A human ESC model for MLL-AF4 leukemic fusion gene reveals an impaired early hematopoietic-endothelial specification

The MLL-AF4 fusion gene is a hallmark genomic aberration in high-risk acute iymphoblastic leukemia in infants. Although it is well established that MLL-AF4 arises prenatally during human development, its effects on hematopoietic development in utero remain unexplored. We have created a human-specifi...

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Veröffentlicht in:Cell research 2012-06, Vol.22 (6), p.986-1002
Hauptverfasser: Bueno, Clara, Montes, Rosa, Melen, Gustavo J, Ramos-Mejia, Verónica, Real, Pedro J, Ayllón, Verónica, Sanchez, Laura, Ligero, Gertrudis, Gutierrez-Aranda, Iván, Fernández, Agustín F, Fraga, Mario F, Moreno-Gimeno, Inmaculada, Burks, Deborah, del Carmen Plaza-Calonge, María, Rodríguez-Manzaneque, Juan C, Menendez, Pablo
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Sprache:eng
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Zusammenfassung:The MLL-AF4 fusion gene is a hallmark genomic aberration in high-risk acute iymphoblastic leukemia in infants. Although it is well established that MLL-AF4 arises prenatally during human development, its effects on hematopoietic development in utero remain unexplored. We have created a human-specific cellular system to study early hemato-endothelial development in MLL-AF4-expressing human embryonic stem cells (hESCs). Functional studies, clonal analysis and gene expression profiling reveal that expression of MLL-AF4 in hESCs has a phenotypic, functional and gene expression impact. MLL-AF4 acts as a global transcriptional activator and a positive regulator of homeobox gene expression in hESCs. Functionally, MLL-AF4 enhances the specification of hemogenic precursors from hESCs
ISSN:1001-0602
1748-7838
DOI:10.1038/cr.2012.4