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首页> 外文期刊>Investigative ophthalmology & visual science >A high-resolution RNA expression atlas of retinitis pigmentosa genes in human and mouse retinas.
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A high-resolution RNA expression atlas of retinitis pigmentosa genes in human and mouse retinas.

机译:视网膜色素变性基因在人和小鼠视网膜中的高分辨率RNA表达图谱。

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PURPOSE: Retinitis pigmentosa (RP) is one of the leading causes of visual handicap in the world population and is characterized by high genetic heterogeneity. The study of the disease mechanisms and the development of efficient therapeutic approaches have mostly relied on the availability of animal models for this condition, so far. Nevertheless, little information is available about the RNA expression profiles of RP genes in the human retina. An expression atlas of 34 known RP genes in human and murine retinas was generated to overcome this lack of information. METHODS: Appropriate templates were retrieved for 34 RP genes that were used to perform RNA in situ hybridization studies on human and murine adult eyes. RESULTS: Most of the genes displayed similar patterns between human and mouse retina. Different expression patterns were observed for the CNGB1, USH2A, and FSCN2 genes, compared with those in previously reported profiles. In addition, different expression profiles were detected for the RPGR, CA4, PAP1, RGR, and RLBP1 genes in human and mouse retinas. CONCLUSIONS: The first gene expression atlas has been generated of RP genes in human and murine retinas. Differences observed in the expression patterns of some genes in humans and mice, will open new perspectives on the function of these genes and their putative roles in disease pathogenesis.
机译:目的:色素性视网膜炎(RP)是世界人口视力障碍的主要原因之一,其特征是高度的遗传异质性。迄今为止,对疾病机制的研究和有效治疗方法的发展主要依赖于针对这种情况的动物模型的可用性。然而,关于人视网膜中RP基因的RNA表达谱的信息很少。为了克服这种信息缺乏,在人类和鼠类视网膜中生成了34个已知RP基因的表达图谱。方法:检索了34个RP基因的适当模板,这些基因用于在人和鼠的成年眼睛上进行RNA原位杂交研究。结果:大多数基因在人和小鼠视网膜之间显示出相似的模式。与先前报道的谱图中的那些相比,观察到CNGB1,USH2A和FSCN2基因的不同表达模式。此外,在人和小鼠视网膜中检测到RPGR,CA4,PAP1,RGR和RLBP1基因的不同表达谱。结论:人类和鼠类视网膜中已经产生了RP基因的第一个基因表达图谱。在人类和小鼠中某些基因的表达模式上观察到的差异,将为这些基因的功能及其在疾病发病机理中的假定作用打开新的视野。

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