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,

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37AG011119-18
Application #
7798020
Study Section
Special Emphasis Panel (NSS)
Program Officer
Mccormick, Anna M
Project Start
1993-03-01
Project End
2012-03-31
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
18
Fiscal Year
2010
Total Cost
$462,178
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
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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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