Polymorphic GGC repeat differentially regulates human reelin gene expression levels

被引:33
作者
Persico, A. M.
Levitt, P.
Pimenta, A. F.
机构
[1] Univ Rome, Lab Mol Psychiat & Neurogenet, I-00155 Rome, Italy
[2] IRCCS, Fdn S Lucia, Rome, Italy
[3] Vanderbilt Univ, Vanderbilt Kennedy Ctr Res Human Dev, Nashville, TN USA
[4] Vanderbilt Univ, Dept Pharmacol, Nashville, TN USA
关键词
autism; gene expression; reelin; schizophrenia; transcription; translation; triplet repeat;
D O I
10.1007/s00702-006-0441-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The human gene encoding Reelin (RELN), a pivotal protein in neurodevelopment, includes a polymorphic GGC repeat in its 5' untranslated region (UTR). CHO cells transfected with constructs encompassing the RELN 5'UTR with 4-to-13 GGC repeats upstream of the luciferase reporter gene show declining luciferase activity with increasing GGC repeat number (P < 0.005), as predicted by computer-based simulations. Conversely, RELN 5'UTR sequences boost reporter gene expression above control levels in neuronal SN56 and N2A cell lines, but 12- and 13-repeat alleles still yield 50-60% less luciferase activity compared to the more common 8- and 10-repeat alleles (P < 0.0001). RELN "long" GGC alleles significantly blunt gene expression and may, through this effect, confer vulnerability to human disorders, such as schizophrenia and autism.
引用
收藏
页码:1373 / 1382
页数:10
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