• 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

一个新的胰岛素依赖型糖尿病易感性基因(IDDM8)在6号染色体q25-q27区域的受累同胞对定位研究。

Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27.

作者信息

Luo D F, Bui M M, Muir A, Maclaren N K, Thomson G, She J X

机构信息

Department of Pathology, College of Medicine, University of Florida, Gainesville 32610, USA.

出版信息

Am J Hum Genet. 1995 Oct;57(4):911-9.

PMID:7573053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1801491/
Abstract

Affected-sib-pair analyses were performed using 104 Caucasian families to map genes that predispose to insulin-dependent diabetes mellitus (IDDM). We have obtained linkage evidence for D6S446 (maximum lod score [MLS] = 2.8) and for D6S264 (MLS = 2.0) on 6q25-q27. Together with a previously reported data set, linkage can be firmly established (MLS = 3.4 for D6S264), and the disease locus has been designated IDDM8. With analysis of independent families, we confirmed linkage evidence for the previously identified IDDM3 (15q) and DDM7 (2q). We also typed additional markers in the regions containing IDDM3, IDDM4, IDDM5, and IDDM8. Preliminary linkage evidence for a novel region on chromosome 4q (D4S1566) has been found in 47 Florida families (P < .03). We also found evidence of linkage for two regions previously identified as potential linkages in the Florida subset: D3S1303 on 3q (P < .04) and D7S486 on 7q (P < .03). We could not confirm linkage with eight other regions (D1S191, D1S412, D4S1604, D8S264, D8S556, D10S193, D13S158, and D18S64) previously identified as potential linkages.

摘要

采用104个高加索家庭进行了受累同胞对分析,以定位易患胰岛素依赖型糖尿病(IDDM)的基因。我们在6q25 - q27区域获得了D6S446(最大对数优势分数[MLS]=2.8)和D6S264(MLS = 2.0)的连锁证据。结合之前报道的数据集,可以确定连锁关系(D6S264的MLS = 3.4),该疾病位点已被命名为IDDM8。通过对独立家庭的分析,我们证实了之前确定的IDDM3(15q)和IDDM7(2q)的连锁证据。我们还在包含IDDM3、IDDM4、IDDM5和IDDM8的区域中检测了其他标记。在47个佛罗里达家庭中发现了4号染色体q区域(D4S1566)一个新区域的初步连锁证据(P < 0.03)。我们还发现了之前在佛罗里达亚组中被确定为潜在连锁区域的两个区域的连锁证据:3q上的D3S1303(P < 0.04)和7q上的D7S486(P < 0.03)。我们无法证实与之前确定为潜在连锁区域的其他八个区域(D1S191、D1S412、D4S1604、D8S264、D8S556、D10S193、D13S158和D18S64)的连锁关系。

