Literature DB >> 20542140

DNA polymerases involved in the incorporation of oxidized nucleotides into DNA: their efficiency and template base preference.

Atsushi Katafuchi1, Takehiko Nohmi.   

Abstract

Genetic information must be duplicated with precision and accurately passed on to daughter cells and later generations. In order to achieve this goal, DNA polymerases (Pols) have to faithfully execute DNA synthesis during chromosome replication and repair. However, the conditions under which Pols synthesize DNA are not always optimal; the template DNA can be damaged by various endogenous and exogenous genotoxic agents including reactive oxygen species (ROS), and ROS oxidize dNTPs in the nucleotide pool from which Pols elongate DNA strands. Both damaged DNA and oxidized dNTPs interfere with faithful DNA synthesis by Pols, inducing various cellular abnormalities, such as mutations, cancer, neurological diseases, and cellular senescence. In this review, we focus on the process by which Pols incorporate oxidized dNTPs into DNA and compare the properties of Pols: efficiency, i.e., k(cat)/K(m), k(pol)/K(d) or V(max)/K(m), and template base preference for the incorporation of 8-oxo-dGTP, an oxidized form of dGTP. In general, Pols involved in chromosome replication, the A- and B-family Pols, are resistant to the incorporation of 8-oxo-dGTP, whereas Pols involved in repair and/or translesion synthesis, the X- and Y-family Pols, incorporate nucleotides in a relatively efficient manner and tend to incorporate it opposite template dA rather than template dC, though there are several exceptions. We discuss the molecular mechanisms by which Pols exhibit different template base preferences for the incorporation of 8-oxo-dGTP and how Pols are involved in the induction of mutations via the incorporation of oxidized nucleotides under oxidative stress. 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20542140     DOI: 10.1016/j.mrgentox.2010.06.004

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  21 in total

Review 1.  Non-canonical actions of mismatch repair.

Authors:  Gray F Crouse
Journal:  DNA Repair (Amst)       Date:  2015-12-02

Review 2.  Translesion DNA polymerases in eukaryotes: what makes them tick?

Authors:  Alexandra Vaisman; Roger Woodgate
Journal:  Crit Rev Biochem Mol Biol       Date:  2017-03-09       Impact factor: 8.250

3.  Role of AtPolζ, AtRev1 and AtPolη in γ ray-induced mutagenesis.

Authors:  Mayu Nakagawa; Shinya Takahashi; Issay Narumi; Ayako N Sakamoto
Journal:  Plant Signal Behav       Date:  2011-05-01

4.  Insights into the substrate specificity of the MutT pyrophosphohydrolase using structural analogues of 8-oxo-2'-deoxyguanosine nucleotide.

Authors:  Michelle L Hamm; Emily J McFadden; Michael Ghio; Maria A M Lindell; Kenneth S Gerien; Suzanne F O'Handley
Journal:  Bioorg Med Chem Lett       Date:  2016-03-02       Impact factor: 2.823

Review 5.  Chemical and biological consequences of oxidatively damaged guanine in DNA.

Authors:  Sarah Delaney; Daniel A Jarem; Catherine B Volle; Craig J Yennie
Journal:  Free Radic Res       Date:  2012-02-22

6.  Klenow Fragment Discriminates against the Incorporation of the Hyperoxidized dGTP Lesion Spiroiminodihydantoin into DNA.

Authors:  Ji Huang; Craig J Yennie; Sarah Delaney
Journal:  Chem Res Toxicol       Date:  2015-11-24       Impact factor: 3.739

7.  Role of DNA polymerase β oxidized nucleotide insertion in DNA ligation failure.

Authors:  Melike Çaglayan; Samuel H Wilson
Journal:  J Radiat Res       Date:  2017-09-01       Impact factor: 2.724

Review 8.  Cellular levels of 8-oxoguanine in either DNA or the nucleotide pool play pivotal roles in carcinogenesis and survival of cancer cells.

Authors:  Yusaku Nakabeppu
Journal:  Int J Mol Sci       Date:  2014-07-15       Impact factor: 5.923

9.  How DNA damage and non-canonical nucleotides alter the telomerase catalytic cycle.

Authors:  Samantha L Sanford; Griffin A Welfer; Bret D Freudenthal; Patricia L Opresko
Journal:  DNA Repair (Amst)       Date:  2021-07-31

10.  Escherichia coli DNA polymerase III is responsible for the high level of spontaneous mutations in mutT strains.

Authors:  Masami Yamada; Masatomi Shimizu; Atsushi Katafuchi; Petr Grúz; Shingo Fujii; Yukio Usui; Robert P Fuchs; Takehiko Nohmi
Journal:  Mol Microbiol       Date:  2012-11-01       Impact factor: 3.501

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