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关联研究中微卫星标记物的评估:寻找结节病中与免疫相关的易感基因。

Evaluation of microsatellite markers in association studies: a search for an immune-related susceptibility gene in sarcoidosis.

作者信息

Tanaka Goh, Matsushita Ikumi, Ohashi Jun, Tsuchiya Naoyuki, Ikushima Soichiro, Oritsu Masaru, Hijikata Minako, Nagata Taiji, Yamamoto Kazuhiko, Tokunaga Katsushi, Keicho Naoto

机构信息

Department of Respiratory Diseases, Research Institute, International Medical Center of Japan, Tokyo 162-8655, Japan.

出版信息

Immunogenetics. 2005 Mar;56(12):861-70. doi: 10.1007/s00251-004-0753-3. Epub 2005 Jan 27.

Abstract

Association studies using linkage disequilibrium (LD) between candidate loci and nearby markers have been proposed to identify susceptibility genes for complex diseases. We analyzed polymorphisms of microsatellites (MSs) and LD patterns of the regions in which candidate genes related to the Th1 immune response have been annotated and attempted to identify a susceptibility gene for sarcoidosis in a marker-based association study. Nineteen MSs were identified in six Th1-related genes (IFNGR1, IFNGR2, IL12RB1, IL12RB2, STAT1 and STAT4) and then eight were further characterized as useful polymorphic markers. Most of these MSs showed LD with single nucleotide polymorphisms (SNPs) on both 5' and 3' ends of these candidate genes, in which r(2) values between at least one of the MS marker alleles and the SNPs were higher than 0.1. A significant association with one MS allele near STAT4 was shown and a cluster of SNPs in LD with the MS marker was associated with sarcoidosis. These results suggest that association studies using not only SNPs but also multi-allelic MS within or near candidate loci would be useful markers to search for a disease susceptibility gene, especially in populations with unknown LD structure.

摘要

利用候选基因座与附近标记之间的连锁不平衡(LD)进行关联研究,已被用于识别复杂疾病的易感基因。我们分析了微卫星(MS)的多态性以及已注释的与Th1免疫反应相关候选基因区域的LD模式,并试图在一项基于标记的关联研究中识别结节病的易感基因。在六个与Th1相关的基因(IFNGR1、IFNGR2、IL12RB1、IL12RB2、STAT1和STAT4)中鉴定出19个MS,然后进一步将其中8个表征为有用的多态性标记。这些MS中的大多数在这些候选基因的5'和3'末端均与单核苷酸多态性(SNP)显示出LD,其中至少一个MS标记等位基因与SNP之间的r(2)值高于0.1。结果显示与STAT4附近的一个MS等位基因存在显著关联,并且与该MS标记处于LD状态的一组SNP与结节病相关。这些结果表明,不仅使用SNP,而且使用候选基因座内或附近的多等位基因MS进行关联研究,将是寻找疾病易感基因的有用标记,尤其是在LD结构未知的人群中。

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