationship to mammalian Sirt genes will flesh out the workings of thissalutary diet, the benefits of which have been known for 70 years. Importantly, CR is known to forestall orprevent many diseases of aging in rodent models. Therefore, drugs that are developed against targets we identify may open new strategies to treat diseases of aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
4R37AG011119-15
Application #
7163656
Study Section
Special Emphasis Panel (NSS)
Program Officer
Mccormick, Anna M
Project Start
1993-03-01
Project End
2012-03-31
Budget Start
2007-04-01
Budget End
2008-03-31
Support Year
15
Fiscal Year
2007
Total Cost
$436,159
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Guarente, Leonard (2013) Calorie restriction and sirtuins revisited. Genes Dev 27:2072-85
Libert, Sergiy; Guarente, Leonard (2013) Metabolic and neuropsychiatric effects of calorie restriction and sirtuins. Annu Rev Physiol 75:669-84
Guarente, Leonard (2013) Sirtuins and ageing--new findings. EMBO Rep 14:750
Herskovits, Adrianna Z; Guarente, Leonard (2013) Sirtuin deacetylases in neurodegenerative diseases of aging. Cell Res 23:746-58
Simic, Petra; Williams, Eric O; Bell, Eric L et al. (2013) SIRT1 suppresses the epithelial-to-mesenchymal transition in cancer metastasis and organ fibrosis. Cell Rep 3:1175-86
Libert, Sergiy; Bonkowski, Michael S; Pointer, Kelli et al. (2012) Deviation of innate circadian period from 24 h reduces longevity in mice. Aging Cell 11:794-800
Chalkiadaki, Angeliki; Guarente, Leonard (2012) High-fat diet triggers inflammation-induced cleavage of SIRT1 in adipose tissue to promote metabolic dysfunction. Cell Metab 16:180-8
Blander, Gil; Bhimavarapu, Anupama; Mammone, Thomas et al. (2009) SIRT1 promotes differentiation of normal human keratinocytes. J Invest Dermatol 129:41-9
Nakahata, Yasukazu; Kaluzova, Milota; Grimaldi, Benedetto et al. (2008) The NAD+-dependent deacetylase SIRT1 modulates CLOCK-mediated chromatin remodeling and circadian control. Cell 134:329-40
Blander, Gil; Olejnik, Jerzy; Krzymanska-Olejnik, Edyta et al. (2005) SIRT1 shows no substrate specificity in vitro. J Biol Chem 280:9780-5

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