Department of Medicine, Section of Rheumatology and Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, Illinois, USA.
Core for Research Informatics, University of Illinois at Chicago, Chicago, Illinois, USA.
Nat Commun. 2018 Sep 24;9(1):3888. doi: 10.1038/s41467-018-06165-6.
Transcription factor (TF) networks determine cell fate in hematopoiesis. However, how TFs cooperate with other regulatory mechanisms to instruct transcription remains poorly understood. Here we show that in small pre-B cells, the lineage restricted epigenetic reader BRWD1 closes early development enhancers and opens the enhancers of late B lymphopoiesis to TF binding. BRWD1 regulates over 7000 genes to repress proliferative and induce differentiation programs. However, BRWD1 does not regulate the expression of TFs required for B lymphopoiesis. Hypogammaglobulinemia patients with BRWD1 mutations have B-cell transcriptional profiles and enhancer landscapes similar to those observed in Brwd1 mice. These data indicate that, in both mice and humans, BRWD1 is a master orchestrator of enhancer accessibility that cooperates with TF networks to drive late B-cell development.
转录因子 (TF) 网络决定了造血过程中的细胞命运。然而,TF 如何与其他调控机制合作来指导转录仍知之甚少。在这里,我们表明在小前 B 细胞中,谱系限制的表观遗传阅读器 BRWD1 关闭早期发育增强子,并打开晚期 B 淋巴发生的增强子以进行 TF 结合。BRWD1 调节超过 7000 个基因,以抑制增殖并诱导分化程序。然而,BRWD1 不调节 B 淋巴发生所需的 TF 的表达。BRWD1 突变的低丙种球蛋白血症患者具有与 Brwd1 小鼠观察到的相似的 B 细胞转录谱和增强子景观。这些数据表明,在小鼠和人类中,BRWD1 是增强子可及性的主要协调因子,它与 TF 网络合作驱动晚期 B 细胞发育。