This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yamada, M.
Right arrow Articles by Nohmi, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yamada, M.
Right arrow Articles by Nohmi, T.

 Previous Article  |  Next Article 

Journal of Bacteriology, July 2006, p. 4992-4995, Vol. 188, No. 13
0021-9193/06/$08.00+0     doi:10.1128/JB.00281-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Involvement of Y-Family DNA Polymerases in Mutagenesis Caused by Oxidized Nucleotides in Escherichia coli

Masami Yamada,1 Tatsuo Nunoshiba,2 Masatomi Shimizu,1,3 Petr Gruz,1 Hiroyuki Kamiya,4 Hideyoshi Harashima,4 and Takehiko Nohmi1*

Division of Genetics and Mutagenesis, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan,1 Graduate School of Life Sciences, Tohoku University, 2-1-1, Katahira, Aoba-ku, Sendai 980-8577, Japan,2 Tokyo Healthcare University, 3-11-3, Setagaya, Setagaya-ku, Tokyo 154-8568, Japan,3 Graduate School of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nihi-6, Kita-ku, Sapporo 060-0812, Japan4

Received 22 February 2006/ Accepted 11 April 2006

Escherichia coli DNA polymerase IV incorporated 2-hydroxy-dATP opposite template guanine or thymine and 8-hydroxy-dGTP exclusively opposite adenine in vitro. Mutator phenotypes in sod/fur strains were substantially diminished by deletion of dinB and/or umuDC. DNA polymerases IV and V may be involved in mutagenesis caused by incorporation of the oxidized deoxynucleoside triphosphates.


* Corresponding author. Mailing address: Division of Genetics and Mutagenesis, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan. Phone: (81) 3 3700 9873. Fax: (81) 3 3707 6950. E-mail: nohmi{at}nihs.go.jp.


Journal of Bacteriology, July 2006, p. 4992-4995, Vol. 188, No. 13
0021-9193/06/$08.00+0     doi:10.1128/JB.00281-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Khairnar, N. P., Misra, H. S. (2009). DNA polymerase X from Deinococcus radiodurans implicated in bacterial tolerance to DNA damage is characterized as a short patch base excision repair polymerase. Microbiology 155: 3005-3014 [Abstract] [Full Text]  
  • Cohen, S. E., Godoy, V. G., Walker, G. C. (2009). Transcriptional Modulator NusA Interacts with Translesion DNA Polymerases in Escherichia coli. J. Bacteriol. 191: 665-672 [Abstract] [Full Text]  
  • Saumaa, S., Tover, A., Tark, M., Tegova, R., Kivisaar, M. (2007). Oxidative DNA Damage Defense Systems in Avoidance of Stationary-Phase Mutagenesis in Pseudomonas putida. J. Bacteriol. 189: 5504-5514 [Abstract] [Full Text]