Akman, S.
and Rodriguez, H.
(2021),
Measurement of Oxidative DNA Damage in the Human p53 and PGK1 Gene at Nucleotide Resolution, Annals Of The New York Academy Of Sciences
(Accessed October 10, 2024)
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
Secure .gov websites use HTTPS
A lock (
) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.
Measurement of Oxidative DNA Damage in the Human p53 and PGK1 Gene at Nucleotide Resolution
Published
Author(s)
S A. Akman,
Abstract
Reactive oxygen species (ROS) from normal metabolism cause damage to DNA, protein and lipid (fat). By developing an oxidative DNA damage mapping version of the Ligation Mediated Polymerase Chain Reaction (LMPCR), we investigated the in vivo and in vitro frequencies of DNA base modifications caused by ROS in human p53 and PGK1 gene. In vivo and in vitro DNA base modification patterns were nearly identical. In human male fibroblasts, these patterns were independent of the transition metal used (Cu(II), Fe(II), or Cr(VI). Furthermore, the local probability of H202-mediated DNA base damage was determined primarily by DNA sequence context.Citation
Annals Of The New York Academy Of Sciences
Pub Type
Journals
Keywords
DNA base damage, free radicals, ligation mediated polymerase chain react, LMPCR, mapping, oxidative stress
Citation
Issues
If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.
Created October 12, 2021