The gene encoding DRAP (BACE2), a glycosylated transmembrane protein of the aspartic protease family, maps to the Down critical region

被引:120
作者
Acquati, F
Accarino, M
Nucci, C
Fumagalli, P
Jovine, L
Ottolenghi, S
Taramelli, R
机构
[1] Univ Insubria, Dipartimento Strutturale & Funzionale, Varese, Italy
[2] Univ Milan, Dipartimento Genet & Biol Microrganismi, Milan, Italy
[3] Osped San Raffaele, IRCCS, I-20132 Milan, Italy
[4] MRC, Mol Biol Lab, Struct Studies Div, Cambridge CB2 2QH, England
来源
FEBS LETTERS | 2000年 / 468卷 / 01期
关键词
aspartic protease; enzyme; cDNA; chromosome; 21; Down syndrome;
D O I
10.1016/S0014-5793(00)01192-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We applied cDNA selection methods to a genomic clone (YAC 761B5) from chromosome 21 located in the so-called 'Down critical region' in 21q22.3, Starting from human fetal heart and brain mRNAs we obtained and sequenced several cDWA clones. One of these clones (Down region aspartic protease (DRAP), named also BACE2 according to the gene nomenclature) revealed a striking nucleotide and amino acid sequence identity with several motifs present in members of the aspartic protease family, In particular the amino acid sequences comprising the two catalytic sites found in all mammalian aspartic proteases are perfectly conserved. Interestingly, the predicted protein shows a typical membrane spanning region; this is at variance with most other known aspartic proteases, which are soluble molecules. We present preliminary evidence, on the basis of in vitro translation studies and cell transfection, that this gene encodes a glycosylated protein which localizes mainly intracellularly but to some extent also to the plasma membrane. Furthermore DRAP/BACE2 shares a high homology with a newly described beta-secretase enzyme (BACE-1) which is a transmembrane aspartic protease, The implications of this finding for Down syndrome are discussed. (C) 2000 Federation of European Biochemical Societies.
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页码:59 / 64
页数:6
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