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A novel polymorphic purine complex at the 1.5 kb upstream region of the human caveolin‐1 gene and risk of Alzheimer's disease; Extra‐short alleles and accumulated allele homozygosity
Author(s) -
Heshmati Y.,
Mirabzadeh A.,
Feizzade G.,
Gilanipour M.,
Etminan M.R.,
Khoram Khorshid H.R.,
Kamali K.,
Fakhri M.,
Moghimi N.,
Najmabadi H.,
Ohadi M.
Publication year - 2008
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30805
Subject(s) - allele , genetics , gene , biology , genotype , disease , medicine
Crucial interaction of caveolin‐1 (CAV1) with β‐ and γ‐secretases, and aberrant expression of the gene encoding this protein in Alzheimer's disease (AD) support a role for CAV1 in the pathophysiology of this disease. We report a novel polymorphic purine complex stretching ∼150 bp of genomic DNA at the 1.5 kb upstream region of the human CAV1 gene, alleles and genotypes of which are associated with sporadic late‐onset AD. Extra‐short alleles were observed in the case group that were absent in the control subjects. Remarkably, 63% of these alleles were observed to be homozygous in length, forming 23.7% of the homozygote length compartment in the AD cases (χ 2 = 19.08, df = 1, P < 0.7). Increased homozygosity for length was also observed at this region in the Alzheimer's cases, for the allele lengths shared by the case and control groups [(χ 2 = 30.75, df = 1, P < 0., OR = 4.54, CI 95% (2.56–8.3)]. This region contains GGAA and GAAA motifs, the consensus binding sites for the Ets and IRF family transcription factors, respectively, and is highly conserved in distantly related non‐human primates in respect with location and motif sequence. The effect of this complex sequence on the expression of CAV1, and the related mechanisms in the pathophysiology of AD remain to be clarified. © 2008 Wiley‐Liss, Inc.