| Literature DB >> 27658901 |
Cyril Pottier1, Thomas A Ravenscroft1, Patricia H Brown1, NiCole A Finch1, Matt Baker1, Meeia Parsons1, Yan W Asmann2, Yingxue Ren1, Elizabeth Christopher1, Denise Levitch1, Marka van Blitterswijk1, Carlos Cruchaga3, Dominique Campion4, Gaël Nicolas5, Anne-Claire Richard6, Rita Guerreiro7, Jose T Bras7, Stephan Zuchner8, Michael A Gonzalez9, Guojun Bu1, Steven Younkin1, David S Knopman10, Keith A Josephs10, Joseph E Parisi10, Ronald C Petersen10, Nilüfer Ertekin-Taner11, Neill R Graff-Radford12, Bradley F Boeve10, Dennis W Dickson1, Rosa Rademakers13.
Abstract
We aimed to identify new candidate genes potentially involved in early-onset Alzheimer's disease (EOAD). Exome sequencing was conducted on 45 EOAD patients with either a family history of Alzheimer's disease (AD, <65 years) or an extremely early age at the onset (≤55 years) followed by multiple variant filtering according to different modes of inheritance. We identified 29 candidate genes potentially involved in EOAD, of which the gene TYROBP, previously implicated in AD, was selected for genetic and functional follow-up. Using 3 patient cohorts, we observed rare coding TYROBP variants in 9 out of 1110 EOAD patients, whereas no such variants were detected in 1826 controls (p = 0.0001), suggesting that at least some rare TYROBP variants might contribute to EOAD risk. Overexpression of the p.D50_L51ins14 TYROBP mutant led to a profound reduction of TREM2 expression, a well-established risk factor for AD. This is the first study supporting a role for genetic variation in TYROBP in EOAD, with in vitro support for a functional effect of the p.D50_L51ins14 TYROBP mutation on TREM2 expression.Entities:
Keywords: Alzheimer's disease; Burden test; Exome sequencing; TREM2; TYROBP
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Year: 2016 PMID: 27658901 PMCID: PMC5159294 DOI: 10.1016/j.neurobiolaging.2016.07.028
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673