Unknown

Dataset Information

0

Specific Mutations in Aph1 Cause γ-Secretase Activation.


ABSTRACT: Amyloid beta peptides (Aβs) are generated from amyloid precursor protein (APP) through multiple cleavage steps mediated by γ-secretase, including endoproteolysis and carboxypeptidase-like trimming. The generation of neurotoxic Aβ42/43 species is enhanced by familial Alzheimer's disease (FAD) mutations within the catalytic subunit of γ-secretase, presenilin 1 (PS1). FAD mutations of PS1 cause partial loss-of-function and decrease the cleavage activity. Activating mutations, which have the opposite effect of FAD mutations, are important for studying Aβ production. Aph1 is a regulatory subunit of γ-secretase; it is presumed to function as a scaffold of the complex. In this study, we identified Aph1 mutations that are active in the absence of nicastrin (NCT) using a yeast γ-secretase assay. We analyzed these Aph1 mutations in the presence of NCT; we found that the L30F/T164A mutation is activating. When introduced in mouse embryonic fibroblasts, the mutation enhanced cleavage. The Aph1 mutants produced more short and long Aβs than did the wild-type Aph1, without an apparent modulatory function. The mutants did not change the amount of γ-secretase complex, suggesting that L30F/T164A enhances catalytic activity. Our results provide insights into the regulatory function of Aph1 in γ-secretase activity.

SUBMITTER: Watanabe H 

PROVIDER: S-EPMC8745412 | biostudies-literature |

REPOSITORIES: biostudies-literature

Similar Datasets

| S-EPMC2740474 | biostudies-literature
| S-EPMC547495 | biostudies-literature
| S-EPMC2118656 | biostudies-literature
| S-EPMC2676034 | biostudies-literature
| S-EPMC7318072 | biostudies-literature
| S-EPMC3003001 | biostudies-literature
| S-EPMC9929099 | biostudies-literature
| S-EPMC2732195 | biostudies-literature
| S-EPMC4115564 | biostudies-literature
| S-EPMC2427353 | biostudies-literature