Stenkamp Deborah L, Calderwood John L, Van Niel Ellen E, Daniels Lawrence M, Gonzalez-Fernandez Federico
Department of Biological Sciences, University of Idaho, Moscow, ID 83844-3051, USA.
Mol Vis. 2005 Sep 30;11:833-45.
Despite decades of investigation, the function of interphotoreceptor retinoid binding protein (IRBP), the most abundant protein in the interphotoreceptor matrix of vertebrates, remains enigmatic. Roles for IRBP in the visual cycle of rod photoreceptors and in the independent visual cycle of cone photoreceptors have been suggested, yet very little is known of the biology of IRBP in cone-dominant retinas, such as those of diurnal birds. Our aim was to identify and characterize expression of the IRBP of the cone-dominant chicken (Gallus gallus domesticus).
Chicken IRBP mRNA was identified by PCR cloning. Primary protein structure, genomic organization, and phylogenies were determined through comparative sequence analyses. Expression of IRBP mRNA was characterized by northern analysis and by in situ hybridization on cryosectioned chicken retina. Expression of the IRBP protein was characterized by western blotting and by indirect immunofluorescence on cryosectioned retina and on retinal whole mounts.
The chicken IRBP gene encodes a secreted protein with a predicted 1,252 amino acid length. The gene structure for chicken IRBP resembles that of most other vertebrates, with four homologous, modular repeats and introns within only the fourth module. Each module is more homologous with the corresponding module in other species than it is with the remaining chicken modules. Chicken retinal tissue contains a single IRBP mRNA transcript of approximately 4.8 kb and western analysis of chicken retina shows a single major band of 140 kDa. Chicken IRBP mRNA is expressed exclusively by retinal photoreceptor cells and the intensity of the hybridization signal shows light/dark rhythmicity. The IRBP protein is localized to the interphotoreceptor matrix of the chicken retina and to intracellular regions of photoreceptors, with a spatial distribution indicating an association with cone outer segments.
The high degree of conservation of IRBP's primary structure, genomic organization, and cell-specific expression within the retinas of all vertebrates examined to date, including those with cone-dominant retinas, implies a conserved role for IRBP in photoreceptor function and/or health. Expression of chicken IRBP and its mRNA are functionally regulated. This report provides a necessary first step to explore a specific function for IRBP in the cone visual cycle.
尽管经过了数十年的研究,但脊椎动物光感受器间基质中最丰富的蛋白质——光感受器间类视黄醇结合蛋白(IRBP)的功能仍然成谜。有人提出IRBP在视杆光感受器的视觉循环以及视锥光感受器独立的视觉循环中发挥作用,但对于像昼行性鸟类这样以视锥细胞为主的视网膜中IRBP的生物学特性却知之甚少。我们的目的是鉴定并描述以视锥细胞为主的鸡(家鸡)IRBP的表达情况。
通过PCR克隆鉴定鸡IRBP mRNA。通过比较序列分析确定其一级蛋白质结构、基因组组织和系统发育。通过Northern分析以及对冷冻切片鸡视网膜进行原位杂交来表征IRBP mRNA的表达。通过蛋白质印迹以及对冷冻切片视网膜和视网膜整装片进行间接免疫荧光来表征IRBP蛋白的表达。
鸡IRBP基因编码一种预测长度为1252个氨基酸的分泌蛋白。鸡IRBP的基因结构与大多数其他脊椎动物相似,有四个同源的模块化重复序列,且仅在第四个模块中有内含子。每个模块与其他物种中相应模块的同源性高于与鸡的其他模块的同源性。鸡视网膜组织含有一条约4.8 kb的单一IRBP mRNA转录本,对鸡视网膜进行的蛋白质印迹分析显示有一条140 kDa的主要条带。鸡IRBP mRNA仅由视网膜光感受器细胞表达,杂交信号强度呈现明/暗节律性。IRBP蛋白定位于鸡视网膜的光感受器间基质以及光感受器的细胞内区域,其空间分布表明与视锥细胞外段有关联。
迄今为止,在所有被检测的脊椎动物视网膜中,包括那些以视锥细胞为主的视网膜,IRBP的一级结构、基因组组织和细胞特异性表达都具有高度保守性,这意味着IRBP在光感受器功能和/或健康方面具有保守作用。鸡IRBP及其mRNA的表达受到功能调控。本报告为探索IRBP在视锥细胞视觉循环中的特定功能提供了必要的第一步。