Department of Developmental Biology, Albert-Ludwigs-University of Freiburg, 79104, Freiburg, Germany.
Epigenetics and Neurobiology Unit, European Molecular Biology Laboratory, EMBL Rome, Adriano Buzzati-Traverso Campus, Via Ramarini 32, 00015, Monterotondo, RM, Italy.
Nat Commun. 2023 Sep 14;14(1):5677. doi: 10.1038/s41467-023-41507-z.
Zygotic genome activation (ZGA) in the development of flies, fish, frogs and mammals depends on pioneer-like transcription factors (TFs). Those TFs create open chromatin regions, promote histone acetylation on enhancers, and activate transcription. Here, we use the panel of single, double and triple mutants for zebrafish genome activators Pou5f3, Sox19b and Nanog, multi-omics and mathematical modeling to investigate the combinatorial mechanisms of genome activation. We show that Pou5f3 and Nanog act differently on synergistic and antagonistic enhancer types. Pou5f3 and Nanog both bind as pioneer-like TFs on synergistic enhancers, promote histone acetylation and activate transcription. Antagonistic enhancers are activated by binding of one of these factors. The other TF binds as non-pioneer-like TF, competes with the activator and blocks all its effects, partially or completely. This activator-blocker mechanism mutually restricts widespread transcriptional activation by Pou5f3 and Nanog and prevents premature expression of late developmental regulators in the early embryo.
合子基因组激活(ZGA)在果蝇、鱼类、青蛙和哺乳动物的发育过程中依赖于先驱样转录因子(TFs)。这些 TFs 可以创建开放染色质区域,促进增强子上的组蛋白乙酰化,并激活转录。在这里,我们使用斑马鱼基因组激活剂 Pou5f3、Sox19b 和 Nanog 的单、双和三突变体面板、多组学和数学建模来研究基因组激活的组合机制。我们表明,Pou5f3 和 Nanog 对协同和拮抗增强子类型的作用不同。Pou5f3 和 Nanog 都作为先驱样 TFs 结合在协同增强子上,促进组蛋白乙酰化并激活转录。拮抗增强子通过其中一个因子的结合而被激活。另一个 TF 作为非先驱样 TF 结合,与激活剂竞争并阻断其所有作用,部分或完全阻断。这种激活剂-阻断剂机制相互限制了 Pou5f3 和 Nanog 的广泛转录激活,并防止了晚期发育调节剂在早期胚胎中过早表达。