The ins and outs of presenilin 1 membrane topology.

M utations of presenilin 1 (PS1) account for up to 60% of early-onset familial Alzheimer’s disease (AD) (1). Because PS1 is a polytopic membrane protein, deciphering its topology is crucial to understanding its important functions. Hydropathy analysis of the PS1 primary amino acid sequence identified 10 hydrophobic regions (HR) [see figure 1A of Dewji et al. (2) in this issue of PNAS]. An eight transmembrane domain (TM) topology, where only 8 of 10 HRs traverse membranes with amino (N) and carboxy (C) tails facing the cytoplasm, has been proposed and is generally accepted by most investigators in this field (Fig. 1 A) (3, 4). In contrast, Dewji and Singer (5) have suggested an alternative in which PS1 has seven TMs with the N tail facing the extracellular space and the C tail facing the cytoplasm (Fig. 1B). This view is now confirmed in studies employing immunofluorescence microscopy with monoclonal antibodies specific either to the N tail or the loop, and polyclonal antipeptide antibodies to the C tail of PS1. The authors offer a provocative suggestion that PS1 may be a member of the superfamily of seven-TM heterotrimeric G protein-coupled receptors (2). PS1 is believed to be a catalytic subunit of -secretase (see ref. 6 for review). A slightly altered proteolytic activity of this enzyme, in concert with -secretase, increases production of a more aggregation-prone peptide, A 42, rather than A 40 from a type I membrane protein, amyloid precursor protein (APP) (6). This increased level of A 42 fragments induces formation of plaques in the brains of AD patients (6). Two conserved aspartate residues, D257 and D385, on the sixth and eighth HRs of human PS1, respectively, are suggested to serve as active site residues, defining -secretase as an aspartyl protease (Fig. 1) (7). Recent studies suggest that -secretase is a multisubunit protease composed of the membrane proteins PS1, APH-1, nicastrin (Nct), and PEN-2 (see literatures in ref. 8). Expression of these four genes in yeast successfully reconstituted the -secretase activity, confirming that they are the minimal constituents of this enzyme (8). However, because -secretase has not been purified to homogeneity, a stoichiometry of each component in the complex and the catalytic properties of this enzyme remain unclear. Clearly, the topology of the PS1 subunit of -secretase will influence the interpretation of the role of the conserved aspartates in the enzyme complex. Thus, a review of the evidence for the accepted view and possible alternatives is instructive. The standard model was first proposed based on gene fusion studies with truncated SEL-12, a Caenorhabditis elegans PS1 homologue, fused to galactosidase after each HR of SEL-12 and corresponding fusions of truncated human PS1 (3, 4). This approach takes advantage of the observation that galactosidase is active within the cytoplasm but not in the extracytosolic compartment. Briefly, the activity of -galactosidase was detected when this enzyme was fused after HR2, -4, -6, -7, -9, and -10 (Fig. 1 A), suggesting that PS1 has an eight-TM topology. This interpretation was further supported by the analysis of intracellular immunostaining profiles of cells transfected with intact PS1 by using polyclonal antibodies specific for the N tail, the loop, and the C tail (9). In a similar approach, using fusion to the cytoplasmic portion of Escherichia coli leader peptidase (LP) or to newt growth hormone, Nakai et al. (10) provided independent evidence that PS1 has a seven-TM topology (Fig. 1C), however, quite different from that proposed by Dewji and colleagues (Fig. 1B). Because the cytoplasmic region of LP possesses N-glycosylation acceptor sites, glycosylation of a fusion protein indicates exposure to the lumen of endoplasmic reticulum (ER) and therefore translocation to the ER. Consistent with their seven-TM model, LP fusion constructs after HR1, -3, and -5 of PS1 produced glycoproteins. However, LP fused after HR10 was glycosylated, but fusions after HR7, -8, and -9 were not. Thus, their seven-TM model was altered to suggest that HR9 is membrane embedded but does not span the bilayer and that the C tail is extracellular. In all models other than that of Nakai et al., the C tail is cytoplasmic. Somewhat different results were reported by Lehmann et al. (11) (Fig. 1D). They fused a portion of prolactin containing glycosylation sites after each HR of PS1 and monitored glycosylation patterns of the chimeric proteins. Glycoproteins were formed in chimeras with fusion junctions after HR1, -3, and -5 of PS1. Based on these results, they concluded that PS1 traverses the membrane six times with both N and C termini located in the cytoplasm. One must conclude that the exact topology deduced from fusion studies depends on the nature of the reporter protein. Perhaps, PS1 assumes multiple conformations around HR8, -9, and -10, as contemplated by Nakai et al. (10), and the fate of each of these HRs is directly influenced by the polar sequence that follows. In E. coli, SecG, a