A growing body of evidence suggests that the cellular response to oxidative
and nitrosative stress is primarily regulated at the level of transcriptio
n. Posttranslational modification of transcription factors may provide a me
chanism by which cells sense these redox changes. In bacteria, for example,
OxyR senses redox-related changes via oxidation or nitrosylation of a free
thiol in the DNA binding region. This mode of regulation may serve as a pa
radigm for redox-sensing by eukaryotic transcription factors as most-includ
ing NF-kappa B, AP-1, and p53-contain reactive thiols in their DNA binding
regions, the modification of which alters binding in vitro. Several of thes
e transcription factors have been found to be sensitive to both reactive ox
ygen species and nitric oxide-related species in vivo. It remains entirely
unclear, however, if oxidation or nitrosylation of eukaryotic transcription
factors is an important mode of regulation, or whether transcriptional act
ivating pathways are principally controlled at other redox-sensitive levels
.