Taneyhill Lisa A, Coles Edward G, Bronner-Fraser Marianne
Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
Development. 2007 Apr;134(8):1481-90. doi: 10.1242/dev.02834. Epub 2007 Mar 7.
The neural crest, a transient population of migratory cells, forms the craniofacial skeleton and peripheral nervous system, among other derivatives in vertebrate embryos. The transcriptional repressor Snail2 is thought to be crucial for the epithelial-to-mesenchymal transition (EMT) that promotes neural crest delamination from the neural tube; however, little is known about its downstream targets. To this end, we depleted avian Snail2 in the premigratory neural crest using morpholino antisense oligonucleotides and examined effects on potential targets by quantitative PCR. Several dorsal neural tube genes were upregulated by alleviating Snail2 repression; moreover, the cell adhesion molecule cadherin6B was derepressed within 30 minutes of blocking Snail2 translation. Examination of the chick cadherin6B genomic sequence reveals that the regulatory region contains three pairs of clustered E boxes, representing putative Snail2 binding sites. Furthermore, in vivo and in vitro biochemical analyses demonstrate that Snail2 directly binds to these sites and regulates cadherin6B transcription. These results are the first to describe a direct target of Snail2 repression in vivo and in the context of the EMT that characterizes neural crest development.
神经嵴是一群短暂迁移的细胞,在脊椎动物胚胎中形成颅面骨骼和周围神经系统以及其他衍生物。转录抑制因子Snail2被认为对促进神经嵴从神经管分层的上皮-间充质转化(EMT)至关重要;然而,对其下游靶点知之甚少。为此,我们使用吗啉代反义寡核苷酸在迁移前的神经嵴中耗尽禽源Snail2,并通过定量PCR检测对潜在靶点的影响。通过减轻Snail2的抑制作用,几个背侧神经管基因被上调;此外,在阻断Snail2翻译后30分钟内,细胞粘附分子钙粘蛋白6B的表达被解除抑制。对鸡钙粘蛋白6B基因组序列的研究表明,调控区域包含三对成簇的E盒,代表假定的Snail2结合位点。此外,体内和体外生化分析表明,Snail2直接结合这些位点并调节钙粘蛋白6B的转录。这些结果首次描述了在体内以及在表征神经嵴发育的EMT背景下Snail2抑制的直接靶点。