• 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

胰岛素基因区域的连锁不平衡:5'侧翼多态性的大小变异及“I类”等位基因中的双峰性

Linkage disequilibrium in the insulin gene region: size variation at the 5' flanking polymorphism and bimodality among "class I" alleles.

作者信息

McGinnis R E, Spielman R S

机构信息

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia 19104-6145.

出版信息

Am J Hum Genet. 1994 Sep;55(3):526-32.

PMID:7915880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1918400/
Abstract

The 5' flanking polymorphism (5'FP), a hypervariable region at the 5' end of the insulin gene, has "class 1" alleles (650-900 bp long) that are in positive linkage disequilibrium with insulin-dependent diabetes mellitus (IDDM). We report that precise sizing of the 5'FP yields a bimodal frequency distribution of class 1 allele lengths. Class 1 alleles belonging to the lower component (650-750 bp) of the bimodal distribution were somewhat more highly associated with IDDM than were alleles from the upper component (760-900 bp), but the difference was not statistically significant. We also examined 5'FP length variation in relation to allelic variation at nearby polymorphisms. At biallelic RFLPs on both sides of the 5'FP, we found that one allele exhibits near-total association with the upper component of the 5'FP class 1 distribution. Such associations represent a little-known but potentially widespread form of linkage disequilibrium. In this type of disequilibrium, a flanking allele has near-complete association with a single mode of VNTR alleles whose lengths represent consecutive numbers of tandem repeats (CNTR). Such extreme disequilibrium between a CNTR mode and flanking alleles may originate and persist because length mutations at some VNTR loci usually add or delete only one or two repeat units.

摘要

5'侧翼多态性(5'FP)是胰岛素基因5'端的一个高变区,具有“1类”等位基因(长度为650 - 900 bp),这些等位基因与胰岛素依赖型糖尿病(IDDM)呈正连锁不平衡。我们报告称,对5'FP进行精确大小测定可得到1类等位基因长度的双峰频率分布。双峰分布中属于较低组分(650 - 750 bp)的1类等位基因与IDDM的关联度略高于较高组分(760 - 900 bp)的等位基因,但差异无统计学意义。我们还研究了5'FP长度变异与附近多态性位点等位基因变异的关系。在5'FP两侧的双等位基因限制性片段长度多态性(RFLP)中,我们发现一个等位基因与5'FP 1类分布的较高组分表现出几乎完全的关联。这种关联代表了一种鲜为人知但可能广泛存在的连锁不平衡形式。在这种不平衡类型中,一个侧翼等位基因与可变数目串联重复序列(VNTR)等位基因的单一模式几乎完全关联,其长度代表串联重复的连续数目(CNTR)。CNTR模式与侧翼等位基因之间的这种极端不平衡可能起源并持续存在,因为某些VNTR位点的长度突变通常仅增加或删除一两个重复单元。

相似文献

1
Linkage disequilibrium in the insulin gene region: size variation at the 5' flanking polymorphism and bimodality among "class I" alleles.胰岛素基因区域的连锁不平衡:5'侧翼多态性的大小变异及“I类”等位基因中的双峰性
Am J Hum Genet. 1994 Sep;55(3):526-32.
2
Insulin gene 5' flanking polymorphism. Length of class 1 alleles in number of repeat units.胰岛素基因5'侧翼多态性。1类等位基因的长度(以重复单位数量计)。
Diabetes. 1995 Nov;44(11):1296-302. doi: 10.2337/diab.44.11.1296.
3
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).连锁不平衡的传递测试:胰岛素基因区域与胰岛素依赖型糖尿病(IDDM)
Am J Hum Genet. 1993 Mar;52(3):506-16.
4
Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkage.胰岛素依赖型糖尿病同胞对中的胰岛素基因共享:无连锁证据。
Am J Hum Genet. 1988 Jan;42(1):167-72.
5
Evidence for association between the class I subset of the insulin gene minisatellite (IDDM2 locus) and IDDM in the Japanese population.胰岛素基因小卫星的I类亚群(IDDM2基因座)与日本人群中胰岛素依赖型糖尿病(IDDM)之间关联的证据。
Diabetes. 1997 Oct;46(10):1637-42. doi: 10.2337/diacare.46.10.1637.
6
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.人类染色体2上人类胰岛素/胰岛素样生长因子II区域的连锁不平衡。
Am J Hum Genet. 1988 Oct;43(4):495-501.
7
DNA polymorphisms in the human tyrosine hydroxylase/insulin/insulin-like growth factor II chromosomal region in relation to glucose and insulin responses.人类酪氨酸羟化酶/胰岛素/胰岛素样生长因子II染色体区域的DNA多态性与葡萄糖及胰岛素反应的关系
Diabetologia. 1993 Jan;36(1):25-32. doi: 10.1007/BF00399089.
8
Imprinted and genotype-specific expression of genes at the IDDM2 locus in pancreas and leucocytes.IDDM2基因座上的基因在胰腺和白细胞中的印记及基因型特异性表达。
J Autoimmun. 1996 Jun;9(3):397-403. doi: 10.1006/jaut.1996.0054.
9
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus.IDDM2位点对人类1型糖尿病的易感性由胰岛素基因小卫星位点的串联重复变异决定。
Nat Genet. 1995 Mar;9(3):284-92. doi: 10.1038/ng0395-284.
10
Associations of IGF2 ApaI RFLP and INS VNTR class I allele size with obesity.胰岛素样生长因子2(IGF2)ApaI限制性片段长度多态性(RFLP)及胰岛素基因可变数目串联重复序列(INS VNTR)I类等位基因大小与肥胖的关联
Eur J Hum Genet. 1999 Oct-Nov;7(7):821-7. doi: 10.1038/sj.ejhg.5200381.

