Author ORCID Identifier

Candice M. Etson: 0000-0002-9796-269X

Document Type

Article

Publication Date

2-2-2010

Publication Title

Proceedings of the National Academy of Sciences of the United States of America

Abstract

The DNA polymerases involved in DNA replication achieve high processivity of nucleotide incorporation by forming a complex with processivity factors. A model system for replicative DNA polymerases, the bacteriophage T7 DNA polymerase (gp5), encoded by gene 5, forms a tight, 1:1 complex with Escherichia coli thioredoxin. By a mechanism that is not fully understood, thioredoxin acts as a processivity factor and converts gp5 from a distributive polymerase into a highly processive one. We use a single-molecule imaging approach to visualize the interaction of fluorescently labeled T7 DNA polymerase with double-stranded DNA. We have observed T7 gp5, both with and without thioredoxin, binding nonspecifically to double-stranded DNA and diffusing along the duplex. The gp5/thioredoxin complex remains tightly bound to the DNA while diffusing, whereas gp5 without thioredoxin undergoes frequent dissociation from and rebinding to the DNA. These observations suggest that thioredoxin increases the processivity of T7 DNA polymerase by suppressing microscopic hopping on and off the DNA and keeping the complex tightly bound to the duplex.

Keywords

DNA replication, Facilitated diffusion, Processivity, Single-molecule imaging, Sliding

Volume

107

Issue

5

First Page

1900

Last Page

1905

DOI

10.1073/pnas.0912664107

ISSN

00278424

Comments

Archived as published.

Included in

Physics Commons

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