Department of Molecular & Cell Biology, Center for Integrative Genomics, University of California, Berkeley, 571 Life Sciences Addition, #3200, Berkeley, CA 94720-3200, USA.
Dev Biol. 2011 Jan 15;349(2):378-86. doi: 10.1016/j.ydbio.2010.10.030. Epub 2010 Oct 28.
Neuronal subtypes originate from an undifferentiated neural epithelium that is progressively divided into progenitor domains by homeodomain transcription factors such as members of the Nkx family. Here we report the functional analysis of Nkx6.1 and Nkx6.2 in Xenopus. While Nkx6.2 is expressed early in a large region of the medial neural plate, Nkx6.1 is restricted to a region overlapping with the region of motor neuron formation. By mRNA injection we show that both can inhibit primary neurogenesis as well as expression of intermediate neural plate markers. However, they do not form auto-regulatory loops and fail to induce ectopic motor neurons as they do in the chick. Using morpholino-mediated knockdown in Xenopus laevis and Xenopus tropicalis we show that Nkx6.1 knockdown results in paralyzed tadpoles. Using DiI labeling and immunohistochemistry we show that the underlying mechanism is a failure of spinal motor neurons to extend axons to their targets. Analysis of neural pattern reveals that ventral Lhx3+ and Pax2+ interneurons are dependent on Nkx6.1 function, but overall neural patterning is not. This study illustrates that while important aspects of Nkx6 gene function are conserved in vertebrate neural patterning, others are not.
神经亚型起源于未分化的神经上皮,通过同源域转录因子(如 Nkx 家族成员)的作用逐渐分为祖细胞区。在这里,我们报告了 Nkx6.1 和 Nkx6.2 在非洲爪蟾中的功能分析。虽然 Nkx6.2 在中侧神经板的一个大区域中早期表达,但 Nkx6.1 仅限于与运动神经元形成区域重叠的区域。通过 mRNA 注射,我们表明两者都可以抑制原神经发生以及中间神经板标记物的表达。然而,它们不会形成自我调节回路,也不会像在鸡中那样诱导异位运动神经元。我们使用在非洲爪蟾和热带爪蟾中的 morpholino 介导的敲低实验表明,Nkx6.1 的敲低导致瘫痪的蝌蚪。通过 DiI 标记和免疫组织化学,我们表明潜在的机制是脊髓运动神经元无法将轴突延伸到其靶标。神经模式的分析表明,腹侧 Lhx3+和 Pax2+中间神经元依赖于 Nkx6.1 功能,但总体神经模式不受影响。本研究表明,虽然 Nkx6 基因功能的重要方面在脊椎动物神经模式中是保守的,但其他方面则不是。