ArticleThe Journal of biological chemistry2026
Robust excision of different purine lesions by homologs thymine DNA glycosylase and mismatch-specific uracil DNA-glycosylase.
Article in The Journal of biological chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
DNA bases are subject to alkylation, deamination, and oxidation, yielding mutagenic and cytotoxic lesions implicated in cancer and neurodegenerative disease. The damage is countered by DNA glycosylases, which hydrolyze the N-glycosyl bond to release the lesion and initiate base excision repair. One glycosylase family is represented by human thymine DNA glycosylase (TDG) and Escherichia coli mismatch-specific uracil DNA-glycosylase (MUG), which exhibits 32% sequence identity. TDG excises thymine/uracil from guanine mispairs, 5-formylcytosine, 5-carboxylcytosine, and 3,N
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