Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Division of Developmental Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, 45267, USA.
Dev Biol. 2022 Sep;489:34-46. doi: 10.1016/j.ydbio.2022.05.019. Epub 2022 May 31.
Patterning of the anterior-posterior axis is fundamental to animal development. The Wnt pathway plays a major role in this process by activating the expression of posterior genes in animals from worms to humans. This observation raises the question of whether the Wnt pathway or other regulators control the expression of the many anterior-expressed genes. We found that the expression of five anterior-specific genes in Caenorhabditis elegans embryos depends on the Wnt pathway effectors pop-1/TCF and sys-1/β-catenin. We focused further on one of these anterior genes, ref-2/ZIC, a conserved transcription factor expressed in multiple anterior lineages. Live imaging of ref-2 mutant embryos identified defects in cell division timing and position in anterior lineages. Cis-regulatory dissection identified three ref-2 transcriptional enhancers, one of which is necessary and sufficient for anterior-specific expression. This enhancer is activated by the T-box transcription factors TBX-37 and TBX-38, and surprisingly, concatemerized TBX-37/38 binding sites are sufficient to drive anterior-biased expression alone, despite the broad expression of TBX-37 and TBX-38. Taken together, our results highlight the diverse mechanisms used to regulate anterior expression patterns in the embryo.
前后轴的模式形成对于动物的发育至关重要。Wnt 通路通过在从线虫到人类的动物中激活后基因的表达,在这个过程中发挥着主要作用。这一观察结果提出了这样一个问题:是否是 Wnt 通路或其他调节剂控制着许多前表达基因的表达。我们发现,秀丽隐杆线虫胚胎中五个前体特异性基因的表达依赖于 Wnt 通路效应物 pop-1/TCF 和 sys-1/β-catenin。我们进一步关注了其中一个前体基因 ref-2/ZIC,这是一种在多个前体谱系中表达的保守转录因子。ref-2 突变体胚胎的实时成像鉴定出在前体谱系中细胞分裂时间和位置的缺陷。顺式调控区剖析鉴定出三个 ref-2 转录增强子,其中一个对于前体特异性表达是必需和充分的。这个增强子被 T 盒转录因子 TBX-37 和 TBX-38 激活,令人惊讶的是,串联的 TBX-37/38 结合位点足以单独驱动前体偏向表达,尽管 TBX-37 和 TBX-38 的表达广泛。总之,我们的结果强调了在胚胎中调节前体表达模式的多种机制。