α-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

被引:38
作者
Busby, V
Goossens, S
Nowotny, P
Hamilton, G
Smemo, S
Harold, D
Turic, D
Jehu, L
Myers, A
Womick, M
Woo, D
Compton, D
Doil, LM
Tacey, KM
Lau, KF
Al-Saraj, S
Killick, R
Pickering-Brown, S
Moore, P
Hollingworth, P
Archer, N
Foy, C
Walter, S
Lendon, C
Iwatsubo, T
Morris, JC
Norton, J
Mann, D
Janssens, B
Hardy, J
O'Donovan, M
Jones, L
Williams, J
Holmans, P
Owen, MJ
Grupe, A
Powell, J
van Hengel, J
Goate, A
Van Roy, F
Lovestone, S
机构
[1] Inst Psychiat, Dept Neurosci, London SE5 8AF, England
[2] State Univ Ghent VIB, Dept Mol Biomed Res, Mol Cell Biol Unit, B-9000 Ghent, Belgium
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Neurol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[6] Univ Wales Coll Med, Dept Psychol Med, Cardiff CF4 4XN, S Glam, Wales
[7] NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[8] Univ Birmingham, Queen Elizabeth Psychiat Hosp, Dept Psychiat, Birmingham B15 2QZ, W Midlands, England
[9] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Neuropathol & Neurosci, Bunkyo Ku, Tokyo 1130033, Japan
[10] Hope Hosp, Greater Manchester Neurosci Ctr, Salford M6 8HD, Lancs, England
[11] Inst Publ Hlth, MRC, Biostat Unit, Cambridge CB2 2SR, England
[12] Celera Diagnost, Alameda, CA USA
关键词
CTNNA3; alpha-T-catenin; Alzheimer's disease; chromosome; 10; amyloid; A beta; age of onset; APOE; Wn;
D O I
10.1385/NMM:5:2:133
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The gene encoding alpha-T-catenin, CTNNA3, is positioned within a region on chromosome 10, showing strong evidence of linkage to Alzheimer's disease (AD), and is therefore a good positional candidate gene for this disorder. We have demonstrated that alpha-T-catenin is expressed in human brain, and like other alpha-catenins, it inhibits Wnt signaling and is therefore also a functional candidate. We initially genotyped two single-nucleotide polymorphisms (SNPs) in the gene, in four independent samples comprising over 1200 cases and controls but failed to detect an association with either SNP. Similarly, we found no evidence for association between CTNNA3 and AD in a sample of subjects showing linkage to chromosome 10, nor were these SNPs associated with Abeta deposition in brain. To comprehensively screen the gene, we genotyped 30 additional SNPs in a subset of the cases and controls (n > 700). None of these SNPs was associated with disease. Although an excellent candidate, we conclude that CTNNA3 is unlikely to account for the AD susceptibility locus on chromosome 10.
引用
收藏
页码:133 / 146
页数:14
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