Pan Yi, Nekkalapudi Srivamsi, Kelly Lisa E, El-Hodiri Heithem M
Center for Molecular and Human Genetics, Columbus Children's Research Institute, Ohio State University, Columbus, OH 43205, USA.
Invest Ophthalmol Vis Sci. 2006 Oct;47(10):4245-53. doi: 10.1167/iovs.06-0167.
The retinal homeobox (Rx) gene plays an essential role in retinal development. An Rx-like (Rx-L) gene from Xenopus laevis has been identified. The purpose of this study was to analyze the function of Rx-L in the developing retina.
DNA-binding properties of Rx-L were analyzed by electrophoretic mobility shift assay (EMSA), with in vitro-translated proteins and radiolabeled oligonucleotide probe. The Rx-L expression pattern was analyzed by in situ hybridization using whole or sectioned embryos and digoxigenin-labeled antisense riboprobes. Rx-L loss of function was studied by using antisense morpholino oligonucleotides targeted to the Rx-L translation initiation site. Embryos injected with control or Rx-L morpholinos were analyzed at stage 41 or 45.
Rx-L shares homology with Rx at the homeo-, OAR, and Rx domains, but lacks an octapeptide motif. Rx-L is expressed in the developing retina beginning in the early tailbud stage. In the maturing retina, Rx-L expression is restricted primarily to the developing photoreceptor layer and the ciliary marginal zone. Rx-L can bind a photoreceptor conserved element-1 (PCE-1) oligonucleotide, an element conserved among all known photoreceptor gene promoters. In a promoter activity assay, Rx-L functions as a stronger transcriptional activator than Rx. Antisense morpholino-mediated knockdown of Rx-L expression resulted in a decrease in rhodopsin and red cone opsin expression levels in Xenopus retinas. Injection of the Rx-L antisense morpholino oligonucleotide also resulted in a decrease in the length of both rod and cone outer segments.
The results suggest that Rx-L functions to regulate rod and cone development by activating photoreceptor-specific gene expression.
视网膜同源框(Rx)基因在视网膜发育中起关键作用。已鉴定出非洲爪蟾的一个类Rx(Rx-L)基因。本研究的目的是分析Rx-L在发育中的视网膜中的功能。
通过电泳迁移率变动分析(EMSA),利用体外翻译的蛋白质和放射性标记的寡核苷酸探针分析Rx-L的DNA结合特性。使用完整或切片胚胎以及地高辛标记的反义核糖探针通过原位杂交分析Rx-L的表达模式。通过使用靶向Rx-L翻译起始位点的反义吗啉代寡核苷酸研究Rx-L的功能丧失。在第41或45阶段分析注射了对照或Rx-L吗啉代的胚胎。
Rx-L在同源结构域、OAR结构域和Rx结构域与Rx具有同源性,但缺乏八肽基序。Rx-L从早期尾芽阶段开始在发育中的视网膜中表达。在成熟的视网膜中,Rx-L的表达主要局限于发育中的光感受器层和睫状边缘区。Rx-L可以结合光感受器保守元件-1(PCE-1)寡核苷酸,这是所有已知光感受器基因启动子中保守的元件。在启动子活性测定中,Rx-L作为比Rx更强的转录激活因子发挥作用。反义吗啉代介导的Rx-L表达敲低导致非洲爪蟾视网膜中视紫红质和红锥视蛋白表达水平降低。注射Rx-L反义吗啉代寡核苷酸也导致视杆和视锥外段长度减少。
结果表明,Rx-L通过激活光感受器特异性基因表达来调节视杆和视锥的发育。