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韩国人群中RUNX1基因多态性与IgE水平的潜在关联。

Putative association of RUNX1 polymorphisms with IgE levels in a Korean population.

作者信息

Chae Soo Cheon, Park Byung Lae, Park Choon-Sik, Ryu Ha-Jung, Yang Yun-Sik, Lee Soo Ok, Choi Yoo Hyun, Kim Eun Mi, Uh Soo Taek, Kim Young Hoon, Kim Ka-Kyung, Oh Bermseok, Chung Hun-Taeg, Kimm Kuchan, Shin Hyoung Doo

机构信息

Genome Research Center for Immune Disorders, Wonkwang University School of Medicine, Iksan 570-749, Korea.

出版信息

Exp Mol Med. 2006 Oct 31;38(5):583-8. doi: 10.1038/emm.2006.68.

Abstract

RUNX1, a member of the runt domain gene family of transcription factors, encodes a heterodimeric transcription factor and regulates the expression of various genes related to hematopoiesis and myeloid differentiation. RUNX1 has been one of the target genes for research into various autoimmune diseases due to its properties as a transcription factor and functional distribution for chromosomal translocation. In an effort to identify additional gene polymorphisms in which variants have been implicated in asthma, we investigated the genetic polymorphisms in RUNX1 to evaluate it as a potential candidate gene for a host genetic study of asthma and IgE production. We identified 19 sequence variants by direct DNA sequencing in 24 individuals of which four common variants were selected for genotyping in our asthma cohort (1,055 asthmatic patients, 384 normal controls). Using logistic regression analysis for association with the risk of asthma, while controlling for age, gender, and smoking status as covariates, no significant associations with the risk of asthma were detected. However, two polymorphisms in the promoter region (-2084G>C and -1282G>A) showed a marginal association with total IgE levels (0.03 and 0.03 in recessive models, respectively). Our findings suggest that polymorphisms in RUNX1 might be one of the genetic factors for the regulation of IgE production.

摘要

RUNX1是转录因子 runt 结构域基因家族的成员之一,编码一种异二聚体转录因子,并调节与造血和髓系分化相关的各种基因的表达。由于RUNX1作为转录因子的特性以及其在染色体易位中的功能分布,它一直是各种自身免疫性疾病研究的靶基因之一。为了确定与哮喘相关的其他基因多态性,我们研究了RUNX1的基因多态性,以评估其作为哮喘和IgE产生宿主基因研究的潜在候选基因。我们通过直接DNA测序在24名个体中鉴定出19个序列变异,其中4个常见变异被选择在我们的哮喘队列(1055名哮喘患者,384名正常对照)中进行基因分型。在控制年龄、性别和吸烟状况作为协变量的情况下,使用逻辑回归分析与哮喘风险的关联,未检测到与哮喘风险的显著关联。然而,启动子区域的两个多态性(-2084G>C和-1282G>A)与总IgE水平显示出边缘关联(隐性模型中分别为0.03和0.03)。我们的研究结果表明,RUNX1中的多态性可能是调节IgE产生的遗传因素之一。

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