Department of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Development. 2013 Aug;140(16):3445-55. doi: 10.1242/dev.096164.
The neural crest comprises multipotent precursor cells that are induced at the neural plate border by a series of complex signaling and genetic interactions. Several transcription factors, termed neural crest specifiers, are necessary for early neural crest development; however, the nature of their interactions and regulation is not well understood. Here, we have established that the PR/SET domain-containing transcription factor Prdm1a is co-expressed with two essential neural crest specifiers, foxd3 and tfap2a, at the neural plate border. Through rescue experiments, chromatin immunoprecipitation and reporter assays, we have determined that Prdm1a directly binds to and transcriptionally activates enhancers for foxd3 and tfap2a and that they are functional, direct targets of Prdm1a at the neural plate border. Additionally, analysis of dominant activator and dominant repressor Prdm1a constructs suggests that Prdm1a is required both as a transcriptional activator and transcriptional repressor for neural crest development in zebrafish embryos.
神经嵴由多能前体细胞组成,这些前体细胞在神经板边缘受到一系列复杂的信号和遗传相互作用的诱导。一些转录因子,称为神经嵴特化因子,对于早期神经嵴发育是必需的;然而,它们的相互作用和调控的本质尚不清楚。在这里,我们已经确定 PR/SET 结构域包含的转录因子 Prdm1a 与两个必需的神经嵴特化因子 foxd3 和 tfap2a 在神经板边缘共同表达。通过挽救实验、染色质免疫沉淀和报告基因分析,我们已经确定 Prdm1a 直接结合并转录激活 foxd3 和 tfap2a 的增强子,并且它们是 Prdm1a 在神经板边缘的功能性直接靶标。此外,对显性激活子和显性抑制子 Prdm1a 构建体的分析表明,Prdm1a 对于斑马鱼胚胎的神经嵴发育既需要作为转录激活因子,也需要作为转录抑制因子。
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