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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.
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页码:28488 / 28497
页数:10
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