Functional Analysis of PGC1-a holo-complex in Diabetes
Project Number7K08DK071017-05
Contact PI/Project LeaderCOOPER, MARCUS P
Awardee OrganizationUNIV OF MASSACHUSETTS MED SCH WORCESTER
Description
Abstract Text
DESCRIPTION (provided by applicant):
This proposal details a 5-year training program and is designed to prepare the principal investigator for a career in academic medicine. The principal investigator has fulfilled clinical requirements for internal medicine at the Johns Hopkins Hospital and cardiology fellowship at Brigham and Women's Hospital. The program encourages the acquisition of sound principles and expertise for studying the transcriptional co-activator, PPAR gamma co-activator 1 alpha (PGC1-alpha), as it pertains to metabolism. Bruce M. Spiegelman, Ph.D. is a pioneer in the field of energy metabolism and will mentor the principal investigator by providing career and scientific guidance.
The research endeavors to elucidate the role of the PGC1-alpha holo-complex in diabetes and energy metabolism. Prior genetic studies in the laboratory identified several transcription factors regulated by PGC1- alpha and highlighted the pivotal role of PGC1-alpha in energy homeostasis. The proteome is the final determinant of cellular phenotype, and we hypothesize that characterization of the PGC1-alpha holo-complex will identify novel factors that regulate diabetes and energy metabolism. Specific aims of the project are: 1) Establish a versatile technique to isolate PGC1-alpha holo-complexes. 2) Elucidate the proteins comprising the PGC1-alpha holo-complex from normal and diabetic tissues. 3) Characterize the molecular and biological significance of the PGC1-alpha complex. This study constitutes the first functional and proteomic analysis of the PGC1-alpha holo-complex, and may define new regulatory roles for PGC1-alpha in diabetes.
The department of Cancer Biology at the Dana-Farber Cancer Institute provides a stimulating and scientifically sound base from which the principal investigator can build a career in academic medicine. Ultimately, the environment and the program will foster the development of the principal investigator into an independent physician-scientist.
Public Health Relevance Statement
Data not available.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AnimalsBindingBiochemicalBiogenesisBiologicalBiological AssayCancer BiologyCardiologyCell LineCell physiologyCellsChromatographyClinicalComplexCultured CellsDana-Farber Cancer InstituteDevelopmentDiabetes MellitusDoctor of MedicineDoctor of PhilosophyEnergy MetabolismEnvironmentEpitopesExhibitsFastingFatty AcidsFellowshipFosteringGeneticGenetic TranscriptionHeartHela CellsHomeostasisHospitalsInternal MedicineInvestigationLaboratoriesLiverMedicineMentorsMetabolismMitochondriaMolecularMusMuscleMyocardiumNon-Insulin-Dependent Diabetes MellitusNuclear ExtractPPAR gammaPersonal SatisfactionPhenotypePhysiciansPhysiologyPlayPrincipal InvestigatorProteinsProteomeProteomicsResearchResearch PersonnelRoleScientistSkeletal MuscleSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationSumTechniquesTherapeuticTissuesTraining ProgramsWomanbasecareerdesigndiabeticestablished cell linegain of functioninsightinterestloss of functionmembernovelnovel diagnosticsprogramssoundtooltranscription factor
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
847
DUNS Number
603847393
UEI
MQE2JHHJW9Q8
Project Start Date
01-May-2005
Project End Date
30-April-2010
Budget Start Date
21-July-2008
Budget End Date
30-April-2009
Project Funding Information for 2008
Total Funding
$132,570
Direct Costs
$122,750
Indirect Costs
$9,820
Year
Funding IC
FY Total Cost by IC
2008
National Institute of Diabetes and Digestive and Kidney Diseases
$132,570
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 7K08DK071017-05
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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