Takada Hitomi, Hattori Daisuke, Kitayama Atsushi, Ueno Naoto, Taira Masanori
Department of Biological Sciences, Graduate School of Science, University of Tokyo, Japan.
Dev Biol. 2005 Jul 1;283(1):253-67. doi: 10.1016/j.ydbio.2005.04.020.
The midbrain-hindbrain boundary (MHB) acts as a local organizer in the development of the CNS in vertebrates. Previously, we identified an MHB-specific bHLH-WRPW transcriptional repressor gene, Xenopus Hes-related 1 (XHR1), which is initially expressed in the presumptive MHB (pre-MHB) region at the early gastrula stage. To better understand the gene cascades involved in MHB formation, we investigated the genes downstream from XHR1 by differential screening using a Xenopus cDNA macroarray and a dexamethasone (DEX)-inducible, dominant-negative transcriptional activator construct of XHR1 (XHR1-VP16-GR). Among the newly identified candidate target genes of XHR1 were Enhancer of split-related genes (ESR1, ESR3/7, and ESR9) and Xenopus laevis cleavage 2 (XLCL2). XHR1-VP16-GR induced the expression of the ESR genes and XLCL2 as well as Xdelta1, Xngnr1, and XHR1 itself in the presence of DEX even after pretreatment with the protein synthesis inhibitor, cycloheximide. This suggests that these genes are direct targets of XHR1. XHR1-knockdown experiments with antisense morpholino oligos and ectopic expression of wild-type XHR1 revealed that XHR1 is necessary and sufficient to repress ESR genes in the pre-MHB region. Misexpression of the ESR genes in the pre-MHB region repressed the MHB marker gene, Pax2, suggesting that the repression of the ESR genes by XHR1 is at least partly required for the early development of the pre-MHB. Our data also show that XHR1 is not activated by Notch signaling, differing from ESR genes. Taken together, we propose a model in which XHR1 defines the pre-MHB region as a prepattern gene by repressing those possible direct target genes.
中脑-后脑边界(MHB)在脊椎动物中枢神经系统(CNS)发育过程中起着局部组织者的作用。此前,我们鉴定出一个MHB特异性的bHLH-WRPW转录抑制基因,即非洲爪蟾Hes相关基因1(XHR1),它最初在原肠胚早期的预定MHB(pre-MHB)区域表达。为了更好地理解参与MHB形成的基因级联反应,我们通过使用非洲爪蟾cDNA宏阵列和XHR1的地塞米松(DEX)诱导型显性负性转录激活构建体(XHR1-VP16-GR)进行差异筛选,研究了XHR1下游的基因。在新鉴定出的XHR1候选靶基因中,有分裂相关增强子基因(ESR1、ESR3/7和ESR9)以及非洲爪蟾卵裂2(XLCL2)。即使在用蛋白质合成抑制剂环己酰亚胺预处理后,在DEX存在的情况下,XHR1-VP16-GR仍能诱导ESR基因、XLCL2以及Xdelta1、Xngnr1和XHR1自身的表达。这表明这些基因是XHR1的直接靶标。用反义吗啉代寡核苷酸进行的XHR1敲低实验以及野生型XHR1的异位表达表明,XHR1对于在pre-MHB区域抑制ESR基因是必要且充分的。ESR基因在pre-MHB区域的错误表达抑制了MHB标记基因Pax2,这表明XHR1对ESR基因的抑制至少部分是pre-MHB早期发育所必需的。我们的数据还表明,与ESR基因不同,XHR1不会被Notch信号激活。综上所述,我们提出了一个模型,其中XHR1通过抑制那些可能的直接靶基因,将pre-MHB区域定义为一个前模式基因。