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CUX1 通过 BAF 复合物调节人类造血干细胞染色质可及性。

CUX1 regulates human hematopoietic stem cell chromatin accessibility via the BAF complex.

机构信息

Department of Pathology, The University of Chicago, Chicago, IL 60637, USA; Committee on Cancer Biology, The University of Chicago, Chicago, IL 60637, USA.

Department of Pathology, The University of Chicago, Chicago, IL 60637, USA.

出版信息

Cell Rep. 2024 May 28;43(5):114227. doi: 10.1016/j.celrep.2024.114227. Epub 2024 May 11.

Abstract

CUX1 is a homeodomain-containing transcription factor that is essential for the development and differentiation of multiple tissues. CUX1 is recurrently mutated or deleted in cancer, particularly in myeloid malignancies. However, the mechanism by which CUX1 regulates gene expression and differentiation remains poorly understood, creating a barrier to understanding the tumor-suppressive functions of CUX1. Here, we demonstrate that CUX1 directs the BAF chromatin remodeling complex to DNA to increase chromatin accessibility in hematopoietic cells. CUX1 preferentially regulates lineage-specific enhancers, and CUX1 target genes are predictive of cell fate in vivo. These data indicate that CUX1 regulates hematopoietic lineage commitment and homeostasis via pioneer factor activity, and CUX1 deficiency disrupts these processes in stem and progenitor cells, facilitating transformation.

摘要

CUX1 是一种含有同源结构域的转录因子,对于多种组织的发育和分化至关重要。CUX1 在癌症中经常发生突变或缺失,特别是在髓系恶性肿瘤中。然而,CUX1 调节基因表达和分化的机制仍知之甚少,这成为了理解 CUX1 肿瘤抑制功能的障碍。在这里,我们证明 CUX1 指导 BAF 染色质重塑复合物与 DNA 结合,以增加造血细胞中的染色质可及性。CUX1 优先调节谱系特异性增强子,并且 CUX1 靶基因可预测体内细胞命运。这些数据表明,CUX1 通过启动因子活性调节造血谱系的决定和动态平衡,并且 CUX1 缺失会破坏干细胞和祖细胞中的这些过程,从而促进转化。

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