Base-pairing properties of the oxidized cytosine derivative, 5-hydroxy uracil Academic Article uri icon

Overview

MeSH Major

  • Base Pairing
  • Cytosine
  • DNA
  • Models, Chemical
  • Models, Molecular
  • Uracil

abstract

  • The most abundant base-substitution mutation resulting from oxidative damage to DNA is the GC to AT transition mutation. 5-hydroxyuracil (5-OHU), produced by the oxidative deamination of cystosine, has been established as the major chemical precursor for this most abundant transition mutation. Results from NMR spectroscopy and UV melting experiments show that 5-OHU would form the most stable pair with G, and the least stable pair with C. The hydroxyl group in the 5th position of the 5-OHU residue may play a role in increasing the stability of the 5-OHU:G pair over the normal Watson-Crick pair, the 5-OHU:A. The 5-OHU:C base pair would be least stable, and would destabilize the base-stacking in the duplex. Our results explain why certain DNA polymerases preferentially incorporate G opposite to 5-OHU over A and why C does not get incorporated against 5-OHU during DNA replication in vivo.

publication date

  • February 15, 2008

Research

keywords

  • Academic Article

Identity

Language

  • eng

PubMed Central ID

  • PMC2262052

Digital Object Identifier (DOI)

  • 10.1016/j.bbrc.2007.12.010

PubMed ID

  • 18078807

Additional Document Info

start page

  • 752

end page

  • 7

volume

  • 366

number

  • 3