Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.
Department of Genetics, Yale University School of Medicine, New Haven, CT 06510, USA.
Mol Cell. 2022 Mar 3;82(5):986-1002.e9. doi: 10.1016/j.molcel.2022.01.024. Epub 2022 Feb 18.
Upon fertilization, embryos undergo chromatin reprogramming and genome activation; however, the mechanisms that regulate these processes are poorly understood. Here, we generated a triple mutant for Nanog, Pou5f3, and Sox19b (NPS) in zebrafish and found that NPS pioneer chromatin opening at >50% of active enhancers. NPS regulate acetylation across core histones at enhancers and promoters, and their function in gene activation can be bypassed by recruiting histone acetyltransferase to individual genes. NPS pioneer chromatin opening individually, redundantly, or additively depending on sequence context, and we show that high nucleosome occupancy facilitates NPS pioneering activity. Nucleosome position varies based on the input of different transcription factors (TFs), providing a flexible platform to modulate pioneering activity. Altogether, our results illuminate the sequence of events during genome activation and offer a conceptual framework to understand how pioneer factors interpret the genome and integrate different TF inputs across cell types and developmental transitions.
受精后,胚胎经历染色质重编程和基因组激活;然而,调节这些过程的机制知之甚少。在这里,我们在斑马鱼中生成了 Nanog、Pou5f3 和 Sox19b(NPS)的三重突变体,发现 NPS 在 >50%的活性增强子处开启先驱染色质。NPS 调节增强子和启动子处核心组蛋白的乙酰化,并且通过将组蛋白乙酰转移酶募集到单个基因,可以绕过它们在基因激活中的功能。NPS 先驱染色质根据序列上下文单独、冗余或累加地打开,我们表明高核小体占有率促进了 NPS 的先驱活性。核小体位置基于不同转录因子(TFs)的输入而变化,为调节先驱活性提供了一个灵活的平台。总的来说,我们的结果阐明了基因组激活过程中的事件顺序,并提供了一个概念框架,以了解先驱因子如何解释基因组,并整合不同 TF 在细胞类型和发育转变中的输入。