Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Aberrant Repair of 8-Oxoguanine in Short DNA Bulges. / Eroshenko, D A; Diatlova, E A; Golyshev, V M и др.
в: Doklady. Biochemistry and biophysics, Том 513, № Suppl 1, 2024, стр. S82-S86.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Aberrant Repair of 8-Oxoguanine in Short DNA Bulges
AU - Eroshenko, D A
AU - Diatlova, E A
AU - Golyshev, V M
AU - Endutkin, A V
AU - Zharkov, D O
N1 - The work was supported by the Russian Foundation for Basic Research (project no. 21-54-12025 NNIO_a). © 2023. Pleiades Publishing, Ltd.
PY - 2024
Y1 - 2024
N2 - The presence of DNA damage can increase the likelihood of DNA replication errors and promote mutations. In particular, pauses of DNA polymerase at the site of damage can lead to polymerase slippage and the formation of 1-2-nucleotide bulges. Repair of such structures using an undamaged DNA template leads to small deletions. One of the most abundant oxidative DNA lesions, 8-oxoguanine (oxoG), was shown to induce small deletions, but the mechanism of this phenomenon is currently unknown. We studied the aberrant repair of oxoG located in one- and two-nucleotide bulges by the Escherichia coli and human base excision repair systems. Our results indicate that the repair in such substrates can serve as a mechanism for fixing small deletions in bacteria but not in humans.
AB - The presence of DNA damage can increase the likelihood of DNA replication errors and promote mutations. In particular, pauses of DNA polymerase at the site of damage can lead to polymerase slippage and the formation of 1-2-nucleotide bulges. Repair of such structures using an undamaged DNA template leads to small deletions. One of the most abundant oxidative DNA lesions, 8-oxoguanine (oxoG), was shown to induce small deletions, but the mechanism of this phenomenon is currently unknown. We studied the aberrant repair of oxoG located in one- and two-nucleotide bulges by the Escherichia coli and human base excision repair systems. Our results indicate that the repair in such substrates can serve as a mechanism for fixing small deletions in bacteria but not in humans.
KW - Humans
KW - DNA Repair
KW - DNA Glycosylases/genetics
KW - DNA Damage
KW - DNA/genetics
KW - Escherichia coli/genetics
KW - Nucleotides
KW - Guanine/analogs & derivatives
KW - 8-oxoguanine
KW - DNA damage
KW - OGG1
KW - DNA repair
KW - mutagenesis
KW - DNA glycosylases
KW - Fpg
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85184905819&origin=inward&txGid=dcf4dcb0c6f04b2278c2013b69a41426
UR - https://www.mendeley.com/catalogue/e1a2efa2-c2ec-3e03-88a5-03b844aa4f30/
U2 - 10.1134/S1607672923600355
DO - 10.1134/S1607672923600355
M3 - Article
C2 - 38337103
VL - 513
SP - S82-S86
JO - Doklady Biochemistry and Biophysics
JF - Doklady Biochemistry and Biophysics
SN - 1607-6729
IS - Suppl 1
ER -
ID: 60460910