Browse by author
Lookup NU author(s): Sukhvinder Gill, Dr Rory O'Neill, Professor Rick Lewis, Professor Bernard Connolly
Full text for this publication is not currently held within this repository. Alternative links are provided below where available.
The interaction of archaeal family B DNA polymerases with deaminated bases has been examined. As determined previously by our group, the polymerase binds tightly to uracil (the deamination product of cytosine), in single-stranded DNA, and stalls replication on encountering this base. DNA polymerisation was also inhibited by the presence of hypoxanthine, the deamination product of adenine. Quantitative binding assays showed that the polymerase bound DNA containing uracil 1.5-4.5-fold more strongly than hypoxanthine and site-directed mutagenesis suggested that the same pocket was used for interaction with both deaminated bases. In contrast the polymerase was insensitive to xanthine, the deamination product of guanine. Traces of uracil and hypoxanthine in DNA can lead to inhibition of the PCR by archaeal DNA polymerases, an important consideration for biotechnology applications. Dual recognition of uracil and hypoxanthine may be facilitated by binding the bases with the glycosidic bond in the anti and syn conformation, respectively.
Author(s): Gill S, O'Neill R, Lewis RJ, Connolly BA
Publication type: Article
Publication status: Published
Journal: Journal of Molecular Biology
Year: 2007
Volume: 372
Issue: 4
Pages: 855-863
ISSN (print): 0022-2836
ISSN (electronic): 1089-8638
Publisher: Academic Press
URL: http://dx.doi.org/10.1016/j.jmb.2007.07.015
DOI: 10.1016/j.jmb.2007.07.015
Notes: Journal Article Research Support, Non-U.S. Gov't England
Altmetrics provided by Altmetric