Nickerson J M, Borst D E, Redmond T M, Si J S, Toffenetti J, Chader G J
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In closing, molecular biology has helped us in the study of uveitis, in defining the parts of the IRBP molecule that cause EAU/EAP. Simple northern and Southern blotting experiments can answer significant questions in the study of gene structure and expression and in relating these to genetic eye diseases. Molecular biology has provided answers to several long-standing cell biology question such as: where is IRBP synthesized, where is the gene expressed, and how is the IRBP polypeptide processed? In considering how mother nature invented the IRBP gene, the gene structure suggests some interesting alternative models, and causes us to speculate about how large proteins may have evolved. Finally, the determination of the protein sequence helps to put us in the position to ask and answer questions about the function of IRBP. It also allows us to begin to determine the consequences of a nonfunctional IRBP. We don't know the answers to all these questions yet, but the structural analyses and the isolation of these genes and cDNAs, presented here, united with other powerful biological techniques should provide the answers.
总之,分子生物学在葡萄膜炎的研究中帮助了我们,确定了引起实验性自身免疫性葡萄膜炎/实验性自身免疫性视网膜炎的视网膜间质抗原(IRBP)分子的部分结构。简单的RNA印迹和DNA印迹实验能够解答基因结构与表达研究中的重要问题,并将这些问题与遗传性眼病联系起来。分子生物学为几个长期存在的细胞生物学问题提供了答案,例如:IRBP在哪里合成,基因在哪里表达,以及IRBP多肽是如何加工的?在思考大自然如何创造出IRBP基因时,基因结构提示了一些有趣的替代模型,并促使我们推测大型蛋白质可能是如何进化的。最后,蛋白质序列的确定有助于我们提出并回答有关IRBP功能的问题。这也使我们能够开始确定无功能IRBP的后果。我们尚未知晓所有这些问题的答案,但本文所展示的结构分析以及这些基因和cDNA的分离,与其他强大的生物技术相结合,应该能够提供答案。