Skirball Institute of Biomolecular Medicine, Helen L. and Martin S. Kimmel Center for Biology and Medicine, and Department of Cell Biology, NYU School of Medicine, New York, NY 10016, USA.
Developmental Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Development. 2019 Apr 15;146(8):dev168153. doi: 10.1242/dev.168153.
The sensory nervous system of comprises cells with varied molecular and functional characteristics, and is, therefore, a powerful model for understanding mechanisms that generate neuronal diversity. We report here that VAB-3, a homolog of the homeodomain-containing protein Pax6, has opposing functions in regulating expression of a specific chemosensory fate. A homeodomain-only short isoform of VAB-3 is expressed in BAG chemosensory neurons, where it promotes gene expression and cell function. In other cells, a long isoform of VAB-3, comprising a Paired homology domain and a homeodomain, represses expression of ETS-5, a transcription factor required for expression of BAG fate. Repression of requires the Eyes Absent homolog EYA-1 and the Six-class homeodomain protein CEH-32. We determined sequences that mediate high-affinity binding of ETS-5, VAB-3 and CEH-32. The locus is enriched for ETS-5-binding sites but lacks sequences that bind VAB-3 and CEH-32, suggesting that these factors do not directly repress expression. We propose that a promoter-selection system together with lineage-specific expression of accessory factors allows VAB-3/Pax6 to either promote or repress expression of specific cell fates in a context-dependent manner. This article has an associated 'The people behind the papers' interview.
感觉神经系统由具有不同分子和功能特征的细胞组成,因此是理解产生神经元多样性机制的有力模型。我们在这里报告,VAB-3 是包含同源域的蛋白 Pax6 的同源物,它在调节特定化学感觉命运的表达中具有相反的功能。VAB-3 的仅含同源域的短亚型在 BAG 化学感觉神经元中表达,在那里它促进基因表达和细胞功能。在其他细胞中,VAB-3 的长亚型,包含一个配对同源域和一个同源域,抑制转录因子 ETS-5 的表达,ETS-5 是表达 BAG 命运所必需的。抑制需要 Eyes Absent 同源物 EYA-1 和 Six-class 同源域蛋白 CEH-32。我们确定了介导 ETS-5、VAB-3 和 CEH-32 高亲和力结合的序列。位点富含 ETS-5 结合位点,但缺乏结合 VAB-3 和 CEH-32 的序列,这表明这些因子不会直接抑制 表达。我们提出,启动子选择系统以及辅助因子的谱系特异性表达允许 VAB-3/Pax6 以依赖于上下文的方式促进或抑制特定细胞命运的表达。本文有一个相关的“论文背后的人物”访谈。