首页> 外文期刊>Scientific reports. >Obesity-related CpG Methylation (cg07814318) of Kruppel-like Factor-13 (KLF13) Gene with Childhood Obesity and its cis-Methylation Quantitative Loci
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Obesity-related CpG Methylation (cg07814318) of Kruppel-like Factor-13 (KLF13) Gene with Childhood Obesity and its cis-Methylation Quantitative Loci

机译:Kruppel样因子-13(KLF13)基因的肥胖相关的CpG甲基化(CG07814318)具有儿童肥胖及其顺式 - 甲基化定量基因座

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The cg07814318 hypermethylation of Kruppel-like factor 13 (KLF13) gene has been reported for its relevancy with Body Mass Index (BMI) from European origin. We explored the cg07814318 methylation and its cis-meQTL (cis-methylation quantitative loci) of KLF13 from a childhood obesity cohort. The cg07814318 methylation in blood was significantly associated with obesity and correlated with several obesity-related physical and biochemical traits. We examined the same loci from purified three human cell types (n?=?47), i.e., pre-adipocytes, adipocytes and islets. The cg07814318 methylation pattern in pre-adipocytes and islets were significant higher in cells from subjects with a higher BMI compared with control subjects. By exome sequencing of KLF13 gene in blood with the same cohort, we found nine SNPs (single nucleotide polymorphisms) within its gene body, and two SNPs (rs11537749 and rs12595641) were as cis-meQTL of cg07814318. There was the 2.01% methylation change of cg07814318 between homozygous dominant and recessive genotypes, especially, in rs12595641. The sequencing variations within KLF13 genes could drive dynamic modifications of obesity-related CpG methylation. Differential DNA methylation patterns in the KLF13 gene determined from separate blood samples showed that this criterion could be used as a surrogate for representing overall epigenetic changes in cells related to obesity.
机译:据报道,KRUPPEL样因子13(KLF13)基因的CG07814318高甲基化与来自欧洲起源的体重指数(BMI)的相关性。我们探讨了KLF13的CG07814318甲基化及其CIS-MEQTL(CIS-甲基化定量基因座)来自儿童肥胖队的群体。 CG07814318血液中的甲基化与肥胖显着相关,与几种肥胖相关的物理和生化特征相关。我们检查了来自纯化的三种人细胞类型(n?= 47)的相同基因座,即脂肪细胞前脂肪细胞,脂肪细胞和胰岛。与对照受试者相比,来自脂肪细胞前脂肪细胞和胰岛的甲基化图案在具有较高BMI的受试者的细胞中显着较高。通过在血液中的血液中序列测序具有相同的队列,我们​​发现其基因体内的九个SNP(单核苷酸多态性),两个SNP(RS11537749和RS12595641)是CG07814318的CIS-MEQTL。纯合子占优势和隐性基因型之间的CG07814318甲基化变化2.01%,特别是在RS12595641中。 KLF13基因内的测序变化可以驱动肥胖相关的CpG甲基化的动态修饰。从单独的血液样品中测定的KLF13基因中的差异DNA甲基化模式表明该标准可以用作代表代表与肥胖有关的细胞的整体表观遗传变化。

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