Matsuo T
Department of Ophthalmology, Okayama University Medical School, Japan.
Jpn J Ophthalmol. 1993;37(3):215-51.
The two main ways to identify the genes involved in the process of morphogenesis are: 1) to analyze genetic causes in patients or animal models with developmental anomalies and 2) to elucidate patterns of the expression of genes by in situ hybridization during the normal development. In this report, these two methods were adopted to identify the genes involved in the morphogenesis of the eye. A unique mutation of the paired box (Pax)-6 gene (a kind of homeobox gene) was found in a new rat strain "rSey" which showed no induction of both lens and nasal placodes in the homozygote. One base "G" insertion in an exon of the genomic DNA gave rise to a new sequence, "GT", which served as an abnormal 5' splice site to generate an internal deletion in the messenger RNA. The homozygote was also known to have impaired migration of neural crest cells from the anterior midbrain, indicating that the Pax-6 gene would play a role in conducting migration of these neural crest cells. Neural crest-derived mesenchymal cells located around the lens vesicle in the optic cup of mouse embryos were positive for the expression of retinoic acid receptor genes, showing that retinoic acids played a role in the formation of such eye structures composed of neural crest-derived cells as the primary vitreous, corneal, iris, and ciliary stroma. Transcripts of the fibroblast growth factor receptor type 1 were found mainly in neuroepithelium of the optic cup of chick embryos, whereas those of the type 2 receptor were detected in neural crest-derived mesenchymal cells surrounding the optic cup. In contrast, the type 3 receptor was expressed mainly in the lens vesicles, suggesting that altogether 3 types of the fibroblast growth factor receptor would be involved in signaling among different structures as the optic cup, lens vesicle, and neural crest-derived mesenchyme. Receptors for activin, a member of the transforming growth factor beta superfamily, were expressed in the neuroepithelium of the optic cup and in the lens vesicle. In the light of these molecular biological findings, the roles of neural crest-derived cells and epithelial-mesenchymal interactions as well as the concept of positional information in the morphogenesis of the eye were discussed.
1)分析患有发育异常的患者或动物模型中的遗传原因;2)在正常发育过程中通过原位杂交阐明基因的表达模式。在本报告中,采用这两种方法来鉴定参与眼睛形态发生的基因。在一种新的大鼠品系“rSey”中发现了配对盒(Pax)-6基因(一种同源异型盒基因)的独特突变,该品系的纯合子中晶状体和鼻基板均未诱导形成。基因组DNA外显子中的一个碱基“G”插入产生了一个新序列“GT”,它作为异常的5'剪接位点,导致信使RNA内部缺失。已知纯合子中神经嵴细胞从前脑中部的迁移受损,这表明Pax-6基因在引导这些神经嵴细胞的迁移中起作用。小鼠胚胎视杯中位于晶状体泡周围的神经嵴衍生间充质细胞视黄酸受体基因表达呈阳性,表明视黄酸在由神经嵴衍生细胞组成的眼睛结构如初级玻璃体、角膜、虹膜和睫状体基质的形成中起作用。在鸡胚视杯的神经上皮中主要发现了1型成纤维细胞生长因子受体的转录本,而在视杯周围的神经嵴衍生间充质细胞中检测到了2型受体的转录本。相反,3型受体主要在晶状体泡中表达,这表明总共3种类型的成纤维细胞生长因子受体参与视杯、晶状体泡和神经嵴衍生间充质等不同结构之间的信号传导。激活素(转化生长因子β超家族的成员)的受体在视杯的神经上皮和晶状体泡中表达。根据这些分子生物学发现,讨论了神经嵴衍生细胞和上皮-间充质相互作用的作用以及位置信息概念在眼睛形态发生中的作用。