Matches in SemOpenAlex for { <https://semopenalex.org/work/W1636888051> ?p ?o ?g. }
- W1636888051 endingPage "37" @default.
- W1636888051 startingPage "4229" @default.
- W1636888051 abstract "Although an association between the product of the familial Alzheimer's disease (FAD) gene, presenilin 1 (PS1), and beta-catenin has been reported recently, the cellular consequences of this interaction are unknown. Here, we show that both the full length and the C-terminal fragment of wild-type or FAD mutant PS1 interact with beta-catenin from transfected cells and brains of transgenic mice, whereas E-cadherin and adenomatous polyposis coli (APC) are not detected in this complex. Inducible overexpression of PS1 led to increased association of beta-catenin with glycogen synthase kinase-3beta (GSK-3beta), a negative regulator of beta-catenin, and accelerated the turnover of endogenous beta-catenin. In support of this finding, the beta-catenin half-life was dramatically longer in fibroblasts deficient in PS1, and this phenotype was completely rescued by replacement of PS1, demonstrating that PS1 normally stimulates the degradation of beta-catenin. In contrast, overexpression of FAD-linked PS1 mutants (M146L and DeltaX9) failed to enhance the association between GSK-3beta and beta-catenin and interfered with the constitutive turnover of beta-catenin. In vivo confirmation was demonstrated in the brains of transgenic mice in which the expression of the M146L mutant PS1 was correlated with increased steady-state levels of endogenous beta-catenin. Thus, our results indicate that PS1 normally promotes the turnover of beta-catenin, whereas PS1 mutants partially interfere with this process, possibly by failing to recruit GSK-3beta into the PS1-beta-catenin complex. These findings raise the intriguing possibility that PS1-beta-catenin interactions and subsequent activities may be consequential for the pathogenesis of AD." @default.
- W1636888051 created "2016-06-24" @default.
- W1636888051 creator A5000250440 @default.
- W1636888051 creator A5005004760 @default.
- W1636888051 creator A5010416927 @default.
- W1636888051 creator A5035094672 @default.
- W1636888051 creator A5058401548 @default.
- W1636888051 creator A5069617787 @default.
- W1636888051 creator A5074910689 @default.
- W1636888051 creator A5075857911 @default.
- W1636888051 creator A5084447225 @default.
- W1636888051 date "1999-06-01" @default.
- W1636888051 modified "2023-10-06" @default.
- W1636888051 title "Presenilin 1 facilitates the constitutive turnover of beta-catenin: differential activity of Alzheimer's disease-linked PS1 mutants in the beta-catenin-signaling pathway." @default.
- W1636888051 cites W1487366060 @default.
- W1636888051 cites W1526586150 @default.
- W1636888051 cites W1563440444 @default.
- W1636888051 cites W1920794749 @default.
- W1636888051 cites W1967137553 @default.
- W1636888051 cites W1972706019 @default.
- W1636888051 cites W1979432217 @default.
- W1636888051 cites W1980061153 @default.
- W1636888051 cites W1982825693 @default.
- W1636888051 cites W1989215255 @default.
- W1636888051 cites W1995434077 @default.
- W1636888051 cites W2002041258 @default.
- W1636888051 cites W2014456898 @default.
- W1636888051 cites W2016537990 @default.
- W1636888051 cites W2036864436 @default.
- W1636888051 cites W2046209489 @default.
- W1636888051 cites W2049881581 @default.
- W1636888051 cites W2053156705 @default.
- W1636888051 cites W2053791137 @default.
- W1636888051 cites W2062876006 @default.
- W1636888051 cites W2070068402 @default.
- W1636888051 cites W2070654470 @default.
- W1636888051 cites W2071377606 @default.
- W1636888051 cites W2075175573 @default.
- W1636888051 cites W2081985759 @default.
- W1636888051 cites W2085813622 @default.
- W1636888051 cites W2132475598 @default.
- W1636888051 cites W2139936955 @default.
- W1636888051 cites W2150970420 @default.
- W1636888051 cites W2154196079 @default.
- W1636888051 cites W2156292819 @default.
- W1636888051 cites W2157895955 @default.
- W1636888051 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6782616" @default.
- W1636888051 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10341227" @default.
- W1636888051 hasPublicationYear "1999" @default.
- W1636888051 type Work @default.
- W1636888051 sameAs 1636888051 @default.
- W1636888051 citedByCount "78" @default.
- W1636888051 countsByYear W16368880512013 @default.
- W1636888051 countsByYear W16368880512015 @default.
- W1636888051 countsByYear W16368880512016 @default.
- W1636888051 countsByYear W16368880512017 @default.
- W1636888051 countsByYear W16368880512018 @default.
- W1636888051 countsByYear W16368880512019 @default.
- W1636888051 countsByYear W16368880512021 @default.
- W1636888051 countsByYear W16368880512022 @default.
- W1636888051 countsByYear W16368880512023 @default.
- W1636888051 crossrefType "journal-article" @default.
- W1636888051 hasAuthorship W1636888051A5000250440 @default.
- W1636888051 hasAuthorship W1636888051A5005004760 @default.
- W1636888051 hasAuthorship W1636888051A5010416927 @default.
- W1636888051 hasAuthorship W1636888051A5035094672 @default.
- W1636888051 hasAuthorship W1636888051A5058401548 @default.
- W1636888051 hasAuthorship W1636888051A5069617787 @default.
- W1636888051 hasAuthorship W1636888051A5074910689 @default.
- W1636888051 hasAuthorship W1636888051A5075857911 @default.
- W1636888051 hasAuthorship W1636888051A5084447225 @default.
- W1636888051 hasConcept C102230213 @default.
- W1636888051 hasConcept C104317684 @default.
- W1636888051 hasConcept C104629339 @default.
- W1636888051 hasConcept C126322002 @default.
- W1636888051 hasConcept C137620995 @default.
- W1636888051 hasConcept C141035611 @default.
- W1636888051 hasConcept C143065580 @default.
- W1636888051 hasConcept C153911025 @default.
- W1636888051 hasConcept C175344181 @default.
- W1636888051 hasConcept C182996813 @default.
- W1636888051 hasConcept C199360897 @default.
- W1636888051 hasConcept C2776174256 @default.
- W1636888051 hasConcept C2779134260 @default.
- W1636888051 hasConcept C2779324961 @default.
- W1636888051 hasConcept C30145163 @default.
- W1636888051 hasConcept C41008148 @default.
- W1636888051 hasConcept C502032728 @default.
- W1636888051 hasConcept C54355233 @default.
- W1636888051 hasConcept C62478195 @default.
- W1636888051 hasConcept C71924100 @default.
- W1636888051 hasConcept C86803240 @default.
- W1636888051 hasConcept C95444343 @default.
- W1636888051 hasConceptScore W1636888051C102230213 @default.
- W1636888051 hasConceptScore W1636888051C104317684 @default.
- W1636888051 hasConceptScore W1636888051C104629339 @default.
- W1636888051 hasConceptScore W1636888051C126322002 @default.
- W1636888051 hasConceptScore W1636888051C137620995 @default.