We studied the effect of aging on the repair of a vector containing the chloramphenicol acetyl transferase gene. This methodology more closely approximates in vivo DNA repair than other methods in that only repair of transcribed segments is measured. Techniques employing these shuttle vectors have been proved to be accurate and reproducible in several studies. No differences in repair were found in studies of primary cultured rat embryo fibroblasts from young and old donors. In addition the repair capacity of rat embryo fibroblasts did not display any change with passage level. A study of repair in human fibroblasts from donors of various ages has begun using the shuttle vector system.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000715-01
Application #
3817656
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Maul, Robert W; Gearhart, Patricia J (2009) Women, autoimmunity, and cancer: a dangerous liaison between estrogen and activation-induced deaminase? J Exp Med 206:11-3
Alrefai, Rudaina H; Winter, David B; Bohr, Vilhelm A et al. (2007) Nucleotide excision repair in an immunoglobulin variable gene is less efficient than in a housekeeping gene. Mol Immunol 44:2800-5