Functional screening in Drosophila identifies Alzheimer's disease susceptibility genes and implicates Tau-mediated mechanisms
Year: 2013
Type: article
Abstract: Using a Drosophila model of Alzheimer's disease (AD), we systematically evaluated 67 candidate genes based on AD-associated genomic loci (P < 10(-4)) from published human genome-wide association studies (GWAS). Genetic manipulation of 87 homologous fly genes was tested for modulation of neurotoxicity caused by human Tau, which forms neurofibrillary tangle pathology in AD. RNA interference (RNAi) targeting 9 genes enhanced Tau neurotoxicity, and in most cases reciprocal activation of gene expression suppressed Tau toxicity. Our screen implicates cindr, the fly ortholog of the human CD2AP AD susceptibility gene, as a modulator of Tau-mediated disease mechanisms. Importantly, we also identify the fly orthologs of FERMT2 and CELF1 as Tau modifiers, and these loci have been independently validated as AD susceptibility loci in the latest GWAS meta-analysis. Both CD2AP and FERMT2 have been previously implicated with roles in cell adhesion, and our screen additionally identifies a fly homolog of the human integrin adhesion receptors, ITGAM and ITGA9, as a modifier of Tau neurotoxicity. Our results highlight cell adhesion pathways as important in Tau toxicity and AD susceptibility and demonstrate the power of model organism genetic screens for the functional follow-up of human GWAS.
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddt478
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: bronze
Funders: Burroughs Wellcome Fund, Ellison Medical Foundation, Wellcome Trust, National Institutes of Health, National Institute on Aging, National Institute of General Medical Sciences, National Center for Research Resources, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: Drosophila Transgenic RNAi Resource Project, INITIATIVE FOR MAXIMIZING STUDENT DEVELOPMENT AT UMASS BOSTON, Integrative analysis of genomic and epigenomic architecture in cognitive decline, G3611247453, Exploring the Genetics of Alzheimer's Disease in Humans and Drosophila, NRI Build-out: Advancing Translational Brain Research, Development of Validated Drosophila in vivo RNAi Models of Human Diseases, Mechanisms of adhesion to the extracellular matrix., Core support for the Wellcome Trust Cancer Research UK Gurdon Institute., Intellectual and Developmental Disablities Research Center
OpenAlex ID: W2137709496
