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Action-at-a-distance mutagenesis induced by oxidized guanine in Werner syndrome protein-reduced human cells.

Abstract：

:8-Oxo-7,8-dihydroguanine (G(O), 8-hydroxyguanine) in DNA is one of the most important oxidatively damaged bases and causes G:C → T:A substitution mutations. The Werner syndrome protein (WRN) is a cancer-related RecQ DNA helicase and plays many roles in DNA replication and repair. To examine the relationships between G(O)-induced mutations and WRN, shuttle plasmid DNA containing a G(O):C pair in the supF gene was transfected into human U2OS cells, in which WRN was knocked down. The plasmid DNA replicated in the knockdown cells was introduced into an Escherichia coli indicator strain. The knockdown of WRN increased the mutant frequency of the G(O)-plasmid DNA. Unexpectedly, however, the WRN knockdown only slightly enhanced the targeted G:C → T:A mutation. Instead, base-substitution mutations at various positions were more frequently detected, with statistical significance. The results obtained in this study suggested that the reduction of the cancer-related WRN induced action-at-a-distance mutagenesis by the G(O):C pair in human cells. In addition, the WRN knockdown decreased the G(O):A-induced A:T → C:G mutations, suggesting that WRN may enhance the mutations caused by G(O) in the nucleotide pool.

journal_name

Chem Res Toxicol

journal_title

Chemical research in toxicology

authors

Kamiya H,Yamazaki D,Nakamura E,Makino T,Kobayashi M,Matsuoka I,Harashima H

doi

10.1021/tx500418m

subject

Has Abstract

pub_date

2015-04-20 00:00:00

pages

621-8

issue

4

eissn

0893-228X

issn

1520-5010

journal_volume

28

pub_type

杂志文章

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