| Literature DB >> 28461250 |
Kilan Le Guennec1, Sarah Veugelen2, Olivier Quenez1, Maria Szaruga2, Stéphane Rousseau1, Gaël Nicolas1, David Wallon3, Frédérique Fluchere4, Thierry Frébourg5, Bart De Strooper6, Dominique Campion7, Lucía Chávez-Gutiérrez2, Anne Rovelet-Lecrux8.
Abstract
Presenilin 1 (PSEN1) mutations are the main cause of autosomal dominant Early-onset Alzheimer Disease (EOAD). Among them, deletions of exon 9 have been reported to be associated with a phenotype of spastic paraparesis. Using exome data from a large sample of 522 EOAD cases and 584 controls to search for genomic copy-number variations (CNVs), we report here a novel partial, in-frame deletion of PSEN1, removing both exons 9 and 10. The patient presented with memory impairment associated with spastic paraparesis, both starting from the age of 56years. He presented a positive family history of EOAD. We performed functional analysis to elucidate the impact of this novel deletion on PSEN1 activity as part of the γ-secretase complex. The deletion does not affect the assembly of a mature protease complex but has an extreme impact on its global endopeptidase activity. The mutant carboxypeptidase-like activity is also strongly impaired and the deleterious mutant effect leads to an incomplete digestion of long Aβ peptides and enhances the production of Aβ43, which has been shown to be potently amyloidogenic and neurotoxic in vivo.Entities:
Keywords: Alzheimer Disease; Amyloid; Aβ43; Early-onset; Hydrophilic loop; PSEN1
Mesh:
Substances:
Year: 2017 PMID: 28461250 DOI: 10.1016/j.nbd.2017.04.020
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996