Gonzalez-Fernandez F, Healy J I
Department of Pathology, University of Virginia Medical Center, Charlottesville 22908.
J Cell Biol. 1990 Dec;111(6 Pt 1):2775-84. doi: 10.1083/jcb.111.6.2775.
Interphotoreceptor retinol-binding protein (IRBP), the major protein component of the subretinal space, is in a strategic position to mediate cellular interactions between the retinal pigmented epithelium (RPE) and the neural retina. While IRBP appears to be involved in vitamin A transport during the visual cycle in the adult, the role of this protein during eye development has not been determined. As a first step to understanding the role of IRBP during retinal development, we have studied the expression of the mRNA for this glycolipoprotein during photoreceptor differentiation in the rat. A rat neural retina cDNA library was prepared from which an IRBP clone was isolated. The clone contains an open reading frame followed by a 3' noncoding sequence ending in 10 adenosine residues. The coding region has an identity of 83.9 and 82.5% with the nucleotide sequence of human and bovine IRBP, respectively. Rats (Sprague-Dawley, Wistar, and Royal College of Surgeon pink-eyed controls) have a 6.4 and a 5.2-kb mRNA for IRBP which are present in a 1:4 ratio and thus are the only vertebrate known to definitely have more than one major form of the IRBP message. Genomic Southern blots are consistent with the hypothesis that there is only one allele of the IRBP gene, suggesting that the two forms are produced by alternative processing of the mRNA. To generate an antisense RNA probe for use in molecular titration assays and Northern blots, an Eco RI-Bam HI fragment from the coding region was subcloned in between flanking Sp6 and T7 promoters. Total RNA was prepared from undissected rat globes from postnatal days p0-p22. The expression of the mRNA for IRBP was studied by Northern blots and the level of the transcripts determined by solution hybridization assays. Approximately 10(5) IRBP mRNA transcripts/micrograms total eye RNA are present at birth. This increases to a final level of 3.1 X 10(6) transcripts/micrograms total RNA by p9. The one-half maximal level of the mRNA occurs at p4.2 which is 2 wk before the one-half maximal level of IRBP is reached in the subretinal space (Gonzalez-Fernandez, F., R. A. Landers, P. A. Glazebrook, S.-L. Fong, G. I. Liou, D. M. K. Lam, and C. D. B. Bridges. 1984. J. Cell Biol. 99:2092-2098). The expression of the mRNA for IRBP reflects the developmental emergence of the interphotoreceptor matrix as an important structure within the retina.(ABSTRACT TRUNCATED AT 400 WORDS)
视网膜下腔的主要蛋白质成分——光感受器间视黄醇结合蛋白(IRBP),处于介导视网膜色素上皮(RPE)与神经视网膜之间细胞相互作用的关键位置。虽然IRBP在成体视觉循环中似乎参与维生素A的运输,但该蛋白在眼睛发育过程中的作用尚未明确。作为了解IRBP在视网膜发育中作用的第一步,我们研究了这种糖脂蛋白的mRNA在大鼠光感受器分化过程中的表达。制备了大鼠神经视网膜cDNA文库,并从中分离出一个IRBP克隆。该克隆包含一个开放阅读框,后面是一个3'非编码序列,末端有10个腺苷残基。编码区与人及牛IRBP的核苷酸序列的同源性分别为83.9%和82.5%。大鼠(斯普拉格-道利大鼠、Wistar大鼠和皇家外科医学院粉红眼对照大鼠)有6.4 kb和5.2 kb的IRBP mRNA,其比例为1:4,因此是已知唯一肯定有不止一种主要形式IRBP信息的脊椎动物。基因组Southern印迹分析与IRBP基因只有一个等位基因的假说一致,表明这两种形式是由mRNA的可变加工产生的。为了生成用于分子滴定分析和Northern印迹的反义RNA探针,将编码区的一个Eco RI - Bam HI片段亚克隆到侧翼的Sp6和T7启动子之间。从出生后第0天到第22天未解剖的大鼠眼球中制备总RNA。通过Northern印迹研究IRBP mRNA的表达,并通过溶液杂交分析确定转录本水平。出生时,每微克总眼RNA中约有10⁵个IRBP mRNA转录本。到第9天,这一水平增加到最终的3.1×10⁶转录本/微克总RNA。mRNA的最大水平的一半出现在第4.2天,这比视网膜下腔中IRBP达到最大水平的一半早2周(冈萨雷斯-费尔南德斯,F.,R. A. 兰德斯,P. A. 格拉泽布鲁克,S.-L. 方,G. I. 廖,D. M. K. 林,和C. D. B. 布里奇斯。1984年。《细胞生物学杂志》99:2092 - 2098)。IRBP mRNA的表达反映了光感受器间基质作为视网膜内重要结构在发育过程中的出现。(摘要截断于400字)