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Nested genetic bit analysis (N-GBA) for mutation detection in the p53 tumor suppressor gene.

机译:巢式遗传位分析(N-GBA)用于检测p53抑癌基因中的突变。

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摘要

There is a growing and significant demand for reliable, simple and sensitive methods for repeated scanning of a given gene or gene fragment for detection and characterization of mutations. Solid-phase sequencing by single base primer extension of nested GBATM primers on miniaturized DNA arrays can be used to effectively scan targeted sequences for missense, insertion and deletion mutations. This paper describes the use of N-GBA arrays designed to scan the sequence of a 33 base region of exon 8 of the p53 gene (codons 272-282) encompassing a hot spot for mutations associated with the development of cancer. Synthetic DNA templates containing various missense, insertion and deletion mutations, as well as DNA prepared from pancreatic and biliary tumor cells, were genotyped using the exon 8 arrays.
机译:对可靠,简单和灵敏的方法进行重复扫描给定基因或基因片段以检测和表征突变的需求日益增长,并且对此也有巨大的需求。通过在微型化DNA阵列上嵌套GBATM引物的单碱基引物延伸进行固相测序可用于有效扫描目标序列的错义,插入和缺失突变。本文介绍了N-GBA阵列的用途,该阵列设计用于扫描p53基因第8外显子的33个碱基区域(密码子272-282)的序列,该区域涵盖了与癌症发展相关的突变热点。使用外显子8阵列对包含各种错义,插入和缺失突变的合成DNA模板,以及从胰腺和胆道肿瘤细胞制备的DNA进行基因分型。

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