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Visualizing Single-molecule DNA Replication with Fluorescence Microscopy

We describe a simple fluorescence microscopy-based real-time method for observing DNA replication at the single-molecule level. A circular, forked DNA template is attached to a functionalized glass coverslip and replicated extensively after introduction of replication proteins and nucleotides (Figur...

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Detalles Bibliográficos
Autores principales: Tanner, Nathan A., Loparo, Joseph J., van Oijen, Antoine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142874/
https://www.ncbi.nlm.nih.gov/pubmed/19820685
http://dx.doi.org/10.3791/1529
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author Tanner, Nathan A.
Loparo, Joseph J.
van Oijen, Antoine M.
author_facet Tanner, Nathan A.
Loparo, Joseph J.
van Oijen, Antoine M.
author_sort Tanner, Nathan A.
collection PubMed
description We describe a simple fluorescence microscopy-based real-time method for observing DNA replication at the single-molecule level. A circular, forked DNA template is attached to a functionalized glass coverslip and replicated extensively after introduction of replication proteins and nucleotides (Figure 1). The growing product double-strand DNA (dsDNA) is extended with laminar flow and visualized by using an intercalating dye. Measuring the position of the growing DNA end in real time allows precise determination of replication rate (Figure 2). Furthermore, the length of completed DNA products reports on the processivity of replication. This experiment can be performed very easily and rapidly and requires only a fluorescence microscope with a reasonably sensitive camera.
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spelling pubmed-31428742011-07-27 Visualizing Single-molecule DNA Replication with Fluorescence Microscopy Tanner, Nathan A. Loparo, Joseph J. van Oijen, Antoine M. J Vis Exp Cellular Biology We describe a simple fluorescence microscopy-based real-time method for observing DNA replication at the single-molecule level. A circular, forked DNA template is attached to a functionalized glass coverslip and replicated extensively after introduction of replication proteins and nucleotides (Figure 1). The growing product double-strand DNA (dsDNA) is extended with laminar flow and visualized by using an intercalating dye. Measuring the position of the growing DNA end in real time allows precise determination of replication rate (Figure 2). Furthermore, the length of completed DNA products reports on the processivity of replication. This experiment can be performed very easily and rapidly and requires only a fluorescence microscope with a reasonably sensitive camera. MyJove Corporation 2009-10-09 /pmc/articles/PMC3142874/ /pubmed/19820685 http://dx.doi.org/10.3791/1529 Text en Copyright © 2009, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Cellular Biology
Tanner, Nathan A.
Loparo, Joseph J.
van Oijen, Antoine M.
Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title_full Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title_fullStr Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title_full_unstemmed Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title_short Visualizing Single-molecule DNA Replication with Fluorescence Microscopy
title_sort visualizing single-molecule dna replication with fluorescence microscopy
topic Cellular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142874/
https://www.ncbi.nlm.nih.gov/pubmed/19820685
http://dx.doi.org/10.3791/1529
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