Suster Maximiliano L, Kania Artur, Liao Meijiang, Asakawa Kazuhide, Charron Frederic, Kawakami Koichi, Drapeau Pierre
Centre for Research in Neuroscience, Research Institute of the McGill University Health Centre, Montréal, Québec H3T 1J4 Canada.
Dev Biol. 2009 Jan 15;325(2):422-33. doi: 10.1016/j.ydbio.2008.10.004. Epub 2008 Oct 18.
Spinal interneurons are key components of locomotor circuits, driving such diverse behaviors as swimming in fish and walking in mammals. Recent work has linked the expression of evolutionarily conserved transcription factors to key features of interneurons in diverse species, raising the possibility that these interneurons are functionally related. Consequently, the determinants of interneuron subtypes are predicted to share conserved cis-regulation in vertebrates with very different spinal cords. Here, we establish a link between cis-regulation and morphology of spinal interneurons that express the Evx1 homeodomain transcription factor from fish to mammals. Using comparative genomics, and complementary transgenic approaches, we have identified a novel enhancer of evx1, that includes two non-coding elements conserved in vertebrates. We show that pufferfish evx1 transgenes containing this enhancer direct reporter expression to a subset of spinal commissural interneurons in zebrafish embryos. Pufferfish, zebrafish and mouse evx1 downstream genomic enhancers label selectively Evx1(+) V0 commissural interneurons in chick and rat embryos. By dissecting the zebrafish evx1 enhancer, we identify a role for a 25 bp conserved cis-element in V0-specific gene expression. Our findings support the notion that spinal interneurons shared between distantly related vertebrates, have been maintained in part via the preservation of highly conserved cis-regulatory modules.
脊髓中间神经元是运动回路的关键组成部分,驱动着诸如鱼类游泳和哺乳动物行走等多种行为。最近的研究工作已将进化上保守的转录因子的表达与不同物种中间神经元的关键特征联系起来,这增加了这些中间神经元在功能上相关的可能性。因此,预计中间神经元亚型的决定因素在具有非常不同脊髓的脊椎动物中共享保守的顺式调控。在这里,我们建立了从鱼类到哺乳动物表达Evx1同源结构域转录因子的脊髓中间神经元的顺式调控与形态之间的联系。利用比较基因组学和互补的转基因方法,我们鉴定出了一个新的evx1增强子,它包含在脊椎动物中保守的两个非编码元件。我们表明,含有该增强子的河豚evx1转基因将报告基因表达导向斑马鱼胚胎中的一部分脊髓连合中间神经元。河豚、斑马鱼和小鼠的evx1下游基因组增强子在鸡和大鼠胚胎中选择性地标记Evx1(+) V0连合中间神经元。通过剖析斑马鱼evx1增强子,我们确定了一个25bp保守顺式元件在V0特异性基因表达中的作用。我们的研究结果支持这样一种观点,即远缘相关脊椎动物共有的脊髓中间神经元,部分是通过高度保守的顺式调控模块的保留而得以维持的。