Nucleotide incorporation against 7,8-dihydro-8-oxoguanine is influenced by neighboring base sequences in TLS DNA polymerase reaction
Author(s) -
Cathleen M. Yung,
Tetsuya Suzuki,
Yoshinaga Okugawa,
Atsushi Kawakami,
David Loakes,
Kazuo Negishi,
Tomoe Negishi
Publication year - 2007
Publication title -
nucleic acids symposium series
Language(s) - English
Resource type - Journals
eISSN - 1746-8272
pISSN - 0261-3166
DOI - 10.1093/nass/nrm025
Subject(s) - transversion , oligonucleotide , dna polymerase , microbiology and biotechnology , polymerase , biology , base pair , sequence (biology) , genetics , dna , dna damage , mutation , chemistry , gene
7,8-Dihydro-8-oxoguanine (8-oxoG) is a well-known oxidative lesion in DNA and is related to carcinogenesis and ageing processes. Misincorporation of dATP opposite to 8-oxoG leads to G --> T transversion mutations. DNA sequence has been proved as an important factor influencing the replication and enzymatic repair of various types of damages. To explore the influence of sequence effect on the properties of translesion synthesis (TLS) polymerase bypass of 8-oxoG, oligonucleotides with an 8-oxoG in different sequence contexts were used. We conclude that the 5'-nearest base next to 8-oxoG has significant effects in the G --> T mutation by hpoleta.
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