首页> 外文期刊>The Journal of Urology >Novel urothelium specific gene expression identified by differential display reverse transcriptase-polymerase chain reaction.
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Novel urothelium specific gene expression identified by differential display reverse transcriptase-polymerase chain reaction.

机译:通过差异显示逆转录酶-聚合酶链反应鉴定的新型尿路上皮特异性基因表达。

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PURPOSE: Understanding the molecular basis of differential gene expression among different tissues at various developmental stages and in neoplastic transformation is an important biological goal. The potential clinical applications of this improved understanding are more precise diagnosis of disease, prediction of prognosis, novel targeted therapies and prediction of response to therapy. MATERIALS AND METHODS: Differential display reverse transcriptase-polymerase chain reaction was used to compare gene expression in bovine urothelium to that in autologous lung, esophagus, liver and spleen. Products that appeared to have urothelial specific expression were sequenced and assessed for homology with known sequences. Ribonuclease protection assays were used to further confirm the expression pattern. RESULTS: A total of 32 discrete cDNAs were identified, including 3 products from genes known to be urothelium specific in their expression, 16 with significant homology to bovine, human or mouse expressed sequence tags and 5 with no sequence homology to any currently available sequence. Urothelium specific mRNA expression was confirmed for 3 genes by ribonuclease protection assays and one (Udd06) was further characterized as a urea transporter. CONCLUSIONS: The use of differential display reverse transcriptase-polymerase chain reaction and other complementary techniques for parallel gene expression analysis will permit the complete characterization of the urothelial transcriptome and help identify potential molecular targets for rationally targeted therapy.
机译:目的:了解不同组织在不同发育阶段和肿瘤转化过程中差异基因表达的分子基础是重要的生物学目标。这种更好理解的潜在临床应用是疾病的更精确诊断,预后的预测,新型靶向疗法以及对治疗反应的预测。材料与方法:采用差异显示逆转录聚合酶链反应,比较牛尿路上皮与自体肺,食道,肝,脾中基因表达。对似乎具有尿路上皮特异性表达的产物进行测序,并评估与已知序列的同源性。使用核糖核酸酶保护试验来进一步证实表达模式。结果:总共鉴定出32个离散cDNA,包括3种表达的尿路上皮特异基因的产物,其中16种与牛,人或小鼠表达的序列标签具有显着的同源性,另外5种与任何现有序列均无序列同源性。通过核糖核酸酶保护试验证实了3个基因的尿路上皮特异性mRNA表达,并且其中一个(Udd06)被进一步表征为尿素转运蛋白。结论:差异显示逆转录酶-聚合酶链反应和其他互补技术用于平行基因表达分析的使用将允许尿路上皮转录组的完整表征,并有助于确定合理靶向治疗的潜在分子靶标。

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