Analysis of protocadherin alpha gene enhancer polymorphism in bipolar disorder and schizophrenia

被引:43
|
作者
Pedrosa, Erika [1 ]
Stefanescu, Radu [1 ]
Margolis, Benjamin [1 ]
Petruolo, Oriana [1 ]
Lo, Yungtai [2 ]
Nolan, Karen [3 ]
Novak, Tomas [4 ]
Stopkova, Pavla [4 ]
Lachman, Herbert M. [1 ]
机构
[1] Albert Einstein Coll Med, Dept Psychiat & Behav Sci, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Epidemiol & Populat Hlth, Bronx, NY 10461 USA
[3] Nathan S Kline Inst Psychiat Res, Dept Psychiat, Orangeburg, NY 10962 USA
[4] Prague Psychiat Ctr, Prague, Czech Republic
关键词
protocadherin; cadherin schizophrenia; bipolar disorder; chromatin;
D O I
10.1016/j.schres.2008.04.013
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Cadherins and protocadherins are cell adhesion proteins that play an important role in neuronal migration, differentiation and synaptogenesis, properties that make them targets to consider in schizophrenia (SZ) and bipolar disorder (BD) pathogenesis. Consequently, allelic variation occurring in protocadherin and cadherin encoding genes that map to regions of the genome targeted in SZ and BD linkage studies are particularly strong candidates to consider. One such set of candidate genes is the 5q31-linked PCDH family, which consists of more than 50 exons encoding three related, though distinct family members - alpha, beta, and gamma - which can generate thousands of different protocadherin proteins through alternative promoter usage and cis-alternative splicing. In this study, we focused on a SNP, rs31745, which is located in a putative PCDH alpha enhancer mapped by ChIP-chip, using antibodies to covalently modified histone H3. A striking increase in homozygotes for the minor allele at this locus was detected in patients with BD. Molecular analysis revealed that the SNP causes allele-specific changes in binding to a brain protein. The findings suggest that the 5q31-linked PCDH locus should be more thoroughly considered as a disease-susceptibility locus in psychiatric disorders. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:210 / 219
页数:10
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