A combinatorial system to examine the enzymatic repair of multiply damaged DNA substrates

Chia Wei Hsu, James W. Conrad, Mark L. Sowers, Tuvshintugs Baljinnyam, Jason L. Herring, Linda C. Hackfeld, Sandra S. Hatch, Lawrence C. Sowers

Research output: Contribution to journalArticlepeer-review

2 Scopus citations


DNA damage drives genetic mutations that underlie the development of cancer in humans. Multiple pathways have been described in mammalian cells which can repair this damage. However, most work to date has focused upon single lesions in DNA. We present here a combinatorial system which allows assembly of duplexes containing single or multiple types of damage by ligating together six oligonucleotides containing damaged or modified bases. The combinatorial system has dual fluorescent labels allowing examination of both strands simultaneously, in order to study interactions or competition between different DNA repair pathways. Using this system, we demonstrate how repair of oxidative damage in one DNA strand can convert a mispaired T:G deamination intermediate into a T:A mutation. We also demonstrate that slow repair of a T:G mispair, relative to a U:G mispair, by the human methyl-binding domain 4 DNA glycosylase provides a competitive advantage to competing repair pathways, and could explain why CpG dinucleotides are hotspots for C to T mutations in human tumors. Data is also presented that suggests repair of closely spaced lesions in opposing strands can be repaired by a combination of short and long-patch base excision repair and simultaneous repair of multiply damage sites can potentially lead to lethal double strand breaks.

Original languageEnglish (US)
Pages (from-to)7406-7419
Number of pages14
JournalNucleic acids research
Issue number13
StatePublished - Jul 22 2022

ASJC Scopus subject areas

  • Genetics


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