Alteration in brain presenilin 1 mRNA expression in early onset familial Alzheimer's disease

被引:16
作者
Barton, AJL
Crook, BW
Karran, EH
Brown, F
Dewar, D
Mann, DMA
Pearson, RCA
Graham, DI
Hardy, J
Hutton, M
Duff, K
Goate, AM
Clark, RF
Roberts, GW
机构
[1] UNIV GLASGOW,WELLCOME SURG INST,GLASGOW G61 1QH,LANARK,SCOTLAND
[2] UNIV GLASGOW,HUGH FRASER NEUROSCI LABS,GLASGOW G61 1QH,LANARK,SCOTLAND
[3] UNIV MANCHESTER,DEPT PATHOL SCI,MANCHESTER M13 9PT,LANCS,ENGLAND
[4] UNIV SHEFFIELD,DEPT BIOMED SCI,SHEFFIELD S10 2NT,S YORKSHIRE,ENGLAND
[5] SO GEN HOSP,NHS TRUST,INST NEUROL SCI,GLASGOW G51 4TF,LANARK,SCOTLAND
[6] UNIV S FLORIDA,SUNCOAST ALZHEIMERS DIS LAB,TAMPA,FL 33613
[7] ST LOUIS UNIV,SCH MED,DEPT PSYCHIAT,ST LOUIS,MO 63110
来源
NEURODEGENERATION | 1996年 / 5卷 / 03期
基金
英国惠康基金;
关键词
familial Alzheimer's disease; human brain; in situ hybridization; presenilin; 1; mRNA;
D O I
10.1006/neur.1996.0029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The expression of the presenilin 1 (PS-1) gene has been investigated by in situ hybridization in early onset familial Alzheimer's disease (FAD), late onset Alzheimer's disease (AD) and normal control brain. Mutations in this gene are responsible for chromosome 14-linked FAD. We have found that presenilin 1 mRNA is present throughout the human brain with a distribution consistent with both a glial and neuronal localization. The in situ hybridization pattern was similar for the controls, the early onset FAD cases and the late onset AD cases. However, one of the two forms of the mRNA for PS-1, the long form (which contains a sequence encoding a four amino acid (VRSQ) insert at its 5' end) was significantly reduced in early onset FAD brain compared with late onset AD. We suggest that this long transcript may alter the normal pathway for processing of amyloid precursor protein, the protein which appears to be central in the pathogenesis of AD. (C) 1996 Academic Press Limited
引用
收藏
页码:213 / 218
页数:6
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