SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells

Mechanisms that operate during embryonic development to restrict cell fate are currently under investigation. Here the authors characterise the role of SCL/TAL1 at the onset of blood specification in embryonic development using mouse EB differentiation culture as a model system.

Guardado en:
Detalles Bibliográficos
Autores principales: Hedia Chagraoui, Maiken S. Kristiansen, Juan Pablo Ruiz, Ana Serra-Barros, Johanna Richter, Elisa Hall-Ponselé, Nicki Gray, Dominic Waithe, Kevin Clark, Philip Hublitz, Emmanouela Repapi, Georg Otto, Paul Sopp, Stephen Taylor, Supat Thongjuea, Paresh Vyas, Catherine Porcher
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
Materias:
Q
Acceso en línea:https://doaj.org/article/58afad89e66d460dbd6feaaa3566ef20
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:58afad89e66d460dbd6feaaa3566ef20
record_format dspace
spelling oai:doaj.org-article:58afad89e66d460dbd6feaaa3566ef202021-12-02T15:34:23ZSCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells10.1038/s41467-018-07787-62041-1723https://doaj.org/article/58afad89e66d460dbd6feaaa3566ef202018-12-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-07787-6https://doaj.org/toc/2041-1723Mechanisms that operate during embryonic development to restrict cell fate are currently under investigation. Here the authors characterise the role of SCL/TAL1 at the onset of blood specification in embryonic development using mouse EB differentiation culture as a model system.Hedia ChagraouiMaiken S. KristiansenJuan Pablo RuizAna Serra-BarrosJohanna RichterElisa Hall-PonseléNicki GrayDominic WaitheKevin ClarkPhilip HublitzEmmanouela RepapiGeorg OttoPaul SoppStephen TaylorSupat ThongjueaParesh VyasCatherine PorcherNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-17 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Hedia Chagraoui
Maiken S. Kristiansen
Juan Pablo Ruiz
Ana Serra-Barros
Johanna Richter
Elisa Hall-Ponselé
Nicki Gray
Dominic Waithe
Kevin Clark
Philip Hublitz
Emmanouela Repapi
Georg Otto
Paul Sopp
Stephen Taylor
Supat Thongjuea
Paresh Vyas
Catherine Porcher
SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
description Mechanisms that operate during embryonic development to restrict cell fate are currently under investigation. Here the authors characterise the role of SCL/TAL1 at the onset of blood specification in embryonic development using mouse EB differentiation culture as a model system.
format article
author Hedia Chagraoui
Maiken S. Kristiansen
Juan Pablo Ruiz
Ana Serra-Barros
Johanna Richter
Elisa Hall-Ponselé
Nicki Gray
Dominic Waithe
Kevin Clark
Philip Hublitz
Emmanouela Repapi
Georg Otto
Paul Sopp
Stephen Taylor
Supat Thongjuea
Paresh Vyas
Catherine Porcher
author_facet Hedia Chagraoui
Maiken S. Kristiansen
Juan Pablo Ruiz
Ana Serra-Barros
Johanna Richter
Elisa Hall-Ponselé
Nicki Gray
Dominic Waithe
Kevin Clark
Philip Hublitz
Emmanouela Repapi
Georg Otto
Paul Sopp
Stephen Taylor
Supat Thongjuea
Paresh Vyas
Catherine Porcher
author_sort Hedia Chagraoui
title SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
title_short SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
title_full SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
title_fullStr SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
title_full_unstemmed SCL/TAL1 cooperates with Polycomb RYBP-PRC1 to suppress alternative lineages in blood-fated cells
title_sort scl/tal1 cooperates with polycomb rybp-prc1 to suppress alternative lineages in blood-fated cells
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/58afad89e66d460dbd6feaaa3566ef20
work_keys_str_mv AT hediachagraoui scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT maikenskristiansen scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT juanpabloruiz scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT anaserrabarros scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT johannarichter scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT elisahallponsele scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT nickigray scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT dominicwaithe scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT kevinclark scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT philiphublitz scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT emmanouelarepapi scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT georgotto scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT paulsopp scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT stephentaylor scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT supatthongjuea scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT pareshvyas scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
AT catherineporcher scltal1cooperateswithpolycombrybpprc1tosuppressalternativelineagesinbloodfatedcells
_version_ 1718386837007892480