Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2

Autores
Kaniecki, Kyle; de Tullio, Luisina; Gibb, Bryan; Kwon, Youngho; Sung, Patrick; Greene, Eric C.
Año de publicación
2017
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Srs2 is a superfamily 1 (SF1) helicase and antirecombinase that is required for genome integrity. However, the mechanisms that regulate Srs2 remain poorly understood. Here, we visualize Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. We demonstrate that Srs2 is a processive translocase capable of stripping thousands of Rad51 molecules from ssDNA at a rate of ∼50 monomers/s. We show that Srs2 is recruited to RPA clusters embedded between Rad51 filaments and that multimeric arrays of Srs2 assemble during translocation on ssDNA through a mechanism involving iterative Srs2 loading events at sites cleared of Rad51. We also demonstrate that Srs2 acts on heteroduplex DNA joints through two alternative pathways, both of which result in rapid disruption of the heteroduplex intermediate. On the basis of these findings, we present a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates. Kaniecki et al. develop a single-molecule assay for directly visualizing the behavior of the yeast helicase Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. These experiments lead to a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates.
Fil: Kaniecki, Kyle. Columbia University; Estados Unidos
Fil: de Tullio, Luisina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina. Columbia University; Estados Unidos
Fil: Gibb, Bryan. New York Institute Of Technology; Estados Unidos. Columbia University; Estados Unidos
Fil: Kwon, Youngho. University of Yale. School of Medicine; Estados Unidos
Fil: Sung, Patrick. University of Yale. School of Medicine; Estados Unidos
Fil: Greene, Eric C.. Columbia University; Estados Unidos
Materia
DNA CURTAINS
DNA REPAIR
HELICASE
HOMOLOGOUS RECOMBINATION
RAD51
SINGLE MOLECULE
SRS2
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/57553

id CONICETDig_9051fed1dc362cbc69530fd73c258ea8
oai_identifier_str oai:ri.conicet.gov.ar:11336/57553
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2Kaniecki, Kylede Tullio, LuisinaGibb, BryanKwon, YounghoSung, PatrickGreene, Eric C.DNA CURTAINSDNA REPAIRHELICASEHOMOLOGOUS RECOMBINATIONRAD51SINGLE MOLECULESRS2https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Srs2 is a superfamily 1 (SF1) helicase and antirecombinase that is required for genome integrity. However, the mechanisms that regulate Srs2 remain poorly understood. Here, we visualize Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. We demonstrate that Srs2 is a processive translocase capable of stripping thousands of Rad51 molecules from ssDNA at a rate of ∼50 monomers/s. We show that Srs2 is recruited to RPA clusters embedded between Rad51 filaments and that multimeric arrays of Srs2 assemble during translocation on ssDNA through a mechanism involving iterative Srs2 loading events at sites cleared of Rad51. We also demonstrate that Srs2 acts on heteroduplex DNA joints through two alternative pathways, both of which result in rapid disruption of the heteroduplex intermediate. On the basis of these findings, we present a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates. Kaniecki et al. develop a single-molecule assay for directly visualizing the behavior of the yeast helicase Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. These experiments lead to a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates.Fil: Kaniecki, Kyle. Columbia University; Estados UnidosFil: de Tullio, Luisina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina. Columbia University; Estados UnidosFil: Gibb, Bryan. New York Institute Of Technology; Estados Unidos. Columbia University; Estados UnidosFil: Kwon, Youngho. University of Yale. School of Medicine; Estados UnidosFil: Sung, Patrick. University of Yale. School of Medicine; Estados UnidosFil: Greene, Eric C.. Columbia University; Estados UnidosElsevier2017-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/57553Kaniecki, Kyle; de Tullio, Luisina; Gibb, Bryan; Kwon, Youngho; Sung, Patrick; et al.; Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2; Elsevier; Cell Reports; 21; 11; 12-2017; 3166-31772211-12472211-1247CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2017.11.047info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:54:38Zoai:ri.conicet.gov.ar:11336/57553instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 09:54:38.806CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
title Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
spellingShingle Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
Kaniecki, Kyle
DNA CURTAINS
DNA REPAIR
HELICASE
HOMOLOGOUS RECOMBINATION
RAD51
SINGLE MOLECULE
SRS2
title_short Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
title_full Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
title_fullStr Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
title_full_unstemmed Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
title_sort Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2
dc.creator.none.fl_str_mv Kaniecki, Kyle
de Tullio, Luisina
Gibb, Bryan
Kwon, Youngho
Sung, Patrick
Greene, Eric C.
author Kaniecki, Kyle
author_facet Kaniecki, Kyle
de Tullio, Luisina
Gibb, Bryan
Kwon, Youngho
Sung, Patrick
Greene, Eric C.
author_role author
author2 de Tullio, Luisina
Gibb, Bryan
Kwon, Youngho
Sung, Patrick
Greene, Eric C.
