• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

日本人群中SLC11A1基因启动子Z-DNA形成基序的功能多态性与1型糖尿病:关联研究与荟萃分析

Functional polymorphism in Z-DNA-forming motif of promoter of SLC11A1 gene and type 1 diabetes in Japanese subjects: association study and meta-analysis.

作者信息

Nishino Masanori, Ikegami Hiroshi, Fujisawa Tomomi, Kawaguchi Yoshihiko, Kawabata Yumiko, Shintani Maki, Ono Masaya, Ogihara Toshio

机构信息

Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Osaka 565-0871, Japan.

出版信息

Metabolism. 2005 May;54(5):628-33. doi: 10.1016/j.metabol.2004.12.006.

DOI:10.1016/j.metabol.2004.12.006
PMID:15877293
Abstract

The association of the polymorphism of the Z-DNA-forming repeats in the promoter region of SLC11A1 (solute carrier family 11 member 1), formerly designated NRAMP1 (natural resistance associated macrophage protein 1), with type 1 diabetes was studied in a total of 244 Japanese subjects. Three alleles were detected in Japanese subjects. In diabetic patients, allele 2 was less frequent and allele 3 was more frequent, albeit not significantly, than in control subjects. Allele 2 was significantly ( P < .024) less frequent whereas allele 3 was more, albeit not significantly, frequent in the younger onset group than in the control subjects. In patients with a susceptible HLA allele, DRB10405 or DRB10901 , the frequency of allele 2 was significantly ( P < .013) lower and that of allele 3 tended to be higher than that in patients without either DRB10405 or DRB10901 . The protective effect of allele 2 against type 1 diabetes and other autoimmune diseases was confirmed by meta-analysis (summary odds ratio, 0.71, 95% confidence interval, 0.53-0.96). Because allele 2 was shown to be associated with low expression of SLC11A1 and protection against another autoimmune disease, rheumatoid arthritis, the negative association of allele 2 with autoimmune type 1 diabetes in the present study suggests that a less active immune system in subjects with allele 2 may protect individuals from autoimmune diseases.

摘要

在总共244名日本受试者中,研究了溶质载体家族11成员1(SLC11A1)(以前称为天然抵抗相关巨噬细胞蛋白1,NRAMP1)启动子区域中形成Z-DNA的重复序列多态性与1型糖尿病的关联。在日本受试者中检测到三个等位基因。在糖尿病患者中,与对照组相比,等位基因2的频率较低,等位基因3的频率较高,尽管差异不显著。在发病年龄较小的组中,等位基因2的频率显著低于对照组(P <.024),而等位基因3的频率较高,尽管差异不显著。在携带易感HLA等位基因DRB10405或DRB10901的患者中,等位基因2的频率显著低于(P <.013)且等位基因3的频率倾向于高于不携带DRB10405或DRB10901的患者。通过荟萃分析证实了等位基因2对1型糖尿病和其他自身免疫性疾病的保护作用(汇总比值比,0.71,95%置信区间,0.53 - 0.96)。由于等位基因2与SLC11A1的低表达以及对另一种自身免疫性疾病类风湿关节炎的保护作用相关,本研究中等位基因2与自身免疫性1型糖尿病的负相关表明,携带等位基因2的个体免疫系统活性较低,可能使其免受自身免疫性疾病的影响。

相似文献

1
Functional polymorphism in Z-DNA-forming motif of promoter of SLC11A1 gene and type 1 diabetes in Japanese subjects: association study and meta-analysis.日本人群中SLC11A1基因启动子Z-DNA形成基序的功能多态性与1型糖尿病:关联研究与荟萃分析
Metabolism. 2005 May;54(5):628-33. doi: 10.1016/j.metabol.2004.12.006.
2
Promoter polymorphism of SLC11A1 (formerly NRAMP1) confers susceptibility to autoimmune type 1 diabetes mellitus in Japanese.溶质载体家族11成员1(原名为天然抗性相关巨噬细胞蛋白1)的启动子多态性使日本人易患自身免疫性1型糖尿病。
Tissue Antigens. 2004 Mar;63(3):231-6. doi: 10.1111/j.1399-0039.2004.000172.x.
3
Analysis of tumor necrosis factor-alpha promoter polymorphism in type 1 diabetes: HLA-B and -DRB1 alleles are primarily associated with the disease in Japanese.1型糖尿病中肿瘤坏死因子-α启动子多态性分析:在日本人中,HLA - B和 - DRB1等位基因与该疾病主要相关。
Tissue Antigens. 2000 Jan;55(1):10-6. doi: 10.1034/j.1399-0039.2000.550102.x.
4
HIF-1 regulates heritable variation and allele expression phenotypes of the macrophage immune response gene SLC11A1 from a Z-DNA forming microsatellite.缺氧诱导因子-1调控巨噬细胞免疫反应基因SLC11A1(来自一个形成Z-DNA的微卫星)的遗传变异和等位基因表达表型。
Blood. 2007 Oct 15;110(8):3039-48. doi: 10.1182/blood-2006-12-063289. Epub 2007 Jul 2.
5
HLA DRB1, DQB1 and insulin promoter VNTR polymorphisms: interactions and the association with adult-onset diabetes mellitus in Czech patients.人类白细胞抗原DRB1、DQB1基因及胰岛素启动子可变数目串联重复序列多态性:捷克患者中的相互作用及其与成人发病型糖尿病的关联
Int J Immunogenet. 2008 Apr;35(2):133-40. doi: 10.1111/j.1744-313X.2008.00749.x. Epub 2008 Feb 11.
6
SLC11A1 promoter gene polymorphisms and fibrosis progression in chronic hepatitis C.SLC11A1启动子基因多态性与慢性丙型肝炎纤维化进展
Gut. 2004 Mar;53(3):446-50. doi: 10.1136/gut.2003.028274.
7
Association of SLC11A1 promoter polymorphisms with the incidence of autoimmune and inflammatory diseases: a meta-analysis.SLC11A1启动子多态性与自身免疫性疾病和炎性疾病发病率的关联:一项荟萃分析
J Autoimmun. 2008 Aug;31(1):42-51. doi: 10.1016/j.jaut.2008.02.002. Epub 2008 Mar 28.
8
Polymorphism in gene for islet autoantigen, IA-2, and type 1 diabetes in Japanese subjects.日本人群中胰岛自身抗原IA-2基因多态性与1型糖尿病的关系
Hum Immunol. 2001 May;62(5):518-22. doi: 10.1016/s0198-8859(01)00234-8.
9
SLC11A1 gene polymorphisms in Korean patients with Behçet's disease.
Scand J Rheumatol. 2006 Sep-Oct;35(5):398-401. doi: 10.1080/03009740600704221.
10
Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes.
Immunogenetics. 2002 Jul;54(4):282-5. doi: 10.1007/s00251-002-0459-3. Epub 2002 Jun 14.

