Identification of Cdca7 as a novel Notch transcriptional target involved in hematopoietic stem cell emergence

Hematopoietic stem cell (HSC) specification occurs in the embryonic aorta and requires Notch activation; however, most of the Notch-regulated elements controlling de novo HSC generation are still unknown. Here, we identify putative direct Notch targets in the aorta-gonad-mesonephros (AGM) embryonic...

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Detalles Bibliográficos
Autores: Islam, Abul, 1978-, Guiu Sagarra, Jordi, 1983-, Bergen, Dylan J.M., de Pater, Emma, Ayllon, Verónica, Gama-Norton, Leonor, Ruiz Herguido, Cristina, González, Jessica, López Bigas, Núria, Menéndez, Pablo, Dzierzak, Elaine, Espinosa Blay, Lluís, Bigas Salvans, Anna
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2014
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/23815
Acceso en línea:http://hdl.handle.net/10230/23815
http://dx.doi.org/10.1084/jem.20131857
Access Level:acceso abierto
Palabra clave:Cultius cel·lulars
Peixos zebra (Animals de laboratori)
Descripción
Sumario:Hematopoietic stem cell (HSC) specification occurs in the embryonic aorta and requires Notch activation; however, most of the Notch-regulated elements controlling de novo HSC generation are still unknown. Here, we identify putative direct Notch targets in the aorta-gonad-mesonephros (AGM) embryonic tissue by chromatin precipitation using antibodies against the Notch partner RBPj. By ChIP-on-chip analysis of the precipitated DNA, we identified 701 promoter regions that were candidates to be regulated by Notch in the AGM. One of the most enriched regions corresponded to the Cdca7 gene, which was subsequently confirmed to recruit the RBPj factor but also Notch1 in AGM cells. We found that during embryonic hematopoietic development, expression of Cdca7 is restricted to the hematopoietic clusters of the aorta, and it is strongly up-regulated in the hemogenic population during human embryonic stem cell hematopoietic differentiation in a Notch-dependent manner. Down-regulation of Cdca7 mRNA in cultured AGM cells significantly induces hematopoietic differentiation and loss of the progenitor population. Finally, using loss-of-function experiments in zebrafish, we demonstrate that CDCA7 contributes to HSC emergence in vivo during embryonic development. Thus, our study identifies Cdca7 as an evolutionary conserved Notch target involved in HSC emergence.