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墨西哥东北部α-1抗胰蛋白酶和肿瘤坏死因子α -308启动子多态性的S和Z等位基因频率

Frequency of S and Z alleles for alpha-1-antitrypsin and tumor necrosis factor alpha -308 promoter polymorphism in northeastern Mexico.

作者信息

Sánchez-Domínguez Celia Nohemí, Buenfil-Lozano José Antonio, Molina-Guajardo Carlos Alejandro, Borjas-Almaguer Omar David, Castillo-Lartigue Abraham, Bustamante-Sáenz Adriana, Martínez-Rodríguez Herminia Guadalupe, Alarcón Miguel Angel Villarreal, Reyes-López Miguel Angel, Ortiz-López Rocío

机构信息

Biochemistry Department, School of Medicine, Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, México.

出版信息

Allergy Asthma Proc. 2008 Jul-Aug;29(4):406-10. doi: 10.2500/aap.2008.29.3125. Epub 2008 Jun 4.

DOI:10.2500/aap.2008.29.3125
PMID:18534053
Abstract

Diseases characterized by airway inflammation, excessive secretion, and obstruction affect a substantial proportion of the population. Studies for understanding the mechanisms underlying these processes are focused on the initiation and maintenance of inflammation. Polymorphisms on DNA sequence of response mediators such as alpha-1-antitrypsin (AAT) and tumor necrosis factor (TNF) alpha have the capacity to influence presentation of diseases, affecting protein amount and/or functionality, and can be analyzed as disease modulators. The purpose of this study was to analyze AAT S and Z alleles and -308G/A TNF-alpha polymorphism on the northeast Mexico mestizo population to compare the influence of these genes in several diseases. DNA samples from 103 volunteers (healthy group) were tested for modifier gene variants by polymerase chain reaction-RFLP as follows: AAT gene for S and Z alleles and TNF-alpha promoter -308G/A (TNF1/TNF2) alleles. Allele frequency for S and TNF2 alleles were 1.5 and 2.4%, respectively, whereas the Z allele was not detected. This study shows low frequencies of the AAT S and TNF2 alleles, and the Z allele was not found. Correlation studies in the future will allow to determine if these alleles have some influence in the clinical presentation of diverse diseases in this group of people.

摘要

以气道炎症、分泌物过多和阻塞为特征的疾病影响着相当一部分人群。旨在了解这些过程潜在机制的研究主要集中在炎症的起始和维持方面。诸如α-1抗胰蛋白酶(AAT)和肿瘤坏死因子(TNF)α等反应介质的DNA序列多态性能够影响疾病的表现,影响蛋白质的数量和/或功能,并且可作为疾病调节因子进行分析。本研究的目的是分析墨西哥东北部梅斯蒂索人群中的AAT S和Z等位基因以及-308G/A TNF-α多态性,以比较这些基因在几种疾病中的影响。通过聚合酶链反应-限制性片段长度多态性(polymerase chain reaction-RFLP)对103名志愿者(健康组)的DNA样本进行修饰基因变体检测,具体如下:检测AAT基因的S和Z等位基因以及TNF-α启动子-308G/A(TNF1/TNF2)等位基因。S等位基因和TNF2等位基因的频率分别为1.5%和2.4%,而未检测到Z等位基因。本研究显示AAT S和TNF2等位基因的频率较低,且未发现Z等位基因。未来的相关性研究将有助于确定这些等位基因是否对该人群中多种疾病的临床表现有一定影响。

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The tumor necrosis factor α (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients.肿瘤坏死因子α(-308 A/G)基因多态性与墨西哥患者的囊性纤维化有关。
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