首页> 外文期刊>Journal of cell biology >Early expression of the gene for interphotoreceptor retinol-binding protein during photoreceptor differentiation suggests a critical role for the interphotoreceptor matrix in retinal development.
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Early expression of the gene for interphotoreceptor retinol-binding protein during photoreceptor differentiation suggests a critical role for the interphotoreceptor matrix in retinal development.

机译:在感光细胞分化过程中,感光细胞间视黄醇结合蛋白基因的早期表达表明,感光细胞间基质在视网膜发育中起着至关重要的作用。

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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)
机译:视网膜下空间的主要蛋白质成分感光体视黄醇结合蛋白(IRBP)在介导视网膜色素上皮(RPE)和神经视网膜之间的细胞相互作用中处于战略地位。尽管IRBP似乎在成年人的视觉周期中参与了维生素A的运输,但该蛋白在眼睛发育过程中的作用尚未确定。作为了解IRBP在视网膜发育过程中的作用的第一步,我们研究了该糖脂蛋白在大鼠感光细胞分化过程中mRNA的表达。制备了大鼠神经视网膜cDNA文库,从中分离了IRBP克隆。该克隆包含一个开放阅读框,后接一个以10个腺苷残基结尾的3'非编码序列。编码区与人和牛IRBP的核苷酸序列的同一性分别为83.9和82.5%。大鼠(Sprague-Dawley,Wistar和Royal College of Surgeon粉红眼睛对照)的IRBP的mRNA分别为6.4和5.2-kb,它们的比例为1:4,因此是唯一已知的具有以上特征的脊椎动物IRBP消息的一种主要形式。基因组Southern印迹与IRBP基因只有一个等位基因的假设一致,表明这两种形式是通过mRNA的替代加工产生的。为了产生用于分子滴定测定和Northern印迹的反义RNA探针,将来自编码区的Eco RI-Bam HI片段亚克隆到Sp6和T7启动子之间。从出生后p0-p22的未解剖大鼠球中制备总RNA。通过Northern印迹研究IRBP的mRNA表达,并通过溶液杂交测定法确定转录水平。出生时大约存在10(5)个IRBP mRNA转录本/微克总眼RNA。到p9时,总RNA的最终水平为3.1 X 10(6)转录本/微克总RNA。 mRNA的一半最大水平出现在p4.2,即视网膜下间隙达到IRBP一半最大水平之前的2周(Gonzalez-Fernandez,F.,RA Landers,PA Glazebrook,S.- L.Fong,GI Liou,DMK Lam和CDB Bridges.1984.J.Cell Biol.99:2092-2098)。 IRBP mRNA的表达反映了感光细胞间基质作为视网膜内部重要结构的发育。(摘要截短为400字)

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