Department of Biology, University of South Dakota, Vermillion, South Dakota, USA.
Dev Dyn. 2011 Jul;240(7):1756-68. doi: 10.1002/dvdy.22675.
The spatially restricted expression of cadherin-7 to the intermediate domain of the neural epithelium and in migrating neural crest cells during early neural development is potentially regulated by multiple signaling inputs. To identify the regulatory modules involved in regulation of cadherin-7, evolutionary conserved non-coding sequences in the cadherin-7 locus were analyzed. This led to the identification of an evolutionary conserved region of 606 bp (ECR1) that together with the cadherin-7 promoter recapitulates endogenous cadherin-7 expression in intermediate neural tube, spinal motor neurons, interneurons, and dorsal root ganglia. Deletion analysis of ECR1 revealed a 19-bp block that is essential for ECR1 enhancer activity, while two separate blocks of 10 and 12 bp were found to be essential for ECR1 silencer activity in the dorsal and ventral neural epithelium, respectively. Together, these data provide an insight into tissue-specific regulatory regions that might be involved in regulation of cadherin-7 gene expression.
在早期神经发育过程中,神经上皮的中间域和迁移中的神经嵴细胞中 cadherin-7 的空间限制表达可能受到多种信号输入的调节。为了鉴定参与 cadherin-7 调节的调节模块,分析了 cadherin-7 基因座中的进化保守非编码序列。这导致鉴定了一个 606 bp 的进化保守区域(ECR1),该区域与 cadherin-7 启动子一起在中间神经管、脊髓运动神经元、中间神经元和背根神经节中重新表达内源性 cadherin-7 表达。ECR1 的缺失分析显示,19-bp 块对于 ECR1 增强子活性是必需的,而分别在背侧和腹侧神经上皮中发现了两个独立的 10-bp 和 12-bp 块对于 ECR1 沉默子活性是必需的。这些数据共同提供了对可能参与 cadherin-7 基因表达调节的组织特异性调节区域的深入了解。