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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >A quadruplex tetra-primer ARMS-PCR method for the simultaneous detection of TP53 Arg72Pro, IVS3 16bp Del/Ins and IVS6+62A>G, and NQO1 C609T polymorphisms
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A quadruplex tetra-primer ARMS-PCR method for the simultaneous detection of TP53 Arg72Pro, IVS3 16bp Del/Ins and IVS6+62A>G, and NQO1 C609T polymorphisms

机译:同时检测TP53 Arg72Pro,IVS3 16bp Del / Ins和IVS6 + 62A> G以及NQO1 C609T多态性的四重四引物ARMS-PCR方法

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The apoptotic pathway has been shown to be crucial in the development of cancers in addition to a variety of neurodegenerative disorders. The tumor suppressor gene (TP53) encodes p53, the central protein in the apoptotic pathway. The NAD(P)H:quinone oxidoreductase 1, which is encoded by the NQO1 gene and, plays a direct role in apoptosis in addition to its recently discovered role as a regulator for p53. Three most commonly studied polymorphisms that were shown to affect the biochemical functions of p53 protein are the exon 4 Arg72pro, Intron 3 16 bp Del/Ins, and Intron 6 A>G polymorphisms. The exon 6 C609T polymorphism was shown to significantly affect NQO1 enzymatic activity. The currently used methods for the separate detection of the four polymorphisms are either slow and laborious or extremely expensive. In this paper, a new highly optimized method for the simultaneous detection of the four polymorphisms is described. The proposed method utilizes 13 primers in a single PCR reaction to detect the four polymorphisms simultaneously based on the principle of tetra-primer ARMS-PCR (also known as PCR-CTPP). The proposed method offers extremely fast, economical, and simple detection. The proposed method was successfully applied to a sample of the Syrian population (n = 144), where we found a unique distribution for TP53 polymorphisms that differed from the major ethnic groups. The proposed method is the first to simultaneously detect four polymorphisms including 3 SNPs in a single PCR reaction based on tetra-primer ARMS-PCR or PCR-CTPP, and can serve as an invaluable tool for the investigation of TP53 haplotypes and the combined effects of the TP53 and NQO1 genes with respect to apoptosis and susceptibility for various types of cancers and neurodegenerative disorders.
机译:除多种神经退行性疾病外,细胞凋亡途径已被证明对癌症的发展至关重要。肿瘤抑制基因(TP53)编码p53,这是凋亡途径中的中心蛋白。 NAD(P)H:醌氧化还原酶1由NQO1基因编码,除最近发现的p53调节剂作用外,还直接在凋亡中起作用。已显示出三个最常研究的可影响p53蛋白生化功能的多态性,即外显子4 Arg72pro,内含子3 16 bp Del / Ins和内含子6 A> G多态性。显示外显子6 C609T多态性显着影响NQO1的酶活性。当前用于分离检测四个多态性的方法要么缓慢且费力,要么非常昂贵。在本文中,描述了一种同时检测四个多态性的高度优化的新方法。提出的方法基于四引物ARMS-PCR(也称为PCR-CTPP)的原理,在单个PCR反应中利用13个引物同时检测四个多态性。所提出的方法提供了非常快速,经济和简单的检测。所提出的方法已成功应用于叙利亚人口样本(n = 144),在该样本中我们发现TP53多态性的独特分布与主要民族不同。该方法是首次基于四引物ARMS-PCR或PCR-CTPP在单个PCR反应中同时检测包括3个SNP在内的4个多态性,可作为研究TP53单倍型及其结合效应的宝贵工具。 TP53和NQO1基因在各种癌症和神经退行性疾病中的凋亡和敏感性方面。

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