Chan Kwok Keung, Chen Yuk Shan, Yau Tai On, Fu Ming, Lui Vincent Chi Hang, Tam Paul Kwong Hang, Sham Mai Har
Department of Biochemistry, The University of Hong Kong, Faculty of Medicine Building, Pokfulam, Hong Kong SAR, China.
Dev Dyn. 2005 Jun;233(2):473-83. doi: 10.1002/dvdy.20347.
The neural and glial cells of the intrinsic ganglia of the enteric nervous system (ENS) are derived from the hindbrain neural crest at the vagal level. The Hoxb3 gene is expressed in the vagal neural crest and in the enteric ganglia of the developing gut during embryogenesis. We have identified a cis-acting enhancer element b3IIIa in the Hoxb3 gene locus. In this study, by transgenic mice analysis, we examined the tissue specificity of the b3IIIa enhancer element using the lacZ reporter gene, with emphasis on the vagal neural crest cells and their derivatives in the developing gut. We found that the b3IIIa-lacZ transgene marks only the vagal region and not the trunk or sacral region. Using cellular markers, we showed that the b3IIIa-lacZ transgene was expressed in a subset of enteric neuroblasts during early development of the gut, and the expression was maintained in differentiated neurons of the myenteric plexus at later stages. The specificity of the b3IIIa enhancer in directing gene expression in the developing ENS was further supported by genetic analysis using the Dom mutant, a spontaneous mouse model of Hirschsprung's disease characterized by the absence of enteric ganglia in the distal gut. The colonization of lacZ-expressing cells in the large intestine was incomplete in all the Dom/b3IIIa-lacZ hybrid mutants we examined. To our knowledge, this is the only vagal neural crest-specific genetic regulatory element identified to date. This element could be used for a variety of genetic manipulations and in establishing transgenic mouse models for studying the development of the ENS.
肠神经系统(ENS)内在神经节的神经细胞和神经胶质细胞源自迷走神经水平的后脑神经嵴。Hoxb3基因在胚胎发育过程中于迷走神经嵴以及发育中肠道的肠神经节中表达。我们在Hoxb3基因座中鉴定出一个顺式作用增强子元件b3IIIa。在本研究中,通过转基因小鼠分析,我们利用lacZ报告基因检测了b3IIIa增强子元件的组织特异性,重点关注发育中肠道的迷走神经嵴细胞及其衍生物。我们发现b3IIIa - lacZ转基因仅标记迷走神经区域,而非躯干或骶骨区域。使用细胞标记物,我们表明b3IIIa - lacZ转基因在肠道早期发育过程中在一部分肠成神经细胞中表达,并且在后期的肌间神经丛分化神经元中持续表达。使用Dom突变体进行的遗传分析进一步支持了b3IIIa增强子在发育中的ENS中指导基因表达的特异性,Dom突变体是一种先天性巨结肠的自发小鼠模型,其特征是远端肠道中缺乏肠神经节。在我们检测的所有Dom/b3IIIa - lacZ杂交突变体中,大肠中表达lacZ的细胞定植均不完全。据我们所知,这是迄今为止鉴定出的唯一迷走神经嵴特异性遗传调控元件。该元件可用于各种基因操作以及建立转基因小鼠模型以研究ENS的发育。