This application is for renewal of the Nathan Shock Center of Excellence in the Basic Biology of Aging at the University of Washington and affiliated institutions. This Center has over the past 15 years provided resources in support of our large community of investigators that are funded to study basic biological mechanisms of aging. We continue to build upon a scientific theme that became established in the past funding cycle, in which comparative gerontologic study informed us of conserved genetic pathways of longevity determination (the TOR pathway is an example of one such). The three proposed Research Resources Core components are well suited to assist in such efforts: 1) Transgenic Animal Model Development;2) Functional Assessment;3) Functional Genomics. The Transgenic Animal Model Development Resource Core continues to pursue a focus on inducible gene expression and knockout models, so that organ and age-specific effects of genetic alterations can be assessed. The Functional Assessment Core builds upon technical resources that have been gathered during the past funding period, such that we can now provide investigators with a broad and informative range of physiologic and cellular assays, including those that are most relevant to assessment of the healthspan of mouse models. The Functional Genomics Core provides expert assistance with state of the art technologies for transcriptomics and proteomics. Consistent with our theme, it includes a focus on translational state, protein turnover and post-translational modification. The Research Development Core will continue to support pilot study projects in the basic biology of aging. The Program Enrichment Core supports administrative management, an external advisory panel, a program of courses and seminars and data sharing and dissemination.

Public Health Relevance

Continuation of this Center's support will further the utilization of state-of-the-art research resources to provide the strongest environment for the conduct of research on aging biology at institutions in our geographical neighborhood. It will 1) enhance the quality of research in the basic biology of aging, 2) facilitate the planning and coordination of aging biology research activities, 3) provide support and an enriched environment for investigators new to aging biology and 4) contribute to our being able to provide resources to Biology of Aging investigators across the nation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
3P30AG013280-18S2
Application #
8536985
Study Section
Special Emphasis Panel (ZAG1-ZIJ-2 (M1))
Program Officer
Sierra, Felipe
Project Start
1997-07-15
Project End
2015-06-30
Budget Start
2012-09-15
Budget End
2013-06-30
Support Year
18
Fiscal Year
2012
Total Cost
$55,350
Indirect Cost
$19,525
Name
University of Washington
Department
Pathology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Walters, Ryan O; Arias, Esperanza; Diaz, Antonio et al. (2018) Sarcosine Is Uniquely Modulated by Aging and Dietary Restriction in Rodents and Humans. Cell Rep 25:663-676.e6
Kramer, Philip A; Duan, Jicheng; Gaffrey, Matthew J et al. (2018) Fatiguing contractions increase protein S-glutathionylation occupancy in mouse skeletal muscle. Redox Biol 17:367-376
Kaeberlein, Matt (2018) How healthy is the healthspan concept? Geroscience 40:361-364
Crane, Matthew M; Kaeberlein, Matt (2018) The paths of mortality: how understanding the biology of aging can help explain systems behavior of single cells. Curr Opin Syst Biol 8:25-31
Beaupere, Carine; Dinatto, Leticia; Wasko, Brian M et al. (2018) Genetic screen identifies adaptive aneuploidy as a key mediator of ER stress resistance in yeast. Proc Natl Acad Sci U S A 115:9586-9591
Andeen, Nicole K; Yang, Han-Yin; Dai, Dao-Fu et al. (2018) DnaJ Homolog Subfamily B Member 9 Is a Putative Autoantigen in Fibrillary GN. J Am Soc Nephrol 29:231-239
Miller, Hillary; Fletcher, Marissa; Primitivo, Melissa et al. (2017) Genetic interaction with temperature is an important determinant of nematode longevity. Aging Cell 16:1425-1429
Martin-Perez, Miguel; Villén, Judit (2017) Determinants and Regulation of Protein Turnover in Yeast. Cell Syst 5:283-294.e5
Dennis, Daniel G; McKay-Fleisch, Jill; Eitzen, Kaila et al. (2017) Normally lethal amino acid substitutions suppress an ultramutator DNA Polymerase ? variant. Sci Rep 7:46535
Russell, Joshua Coulter; Burnaevskiy, Nikolay; Ma, Bridget et al. (2017) Electrophysiological measures of aging pharynx function in C. elegans reveal enhanced organ functionality in older, long-lived mutants. J Gerontol A Biol Sci Med Sci :

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