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Allelic mRNA expression of sortilin-1 (SORL1) mRNA in Alzheimer's autopsy brain tissues.

机译:阿尔茨海默氏病尸体脑组织中sortilin-1(SORL1)mRNA的等位基因mRNA表达。

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摘要

Polymorphisms in the gene encoding SORL1, involved in cellular trafficking of APP, have been implicated in late-onset Alzheimer's disease, by a mechanism thought to affect mRNA expression. To search for regulatory polymorphisms, we have measured allele-specific mRNA expression of SORL1 in human autopsy tissues from the prefrontal cortex of 26 Alzheimer's patients, and 51 controls, using two synonymous marker SNPs (rs3824968 in exon 34 (11 heterozygous AD subjects and 16 controls), and rs12364988 in exon 6 (8 heterozygous AD subjects)). Significant allelic expression imbalance (AEI), indicative of the presence of cis-acting regulatory factors, was detected in a single control subject, while allelic ratios were near unity for all other subjects. We genotyped 7 SNPs in two haplotype blocks that had previously been implicated in Alzheimer's disease. Since each of these SNPs was heterozygous in several subjects lacking AEI, this study fails to support a regulatory role for SORL1 polymorphisms in mRNA expression.
机译:编码SORL1的基因的多态性,与APP的细胞运输有关,已通过影响mRNA表达的机制与晚期阿尔茨海默氏病有关。为了寻找调节性多态性,我们使用两个同义标记SNPs(第38外显子(11个杂合子AD和16个外显子)中的rs3824968,测量了26名阿尔茨海默氏病患者和51名对照的人尸体解剖组织中SORL1的等位基因特异性mRNA表达。对照)和第12外显子中的rs12364988(8个杂合AD受试者)。在单个对照受试者中检测到显着的等位基因表达失衡(AEI),表明存在顺式作用调节因子,而其他所有受试者的等位基因比率均接近1。我们对两个单倍型基因组中的7个SNP进行了基因分型,以前它们与阿尔茨海默氏病有关。由于这些SNP中的每一个在缺乏AEI的几个受试者中都是杂合的,因此该研究未能支持SORL1多态性在mRNA表达中的调节作用。

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