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类风湿关节炎中IDDM8区域内基因的精细定位

Fine mapping of genes within the IDDM8 region in rheumatoid arthritis.

作者信息

Hinks Anne, Barton Anne, John Sally, Shephard Neil, Worthington Jane

机构信息

Arthritis Research Campaign Epidemiology Unit, University of Manchester, Manchester M13 9PT, UK.

出版信息

Arthritis Res Ther. 2006;8(5):R145. doi: 10.1186/ar2037.

Abstract

The IDDM8 region on chromosome 6q27, first identified as a susceptibility locus for type 1 diabetes, has previously been linked and associated with rheumatoid arthritis (RA). The region contains a number of potential candidate genes, including programmed cell death 2 (PDCD2), the proteosome subunit beta type 1 (PSMB1), delta-like ligand 1 (DLL-1) and TATA box-binding protein (TBP) amongst others. The aim of this study was to fine map the IDDM8 region on chromosome 6q27, focusing on the genes in the region, to identify polymorphisms that may contribute to susceptibility to RA and potentially to other autoimmune diseases. Validated single nucleotide polymorphisms (SNPs; n = 65) were selected from public databases from the 330 kb region of IDDM8. These were genotyped using Sequenom MassArray genotyping technology in two datasets; the test dataset comprised 180 RA cases and 180 controls. We tested 50 SNPs for association with RA and any significant associations were genotyped in a second dataset of 174 RA cases and 192 controls, and the datasets were combined before analysis. Association analysis was performed by chi-square test implemented in Stata software and linkage disequilibrium and haplotype analysis was performed using Helix tree version 4.1. There was initial weak evidence of association, with RA, of a number of SNPs around the loc154449 putative gene and within the KIAA1838 gene; however, these associations were not significant in the combined dataset. Our study has failed to detect evidence of association with any of the known genes mapping to the IDDM8 locus with RA.

摘要

6号染色体q27区域的IDDM8位点最初被鉴定为1型糖尿病的易感基因座,此前已被证明与类风湿性关节炎(RA)有关联。该区域包含许多潜在的候选基因,包括程序性细胞死亡2(PDCD2)、蛋白酶体亚基β型1(PSMB1)、δ样配体1(DLL-1)和TATA盒结合蛋白(TBP)等。本研究的目的是对6号染色体q27上的IDDM8区域进行精细定位,重点关注该区域的基因,以确定可能导致RA易感性以及潜在地导致其他自身免疫性疾病的多态性。从IDDM8的330 kb区域的公共数据库中选择经过验证的单核苷酸多态性(SNP;n = 65)。使用Sequenom MassArray基因分型技术在两个数据集中对这些SNP进行基因分型;测试数据集包括180例RA患者和180例对照。我们测试了50个SNP与RA的关联性,并在第二个包含174例RA患者和192例对照的数据集中对任何显著关联进行基因分型,并且在分析前将两个数据集合并。使用Stata软件通过卡方检验进行关联分析,并使用Helix tree 4.1版本进行连锁不平衡和单倍型分析。在假定基因loc154449周围和KIAA1838基因内的一些SNP最初有与RA相关联的微弱证据;然而,这些关联在合并数据集中并不显著。我们的研究未能检测到与映射到IDDM8基因座的任何已知基因与RA相关联的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4578/1779440/a67e702acb98/ar2037-1.jpg

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