The aim of this proposal is to understand the molecular basis of aging by SIR2 genes in mammals. This gene determines the life span in yeast and C. elegans. The activity of SIR2, NAD-dependent protein deacetylase, allows cells to couple metabolism to aging. SIR2 appears to slow aging and extend life span in times of stress or scarcity. In particular, SIR2 mediates longevity in yeast in response to calorie restriction (CR). In mammals, there are seven SIR2 homologs. This proposal focuses on the ortholog, SIRT1, which possesses the same enzymatic activity as SIR2. Previous work showed that SIRT1 can promote survival of cultured mammalian cells in response to oxidative stress by deacetylating and down-regulating p53. In this proposal, we undertake a systematic study of the functions of SIRT1 in mammals. This project includes an identification and study of mammalian proteins that interact with SIRTI. Also, the project examines the relationship between SIRT1 and two primary features of CR in mammals; reduction in white fat and sterility. Finally, the project will study genetically altered mice in which SIRT1 is absent or over expressed. This project will enable us to understand the regulation of aging in mammals by SIRTI. It may also have implications for diseases of aging, such as cancer, cardiovascular disease, diabetes, and neurodegenerative disease.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG015339-10
Application #
7440246
Study Section
Special Emphasis Panel (ZRG1-CMAD (01))
Program Officer
Mccormick, Anna M
Project Start
1999-05-01
Project End
2009-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
10
Fiscal Year
2008
Total Cost
$413,534
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
Das, Abhirup; Huang, George X; Bonkowski, Michael S et al. (2018) Impairment of an Endothelial NAD+-H2S Signaling Network Is a Reversible Cause of Vascular Aging. Cell 173:74-89.e20
Ondracek, Caitlin R; Frappier, Vincent; Ringel, Alison E et al. (2017) Mutations that Allow SIR2 Orthologs to Function in a NAD+-Depleted Environment. Cell Rep 18:2310-2319
Guarente, Leonard (2014) Linking DNA damage, NAD(+)/SIRT1, and aging. Cell Metab 20:706-707
Imai, Shin-ichiro; Guarente, Leonard (2014) NAD+ and sirtuins in aging and disease. Trends Cell Biol 24:464-71
Chang, Hung-Chun; Guarente, Leonard (2014) SIRT1 and other sirtuins in metabolism. Trends Endocrinol Metab 25:138-45
Sinclair, David A; Guarente, Leonard (2014) Small-molecule allosteric activators of sirtuins. Annu Rev Pharmacol Toxicol 54:363-80
Herskovits, A Zara; Guarente, Leonard (2014) SIRT1 in neurodevelopment and brain senescence. Neuron 81:471-83
Li, Yu; Wong, Kimberly; Giles, Amber et al. (2014) Hepatic SIRT1 attenuates hepatic steatosis and controls energy balance in mice by inducing fibroblast growth factor 21. Gastroenterology 146:539-49.e7
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

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