Riddiford Nick, Schlosser Gerhard
School of Natural Sciences, National University of Ireland, Galway, Ireland.
Regenerative Medicine Institute (REMEDI), National University of Ireland, Galway, Ireland.
Elife. 2016 Aug 31;5:e17666. doi: 10.7554/eLife.17666.
The pre-placodal ectoderm, marked by the expression of the transcription factor Six1 and its co-activator Eya1, develops into placodes and ultimately into many cranial sensory organs and ganglia. Using RNA-Seq in we screened for presumptive direct placodal target genes of Six1 and Eya1 by overexpressing hormone-inducible constructs of Six1 and Eya1 in pre-placodal explants, and blocking protein synthesis before hormone-inducing nuclear translocation of Six1 or Eya1. Comparing the transcriptome of explants with non-induced controls, we identified hundreds of novel Six1/Eya1 target genes with potentially important roles for placode development. Loss-of-function studies confirmed that target genes encoding known transcriptional regulators of progenitor fates (e.g. Sox2, Hes8) and neuronal/sensory differentiation (e.g. Ngn1, Atoh1, Pou4f1, Gfi1) require Six1 and Eya1 for their placodal expression. Our findings provide insights into the gene regulatory network regulating placodal neurogenesis downstream of Six1 and Eya1 suggesting new avenues of research into placode development and disease.
以转录因子Six1及其共激活因子Eya1的表达为标志的前板层外胚层发育成板层,最终发育成许多颅感觉器官和神经节。我们在[具体实验条件未给出]中使用RNA测序技术,通过在前板层外植体中过表达Six1和Eya1的激素诱导型构建体,并在激素诱导Six1或Eya1核转位之前阻断蛋白质合成,筛选Six1和Eya1可能的直接板层靶基因。将外植体的转录组与未诱导的对照进行比较,我们鉴定出数百个对板层发育具有潜在重要作用的新型Six1/Eya1靶基因。功能丧失研究证实,编码已知祖细胞命运转录调节因子(如Sox2、Hes8)和神经元/感觉分化相关因子(如Ngn1、Atoh1、Pou4f1、Gfi1)的靶基因在板层中的表达需要Six1和Eya1。我们的研究结果为Six1和Eya1下游调节板层神经发生的基因调控网络提供了见解,为板层发育和疾病的研究提出了新的途径。