Chu Leung Wing, Li Yan, Li Zhong, Tang Alan Y B, Cheung Bernard M Y, Leung Raymond Y H, Yik Ping-Yiu, Jin Dong-Yan, Song You-Qiang
Department of Medicine, The University of Hong Kong, Hong Kong.
Am J Med Genet B Neuropsychiatr Genet. 2007 Dec 5;144B(8):1007-13. doi: 10.1002/ajmg.b.30525.
Recent genetic studies have shown that variants of the ATP-binding cassette transporter A1, ABCA1, may be implicated in the pathogenesis of Alzheimer's disease (AD). In this case-control study, a panel of 19 single nucleotide polymorphisms (SNP) (including three amino-acid-coding SNPs used for replication of previous work, and 16 newly selected intronic tag SNPs) was genotyped. Nominally significant single marker P-values were observed in four SNPs, with the highest score of 0.003 for rs2297404 (OR = 1.88, 95%CI 1.23-2.87). In addition, six distinct linkage disequilibrium (LD) blocks were detected. LD block1 harbored three nominally significant SNPs (rs2297404, rs2230808, and rs2020927), and showed a different haplotype structure in the affected and unaffected groups. Of the four haplotypes identified, haplotype2 (CAC) was more prevalent in the disease group (0.323 in AD vs. 0.202 in control); while haplotype1 (TGG) was over-represented in the healthy controls (0.595 in control vs. 0.493 in AD), indicating disease risk conferring possibility of haplotype2. After doubling the sample size, the three nominally significant SNPs were still significantly associated with AD. Although coding SNP (rs2230808) was confirmed to have a significant association with AD, prediction of the effects of an amino acid substitution SNP rs2230808 (R1587K) on the three-dimensional structure and function of the ABCA1 protein using PolyPhen program revealed that it is unlikely to be functionally significant. However, the adjacent rs2297404 in the same LD block is potentially functionally significant because of its position in the immediate vicinity of a splicing branch site. Further functional analysis of this polymorphism should be a high priority.
近期的基因研究表明,ATP结合盒转运体A1(ABCA1)的变体可能与阿尔茨海默病(AD)的发病机制有关。在这项病例对照研究中,对一组19个单核苷酸多态性(SNP)(包括用于重复先前研究的3个氨基酸编码SNP,以及16个新选择的内含子标签SNP)进行了基因分型。在4个SNP中观察到名义上显著的单标记P值,rs2297404的得分最高,为0.003(OR = 1.88,95%CI 1.23 - 2.87)。此外,检测到6个不同的连锁不平衡(LD)块。LD块1包含3个名义上显著的SNP(rs2297404、rs2230808和rs2020927),并且在患病组和未患病组中显示出不同的单倍型结构。在鉴定出的4种单倍型中,单倍型2(CAC)在疾病组中更为常见(AD组为0.323,对照组为0.202);而单倍型1(TGG)在健康对照组中占比过高(对照组为0.595,AD组为0.493),表明单倍型2具有疾病风险。在样本量翻倍后,这3个名义上显著的SNP仍与AD显著相关。尽管编码SNP(rs2230808)被证实与AD有显著关联,但使用PolyPhen程序预测氨基酸替代SNP rs2230808(R1587K)对ABCA1蛋白三维结构和功能的影响表明,它不太可能具有功能显著性。然而,同一LD块中相邻的rs2297404因其紧邻剪接分支位点的位置而可能具有功能显著性。对这种多态性的进一步功能分析应作为高度优先事项。