Institut de Recherches Cliniques de Montréal, Laboratory of Molecular Genetics, Montréal, Quebec, Canada.
Eur J Endocrinol. 2021 Jan;184(1):R1-R15. doi: 10.1530/EJE-20-0866.
Pioneer transcription factors have key roles in development as master regulators of cell fate specification. Only a small fraction of all transcription factors have the pioneer ability that confers access to target genomic DNA sites embedded in so-called 'closed' heterochromatin. This ability to seek and bind target sites within the silenced portion of the epigenome is the basis for their role in changing cell fate. Upon binding heterochromatin sites, pioneer factors trigger remodeling of chromatin from a repressed into an active organization. This action is typically exerted at enhancer regulatory sequences, thus allowing activation of new gene subsets. During pituitary development, the only pioneer with a well-documented role is Pax7 that specifies the intermediate lobe melanotrope cell fate. In this review, a particular focus is placed on this Pax7 function but its properties are also considered within the general context of pioneer factor action. Given their potent activity to reprogram gene expression, it is not surprising that many pioneers are associated with tumor development. Overexpression or chromosomal translocations leading to the production of chimeric pioneers have been implicated in different cancers. We review here the current knowledge on the mechanism of pioneer factor action.
先驱转录因子作为细胞命运特化的主调控因子,在发育中起着关键作用。只有一小部分转录因子具有先驱能力,可以进入所谓的“封闭”异染色质中嵌入的靶基因组 DNA 位点。这种在沉默的表观基因组部分中寻找和结合靶位点的能力是它们改变细胞命运的基础。与异染色质位点结合后,先驱因子触发染色质从抑制状态到活跃状态的重塑。这种作用通常在增强子调控序列中发挥,从而允许新的基因子集的激活。在垂体发育过程中,唯一具有明确记录的先驱因子是 Pax7,它指定中间叶黑色素细胞命运。在这篇综述中,特别关注了 Pax7 的这一功能,但也考虑了其在先驱因子作用的一般背景下的特性。鉴于它们在重新编程基因表达方面的强大活性,许多先驱因子与肿瘤的发展有关也就不足为奇了。过表达或染色体易位导致嵌合先驱因子的产生与不同的癌症有关。我们在这里回顾了先驱因子作用的机制的最新知识。