Mechanistic studies of dinucleotide and oligonucleotide model cyclobutane pyrimidine dimer (CPD) DNA lesions under alkaline conditions

0556554 - ÚOCHB 2023 RIV GB eng J - Článek v odborném periodiku
Chaturvedi, Ritu - Long, E. C.
Mechanistic studies of dinucleotide and oligonucleotide model cyclobutane pyrimidine dimer (CPD) DNA lesions under alkaline conditions.
Bioorganic & Medicinal Chemistry. Roč. 54, January (2022), č. článku 116499. ISSN 0968-0896. E-ISSN 1464-3391
Institucionální podpora: RVO:61388963
Klíčová slova: DNA damage * cyclobutane pyrimidine dimer * alkaline reactivity * hemiaminal * DNA strand break
Obor OECD: Analytical chemistry
Impakt faktor: 3.5, rok: 2022
Způsob publikování: Omezený přístup
https://doi.org/10.1016/j.bmc.2021.116499

Cyclobutane pyrimidine dimers (CPDs) are the most abundant mutagenic DNA lesions formed in mammalian cells upon exposure to UV-B radiation (280-315 nm) in sunlight. These lesions are thought to be chemically stable and to withstand high concentrations of acids and bases.While earlier investigations of DNA lesions containing saturated pyrimidines have shown that the C4 carbonyl is a potential target of nucleophilic attack, similar reactions with thymine nucleobase model CPDs clearly showed that the cis-syn CPD (major isomer) is stable in the presence of a high concentration of alkali at room temperature. Here is described the alkaline reactivity of these lesions when contained within a dinucleotide CPD model system. Results using cis-syn CPD formed from dinucleotide 5 & PRIME,-TpT-3 & PRIME, combined with [O-18]-labelling indicated that CPD undergoes a water addition at the C4=O groups of these now saturated rings. The intermediate formed, however, completely reverts to the starting lesion. Along with confirming the target of water addition within CPD lesions, it was also determined that the two C4 carbonyls present on adjacent saturated pyrimidine rings of the photolesion undergo water exchange at different rates (3 & PRIME, > 5 & PRIME,). Moreover, the difference in reactivity exhibited by these two positions is not limited to a dinucleotide and was observed also in oligonucleotides. Overall, a full understanding of the chemistry of CPD lesions is crucial to our knowledge of naturally-occuring DNA modifications and may lead to further insight into their detection, modification, and biochemical recognition & repair.
Trvalý link: http://hdl.handle.net/11104/0331080