Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions
- Autores
- Swinstead, Erin E.; Miranda, Tina B.; Paakinaho, Ville; Baek, Songjoon; Goldstein, Ido; Hawkins, Mary; Karpova, Tatiana S.; Ball, David; Mazza, Davide; Lavis, Luke D.; Grimm, Jonathan B.; Morisaki, Tatsuya; Grøntved, Lars; Presman, Diego Martin; Hager, Gordon L.
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The estrogen receptor (ER), glucocorticoid receptor (GR), and forkhead box protein 1 (FoxA1) are significant factors in breast cancer progression. FoxA1 has been implicated in establishing ER-binding patterns though its unique ability to serve as a pioneer factor. However, the molecular interplay between ER, GR, and FoxA1 requires further investigation. Here we show that ER and GR both have the ability to alter the genomic distribution of the FoxA1 pioneer factor. Single-molecule tracking experiments in live cells reveal a highly dynamic interaction of FoxA1 with chromatin in vivo. Furthermore, the FoxA1 factor is not associated with detectable footprints at its binding sites throughout the genome. These findings support a model wherein interactions between transcription factors and pioneer factors are highly dynamic. Moreover, at a subset of genomic sites, the role of pioneer can be reversed, with the steroid receptors serving to enhance binding of FoxA1.
Fil: Swinstead, Erin E.. National Institutes of Health; Estados Unidos
Fil: Miranda, Tina B.. National Institutes of Health; Estados Unidos
Fil: Paakinaho, Ville. National Institutes of Health; Estados Unidos
Fil: Baek, Songjoon. National Institutes of Health; Estados Unidos
Fil: Goldstein, Ido. National Institutes of Health; Estados Unidos
Fil: Hawkins, Mary. National Institutes of Health; Estados Unidos
Fil: Karpova, Tatiana S.. National Institutes of Health; Estados Unidos
Fil: Ball, David. National Institutes of Health; Estados Unidos
Fil: Mazza, Davide. Universita Vita-salute San Raffaele; Italia
Fil: Lavis, Luke D.. Howard Hughes Medical Institute; Estados Unidos
Fil: Grimm, Jonathan B.. Howard Hughes Medical Institute; Estados Unidos
Fil: Morisaki, Tatsuya. National Institutes of Health; Estados Unidos. State University of Colorado - Fort Collins; Estados Unidos
Fil: Grøntved, Lars. National Institutes of Health; Estados Unidos
Fil: Presman, Diego Martin. National Institutes of Health; Estados Unidos
Fil: Hager, Gordon L.. National Institutes of Health; Estados Unidos - Materia
-
Foxa1
Chromatin
Single Molecule Tracking
Glucocorticoid Receptor - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/60625
Ver los metadatos del registro completo
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Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin TransitionsSwinstead, Erin E.Miranda, Tina B.Paakinaho, VilleBaek, SongjoonGoldstein, IdoHawkins, MaryKarpova, Tatiana S.Ball, DavidMazza, DavideLavis, Luke D.Grimm, Jonathan B.Morisaki, TatsuyaGrøntved, LarsPresman, Diego MartinHager, Gordon L.Foxa1ChromatinSingle Molecule TrackingGlucocorticoid Receptorhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The estrogen receptor (ER), glucocorticoid receptor (GR), and forkhead box protein 1 (FoxA1) are significant factors in breast cancer progression. FoxA1 has been implicated in establishing ER-binding patterns though its unique ability to serve as a pioneer factor. However, the molecular interplay between ER, GR, and FoxA1 requires further investigation. Here we show that ER and GR both have the ability to alter the genomic distribution of the FoxA1 pioneer factor. Single-molecule tracking experiments in live cells reveal a highly dynamic interaction of FoxA1 with chromatin in vivo. Furthermore, the FoxA1 factor is not associated with detectable footprints at its binding sites throughout the genome. These findings support a model wherein interactions between transcription factors and pioneer factors are highly dynamic. Moreover, at a subset of genomic sites, the role of pioneer can be reversed, with the steroid receptors serving to enhance binding of FoxA1.Fil: Swinstead, Erin E.. National Institutes of Health; Estados UnidosFil: Miranda, Tina B.. National Institutes of Health; Estados UnidosFil: Paakinaho, Ville. National Institutes of Health; Estados UnidosFil: Baek, Songjoon. National Institutes of Health; Estados UnidosFil: Goldstein, Ido. National Institutes of Health; Estados UnidosFil: Hawkins, Mary. National Institutes of Health; Estados UnidosFil: Karpova, Tatiana S.. National Institutes of Health; Estados UnidosFil: Ball, David. National Institutes of Health; Estados UnidosFil: Mazza, Davide. Universita Vita-salute San Raffaele; ItaliaFil: Lavis, Luke D.. Howard Hughes Medical Institute; Estados UnidosFil: Grimm, Jonathan B.. Howard Hughes Medical Institute; Estados UnidosFil: Morisaki, Tatsuya. National Institutes of Health; Estados Unidos. State University of Colorado - Fort Collins; Estados UnidosFil: Grøntved, Lars. National Institutes of Health; Estados UnidosFil: Presman, Diego Martin. National Institutes of Health; Estados UnidosFil: Hager, Gordon L.. National Institutes of Health; Estados UnidosCell Press2016-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/60625Swinstead, Erin E.; Miranda, Tina B.; Paakinaho, Ville; Baek, Songjoon; Goldstein, Ido; et al.; Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions; Cell Press; Cell; 165; 3; 4-2016; 593-6050092-8674CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.cell.2016.02.067info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0092867416302574info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:02:15Zoai:ri.conicet.gov.ar:11336/60625instacron: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 10:02:15.704CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
title |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
