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首页> 外文期刊>BMC Medical Genetics >Genetic association study of selected candidate genes (ApoB, LPL, Leptin) and telomere length in obese and hypertensive individuals
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Genetic association study of selected candidate genes (ApoB, LPL, Leptin) and telomere length in obese and hypertensive individuals

机译:肥胖和高血压个体中所选候选基因(ApoB,LPL,瘦蛋白)和端粒长度的遗传关联研究

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Background A genetic study was carried out among obese and hypertensive individuals from India to assess allelic association, if any, at three candidate loci: Apolipoprotein B (ApoB) minisatellite and two tetranucleotide repeat loci; LPL (Lipoprotein lipase) and Leptin. Attempt has also been made to find out whether telomere length attrition is associated with hypertension and obese individuals. Methods Venous blood samples were collected from 37 normal, 35 obese and 47 hypertensive individuals. Genomic DNA was extracted from peripheral blood mononuclear cells (PBMC) and PCR amplifications were achieved using locus specific primers. Genotyping of ApoB minisatellite was performed using 4% polyacrylamide gel electrophoresis (PAGE) followed by silver staining, whereas LPL and Leptin loci were genotyped using ALF Express? DNA sequencer. Telomere length was determined using a recently developed real time based quantitative PCR, where the relative telomere length was determined by calculating the relative ratio of telomere (T) and single copy gene (S) PCR products which is expressed as T/S ratio. Results All the three loci are highly polymorphic, display high heterozygosity and conform to Hardy-Weinberg's equilibrium expectations. ApoB minisatellite displayed 14 alleles, whereas LPL and Leptin tetranucleotide loci were having 9 and 17 alleles, respectively. Interestingly two new alleles (9 and 11 repeats) were detected at ApoB locus for the first time. The alleles at Leptin locus were classified as Class I (lower alleles: 149-200 bp) and Class II alleles (higher alleles: >217 bp). Higher alleles at ApoB (>39 repeats), predominant allele 9 at LPL and alleles 164 bp and 224 bp at Leptin loci have shown allelic association with hypertensive individuals. After adjusting the influence of age and gender, the analysis of co-variance (ANCOVA) revealed the relative telomere length (T/S ratio) in hypertensive individuals to be (1.01 ± 0.021), which was significantly different (P Conclusion The present study revealed that allelic association at ApoB, LPL, Leptin loci and loss of telomere length may have strong genetic association with hypertensive individuals. However, further study on larger sample size is needed to draw firm conclusions.
机译:背景对来自印度的肥胖和高血压人群进行了一项遗传研究,以评估三个候选基因座的等位基因关联(如果有):载脂蛋白B(ApoB)小卫星和两个四核苷酸重复基因座; LPL(脂蛋白脂肪酶)和瘦素。还试图找出端粒长度减少是否与高血压和肥胖个体有关。方法收集37例正常人,35例肥胖者和47例高血压患者的静脉血。从外周血单核细胞(PBMC)中提取基因组DNA,并使用基因座特异性引物进行PCR扩增。使用4%聚丙烯酰胺凝胶电泳(PAGE)进行ApoB小卫星的基因分型,然后进行银染,而使用ALF Express?对LPL和瘦蛋白基因座进行基因分型。 DNA测序仪。使用最近开发的基于实时的定量PCR确定端粒长度,其中相对端粒长度通过计算端粒(T)和单拷贝基因(S)PCR产物的相对比值(以T / S比表示)来确定。结果这三个基因座均为高度多态性,显示高杂合度,符合Hardy-Weinberg的平衡期望。 ApoB小卫星显示14个等位基因,而LPL和Leptin四核苷酸位点分别具有9和17个等位基因。有趣的是,首次在ApoB位点检测到两个新的等位基因(9和11个重复)。瘦素基因座的等位基因分为I类(低等位基因:149-200 bp)和II类等位基因(高等位基因:> 217 bp)。 ApoB的较高等位基因(> 39个重复),LPL上的主要等位基因9和Leptin基因座上的164 bp和224 bp等位基因已显示出与高血压个体相关的等位基因。调整年龄和性别的影响后,协方差分析(ANCOVA)显示高血压个体的相对端粒长度(T / S比)为(1.01±0.021),差异显着(P结论)揭示ApoB,LPL,Leptin基因座的等位基因关联和端粒长度的丢失可能与高血压个体有很强的遗传关联,但是,需要对更大的样本量进行进一步研究以得出明确的结论。

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