Research output: Contribution to journal › Review article › peer-review
8-Oxoadenine: A «New» Player of the Oxidative Stress in Mammals? / Kruchinin, Alexander A; Kamzeeva, Polina N; Zharkov, Dmitry O et al.
In: International Journal of Molecular Sciences, Vol. 25, No. 2, 1342, 22.01.2024.Research output: Contribution to journal › Review article › peer-review
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TY - JOUR
T1 - 8-Oxoadenine: A «New» Player of the Oxidative Stress in Mammals?
AU - Kruchinin, Alexander A
AU - Kamzeeva, Polina N
AU - Zharkov, Dmitry O
AU - Aralov, Andrey V
AU - Makarova, Alena V
N1 - The study was supported by The Russian Scientific Foundation grant 23-14-00209 to A.V.M. D.O.Z. acknowledges funding from the Russian Ministry of Science and Higher Education (project 075-15-2022-263).
PY - 2024/1/22
Y1 - 2024/1/22
N2 - Numerous studies have shown that oxidative modifications of guanine (7,8-dihydro-8-oxoguanine, 8-oxoG) can affect cellular functions. 7,8-Dihydro-8-oxoadenine (8-oxoA) is another abundant paradigmatic ambiguous nucleobase but findings reported on the mutagenicity of 8-oxoA in bacterial and eukaryotic cells are incomplete and contradictory. Although several genotoxic studies have demonstrated the mutagenic potential of 8-oxoA in eukaryotic cells, very little biochemical and bioinformatics data about the mechanism of 8-oxoA-induced mutagenesis are available. In this review, we discuss dual coding properties of 8-oxoA, summarize historical and recent genotoxicity and biochemical studies, and address the main protective cellular mechanisms of response to 8-oxoA. We also discuss the available structural data for 8-oxoA bypass by different DNA polymerases as well as the mechanisms of 8-oxoA recognition by DNA repair enzymes.
AB - Numerous studies have shown that oxidative modifications of guanine (7,8-dihydro-8-oxoguanine, 8-oxoG) can affect cellular functions. 7,8-Dihydro-8-oxoadenine (8-oxoA) is another abundant paradigmatic ambiguous nucleobase but findings reported on the mutagenicity of 8-oxoA in bacterial and eukaryotic cells are incomplete and contradictory. Although several genotoxic studies have demonstrated the mutagenic potential of 8-oxoA in eukaryotic cells, very little biochemical and bioinformatics data about the mechanism of 8-oxoA-induced mutagenesis are available. In this review, we discuss dual coding properties of 8-oxoA, summarize historical and recent genotoxicity and biochemical studies, and address the main protective cellular mechanisms of response to 8-oxoA. We also discuss the available structural data for 8-oxoA bypass by different DNA polymerases as well as the mechanisms of 8-oxoA recognition by DNA repair enzymes.
KW - Animals
KW - Adenine/chemistry
KW - DNA-Directed DNA Polymerase/metabolism
KW - Oxidative Stress
KW - DNA Damage
KW - Mutagens
KW - Mammals/metabolism
KW - DNA Repair
KW - 7,8-dihydro-8-oxoadenine
KW - translesion DNA synthesis
KW - base excision repair
KW - mutagenesis
KW - DNA polymerases
KW - DNA glycosylases
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85183376672&origin=inward&txGid=7baf402a74d4d73135ff40e30571be22
UR - https://www.mendeley.com/catalogue/01e6bb26-e380-36b7-86e2-7ec5f56f263b/
U2 - 10.3390/ijms25021342
DO - 10.3390/ijms25021342
M3 - Review article
C2 - 38279342
VL - 25
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1661-6596
IS - 2
M1 - 1342
ER -
ID: 60452173