首页> 外文期刊>Investigative ophthalmology & visual science >Gene expression profile studies of human keratoconus cornea for NEIBank: a novel cornea-expressed gene and the absence of transcripts for aquaporin 5.
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Gene expression profile studies of human keratoconus cornea for NEIBank: a novel cornea-expressed gene and the absence of transcripts for aquaporin 5.

机译:NEIBank的人角膜圆锥角膜的基因表达谱研究:一个新的角膜表达基因和水通道蛋白5的转录本缺失。

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PURPOSE: To increase the database of genes expressed in human cornea and to gain insights into the molecular basis of keratoconus (KC). METHODS: A cDNA library was constructed from KC corneas harvested at keratoplasty and used for expressed sequence tag (EST) analysis. Data were analyzed using grouping and identification of sequence tags (GRIST). Expression of selected clones was examined by RT-PCR. RESULTS: A total of 7680 clones was sequenced from the 5' end. After bioinformatics analysis, 4090 clusters of clones, each potentially representing individual genes, were identified. Of these, 887 genes were represented by more than one clone. The five most abundant transcripts, represented by >60 clones each, were for keratin-12, TGFBI (BIGH3), decorin, ALDH3, and enolase 1, all known markers for cornea. Many other markers for epithelial, stromal, and endothelial genes were also present. One cluster of six clones came from an apparently novel gene (designated KC6) located on chromosome 18 at p12.3. RT-PCRof RNA from several human tissues detected KC6 transcripts only in cornea. In addition, no clones were observed for the usually prominent corneal epithelial cell marker aquaporin 5 (AQP5), a water channel protein. Semiquantitative RT-PCR confirmed that expression of AQP5 is much lower in KC cornea than in non-KC cornea. CONCLUSIONS: This analysis increases the database of genes expressed in the human cornea and provides insights into KC. KC6 is a novel gene of unknown function that shows cornea-preferred expression, whereas the suppression of transcripts for AQP5 provides the first clear evidence of a molecular defect identified in KC.
机译:目的:增加在人角膜中表达的基因数据库,并深入了解圆锥角膜(KC)的分子基础。方法:从角膜移植术中收获的角膜角膜构建一个cDNA文库,并将其用于表达序列标签(EST)分析。使用分组和序列标签识别(GRIST)分析数据。通过RT-PCR检查所选克隆的表达。结果:从5'末端开始总共测序了7680个克隆。经过生物信息学分析,鉴定出4090个克隆簇,每个簇潜在代表单个基因。其中,887个基因由一个以上的克隆代表。五个最丰富的转录本,分别由> 60个克隆表示,分别是角蛋白12,TGFBI(BIGH3),核心蛋白聚糖,ALDH3和烯醇酶1(所有已知的角膜标记)。还存在许多其他上皮,基质和内皮基因标记。六个克隆中的一簇来自位于p12.3处第18号染色体上的一个明显的新基因(称为KC6)。来自几个人体组织的RNA的RT-PCR仅在角膜中检测到KC6转录本。此外,没有观察到通常突出的角膜上皮细胞标记水通道蛋白5(AQP5)(一种水通道蛋白)的克隆。半定量RT-PCR证实,AQP5的表达在KC角膜中比在非KC角膜中低得多。结论:该分析增加了人类角膜中表达的基因数据库,并提供了对KC的见解。 KC6是一个功能未知的新基因,显示了角膜优先表达,而抑制AQP5的转录本则为KC中鉴定出的分子缺陷提供了第一个明确证据。

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