相似文献

1
Affected-sib-pair mapping of a novel susceptibility gene to insulin-dependent diabetes mellitus (IDDM8) on chromosome 6q25-q27.一个新的胰岛素依赖型糖尿病易感性基因(IDDM8)在6号染色体q25-q27区域的受累同胞对定位研究。
Am J Hum Genet. 1995 Oct;57(4):911-9.
2
Confirmation of three susceptibility genes to insulin-dependent diabetes mellitus: IDDM4, IDDM5 and IDDM8.胰岛素依赖型糖尿病三个易感基因的确认:IDDM4、IDDM5和IDDM8。
Hum Mol Genet. 1996 May;5(5):693-8. doi: 10.1093/hmg/5.5.693.
3
A locus on chromosome 15q26 (IDDM3) produces susceptibility to insulin-dependent diabetes mellitus.位于15号染色体q26区域(IDDM3)的一个基因座会导致对胰岛素依赖型糖尿病的易感性。
Nat Genet. 1994 Oct;8(2):189-94. doi: 10.1038/ng1094-189.
4
Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes.1型糖尿病中6号染色体长臂的饱和多点连锁图谱分析
Hum Mol Genet. 1996 Jul;5(7):1071-4. doi: 10.1093/hmg/5.7.1071.
5
Preliminary studies on associations of IDDM3, IDDM4, IDDM5 and IDDM8 with IDDM in Chengdu population.成都人群中IDDM3、IDDM4、IDDM5和IDDM8与胰岛素依赖型糖尿病关联的初步研究。
Chin Med Sci J. 2001 Jun;16(2):120-2.
6
Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci.类风湿关节炎与胰岛素依赖型糖尿病位点的连锁:支持存在共同自身免疫易感性位点假说的证据。
Arthritis Rheum. 2000 Dec;43(12):2771-5. doi: 10.1002/1529-0131(200012)43:12<2771::AID-ANR17>3.0.CO;2-V.
7
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.位于11号染色体q13区的糖尿病易感基因座IDDM4的精细定位。
Am J Hum Genet. 1998 Aug;63(2):547-56. doi: 10.1086/301974.
8
Do non-insulin-dependent diabetes mellitus (NIDDM) and insulin-dependent diabetes mellitus (IDDM) share genetic susceptibility loci? An analysis of putative IDDM susceptibility regions in familial NIDDM.非胰岛素依赖型糖尿病(NIDDM)和胰岛素依赖型糖尿病(IDDM)是否共享遗传易感性位点?对家族性NIDDM中假定的IDDM易感性区域的分析。
Metabolism. 1997 Jan;46(1):48-52. doi: 10.1016/s0026-0495(97)90166-9.
9
Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.1型糖尿病中与6号染色体上HLA相关的非MHC易感基因座的证据。
Am J Hum Genet. 1997 Jan;60(1):174-87.
10
A genome-wide search for human type 1 diabetes susceptibility genes.一项针对人类1型糖尿病易感基因的全基因组搜索。
Nature. 1994 Sep 8;371(6493):130-6. doi: 10.1038/371130a0.

引用本文的文献

1
From markers to molecular mechanisms: type 1 diabetes in the post-GWAS era.从标志物到分子机制:全基因组关联研究时代后的1型糖尿病
Rev Diabet Stud. 2012 Winter;9(4):201-23. doi: 10.1900/RDS.2012.9.201. Epub 2012 Dec 28.
2
Variants in PTPN22 and SMOC2 genes and the risk of thyroid disease in the Jordanian Arab population.PTPN22 和 SMOC2 基因变异与约旦阿拉伯人群甲状腺疾病的风险。
Endocrine. 2013 Dec;44(3):702-9. doi: 10.1007/s12020-013-9908-z. Epub 2013 Mar 6.
3
Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.全基因组关联分析表明,NELL1影响非裔美国人对氢氯噻嗪的不良代谢反应。
Pharmacogenomics J. 2014 Feb;14(1):35-40. doi: 10.1038/tpj.2013.3. Epub 2013 Feb 12.
4
Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs.1 型糖尿病遗传相互作用的检测:4422 对患病同胞对的连锁和分层分析。
Diabetes. 2011 Mar;60(3):1030-40. doi: 10.2337/db10-1195. Epub 2011 Jan 24.
5
Common variants in FOXP1 are associated with generalized vitiligo.FOXP1 常见变异与泛发性白癜风有关。
Nat Genet. 2010 Jul;42(7):576-8. doi: 10.1038/ng.602. Epub 2010 Jun 6.
6
Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.全基因组关联研究在一个孤立的欧洲创始人群体中的泛发性白癜风中确定了 SMOC2,它与 IDDM8 密切相关。
J Invest Dermatol. 2010 Mar;130(3):798-803. doi: 10.1038/jid.2009.347. Epub 2009 Nov 5.
7
Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium.对来自1型糖尿病遗传协会的2496个多位点家庭进行全基因组扫描以寻找与1型糖尿病的连锁关系。
Diabetes. 2009 Apr;58(4):1018-22. doi: 10.2337/db08-1551. Epub 2009 Jan 9.
8
The mutation of the LEW.1AR1-iddm rat maps to the telomeric end of rat chromosome 1.LEW.1AR1 - iddm大鼠的突变定位在大鼠1号染色体的端粒末端。
Mamm Genome. 2008 Apr;19(4):292-7. doi: 10.1007/s00335-008-9102-4. Epub 2008 Mar 21.
9
Genetic analysis of the LEW.1AR1-iddm rat: an animal model for spontaneous diabetes mellitus.LEW.1AR1-iddm大鼠的遗传分析:一种自发性糖尿病的动物模型。
Mamm Genome. 2005 Jun;16(6):432-41. doi: 10.1007/s00335-004-3022-8.
10
ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.ZAC、LIT1(KCNQ1OT1)和p57KIP2(CDKN1C)处于一个可能在贝克威思-维德曼综合征中起作用的印记基因网络中。
Nucleic Acids Res. 2005 May 11;33(8):2650-60. doi: 10.1093/nar/gki555. Print 2005.

