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利用微卫星和荧光DNA技术快速检测结直肠肿瘤中的等位基因缺失

Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology.

作者信息

Cawkwell L, Bell S M, Lewis F A, Dixon M F, Taylor G R, Quirke P

机构信息

Academic Unit of Pathological Sciences, University of Leeds, UK.

出版信息

Br J Cancer. 1993 Jun;67(6):1262-7. doi: 10.1038/bjc.1993.236.

Abstract

In order to investigate allele loss in colorectal tumours we have developed a rapid technique which overcomes most of the problems associated with radioactive Restriction Fragment Length Polymorphism (RFLP) analysis of allele loss. We utilise microsatellite length polymorphisms which are highly informative and are closely linked to loci of interest. Sequences containing microsatellites can be amplified from normal and tumour DNA pairs by a polymerase chain reaction (PCR) in which one of the primers is fluorescently labelled. This enables us to detect the products on polyacrylamide gels run on an automated DNA sequencer using dedicated software, by which results are automatically quantitated in terms of peak size, height, and area. Using this technique we have analysed 26 normal tissue: cancer pairs for allele loss at two loci linked to the adenomatous polyposis coli (APC) gene on chromosome 5q. Repeated assays yielded identical results for each pair. Allele loss was found in 10 out of 25 informative samples (40%).

摘要

为了研究结肠直肠肿瘤中的等位基因缺失,我们开发了一种快速技术,该技术克服了与放射性限制性片段长度多态性(RFLP)分析等位基因缺失相关的大多数问题。我们利用微卫星长度多态性,其信息丰富且与感兴趣的基因座紧密连锁。含有微卫星的序列可通过聚合酶链反应(PCR)从正常和肿瘤DNA对中扩增,其中一个引物用荧光标记。这使我们能够使用专用软件在自动DNA测序仪上运行的聚丙烯酰胺凝胶上检测产物,通过该软件可根据峰大小、高度和面积自动定量结果。使用该技术,我们分析了26对正常组织与癌组织,以检测位于5号染色体上与腺瘤性息肉病大肠杆菌(APC)基因连锁的两个基因座的等位基因缺失情况。对每一对样本进行重复检测均得到相同结果。在25个信息性样本中的10个(40%)发现了等位基因缺失。

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Cancer. Gene losses in human tumours.癌症。人类肿瘤中的基因缺失。
Nature. 1988 Sep 29;335(6189):400-2. doi: 10.1038/335400a0.

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