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GATA2 Promotes Hematopoietic Development and Represses Cardiac Differentiation of Human Mesoderm

In vertebrates, GATA2 is a master regulator of hematopoiesis and is expressed throughout embryo development and in adult life. Although the essential role of GATA2 in mouse hematopoiesis is well established, its involvement during early human hematopoietic development is not clear. By combining time...

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Detalles Bibliográficos
Autores principales: Castaño, Julio, Aranda, Sergi, Bueno, Clara, Calero-Nieto, Fernando J., Mejia-Ramirez, Eva, Mosquera, Jose Luis, Blanco, Enrique, Wang, Xiaonan, Prieto, Cristina, Zabaleta, Lorea, Mereu, Elisabetta, Rovira, Meritxell, Jiménez-Delgado, Senda, Matson, Daniel R., Heyn, Holger, Bresnick, Emery H., Göttgens, Berthold, Di Croce, Luciano, Menendez, Pablo, Raya, Angel, Giorgetti, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6742600/
https://www.ncbi.nlm.nih.gov/pubmed/31402335
http://dx.doi.org/10.1016/j.stemcr.2019.07.009
Descripción
Sumario:In vertebrates, GATA2 is a master regulator of hematopoiesis and is expressed throughout embryo development and in adult life. Although the essential role of GATA2 in mouse hematopoiesis is well established, its involvement during early human hematopoietic development is not clear. By combining time-controlled overexpression of GATA2 with genetic knockout experiments, we found that GATA2, at the mesoderm specification stage, promotes the generation of hemogenic endothelial progenitors and their further differentiation to hematopoietic progenitor cells, and negatively regulates cardiac differentiation. Surprisingly, genome-wide transcriptional and chromatin immunoprecipitation analysis showed that GATA2 bound to regulatory regions, and repressed the expression of cardiac development-related genes. Moreover, genes important for hematopoietic differentiation were upregulated by GATA2 in a mostly indirect manner. Collectively, our data reveal a hitherto unrecognized role of GATA2 as a repressor of cardiac fates, and highlight the importance of coordinating the specification and repression of alternative cell fates.