Abstract
The loss of a coding nucleobase from the structure of DNA is a common event that generates an abasic (Ap) site (1). Ap sites exist as an equilibrating mixture of a cyclic hemiacetal and a ring-opened aldehyde. Aldehydes are electrophilic functional groups that can form covalent adducts with nucleophilic sites in DNA. Thus, Ap sites present a potentially reactive aldehyde as part of the internal structure of DNA. Here we report evidence that the aldehyde group of Ap sites in duplex DNA can form a covalent adduct with the N 6-amino group of adenine residues on the opposing strand. The resulting interstrand DNA-DNA cross-link occurs at 5′-ApT/5′-AA sequences in remarkably high yields (15-70%) under physiologically relevant conditions. This naturally occurring DNA-templated reaction has the potential to generate cross-links in the genetic material of living cells. © 2014 American Chemical Society.
Cite
CITATION STYLE
Price, N. E., Johnson, K. M., Wang, J., Fekry, M. I., Wang, Y., & Gates, K. S. (2014). Interstrand DNA-DNA cross-link formation between adenine residues and abasic sites in duplex dna. Journal of the American Chemical Society, 136(9), 3483–3490. https://doi.org/10.1021/ja410969x
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.