PCR-DGGE分析筛选人肿瘤坏死因子-α基因启动子多态性

A Patiño-Garcı́a , E Sotillo-Piñeiro , C Modesto , L Sierrasesúmaga
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引用次数: 11

摘要

我们设计了一种新的PCR–DGGE技术,能够检测TNF-α基因启动子的碱基变化。对来自西班牙儿童的130个样本的筛选表明,这项技术准确地检测到启动子序列−376、−308、−238和−163位置多态性引起的带型改变。尽管需要进一步的分析来完全表征检测到的改变,但我们相信这种PCR–DGGE技术是对TNF-α启动子的遗传特征进行快速而敏感的第一种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening of the human tumor necrosis factor-alpha (TNF-α) gene promoter polymorphisms by PCR–DGGE analysis

We have designed a new PCR–DGGE technique that enables detection of base changes in the TNF-α gene promoter. Screening of 130 samples from Spanish children has shown that this technique accurately detects the altered band patterns induced by the presence of the polymorphisms at positions −376, −308, −238 and −163 of the promoter sequence. Although further analysis are needed to fully characterise the alterations detected, we believe that this PCR–DGGE technique is a rapid and sensitive first approach to the genetic characterisation of the TNF-α promoter.

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