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通过cDNA代表性差异分析鉴定胰腺癌中具有特异性表达的基因。

Identification of genes with specific expression in pancreatic cancer by cDNA representational difference analysis.

作者信息

Gress T M, Wallrapp C, Frohme M, Müller-Pillasch F, Lacher U, Friess H, Büchler M, Adler G, Hoheisel J D

机构信息

Department of Internal Medicine I, University of Ulm, Germany.

出版信息

Genes Chromosomes Cancer. 1997 Jun;19(2):97-103. doi: 10.1002/(sici)1098-2264(199706)19:2<97::aid-gcc5>3.0.co;2-v.

Abstract

cDNA representational difference analysis (cDNA-RDA) is a polymerase-chain-reaction-coupled subtractive and kinetic enrichment procedure for the isolation of differentially expressed genes. In this study, the technique was used to isolate novel genes specifically expressed in pancreatic cancer. cDNA-RDA was done on cDNA reverse transcribed from a poly(A)+ mRNA pool made from 10 cancer tissues (tester) by using as a driver a cDNA from a poly(A)+ mRNA pool made from a combination of 10 tissues of chronic pancreatitis and 10 healthy pancreatic tissues. The use of chronic pancreatitis in addition to healthy pancreas mRNA in the driver preparation eliminated the influence of stromal tissue components present as contamination in the cancer-specific preparations. Such cDNA-RDA led to the isolation of 16 distinct, cancer-specific gene fragments. These were confirmed to be overexpressed in pancreatic cancer tissues by Northern blot analysis. Sequence analysis revealed homologies to five genes previously implicated in the carcinogenesis of the pancreas or other tissues. Eleven fragments had no significant homology to any known gene and thus represent novel candidate disease genes. The experiments demonstrate that cDNA-RDA is a reproducible and highly efficient method for the identification of novel genes with cancer-specific expression.

摘要

互补DNA代表性差异分析(cDNA-RDA)是一种与聚合酶链反应相结合的消减和动力学富集程序,用于分离差异表达基因。在本研究中,该技术被用于分离在胰腺癌中特异性表达的新基因。通过使用由10个慢性胰腺炎组织和10个健康胰腺组织组合而成的聚腺苷酸加尾(poly(A)+)mRNA池制备的互补DNA作为驱动子,对从10个癌组织(测试子)制成的聚腺苷酸加尾mRNA池逆转录得到的互补DNA进行cDNA-RDA。在驱动子制备中除了使用健康胰腺mRNA外还加入慢性胰腺炎,消除了癌特异性制备物中作为污染物存在基质组织成分的影响。这种cDNA-RDA导致分离出16个不同的、癌特异性基因片段。通过Northern印迹分析证实这些片段在胰腺癌组织中过表达。序列分析显示与先前涉及胰腺或其他组织致癌作用的五个基因具有同源性。11个片段与任何已知基因均无明显同源性,因此代表新的候选疾病基因。实验表明,cDNA-RDA是一种可重复且高效的方法,用于鉴定具有癌特异性表达的新基因。

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