Literature DB >> 7596406

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.

R Sherrington1, E I Rogaev, Y Liang, E A Rogaeva, G Levesque, M Ikeda, H Chi, C Lin, G Li, K Holman, T Tsuda, L Mar, J F Foncin, A C Bruni, M P Montesi, S Sorbi, I Rainero, L Pinessi, L Nee, I Chumakov, D Pollen, A Brookes, P Sanseau, R J Polinsky, W Wasco, H A Da Silva, J L Haines, M A Perkicak-Vance, R E Tanzi, A D Roses, P E Fraser, J M Rommens, P H St George-Hyslop.   

Abstract

Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic linkage studies have mapped a locus (AD3) associated with susceptibility to a very aggressive form of Alzheimer's disease to chromosome 14q24.3. We have defined a minimal cosegregating region containing the AD3 gene, and isolated at least 19 different transcripts encoded within this region. One of these transcripts (S182) corresponds to a novel gene whose product is predicted to contain multiple transmembrane domains and resembles an integral membrane protein. Five different missense mutations have been found that cosegregate with early-onset familial Alzheimer's disease. Because these changes occurred in conserved domains of this gene, and are not present in normal controls, they are likely to be causative of AD3.

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Year:  1995        PMID: 7596406     DOI: 10.1038/375754a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


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