Abstract
Presenilin-1 (PS1) and presenilin-2 (PS2) are associated with a majority of early onset familial Alzheimer's disease (FAD). Sequence analysis of PS1/2 has revealed integral transmembrane proteins which are highly homologous to the protein coded by sel-12, a Caenorhabditis elegans gene involved in the lin-12/Notch signaling pathway. The normal function of PS1/2, as well as the pathogenesis caused by mutations of these genes in FAD, are unknown however. We have identified a Drosophila presenilin homolog (DPS) and mapped the chromosomal location of this gene. DPS shows 53% amino acid identity to PS1/2 and 45% to the sel-12 product. Strong amino acid conservations appear at the position associated with FAD. In embryonic stages, DPS is expressed primarily in the CNS.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alzheimer Disease / physiopathology
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Amino Acid Sequence
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Animals
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Caenorhabditis elegans / genetics
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Caenorhabditis elegans Proteins*
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Drosophila / physiology*
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Drosophila Proteins*
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Embryo, Nonmammalian
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Gene Expression Regulation, Developmental
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Helminth Proteins / chemistry
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Humans
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Membrane Proteins / biosynthesis
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Membrane Proteins / chemistry*
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Membrane Proteins / genetics
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Molecular Sequence Data
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Nervous System / metabolism*
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Presenilin-1
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Presenilin-2
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Presenilins
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Sequence Homology, Amino Acid
Substances
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Caenorhabditis elegans Proteins
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Drosophila Proteins
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Helminth Proteins
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Membrane Proteins
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PSEN1 protein, human
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PSEN2 protein, human
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Presenilin-1
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Presenilin-2
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Presenilins
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Psn protein, Drosophila
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SEL-12 protein, C elegans