Aging is inevitable. It is governed by both inheritance and environmental factors. A deeper understanding of the aging process might allow us to slow its progression or at least delay the onset of age-associated diseases, and thus extend the well being of individuals. The universality in the decline of energy with age highlights energy metabolism and the role of role mitochondria (mt) in aging. A widely accepted but still unproven theory of aging centers on the accumulation of cellular damage by the generation of reactive oxygen species. In cells, reactive oxygen species are generated in mitochondria and have been demonstrated to damage mitochondrial DNA. Since DNA repair is limited in mitochondria, some of this damage may go on to cause mutations when the DNA is replicated. We have developed, established, and validated exceptionally sensitive assays to quantify mutations in nuclear and mitochondrial DNA.
Our specific aims will be focused in two directions: 1) We will determine the frequency and types of mutations that increase in different tissues during aging in humans. We will analyze the mechanism by which specific mitochondrial mutations are be selective amplified. 2) Our focus will be on Parkinson syndrome, one of the most prevalent age-dependent neurological diseases. Using cell culture and mouse models, we will examine the contribution of reactive oxygen species to mitochondrial mutagenesis. Most importantly, we will ascertain if selectively amplified mitochondrial mutations can provide a marker for diagnosis of Parkinson syndrome and or monitoring of disease progression and response to treatment.

Public Health Relevance

The goal of this project is to determine the mechanism for the generation of mitochondial DNA mutations during normal aging and in age-associated diseases. If these mutations are generated by oxygen metabolism, it should be feasible to decrease their production by specific anti-oxidants that target mitochondria, and thus the progression of age-associated diseases. We will investigate the generation of mitochondrial mutations in one of the most prevalent age-associated neurological diseases. Parkinson.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG001751-30
Application #
8431785
Study Section
Special Emphasis Panel (ZAG1-ZIJ-6)
Project Start
Project End
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
30
Fiscal Year
2013
Total Cost
$285,910
Indirect Cost
$100,856
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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