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Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA

Escherichia coli RecA is the defining member of a ubiquitous class of DNA strand exchange proteins that are essential for homologous recombination, a pathway that maintains genomic integrity by repairing broken DNA(1). To function, filaments of RecA must nucleate and grow on single-stranded DNA (ssD...

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Autores principales: Bell, Jason C., Plank, Jody L., Dombrowski, Christopher C., Kowalczykowski, Stephen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112059/
https://www.ncbi.nlm.nih.gov/pubmed/23103864
http://dx.doi.org/10.1038/nature11598
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author Bell, Jason C.
Plank, Jody L.
Dombrowski, Christopher C.
Kowalczykowski, Stephen C.
author_facet Bell, Jason C.
Plank, Jody L.
Dombrowski, Christopher C.
Kowalczykowski, Stephen C.
author_sort Bell, Jason C.
collection PubMed
description Escherichia coli RecA is the defining member of a ubiquitous class of DNA strand exchange proteins that are essential for homologous recombination, a pathway that maintains genomic integrity by repairing broken DNA(1). To function, filaments of RecA must nucleate and grow on single-stranded DNA (ssDNA) in direct competition with ssDNA-binding protein (SSB), which rapidly binds and continuously sequesters ssDNA, kinetically blocking RecA assembly(2,3). This dynamic self-assembly on a DNA lattice, in competition with another protein, is unique for the RecA-family relative to other filament-forming proteins such as actin and tubulin. The complexity of this process has hindered our understanding of RecA filament assembly because ensemble measurements cannot reliably distinguish between the nucleation and growth phases, despite extensive and diverse attempts(2–5). Previous single-molecule assays have measured nucleation and growth of RecA—and its eukaryotic homolog RAD51—on naked dsDNA and ssDNA(6–12); however, the template for RecA self-assembly in vivo is SSB-coated ssDNA(3). Using single-molecule microscopy, we directly visualized RecA filament assembly on single molecules of SSB-coated ssDNA, simultaneously measuring nucleation and growth. We establish that a dimer of RecA is required for nucleation, followed by growth of the filament through monomer addition, consistent with the finding that nucleation, but not growth, is modulated by nucleotide and magnesium ion cofactors. Filament growth is bidirectional, albeit faster in the 5′→3′ direction. Both nucleation and growth are repressed at physiological conditions, highlighting the essential role of recombination mediators in potentiating assembly in vivo. We define a two-step kinetic mechanism where RecA nucleates on transiently exposed ssDNA during SSB sliding and/or partial dissociation (i.e., DNA unwrapping) and then grows. We further demonstrate that the recombination mediator protein pair, RecOR, accelerates both RecA nucleation and filament growth, and that introduction of RecF further stimulates RecA nucleation.
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spelling pubmed-41120592014-07-27 Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA Bell, Jason C. Plank, Jody L. Dombrowski, Christopher C. Kowalczykowski, Stephen C. Nature Article Escherichia coli RecA is the defining member of a ubiquitous class of DNA strand exchange proteins that are essential for homologous recombination, a pathway that maintains genomic integrity by repairing broken DNA(1). To function, filaments of RecA must nucleate and grow on single-stranded DNA (ssDNA) in direct competition with ssDNA-binding protein (SSB), which rapidly binds and continuously sequesters ssDNA, kinetically blocking RecA assembly(2,3). This dynamic self-assembly on a DNA lattice, in competition with another protein, is unique for the RecA-family relative to other filament-forming proteins such as actin and tubulin. The complexity of this process has hindered our understanding of RecA filament assembly because ensemble measurements cannot reliably distinguish between the nucleation and growth phases, despite extensive and diverse attempts(2–5). Previous single-molecule assays have measured nucleation and growth of RecA—and its eukaryotic homolog RAD51—on naked dsDNA and ssDNA(6–12); however, the template for RecA self-assembly in vivo is SSB-coated ssDNA(3). Using single-molecule microscopy, we directly visualized RecA filament assembly on single molecules of SSB-coated ssDNA, simultaneously measuring nucleation and growth. We establish that a dimer of RecA is required for nucleation, followed by growth of the filament through monomer addition, consistent with the finding that nucleation, but not growth, is modulated by nucleotide and magnesium ion cofactors. Filament growth is bidirectional, albeit faster in the 5′→3′ direction. Both nucleation and growth are repressed at physiological conditions, highlighting the essential role of recombination mediators in potentiating assembly in vivo. We define a two-step kinetic mechanism where RecA nucleates on transiently exposed ssDNA during SSB sliding and/or partial dissociation (i.e., DNA unwrapping) and then grows. We further demonstrate that the recombination mediator protein pair, RecOR, accelerates both RecA nucleation and filament growth, and that introduction of RecF further stimulates RecA nucleation. 2012-10-24 2012-11-08 /pmc/articles/PMC4112059/ /pubmed/23103864 http://dx.doi.org/10.1038/nature11598 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
Bell, Jason C.
Plank, Jody L.
Dombrowski, Christopher C.
Kowalczykowski, Stephen C.
Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title_full Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title_fullStr Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title_full_unstemmed Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title_short Direct imaging of RecA nucleation and growth on single molecules of SSB-coated ssDNA
title_sort direct imaging of reca nucleation and growth on single molecules of ssb-coated ssdna
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4112059/
https://www.ncbi.nlm.nih.gov/pubmed/23103864
http://dx.doi.org/10.1038/nature11598
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