Institute for Regenerative Medicine, Epigenetics Institute, Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104-5157, USA; email:
Annu Rev Genet. 2020 Nov 23;54:367-385. doi: 10.1146/annurev-genet-030220-015007. Epub 2020 Sep 4.
Pioneer transcription factors have the intrinsic biochemical ability to scan partial DNA sequence motifs that are exposed on the surface of a nucleosome and thus access silent genes that are inaccessible to other transcription factors. Pioneer factors subsequently enable other transcription factors, nucleosome remodeling complexes, and histone modifiers to engage chromatin, thereby initiating the formation of an activating or repressive regulatory sequence. Thus, pioneer factors endow the competence for fate changes in embryonic development, are essential for cellular reprogramming, and rewire gene networks in cancer cells. Recent studies with reconstituted nucleosomes in vitro and chromatin binding in vivo reveal that pioneer factors can directly perturb nucleosome structure and chromatin accessibility in different ways. This review focuses on our current understanding of the mechanisms by which pioneer factors initiate gene network changes and will ultimately contribute to our ability to control cell fates at will.
先驱转录因子具有内在的生化能力,可以扫描核小体表面暴露的部分 DNA 序列基序,从而接触到其他转录因子无法接触的沉默基因。先驱因子随后使其他转录因子、核小体重塑复合物和组蛋白修饰因子与染色质结合,从而启动激活或抑制性调节序列的形成。因此,先驱因子赋予胚胎发育中命运变化的能力,对于细胞重编程和癌细胞中的基因网络重排至关重要。最近在体外重建核小体和体内染色质结合的研究表明,先驱因子可以以不同的方式直接干扰核小体结构和染色质可及性。本综述重点介绍了我们目前对先驱因子启动基因网络变化机制的理解,这最终将有助于我们随心所欲地控制细胞命运。