中尺度染色质封闭促进了活细胞中先驱转录因子的目标搜索

Zuhui Wang, Bo Wang, Di Niu, Chao Yin, Ying Bi, Claudia Cattoglio, Kyle M. Loh, Luke D. Lavis, Hao Ge, Wulan Deng
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摘要

先锋转录因子(PTFs)具有进入封闭染色质区域并启动细胞命运变化的独特能力,但其潜在机制仍然难以捉摸。在这里,我们描述了活细胞中以染色质为目标的 PTFs 的单分子动力学特征,揭示了一种显著的 "封闭目标搜索 "机制。FOXA1、FOXA2、SOX2、OCT4和KLF4等PTF比非PTF MYC更频繁地取样染色质,在细胞核内快速自由扩散和中尺度区内较慢的封闭扩散之间交替进行。超分辨显微镜显示,封闭染色质组织为中尺度核糖体致密域,在局部限制了 FOXA2 的扩散并丰富了其结合。我们确定了有别于DNA结合域的特定组蛋白相互作用无序区,它们对封闭染色质内的封闭目标搜索动力学和先驱活动至关重要。与其他因子的融合增强了先锋活性。动力学模拟表明,瞬时封闭可以通过缩短搜索时间和重复结合来提高目标结合率。我们的研究结果阐明了 PTF 如何识别并利用封闭染色质组织来访问靶标,揭示了基因调控的一个关键方面。
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Mesoscale chromatin confinement facilitates target search of pioneer transcription factors in live cells

Pioneer transcription factors (PTFs) possess the unique capability to access closed chromatin regions and initiate cell fate changes, yet the underlying mechanisms remain elusive. Here, we characterized the single-molecule dynamics of PTFs targeting chromatin in living cells, revealing a notable ‘confined target search’ mechanism. PTFs such as FOXA1, FOXA2, SOX2, OCT4 and KLF4 sampled chromatin more frequently than non-PTF MYC, alternating between fast free diffusion in the nucleus and slower confined diffusion within mesoscale zones. Super-resolved microscopy showed closed chromatin organized as mesoscale nucleosome-dense domains, confining FOXA2 diffusion locally and enriching its binding. We pinpointed specific histone-interacting disordered regions, distinct from DNA-binding domains, crucial for confined target search kinetics and pioneer activity within closed chromatin. Fusion to other factors enhanced pioneer activity. Kinetic simulations suggested that transient confinement could increase target association rate by shortening search time and binding repeatedly. Our findings illuminate how PTFs recognize and exploit closed chromatin organization to access targets, revealing a pivotal aspect of gene regulation.

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