spellingShingle |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions Swinstead, Erin E. Foxa1 Chromatin Single Molecule Tracking Glucocorticoid Receptor |
title_short |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
title_full |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
title_fullStr |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
title_full_unstemmed |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
title_sort |
Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions |
dc.creator.none.fl_str_mv |
Swinstead, Erin E. Miranda, Tina B. Paakinaho, Ville Baek, Songjoon Goldstein, Ido Hawkins, Mary Karpova, Tatiana S. Ball, David Mazza, Davide Lavis, Luke D. Grimm, Jonathan B. Morisaki, Tatsuya Grøntved, Lars Presman, Diego Martin Hager, Gordon L. |
author |
Swinstead, Erin E. |
author_facet |
Swinstead, Erin E. Miranda, Tina B. Paakinaho, Ville Baek, Songjoon Goldstein, Ido Hawkins, Mary Karpova, Tatiana S. Ball, David Mazza, Davide Lavis, Luke D. Grimm, Jonathan B. Morisaki, Tatsuya Grøntved, Lars Presman, Diego Martin Hager, Gordon L. |
author_role |
author |
author2 |
Miranda, Tina B. Paakinaho, Ville Baek, Songjoon Goldstein, Ido Hawkins, Mary Karpova, Tatiana S. Ball, David Mazza, Davide Lavis, Luke D. Grimm, Jonathan B. Morisaki, Tatsuya Grøntved, Lars Presman, Diego Martin Hager, Gordon L. |
author2_role |
author author author author author author author author author author author author author author |
dc.subject.none.fl_str_mv |
Foxa1 Chromatin Single Molecule Tracking Glucocorticoid Receptor |
topic |
Foxa1 Chromatin Single Molecule Tracking Glucocorticoid Receptor |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The estrogen receptor (ER), glucocorticoid receptor (GR), and forkhead box protein 1 (FoxA1) are significant factors in breast cancer progression. FoxA1 has been implicated in establishing ER-binding patterns though its unique ability to serve as a pioneer factor. However, the molecular interplay between ER, GR, and FoxA1 requires further investigation. Here we show that ER and GR both have the ability to alter the genomic distribution of the FoxA1 pioneer factor. Single-molecule tracking experiments in live cells reveal a highly dynamic interaction of FoxA1 with chromatin in vivo. Furthermore, the FoxA1 factor is not associated with detectable footprints at its binding sites throughout the genome. These findings support a model wherein interactions between transcription factors and pioneer factors are highly dynamic. Moreover, at a subset of genomic sites, the role of pioneer can be reversed, with the steroid receptors serving to enhance binding of FoxA1. Fil: Swinstead, Erin E.. National Institutes of Health; Estados Unidos Fil: Miranda, Tina B.. National Institutes of Health; Estados Unidos Fil: Paakinaho, Ville. National Institutes of Health; Estados Unidos Fil: Baek, Songjoon. National Institutes of Health; Estados Unidos Fil: Goldstein, Ido. National Institutes of Health; Estados Unidos Fil: Hawkins, Mary. National Institutes of Health; Estados Unidos Fil: Karpova, Tatiana S.. National Institutes of Health; Estados Unidos Fil: Ball, David. National Institutes of Health; Estados Unidos Fil: Mazza, Davide. Universita Vita-salute San Raffaele; Italia Fil: Lavis, Luke D.. Howard Hughes Medical Institute; Estados Unidos Fil: Grimm, Jonathan B.. Howard Hughes Medical Institute; Estados Unidos Fil: Morisaki, Tatsuya. National Institutes of Health; Estados Unidos. State University of Colorado - Fort Collins; Estados Unidos Fil: Grøntved, Lars. National Institutes of Health; Estados Unidos Fil: Presman, Diego Martin. National Institutes of Health; Estados Unidos Fil: Hager, Gordon L.. National Institutes of Health; Estados Unidos |
description |
The estrogen receptor (ER), glucocorticoid receptor (GR), and forkhead box protein 1 (FoxA1) are significant factors in breast cancer progression. FoxA1 has been implicated in establishing ER-binding patterns though its unique ability to serve as a pioneer factor. However, the molecular interplay between ER, GR, and FoxA1 requires further investigation. Here we show that ER and GR both have the ability to alter the genomic distribution of the FoxA1 pioneer factor. Single-molecule tracking experiments in live cells reveal a highly dynamic interaction of FoxA1 with chromatin in vivo. Furthermore, the FoxA1 factor is not associated with detectable footprints at its binding sites throughout the genome. These findings support a model wherein interactions between transcription factors and pioneer factors are highly dynamic. Moreover, at a subset of genomic sites, the role of pioneer can be reversed, with the steroid receptors serving to enhance binding of FoxA1. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-04 |
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/11336/60625 Swinstead, Erin E.; Miranda, Tina B.; Paakinaho, Ville; Baek, Songjoon; Goldstein, Ido; et al.; Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions; Cell Press; Cell; 165; 3; 4-2016; 593-605 0092-8674 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/60625 |
identifier_str_mv |
Swinstead, Erin E.; Miranda, Tina B.; Paakinaho, Ville; Baek, Songjoon; Goldstein, Ido; et al.; Steroid Receptors Reprogram FoxA1 Occupancy through Dynamic Chromatin Transitions; Cell Press; Cell; 165; 3; 4-2016; 593-605 0092-8674 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.cell.2016.02.067 info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0092867416302574 |
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 |
Cell Press |
publisher.none.fl_str_mv |
Cell Press |
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 |
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1842269746589859840 |
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13.13397 |