首页> 外文期刊>Journal of diabetes and its complications >A single nucleotide polymorphism alters the sequence of SP1 binding site in the adiponectin promoter region and is associated with diabetic nephropathy among type 1 diabetic patients in the Genetics of Kidneys in Diabetes Study.
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A single nucleotide polymorphism alters the sequence of SP1 binding site in the adiponectin promoter region and is associated with diabetic nephropathy among type 1 diabetic patients in the Genetics of Kidneys in Diabetes Study.

机译:在糖尿病的肾脏遗传学研究中,单核苷酸多态性改变了脂联素启动子区域中SP1结合位点的序列,并与1型糖尿病患者的糖尿病肾病有关。

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OBJECTIVE: The adiponectin promoter single nucleotide polymorphism (SNP) -11391G/A is found to be associated with nephropathy in type 1 diabetic (T1D) patients among Danish, but not French, Finnish, and Swedish populations. In the present study, we identified the binding sites for transcriptional factors in the adiponectin promoter region and also evaluated the association between adiponectin promoter polymorphisms and diabetic nephropathy (DN) in T1D patients. MATERIALS AND METHODS: Three adiponectin promoter SNPs, including -11377C/G, -11391G/A, and -11426A/G, were genotyped with dynamic allele-specific hybridization. The subjects included 1177 American T1D patients (622 females/555 males) with or without DN. All patients are of European descent and selected from the Genetics of Kidneys in Diabetes (GoKinD) study. RESULTS: We identified four binding sites of transcriptional stimulatory protein (SP1) in the adiponectin putative promoter and found that the G allele of SNP -11377C/G altered the sequence for one of the SP1 binding sites. This polymorphism was significantly associated with DN in female T1D patients (P=.022, OR=1.352, 95% CI=1.044-1.752). Further analyses indicated the common diplotype (haplotypic genotype) H1/H1, constructed with SNPs -11377C/G and -11391G/A, was significantly associated with DN in females (P=.013), while the association of another diplotype H1/H2 with DN in females was of borderline significance (P=.071). CONCLUSIONS: The present study thus provides the first evidence that SNP -11377C/G alters the sequence in one of the SP1 binding sites in the adiponectin promoter region. This polymorphism, together with another promoter SNP -11391G/A, may confer susceptibility to the development of DN in T1D patients among the GoKinD population.
机译:目的:脂联素启动子单核苷酸多态性(SNP)-11391G / A被发现与丹麦人(而非法国,芬兰和瑞典)的1型糖尿病(T1D)患者的肾病有关。在本研究中,我们确定了脂联素启动子区域中转录因子的结合位点,并评估了脂联素启动子多态性与T1D患者的糖尿病肾病(DN)之间的关联。材料与方法:采用动态等位基因特异性杂交对三种脂联素启动子SNP,包括-11377C / G,-11391G / A和-11426A / G进行基因分型。受试者包括1177名患有DN或不患有DN的美国T1D患者(622名女性/ 555名男性)。所有患者均为欧洲人血统,选自糖尿病肾脏遗传学(GoKinD)研究。结果:我们在脂联素推定的启动子中鉴定了四个转录刺激蛋白(SP1)结合位点,发现SNP -11377C / G的G等位基因改变了其中一个SP1结合位点的序列。在女性T1D患者中,这种多态性与DN显着相关(P = .022,OR = 1.352,95%CI = 1.044-1.752)。进一步的分析表明,由SNP -11377C / G和-11391G / A构建的常见双倍型(单倍型基因型)H1 / H1与女性的DN显着相关(P = .013),而另一个双倍型H1 / H2的关联DN在女性中具有临界意义(P = .071)。结论:本研究因此提供了第一个证据,即SNP -11377C / G改变了脂联素启动子区域SP1结合位点中的一个序列。这种多态性,与另一个启动子SNP -11391G / A一起,可能使GoKinD人群中T1D患者的DN易感性增加。

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