Core C: Animal Production and Specimen Preparation The goal of this core is to produce all of the mice needed in the Program Project, to assess their health status, and to generate the biopsy and necropsy specimens needed by each of the component projects within the program.
Specific Aims i nclude: 1. Breeding the 600 UM-HET3 mice of Population 1. 2. Providing tail tip DNA specimen for genotyping by Genotyping Core. 3. Providing biopsy specimens (blood cells, plasma, skin, etc.) needed at defined ages by Projects 1 and 5. 4. Providing body weight data at 3 month intervals to the Analysis ore. 5. Sacrificing each mouse in Population 1 at 18 months of age, and providing tissue specimens needed by each of the projects for physiological and/or biochemical analysis. Data on pathological lesions will be provided to each investigation and to the Analysis Core for use as a co-variate or exclusion criterion in statistical tests. 6. Producing the 180 mice in Population 2 (half of which are selected for genetic alleles associated with prolonged lifespan), and providing biopsy and necropsy specimens for these mice to each project. 7. Breeding UM-HET3 mice needed at various ages as controls by several of the component projects. The Core will be directed by Dr. Richard Miller, who will be assisted by the effort of a half-time research technician. All mice will be housed in the specific pathogen free vivarium of the newly opened Cancer Center and Geriatrics Center Building, and will be protected from infectious illness by use of individual micro-isolator caging. Husbandry procedures in use by the Geriatrics animal colonies have been able to maintain documented specific-pathogen free status since 1993, and should ensure a supply of high quality research animals for use in this program.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG016699-03
Application #
6458993
Study Section
Project Start
2001-06-05
Project End
2002-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
3
Fiscal Year
2001
Total Cost
$312,755
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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Chisa, Jennifer L; Burke, David T (2007) Mammalian mRNA splice-isoform selection is tightly controlled. Genetics 175:1079-87
Hanlon, Philip; Lorenz, William Andrew; Shao, Zhihong et al. (2006) Three-locus and four-locus QTL interactions influence mouse insulin-like growth factor-I. Physiol Genomics 26:46-54
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Harper, James M; Durkee, Stephen J; Smith-Wheelock, Michael et al. (2005) Hyperglycemia, impaired glucose tolerance and elevated glycated hemoglobin levels in a long-lived mouse stock. Exp Gerontol 40:303-14
Volkman, Suzanne K; Galecki, Andrzej T; Burke, David T et al. (2004) Quantitative trait loci that modulate femoral mechanical properties in a genetically heterogeneous mouse population. J Bone Miner Res 19:1497-505
Harper, James M; Galecki, Andrzej T; Burke, David T et al. (2004) Body weight, hormones and T cell subsets as predictors of life span in genetically heterogeneous mice. Mech Ageing Dev 125:381-90
Wisser, Kathleen C; Schauerte, Joseph A; Burke, David T et al. (2004) Mapping tissue-specific genes correlated with age-dependent changes in protein stability and function. Arch Biochem Biophys 432:58-70
Harper, James M; Galecki, Andrzej T; Burke, David T et al. (2003) Quantitative trait loci for insulin-like growth factor I, leptin, thyroxine, and corticosterone in genetically heterogeneous mice. Physiol Genomics 15:44-51
Bennett-Baker, Pamela E; Wilkowski, Jodi; Burke, David T (2003) Age-associated activation of epigenetically repressed genes in the mouse. Genetics 165:2055-62

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