Positional Cloning Of A Diabetes Gene On Chromosome 11
Positional Cloning Of A Diabetes Gene On Chromosome 11
批准号:
6810609
负责人:
Leslie J Baier
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
artificial chromosomes biotechnology body composition chromosomes clinical research diabetes mellitus genetics family genetics genetic mapping genetic markers genetic polymorphism genetic susceptibility genotype glucose metabolism human genetic material tag human subject insulin linkage disequilibriums linkage mapping microarray technology molecular cloning nucleic acid sequence phenotype single nucleotide polymorphism
中文摘要
先前对居住在美国的皮马印第安人进行的基因组扫描表明,染色体11 q23 -24(LOD=3.6)上存在肥胖易感基因座。还有证据表明,相同的基因组区域包含2型糖尿病(T2 DM)的易感基因座(LOD=1.7)。双变量连锁分析的组合表型糖尿病的易感位点(LOD= 5.2)的最强有力的证据。在这个精确的基因组区域(D11 S4464)与体重指数(BMI)的联系已经在来自心脏病研究的高加索人和来自犹他州(Myriad Genetics)的家系中的病态肥胖男性中得到了复制。皮马印第安人的连锁区域跨越约24 Mb。我们目前的目标是定位克隆负责连锁的基因。正在对整个连锁区域的位置候选基因进行测序,以确定遗传变异。此外,连锁不平衡(LD)定位被用来缩小易感区域。对于LD作图,单核苷酸多态性(SNP)被系统地鉴定,并在整个连锁区域以25 kB的间隔进行基因分型。到目前为止,已经在1229个DNA样本中对跨越我们连锁区域的大约700个SNP进行了单独的基因分型,并测试了与BMI或T2 DM的相关性。已经初步鉴定了两个独立的区域,其含有与BMI和糖尿病显著相关的多个SNP。对我们目前的L.D.作图数据表明,染色体11 q23 -24上不止一个基因与糖尿病和BMI相关。
英文摘要
A prior genomic scan in Pima Indians living in the United States indicated an obesity susceptibility locus on chromosome 11q23-24 (LOD=3.6). There was also evidence that the same genomic region contained a susceptibility locus for type 2 diabetes mellitus (T2DM)(LOD=1.7). Bivariate linkage analysis for the combined phenotype diabesity gave the strongest evidence for a susceptibility locus (LOD= 5.2). Linkage to body mass index (BMI) at this precise genomic region (D11S4464) has been replicated in Caucasians from the Framingham Heart Study and in morbidly obese males in pedigrees from Utah (Myriad Genetics). The region of linkage in Pima Indians spans approximately 24 Mb. Our current goal is to positionally clone the gene(s) responsible for the linkage. Positional candidate genes across the region of linkage are being sequenced to identify genetic variants. In addition, linkage disequilibrium (LD) mapping is being used to narrow the susceptibility region. For LD mapping, single nucleotide polymorphisms (SNPs) are being systematically identified and genotyped at 25 kB intervals across the region of linkage. To date, approximately 700 SNPs that span our region of linkage have been individually genotyped in 1229 DNA samples, and tested for association with either BMI or T2DM. Two separate regions have been preliminarily identified that contain multiple SNPs significantly associated with BMI and diabetes. A preliminary interpretation of our current L.D. mapping data is that more than one gene is responsible for the linkage to diabetes and BMI on chromosome 11q23-24.
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