本文引用的文献

1
Polygenic control of autoimmune diabetes in nonobese diabetic mice.非肥胖糖尿病小鼠自身免疫性糖尿病的多基因控制
Nat Genet. 1993 Aug;4(4):404-9. doi: 10.1038/ng0893-404.
2
Susceptibility to insulin dependent diabetes mellitus maps to a 4.1 kb segment of DNA spanning the insulin gene and associated VNTR.胰岛素依赖型糖尿病的易感性定位到一段跨越胰岛素基因及相关可变数目串联重复序列的4.1 kb DNA片段。
Nat Genet. 1993 Jul;4(3):305-10. doi: 10.1038/ng0793-305.
3
Protection from insulin-dependent diabetes mellitus is linked to a peptide transporter gene.对胰岛素依赖型糖尿病的防护与一种肽转运蛋白基因有关。
Eur J Immunol. 1993 Aug;23(8):1784-8. doi: 10.1002/eji.1830230808.
4
Genetic dissection of complex traits.复杂性状的基因剖析
Science. 1994 Sep 30;265(5181):2037-48. doi: 10.1126/science.8091226.
5
Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q.11号染色体q臂上胰岛素依赖型糖尿病易感性位点的基因定位
Nature. 1994 Sep 8;371(6493):161-4. doi: 10.1038/371161a0.
6
A genome-wide search for human type 1 diabetes susceptibility genes.一项针对人类1型糖尿病易感基因的全基因组搜索。
Nature. 1994 Sep 8;371(6493):130-6. doi: 10.1038/371130a0.
7
Linkage of the VNTR/insulin-gene and type I diabetes mellitus: increased gene sharing in affected sibling pairs.可变数目串联重复序列/胰岛素基因与Ⅰ型糖尿病的连锁关系:患病同胞对中基因共享增加。
Am J Hum Genet. 1994 May;54(5):909-12.
8
Additive susceptibility to insulin-dependent diabetes conferred by HLA-DQB1 and insulin genes.由HLA - DQB1基因和胰岛素基因共同导致的胰岛素依赖型糖尿病易感性增加。
Autoimmunity. 1994;18(3):195-203. doi: 10.3109/08916939409007996.
9
Association of LMP2 and LMP7 genes within the major histocompatibility complex with insulin-dependent diabetes mellitus: population and family studies.主要组织相容性复合体中LMP2和LMP7基因与胰岛素依赖型糖尿病的关联:人群和家族研究。
Am J Hum Genet. 1995 Feb;56(2):528-34.
10
A locus on chromosome 15q26 (IDDM3) produces susceptibility to insulin-dependent diabetes mellitus.位于15号染色体q26区域(IDDM3)的一个基因座会导致对胰岛素依赖型糖尿病的易感性。
Nat Genet. 1994 Oct;8(2):189-94. doi: 10.1038/ng1094-189.