Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/1170
Title: Evaluation of phosphodiesterase I-based protocols for the detection of multiply damaged sites in DNA : the detection of abasic, oxidative and alkylative tandem damage in DNA oligonucleotides
Authors: Bowman, Karen J.
Le Pla, Rachel
Guichard, Yves.
Farmer, Peter B.
Jones, George D. D.
First Published: 2001
Publisher: Oxford University Press (OUP)
Citation: Nucleic Acids Research, 2001, 29 (20), e101-e112
Abstract: It has been proposed that DNA multiply damaged sites (MDS), where more than one moiety in a local region (∼1 helical turn, 10 bp) of the DNA is damaged, are lesions of enhanced biological significance. However, other than indirect measures, there are few analytical techniques that allow direct detection of MDS in DNA. In the present study we demonstrate the potential of protocols incorporating an exonucleolytic snake venom phosphodiesterase (SVPD) digestion stage to permit the direct detection of certain tandem damage, in which two lesions are immediately adjacent to each other on the same DNA strand. A series of prepared oligonucleotides containing either single or pairs of tetrahydrofuran moieties (F), thymine glycol lesions (T[superscript g]) or methylphosphotriester adducts (Me-PTE) were digested with SVPD and the digests examined by either [superscript 32]P-end-labelling or electrospray mass spectrometry. The unambiguous observation of SVPD-resistant ‘trimer’ species in the digests of oligonucleotides containing adjacent F, T[superscript g] and Me-PTE demonstrates that the SVPD digestion strategy is capable of allowing direct detection of certain tandem damage. Furthermore, in studies to determine the specificity of SVPD in dealing with pairs of lesions on the same strand, it was found mandatory to have the two lesions immediately adjacent to each other in order to generate the trimer species; pairs of lesions separated by as few as one or two normal nucleotides behave principally as single lesions towards SVPD.
DOI Link: 10.1093/nar/29.20.e101
ISSN: 0305-1048
eISSN: 1362-4962
Links: http://hdl.handle.net/2381/1170
http://nar.oxfordjournals.org/content/29/20/e101
Version: Publisher Version
Status: Peer-reviewed
Type: Article
Rights: Copyright © 2001, Oxford University Press (OUP). Deposited with reference to the publisher’s open access archiving policy.
Appears in Collections:Published Articles, Dept. of Cancer Studies and Molecular Medicine

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