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

机译:ERG通过限制其分化来促进造血干细胞的维持

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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.
机译:自我更新和分化之间的平衡对于维持造血干细胞(HSC)至关重要。尽管许多基因调控因子已显示出可控制HSC自我更新或驱动其分化,但我们对于限制HSC分化的转录因子的见解相对较少。在目前的工作中,我们确定与ETS(E-26)相关的基因(ERG)是保护HSC免受分化的关键因素。具体来说,Erg的损失将使HSC分化加速> 20倍,从而导致免疫表型和功能性HSC迅速耗竭。从分子上讲,我们可以证明ERG除了促进HSC自我更新基因的表达外,还可以抑制一组MYC靶标,从而解释了Erg丧失为何紧密模仿Myc的过表达。一致地,已知抑制Myc表达的BET域抑制剂CPI-203具有部分表型拯救作用。总之,ERG在协调自我更新和HSC分化之间的平衡中起着至关重要的作用。

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