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子宫球蛋白相关蛋白1与支气管哮喘的关联

Association of uteroglobulin-related protein 1 with bronchial asthma.

作者信息

Heinzmann Andrea, Dietrich Henriette, Deichmann Klaus A

机构信息

University Children's Hospital, University of Freiburg, Freiburg, Germany.

出版信息

Int Arch Allergy Immunol. 2003 Aug;131(4):291-5. doi: 10.1159/000072141.

Abstract

BACKGROUND

Chromosomal region 5q31 harbours a number of genes associated with atopic phenotypes, for example the genes coding for interleukin (IL) 4, IL13 and the beta(2)-adrenoreceptor. A new gene within this region was identified only very recently. The encoded protein - uteroglobin-related protein 1 (UGRP1) - is thought to act as an anti-inflammatory agent and is mainly expressed in the lung and trachea. The functional promoter polymorphism A-112G in UGRP1 was shown to be associated with bronchial asthma in a Japanese population. We were thus interested in finding out whether the polymorphism so far identified or others within UGRP1 were associated with bronchial asthma in a German Caucasian population.

METHODS

We performed direct genomic sequencing of the promoter and coding region of UGRP1 in 15 asthmatic children and 15 controls. The identified polymorphisms were genotyped by means of RFLP. Statistical analysis was performed with the Armitage trend test.

RESULTS

We identified 5 non-coding variants, 4 of which being described for the first time. Three polymorphisms were common and typed in 182 asthmatic children and 270 controls. None of the polymorphisms were associated with bronchial asthma in our population.

CONCLUSIONS

We conclude from our data that UGRP1 does not play a major role in the development of bronchial asthma in our Caucasian population.

摘要

背景

染色体区域5q31包含许多与特应性表型相关的基因,例如编码白细胞介素(IL)4、IL13和β₂ - 肾上腺素能受体的基因。该区域内的一个新基因直到最近才被发现。编码的蛋白质——子宫珠蛋白相关蛋白1(UGRP1)——被认为具有抗炎作用,主要在肺和气管中表达。UGRP1中功能性启动子多态性A - 112G在日本人群中显示与支气管哮喘相关。因此,我们有兴趣了解到目前为止所鉴定的多态性或UGRP1内的其他多态性在德国白种人群中是否与支气管哮喘相关。

方法

我们对15名哮喘儿童和15名对照者的UGRP1启动子和编码区进行了直接基因组测序。通过限制性片段长度多态性(RFLP)对鉴定出的多态性进行基因分型。采用阿米蒂奇趋势检验进行统计分析。

结果

我们鉴定出5个非编码变异,其中4个是首次被描述。三种多态性较为常见,并在182名哮喘儿童和270名对照者中进行了分型。在我们的研究人群中,没有一种多态性与支气管哮喘相关。

结论

根据我们的数据,我们得出结论,UGRP1在我们白种人群支气管哮喘的发病过程中不发挥主要作用。

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