Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene

被引:130
作者
Artiga, MJ
Bullido, MJ
Frank, A
Sastre, I
Recuero, M
Garcia, MA
Lendon, CL
Han, SW
Morris, JC
Vázquez, J
Goate, A
Valdivieso, F [1 ]
机构
[1] Univ Autonoma Madrid, CSIC, Dept Mol Biol, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, CSIC, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
[3] Univ Madrid, Hosp La Paz, Neurol Serv, Madrid 28034, Spain
[4] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[6] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
关键词
D O I
10.1093/hmg/7.12.1887
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While the epsilon 4 allele of apolipoprotein E (APOE, gene; ApoE, protein) is widely accepted as a major genetic risk factor for the late onset form of Alzheimer's disease (AD), recent evidence points to variations in ApoE levels as another important factor. We have previously reported that a common variant in the regulatory region of APOE(-491A) is associated with risk for late onset AD. In this report we analyze the association of another APOE promoter polymorphism (-427T/C) with AD in two case-control clinical samples and demonstrate a correlation between APOE promoter transcriptional activity and risk for AD. The association studies show that the allelic variant (-427C) and the haplotype [-491A-427C] of the APOE promoter are associated with increased risk for AD. Study of the transcriptional activity of the common haplotypes defined by combination of the -491 and -427 alleles indicated that the risk for late onset AD positively correlates with transcriptional activity of the APOE gene, suggesting that increases in the local expression of ApoE could be responsible for the association of APOE promoter polymorphism with AD.
引用
收藏
页码:1887 / 1892
页数:6
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