引用本文的文献

1
Polymorphism in regulatory gene sequences.调控基因序列中的多态性。
Genome Biol. 2001;2(1):COMMENT2001. doi: 10.1186/gb-2000-2-1-comment2001. Epub 2000 Dec 20.
2
Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.在跨越RNU2 - BRCA1的17号染色体q21区段有效抑制重组的证据。
Am J Hum Genet. 1999 May;64(5):1427-39. doi: 10.1086/302358.
3
Diabetes susceptibility at IDDM2 cannot be positively mapped to the VNTR locus of the insulin gene.胰岛素依赖型糖尿病2型(IDDM2)的糖尿病易感性不能正向定位到胰岛素基因的可变数目串联重复序列(VNTR)位点。
Diabetologia. 1996 May;39(5):594-9. doi: 10.1007/BF00403307.
4
HLA DQA1-DQB1-TAP2 haplotypes in IDDM families: no evidence for an additional contribution to disease risk by the TAP2 locus.胰岛素依赖型糖尿病家族中的HLA DQA1 - DQB1 - TAP2单倍型:无证据表明TAP2基因座对疾病风险有额外影响。
Diabetologia. 1995 Aug;38(8):968-74. doi: 10.1007/BF00400587.

本文引用的文献

1
The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models.选择与连锁的相互作用。I. 一般考量;杂种优势模型。
Genetics. 1964 Jan;49(1):49-67. doi: 10.1093/genetics/49.1.49.
2
Mutation of human short tandem repeats.人类短串联重复序列的突变
Hum Mol Genet. 1993 Aug;2(8):1123-8. doi: 10.1093/hmg/2.8.1123.
3
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.脆性X突变与两个紧密连锁的CA重复序列之间的连锁不平衡表明,脆性X染色体源自少数几个奠基者染色体。
Am J Hum Genet. 1993 Feb;52(2):297-304.
4
The highly polymorphic region near the human insulin gene is composed of simple tandemly repeating sequences.人类胰岛素基因附近的高度多态性区域由简单串联重复序列组成。
Nature. 1982 Jan 7;295(5844):31-5. doi: 10.1038/295031a0.
5
A polymorphic locus near the human insulin gene is associated with insulin-dependent diabetes mellitus.人类胰岛素基因附近的一个多态性位点与胰岛素依赖型糖尿病相关。
Diabetes. 1984 Feb;33(2):176-83. doi: 10.2337/diab.33.2.176.
6
Analysis of endonuclease R-EcoRI fragments of DNA from lambdoid bacteriophages and other viruses by agarose-gel electrophoresis.通过琼脂糖凝胶电泳分析来自λ样噬菌体和其他病毒的DNA的核酸内切酶R-EcoRI片段。
J Virol. 1974 Nov;14(5):1235-44. doi: 10.1128/JVI.14.5.1235-1244.1974.
7
HLA-DR effects in a large German IDDM dataset.在一个大型德国胰岛素依赖型糖尿病数据集中的HLA - DR效应
Genet Epidemiol Suppl. 1986;1:323-8. doi: 10.1002/gepi.1370030749.
8
Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.人类DNA串联重复高变位点上新长度等位基因的自发突变率。
Nature. 1988 Mar 17;332(6161):278-81. doi: 10.1038/332278a0.
9
Evidence for increased recombination near the human insulin gene: implication for disease association studies.人类胰岛素基因附近重组增加的证据:对疾病关联研究的启示。
Proc Natl Acad Sci U S A. 1986 Feb;83(4):1045-9. doi: 10.1073/pnas.83.4.1045.
10
Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.人类染色体2上人类胰岛素/胰岛素样生长因子II区域的连锁不平衡。
Am J Hum Genet. 1988 Oct;43(4):495-501.