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv DNA CURTAINS
DNA REPAIR
HELICASE
HOMOLOGOUS RECOMBINATION
RAD51
SINGLE MOLECULE
SRS2
topic DNA CURTAINS
DNA REPAIR
HELICASE
HOMOLOGOUS RECOMBINATION
RAD51
SINGLE MOLECULE
SRS2
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Srs2 is a superfamily 1 (SF1) helicase and antirecombinase that is required for genome integrity. However, the mechanisms that regulate Srs2 remain poorly understood. Here, we visualize Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. We demonstrate that Srs2 is a processive translocase capable of stripping thousands of Rad51 molecules from ssDNA at a rate of ∼50 monomers/s. We show that Srs2 is recruited to RPA clusters embedded between Rad51 filaments and that multimeric arrays of Srs2 assemble during translocation on ssDNA through a mechanism involving iterative Srs2 loading events at sites cleared of Rad51. We also demonstrate that Srs2 acts on heteroduplex DNA joints through two alternative pathways, both of which result in rapid disruption of the heteroduplex intermediate. On the basis of these findings, we present a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates. Kaniecki et al. develop a single-molecule assay for directly visualizing the behavior of the yeast helicase Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. These experiments lead to a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates.
Fil: Kaniecki, Kyle. Columbia University; Estados Unidos
Fil: de Tullio, Luisina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Centro de Investigaciones en Química Biológica de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Centro de Investigaciones en Química Biológica de Córdoba; Argentina. Columbia University; Estados Unidos
Fil: Gibb, Bryan. New York Institute Of Technology; Estados Unidos. Columbia University; Estados Unidos
Fil: Kwon, Youngho. University of Yale. School of Medicine; Estados Unidos
Fil: Sung, Patrick. University of Yale. School of Medicine; Estados Unidos
Fil: Greene, Eric C.. Columbia University; Estados Unidos
description Srs2 is a superfamily 1 (SF1) helicase and antirecombinase that is required for genome integrity. However, the mechanisms that regulate Srs2 remain poorly understood. Here, we visualize Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. We demonstrate that Srs2 is a processive translocase capable of stripping thousands of Rad51 molecules from ssDNA at a rate of ∼50 monomers/s. We show that Srs2 is recruited to RPA clusters embedded between Rad51 filaments and that multimeric arrays of Srs2 assemble during translocation on ssDNA through a mechanism involving iterative Srs2 loading events at sites cleared of Rad51. We also demonstrate that Srs2 acts on heteroduplex DNA joints through two alternative pathways, both of which result in rapid disruption of the heteroduplex intermediate. On the basis of these findings, we present a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates. Kaniecki et al. develop a single-molecule assay for directly visualizing the behavior of the yeast helicase Srs2 as it acts upon single-stranded DNA (ssDNA) bound by the Rad51 recombinase. These experiments lead to a model describing the recruitment and regulation of Srs2 as it acts upon homologous recombination intermediates.
publishDate 2017
dc.date.none.fl_str_mv 2017-12
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/57553
Kaniecki, Kyle; de Tullio, Luisina; Gibb, Bryan; Kwon, Youngho; Sung, Patrick; et al.; Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2; Elsevier; Cell Reports; 21; 11; 12-2017; 3166-3177
2211-1247
2211-1247
CONICET Digital
CONICET
url http://hdl.handle.net/11336/57553
identifier_str_mv Kaniecki, Kyle; de Tullio, Luisina; Gibb, Bryan; Kwon, Youngho; Sung, Patrick; et al.; Dissociation of Rad51 Presynaptic Complexes and Heteroduplex DNA Joints by Tandem Assemblies of Srs2; Elsevier; Cell Reports; 21; 11; 12-2017; 3166-3177
2211-1247
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2017.11.047
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1842269297960812544
score 13.13397