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ERG promotes the maintenance of hematopoietic stem cells by restricting their differentiation

The balance between self-renewal and differentiation is crucial for the maintenance of hematopoietic stem cells (HSCs). Whereas numerous gene regulatory factors have been shown to control HSC self-renewal or drive their differentiation, we have relatively few insights into transcription factors that...

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Detalles Bibliográficos
Autores principales: Knudsen, Kasper Jermiin, Rehn, Matilda, Hasemann, Marie Sigurd, Rapin, Nicolas, Bagger, Frederik Otzen, Ohlsson, Ewa, Willer, Anton, Frank, Anne-Katrine, Søndergaard, Elisabeth, Jendholm, Johan, Thorén, Lina, Lee, Julie, Rak, Justyna, Theilgaard-Mönch, Kim, Porse, Bo Torben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579349/
https://www.ncbi.nlm.nih.gov/pubmed/26385962
http://dx.doi.org/10.1101/gad.268409.115
Descripción
Sumario:The balance between self-renewal and differentiation is crucial for the maintenance of hematopoietic stem cells (HSCs). Whereas numerous gene regulatory factors have been shown to control HSC self-renewal or drive their differentiation, we have relatively few insights into transcription factors that serve to restrict HSC differentiation. In the present work, we identify ETS (E-twenty-six)-related gene (ERG) as a critical factor protecting HSCs from differentiation. Specifically, loss of Erg accelerates HSC differentiation by >20-fold, thus leading to rapid depletion of immunophenotypic and functional HSCs. Molecularly, we could demonstrate that ERG, in addition to promoting the expression of HSC self-renewal genes, also represses a group of MYC targets, thereby explaining why Erg loss closely mimics Myc overexpression. Consistently, the BET domain inhibitor CPI-203, known to repress Myc expression, confers a partial phenotypic rescue. In summary, ERG plays a critical role in coordinating the balance between self-renewal and differentiation of HSCs.