Everyone ages, and many diseases that affect humans, such as cancer, are correlated with aging. Thus, understanding the regulation of aging may also help elucidate the causes behind the predisposition of older humans to diseases like cancer. Caenorhabditis elegans is an excellent organism in which to investigate the regulation of aging. Genetic analyses have already shown that an insulin/lGF-like hormonal control system regulates aging in the worm. However, many components of this system have not been identified. Thus, the characterization of additional lifespan control genes should increase the understanding of the pathways that regulate the rate of aging in worms. Long-lived mutants from the EMS mutagenesis lifespan screen previously performed by the Kenyon group will be characterized in the hope of finding new molecules that control lifespan. Furthermore, some long-lived worms isolated from the screen exhibit sensory defects. However, little is still known on how the worm?s sensory system controls its lifespan, and thus will be a focus of this study to provide exciting insight on the role of the environment on regulating an animal?s lifespan, which should lead to a better understanding of the mechanisms of aging.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32AG005860-01A1
Application #
6370225
Study Section
Biological Sciences 2 (BIOL)
Program Officer
Mccormick, Anna M
Project Start
2001-07-01
Project End
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
1
Fiscal Year
2001
Total Cost
$41,996
Indirect Cost
Name
University of California San Francisco
Department
Biochemistry
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143