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lüll Sequence analyses of presenilin mutations linked to familial Alzheimer s disease Kim SD; Kim JCell Stress Chaperones 2008[Dec]; 13 (4): 401-12Familial Alzheimer's disease (FAD)-linked presenilin (PS) mutations show gain-of-toxic-function characteristics. These FAD PS mutations are scattered throughout the PS molecule, reminiscent of the distribution of cystic fibrosis transmembrane conductance regulator and p53 mutations. Because of the scattered distribution of PS mutations, it is difficult to infer mechanistic insights about how these mutations cause the disease similarly. Recent careful reexamination of gamma-secretase activity indicates that some PS mutations decrease the proteolytic activity of gamma-secretase, suggesting a loss-of-function nature of PS mutations. To extend this observation to all known PS mutations, a large number of PS mutations were evaluated using bioinformatic tools. The analyses reveal that as many as one third of PS1 residues are highly conserved, that about 75% of FAD mutations are located to the highly conserved residues, and that most PS mutations likely damage the activity of PS. These results are consistent with the idea that the majority of PS mutations lower the activity of PS/gamma-secretase.|*Sequence Analysis, DNA[MESH]|Alzheimer Disease/*genetics[MESH]|Amino Acid Sequence[MESH]|Conserved Sequence[MESH]|Humans[MESH]|Molecular Sequence Data[MESH]|Mutation/*genetics[MESH]|Presenilins/chemistry/*genetics[MESH]|Protein Folding[MESH] |