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High-Speed Apolipoprotein E Genotyping and Apolipoprotein B3500 Mutation Detection Using Real-Time Fluorescence PCR and Melting Curves

机译:实时荧光PCR和熔解曲线检测高速载脂蛋白E基因型和载脂蛋白B3500突变

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Apolipoproteins play a central role in cholesterol transport by their association to lipoproteins and their function as ligands for receptors, cofactors, or structural proteins. Mutations and polymorphisms in a variety of apolipoproteins lead to lipoprotein metabolism disorders and/or susceptibility to cardiovascular disease. In familial defective apolipoprotein B-100, the clearance of LDL particles from the circulation is impaired because of reduced affinity of the apolipoprotein (apo) B component of LDL for the LDL receptor as a result of a G-to-A mutation at nucleotide 10708 in exon 26 of the apoB gene, which causes substitution of Arg3500 for Gln (1)(2). The frequency of the mutation is 1 in 700 in the general population (3). Heterozygous individuals have increased serum concentrations of cholesterol. Apolipoprotein E (apoE) likewise is involved in the clearance of HDL, contributing to reverse cholesterol transport (4). Genetic variation at the APOE locus in humans is an important determinant of plasma lipid concentrations and relative risk of atherosclerosis (5). Among several rare variants, three major alleles have been identified in the population: E2 , E3 , and E4 . The most common E3 isoform is distinguished by cysteine at position 112 and arginine at position 158 in the receptor-binding region of apoE. The E4 isoform (Arg112 and Arg158) is associated with increased cholesterol, thus enhancing the risk of heart disease (5). In addition, E4 / E4 individuals have a very high risk for developing Alzheimer disease(6). Most patients with type III hyperlipidemia are homozygous for the E2 allele (Cys112 and Cys158).To date, genotyping for apoE is mainly performed by PCR, followed by digestion with restriction enzymes and restriction fragment length polymorphism (RFLP) analysis, and separation of the resulting DNA fragments on agarose or acrylamide gels (7). For apoB3500, an allele-specific …
机译:载脂蛋白通过与脂蛋白缔合,并作为受体,辅因子或结构蛋白的配体起作用,在胆固醇运输中起着核心作用。多种载脂蛋白的突变和多态性会导致脂蛋白代谢异常和/或易患心血管疾病。在家族性缺陷载脂蛋白B-100中,由于核苷酸10708上的G-A突变导致LDL载脂蛋白(apo)B组分对LDL受体的亲和力降低,因此LDL颗粒从循环中的清除受到损害在apoB基因的第26外显子中,它导致Arg3500取代Gln(1)(2)。在一般人群中,突变频率为700分之一(3)。杂合子个体的血清胆固醇浓度升高。载脂蛋白E(apoE)同样也参与了HDL的清除,从而促进了胆固醇的逆向转运(4)。人类APOE位点的遗传变异是血浆脂质浓度和动脉粥样硬化相对危险性的重要决定因素(5)。在几个罕见的变体中,已在种群中鉴定出三个主要等位基因:E2,E3和E4。最常见的E3亚型的特征是apoE受体结合区域中112位的半胱氨酸和158位的精氨酸。 E4亚型(Arg112和Arg158)与胆固醇升高有关,因此增加了患心脏病的风险(5)。此外,E4 / E4个体患阿尔茨海默氏病的风险很高(6)。多数III型高脂血症患者的E2等位基因是纯合的(Cys112和Cys158)。琼脂糖或丙烯酰胺凝胶上产生的DNA片段(7)。对于apoB3500,一个等位基因特异性…

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