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。
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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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VOLUME CONTENTS Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locus Mutational analysis within the 3′ region of the PKD1 gene in Japanese families Allelic polymorphisms in the transcriptional regulatory region of human SEL1L CUMULATIVE AUTHOR INDEX FOR MUTNOM 2000
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