Isolation and functional characterisation of the promoter region of the human prion protein gene

被引:39
作者
Mahal, SP
Asante, EA
Antoniou, M
Collinge, J [1 ]
机构
[1] Imperial Coll Sch Med St Marys, MRC, Prion Unit, London W2 1PG, England
[2] Imperial Coll Sch Med St Marys, Dept Neurogenet, London W2 1PG, England
[3] Guys Hosp, GKT Sch Med, Div Med & Mol Genet, London SE1 9RT, England
基金
英国医学研究理事会;
关键词
brain; expression; prion disease; regulatory elements;
D O I
10.1016/S0378-1119(01)00424-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human prion protein gene (PRNP) encodes a 33-35 kDa cell surface protein that is highly expressed in the central nervous system and is vital to the pathogenesis of prion diseases. We have characterised the promoter region of PRNP as a first step towards defining the mechanisms regulating its expression. Sequence analysis of a 2.7 kb genomic DNA fragment containing exon I and the 5 ' -flanking region of PRNP, revealed a number of putative transcriptional factor binding sites, including Sp1, Ap-1, Ap-2 and a CCAAT box. Transient transfection assays in tissue culture cells with constructs consisting of the wild-type and deletion mutants of the PRNP 2.7 kb genomic fragment driving a luciferase reporter gene, demonstrate an active promoter within a 273 bp region (-148 to + 125, relative to the cap site). (C) 2001 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 114
页数:10
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