Bypass of a Nick by the Replisome of Bacteriophage T7

被引:13
|
作者
Zhu, Bin [1 ]
Lee, Seung-Joo [1 ]
Richardson, Charles C. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
DNA-REPLICATION FORK; GENE; 4; PROTEIN; STRAND-DISPLACEMENT; ESCHERICHIA-COLI; PRIMASE DOMAINS; BINDING PROTEIN; DEOXYRIBONUCLEIC-ACID; POLYMERASE-ACTIVITY; HELICASE ACTIVITY; SINGLE-MOLECULE;
D O I
10.1074/jbc.M111.252023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA polymerase and DNA helicase are essential components of DNA replication. The helicase unwinds duplex DNA to provide single-stranded templates for DNA synthesis by the DNA polymerase. In bacteriophage T7, movement of either the DNA helicase or the DNA polymerase alone terminates upon encountering a nick in duplex DNA. Using a minicircular DNA, we show that the helicase.polymerase complex can bypass a nick, albeit at reduced efficiency of 7%, on the non-template strand to continue rolling circle DNA synthesis. A gap in the non-template strand cannot be bypassed. The efficiency of bypass synthesis depends on the DNA sequence downstream of the nick. A nick on the template strand cannot be bypassed. Addition of T7 single-stranded DNA-binding protein to the complex stimulates nick bypass 2-fold. We propose that the association of helicase with the polymerase prevents dissociation of the helicase upon encountering a nick, allowing the helicase to continue unwinding of the duplex downstream of the nick.
引用
收藏
页码:28488 / 28497
页数:10
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