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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Novel polymorphisms of the amyloid precursor protein (APP) gene in Chinese/Taiwanese patients with Alzheimer's disease.
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Novel polymorphisms of the amyloid precursor protein (APP) gene in Chinese/Taiwanese patients with Alzheimer's disease.

机译:中国/台湾阿尔茨海默氏病患者淀粉样蛋白前体蛋白(APP)基因的新型多态性。

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We aimed to determine if the amyloid precursor protein (APP) gene polymorphism is present in Chinese/Taiwanese patients with Alzheimer's disease (AD). This is a 3-year prospective assessment of the genotypes of the APP gene among Chinese/Taiwanese patients with AD. The sample consisted of 50 AD patients and 50 unaffected controls. Participants were recruited from the practices of the authors. Controls were comprised of 45 unrelated healthy subjects and 5 unaffected family members of AD patients. Data were collected in a university-based research unit of a tertiary medical center. Sequencing of the APP gene from exon 15 to exon 18 was performed on the peripheral blood of the patients and the unaffected controls after their informed consent was obtained. Among 50 AD subjects, 11 (7 men, 4 women) had APP gene polymorphisms. Mean age of onset was 72 years (range 65-82 years). Polymorphism of APP gene with A to C substitution at nucleotide position (nt) 284490 (A284490C) was found in 8 AD patients, at nt 284493 (A284493C) in 5, T284497C in 3 patients, and T284500C in 1 patient. These single nucleotide substitutions of the APP gene corresponded to the amino acid substitutions I718L, L720S, and V710G. These polymorphisms were not found in the unaffected controls. The mutations were confirmed by StyI restriction enzyme digestion assay using the subclone from polymerase chain reaction (PCR) products of the mutated APP gene. Thus, APP gene polymorphisms at codon 718 (I>L), 720 (L>S), and 710 (V>G) can be found in certain Chinese/Taiwanese patients with Alzheimer's disease.
机译:我们旨在确定淀粉样蛋白前体蛋白(APP)基因多态性是否存在于中国/台湾患有阿尔茨海默氏病(AD)的患者中。这是对中国/台湾AD病人APP基因型进行的为期3年的前瞻性评估。样本由50位AD患者和50位未受影响的对照组组成。参与者是从作者的实践中招募的。对照组由45位不相关的健康受试者和5位未受影响的AD患者家庭成员组成。数据是在三级医疗中心的大学级研究部门中收集的。在获得患者的知情同意后,对患者和未患病对照的外周血进行第15外显子至第18外显子APP基因的测序。在50名AD受试者中,有11名(男性7名,女性4名)具有APP基因多态性。平均发病年龄为72岁(65-82岁)。在8位AD患者,5位患者nt 284493(A284493C),5位患者的T284497C和1位患者的T284500C的核苷酸位置(nt)284490(A284490C)具有A到C取代的APP基因的多态性。 APP基因的这些单核苷酸取代对应于氨基酸取代I718L,L720S和V710G。在未受影响的对照中未发现这些多态性。使用来自突变APP基因的聚合酶链反应(PCR)产物的亚克隆,通过StyI限制性内切酶消化测定法确认了突变。因此,在某些患有阿尔茨海默氏病的中国/台湾患者中可以发现密码子为718(I> L),720(L> S)和710(V> G)的APP基因多态性。

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