In the past granting period, we learned that a fundamental mechanismof aging is conserved from yeast to animals. Thus, yeast is a valuable model for at least some important aspects of aging in higher organisms. A specific gene, SIR2, is conserved in organisms from bacteria to humans. This gene clearly regulates aging by promoting longevity in yeast and C. elegans, suggesting that its effects will prove to be general. The activity of Sir2p is to deacetylate proteins when provided with the co-substrate, NAD (nicotinamide-adenine dinucleotide). Our studies in yeast indicate that the replicative aging of mother cells can be extended by calorie restriction, and that this extension requires Sir2p. Since calorie restriction is the only intervention known to extend life span in mammals, these findingsmay have broad implications. We have further learned that the known effects of Sir2p on genomic silencing are pertinent to yeast aging. In the next period we propose to study the mechanism of Sir2p-mediated silencing in greater detail by analyzingsir2 mutations genetically and biochemically. We further propose to use a combination of yeast genetic and molecular approaches to define the specificmetabolic mechanism by which calorie restriction extends life span and how this might relate to Sir2p. In addition, we will probe the intriguing link between sojourns in stationary phase and yeast replicative aging. This particularstudy might provide a conceptual link between the aging of dividing and post-mitotic cells. Finally, we will begin an analysis of two new genes, SSD1 and MPT5, that affect yeast aging in a SIR2-independent way. These experiments will add to a substantial base of knowledge of aging in the simple budding yeast and will be a platform for studies of aging in higher organisms, includingmammals. 3ERFCRMANCE SITE(S) (organization, city, state) Massachusetts Institute of Technology 77 Massachusetts Avenue, 68-280 Cambridge, MA 02139 KEY PERSONNEL. See instructions on Page 11. Usecontinuationpages as neededto provide the required information in the format shown below. Name Organization Role on Project (/ Leonard Guarente Massachusetts Institute of Technology P.I. PHS CI98 (Rev. 4/98) Page 2 BB Numbisr pages consecutively at the bottom throughout the application. Do QQJ use suffixes such as 3a, 3b. CC Principa^Plstigator/Program Director (Last, first, middle): ^B Type frie name of the principal investigator/program director at the top of each printed page and each continuation instructions on page 6.) RESEARCH GRANT TABLE OF CONTENTS Face Page Description,
| 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 |
| 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 |
| 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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