Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's disease

dc.contributor.authorMiller, Jason E.
dc.contributor.authorShivakumar, Manu K.
dc.contributor.authorLee, Younghee
dc.contributor.authorHan, Seonggyun
dc.contributor.authorHorgousluoglu, Emrin
dc.contributor.authorRisacher, Shannon L.
dc.contributor.authorSaykin, Andrew J.
dc.contributor.authorNho, Kwangsik
dc.contributor.authorKim, Dokyoon
dc.contributor.departmentRadiology and Imaging Sciences, School of Medicineen_US
dc.date.accessioned2019-05-01T17:57:00Z
dc.date.available2019-05-01T17:57:00Z
dc.date.issued2018-09-14
dc.description.abstractBACKGROUND: Alzheimer's disease (AD) is one of the most common neurodegenerative diseases that causes problems related to brain function. To some extent it is understood on a molecular level how AD arises, however there are a lack of biomarkers that can be used for early diagnosis. Two popular methods to identify AD-related biomarkers use genetics and neuroimaging. Genes and neuroimaging phenotypes have provided some insights as to the potential for AD biomarkers. While the field of imaging-genomics has identified genetic features associated with structural and functional neuroimaging phenotypes, it remains unclear how variants that affect splicing could be important for understanding the genetic etiology of AD. METHODS: In this study, rare variants (minor allele frequency < 0.01) in splicing regulatory element (SRE) loci from whole genome sequencing (WGS) in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort, were used to identify genes that are associated with global brain cortical glucose metabolism in AD measured by FDG PET-scans. Gene-based associated analyses of rare variants were performed using the program BioBin and the optimal Sequence Kernel Association Test (SKAT-O). RESULTS: The gene, EXOC3L4, was identified as significantly associated with global cortical glucose metabolism (FDR (false discovery rate) corrected p < 0.05) using SRE coding variants only. Three loci that may affect splicing within EXOC3L4 contribute to the association. CONCLUSION: Based on sequence homology, EXOC3L4 is likely a part of the exocyst complex. Our results suggest the possibility that variants which affect proper splicing of EXOC3L4 via SREs may impact vesicle transport, giving rise to AD related phenotypes. Overall, by utilizing WGS and functional neuroimaging we have identified a gene significantly associated with an AD related endophenotype, potentially through a mechanism that involves splicing.en_US
dc.identifier.citationMiller, J. E., Shivakumar, M. K., Lee, Y., Han, S., Horgousluoglu, E., Risacher, S. L., … Alzheimer’s Disease Neuroimaging Initiative (2018). Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's disease. BMC medical genomics, 11(Suppl 3), 76. doi:10.1186/s12920-018-0390-6en_US
dc.identifier.urihttps://hdl.handle.net/1805/19059
dc.language.isoen_USen_US
dc.publisherBiomed Centralen_US
dc.relation.isversionof10.1186/s12920-018-0390-6en_US
dc.relation.journalBMC Medical Geneticsen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourcePMCen_US
dc.subjectAlternative splicingen_US
dc.subjectImaging genomicsen_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectWhole genome sequencingen_US
dc.subjectRare variantsen_US
dc.titleRare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's diseaseen_US
dc.typeArticleen_US
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