A novel functional low-density lipoprotein receptor-related protein 6 gene alternative splice variant is associated with Alzheimer's disease

被引:37
作者
Alarcon, Marcelo A. [1 ,2 ,3 ]
Medina, Matias A. [1 ,2 ]
Hu, Qubai [4 ]
Avila, Miguel E. [1 ,2 ,3 ]
Bustos, Bernabe I. [1 ,2 ]
Perez-Palma, Eduardo [1 ,2 ]
Peralta, Alexis [1 ,2 ]
Salazar, Paulina [1 ,2 ]
Ugarte, Giorgia D. [1 ,2 ,3 ]
Reyes, Ariel E. [1 ,2 ]
Martin, George M. [4 ]
Opazo, Carlos [3 ,5 ]
Moon, Randall T. [6 ,7 ]
De Ferrari, Giancarlo V. [1 ,2 ]
机构
[1] Univ Andres Bello, Ctr Biomed Res, Santiago, Chile
[2] Univ Andres Bello, FONDAP Ctr Genome Regulat, Santiago, Chile
[3] Univ Concepcion, Fac Biol Sci, Concepcion, Chile
[4] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
[5] Univ Melbourne, Oxidat Biol Lab, Florey Inst Neurosci & Mental Hlth, Melbourne, Vic, Australia
[6] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
[7] Univ Washington, Sch Med, Inst Stem Cell & Regenerat Med, Seattle, WA USA
关键词
Alternative splicing; Alzheimer's disease; LRP6; Wnt/beta-catenin signaling; GLYCOGEN-SYNTHASE KINASE-3-BETA; WNT SIGNALING PATHWAY; AMYLOID PRECURSOR PROTEIN; ALPHA-T-CATENIN; BETA-CATENIN; TRANSCRIPT EXPRESSION; TAU PHOSPHORYLATION; SEQUENCE VARIANTS; TARGET GENES; HUMAN BRAIN;
D O I
10.1016/j.neurobiolaging.2012.11.004
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We previously found that single nucleotide polymorphisms in the low-density lipoprotein receptor-related protein 6 (LRP6) gene are associated with Alzheimer's disease (AD). Here, we studied the post-transcriptional metabolism of the LRP6 message scanning sequentially the 23 LRP6 exons in human tissues and found a novel LRP6 isoform that completely skips exon 3 (LRP6 Delta 3) in all tissues examined and was also conserved in mice. Expression levels of the LRP6 isoforms were determined in 47 cortical brain messenger (m) RNA samples including 22 AD cases, 11 control subjects, and 14 individuals with other neurological disorders. LRP6 Delta 3 mRNA levels were significantly augmented in AD brains compared with controls (1.6-fold; p = 0.037) or other pathological samples (2-fold; p = 0.007). Functional analysis in Wnt/beta-catenin signaling assays revealed that skipping of exon 3 reduced significantly the signaling activity of the LRP6 coreceptor. We conclude that the LRP6 Delta 3 isoform is a novel splice variant, which shows diminished Wnt/beta-catenin signaling activity and might have a functional role in individuals with AD. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1709.e9 / 1709.e18
页数:10
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