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SSB diffusion on single stranded DNA stimulates RecA filament formation

Single stranded (ss)DNA generated in the cell during DNA metabolism is stabilized and protected by binding of single stranded DNA binding (SSB) proteins. E. coli SSB, a representative homotetrameric SSB, binds to ssDNA by wrapping the DNA using its four subunits. However, such a tightly wrapped, hig...

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Detalles Bibliográficos
Autores principales: Roy, Rahul, Kozlov, Alexander G., Lohman, Timothy M., Ha, Taekjip
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782680/
https://www.ncbi.nlm.nih.gov/pubmed/19820696
http://dx.doi.org/10.1038/nature08442
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author Roy, Rahul
Kozlov, Alexander G.
Lohman, Timothy M.
Ha, Taekjip
author_facet Roy, Rahul
Kozlov, Alexander G.
Lohman, Timothy M.
Ha, Taekjip
author_sort Roy, Rahul
collection PubMed
description Single stranded (ss)DNA generated in the cell during DNA metabolism is stabilized and protected by binding of single stranded DNA binding (SSB) proteins. E. coli SSB, a representative homotetrameric SSB, binds to ssDNA by wrapping the DNA using its four subunits. However, such a tightly wrapped, high affinity protein-DNA complex still needs to be removed or repositioned quickly for unhindered action of other proteins. Here, we show, using single molecule two and three-color FRET, that tetrameric SSB can spontaneously migrate along ssDNA. Diffusional migration of SSB helps in the local displacement of SSB by an elongating RecA filament. SSB diffusion also melts short DNA hairpins transiently and stimulates RecA filament elongation on DNA with secondary structure. This first observation of diffusional movement of a protein on ssDNA introduces a new paradigm for how an SSB protein can be redistributed, while remaining tightly bound to ssDNA during recombination and repair processes.
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spelling pubmed-27826802010-04-22 SSB diffusion on single stranded DNA stimulates RecA filament formation Roy, Rahul Kozlov, Alexander G. Lohman, Timothy M. Ha, Taekjip Nature Article Single stranded (ss)DNA generated in the cell during DNA metabolism is stabilized and protected by binding of single stranded DNA binding (SSB) proteins. E. coli SSB, a representative homotetrameric SSB, binds to ssDNA by wrapping the DNA using its four subunits. However, such a tightly wrapped, high affinity protein-DNA complex still needs to be removed or repositioned quickly for unhindered action of other proteins. Here, we show, using single molecule two and three-color FRET, that tetrameric SSB can spontaneously migrate along ssDNA. Diffusional migration of SSB helps in the local displacement of SSB by an elongating RecA filament. SSB diffusion also melts short DNA hairpins transiently and stimulates RecA filament elongation on DNA with secondary structure. This first observation of diffusional movement of a protein on ssDNA introduces a new paradigm for how an SSB protein can be redistributed, while remaining tightly bound to ssDNA during recombination and repair processes. 2009-10-11 2009-10-22 /pmc/articles/PMC2782680/ /pubmed/19820696 http://dx.doi.org/10.1038/nature08442 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Roy, Rahul
Kozlov, Alexander G.
Lohman, Timothy M.
Ha, Taekjip
SSB diffusion on single stranded DNA stimulates RecA filament formation
title SSB diffusion on single stranded DNA stimulates RecA filament formation
title_full SSB diffusion on single stranded DNA stimulates RecA filament formation
title_fullStr SSB diffusion on single stranded DNA stimulates RecA filament formation
title_full_unstemmed SSB diffusion on single stranded DNA stimulates RecA filament formation
title_short SSB diffusion on single stranded DNA stimulates RecA filament formation
title_sort ssb diffusion on single stranded dna stimulates reca filament formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782680/
https://www.ncbi.nlm.nih.gov/pubmed/19820696
http://dx.doi.org/10.1038/nature08442
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