引用本文的文献

1
Systemic lupus erythematosus and pulmonary tuberculosis in a patient developing acute-onset type 1 diabetes.一名急性起病的1型糖尿病患者合并系统性红斑狼疮和肺结核。
Diabetol Int. 2024 Nov 12;16(1):175-181. doi: 10.1007/s13340-024-00772-z. eCollection 2025 Jan.
2
Construction of ssDNA-Attached LR-Chimera Involving Z-DNA for ZBP1 Binding Analysis.构建 ssDNA 连接的 LR-Chimera 涉及 Z-DNA 以用于 ZBP1 结合分析。
Molecules. 2022 Jun 9;27(12):3706. doi: 10.3390/molecules27123706.
3
Nonalternating purine pyrimidine sequences can form stable left-handed DNA duplex by strong topological constraint.
非交替嘌呤嘧啶序列可以通过强大的拓扑约束形成稳定的左手 DNA 双链。
Nucleic Acids Res. 2022 Jan 25;50(2):684-696. doi: 10.1093/nar/gkab1283.
4
Correlation of Polymorphisms of Natural Resistance-Associated Macrophage Protein 1 (NRAMP1) Gene and Smoking with the Risk of Rheumatoid Arthritis in Chinese Han People.自然抗性相关巨噬细胞蛋白 1(NRAMP1)基因多态性与吸烟和类风湿关节炎风险在中国汉族人群中的相关性。
Med Sci Monit. 2019 Jul 18;25:5321-5326. doi: 10.12659/MSM.913585.
5
Genetic variants of SLC11A1 are associated with both autoimmune and infectious diseases: systematic review and meta-analysis.溶质载体家族11成员1(SLC11A1)的基因变异与自身免疫性疾病和感染性疾病均相关:系统评价与荟萃分析。
Genes Immun. 2015 Jun;16(4):275-83. doi: 10.1038/gene.2015.8. Epub 2015 Apr 9.
6
Improving power of genome-wide association studies with weighted false discovery rate control and prioritized subset analysis.利用加权假发现率控制和优先子集分析提高全基因组关联研究的效能。
PLoS One. 2012;7(4):e33716. doi: 10.1371/journal.pone.0033716. Epub 2012 Apr 9.
7
Evidence of association with type 1 diabetes in the SLC11A1 gene region.SLC11A1 基因区域与 1 型糖尿病关联的证据。
BMC Med Genet. 2011 Apr 27;12:59. doi: 10.1186/1471-2350-12-59.
8
NRAMP1 (SLC11A1) variants: genetic susceptibility to multiple Sclerosis.NRAMP1(SLC11A1)变体:多发性硬化症的遗传易感性。
J Clin Immunol. 2010 Jul;30(4):583-6. doi: 10.1007/s10875-010-9422-5. Epub 2010 Apr 20.
9
Linking chronic infection and autoimmune diseases: Mycobacterium avium subspecies paratuberculosis, SLC11A1 polymorphisms and type-1 diabetes mellitus.将慢性感染与自身免疫性疾病联系起来:鸟分枝杆菌亚种副结核分枝杆菌、SLC11A1 多态性与 1 型糖尿病。
PLoS One. 2009 Sep 21;4(9):e7109. doi: 10.1371/journal.pone.0007109.
10
Genetic susceptibility to Behçet's syndrome is associated with NRAMP1 (SLC11A1) polymorphism in Turkish patients.土耳其患者中,白塞病的遗传易感性与天然抗性相关巨噬细胞蛋白1(SLC11A1)基因多态性有关。
Rheumatol Int. 2009 May;29(7):787-91. doi: 10.1007/s00296-008-0763-9. Epub 2008 Nov 8.