| Literature DB >> 8938132 |
X Li1, I Greenwald.
Abstract
Mutant presenilins cause Alzheimer's disease. Presenilins have multiple hydrophobic regions that could theoretically span a membrane, and a knowledge of the membrane topology is crucial for deducing the mechanism of presenilin function. By analyzing the activity of beta-galactosidase hybrid proteins expressed in C. elegans, we show that the C. elegans SEL-12 presenilin has eight transmembrane domains and that there is a cleavage site after the sixth transmembrane domain. We examine the presenilin sequence in view of the predicted topology and discuss possible mechanisms for presenilin function.Entities:
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Year: 1996 PMID: 8938132 DOI: 10.1016/s0896-6273(00)80231-7
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173