Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans
Bakken, Trygve E. ; Roddey, J. Cooper ; Djurovic, Srdjan ; Akshoomoff, Natacha ; Amaral, David G. ; Bloss, Cinnamon S. ; Casey, B. J. ; Chang, Linda ; Ernst, Thomas M. ; Gruen, Jeffrey R. ... show 10 more
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Authors
Roddey, J. Cooper
Djurovic, Srdjan
Akshoomoff, Natacha
Amaral, David G.
Bloss, Cinnamon S.
Casey, B. J.
Chang, Linda
Ernst, Thomas M.
Gruen, Jeffrey R.
Jernigan, Terry L.
Kaufmann, Walter E.
Kenet, Tal
Kennedy, David N
Kuperman, Joshua M.
Murray, Sarah S.
Sowell, Elizabeth R.
Rimol, Lars M.
Mattingsdal, Morten
Melle, Ingrid
Agartz, Ingrid
Andreassen, Ole A.
Schork, Nicholas J.
Dale, Anders M.
Alzheimer’s Disease Neuroimaging Initiative
Pediatric Imaging, Neurocognition, and Genetics Study
Frazier, Jean A.
Yakutis, Lauren
Student Authors
Faculty Advisor
Academic Program
UMass Chan Affiliations
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Keywords
Adult
Aged
Brain
Brain Mapping
Cohort Studies
Diagnostic Imaging
Female
Genetic Variation
Genome-Wide Association Study
Genomics
Genotype
Humans
Male
Middle Aged
Models, Genetic
Phosphoric Diester Hydrolases
Polymorphism, Single Nucleotide
Saccharomyces cerevisiae
Visual Cortex
Genetics and Genomics
Neuroscience and Neurobiology
Psychiatry
Psychiatry and Psychology
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Embargo Expiration Date
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Abstract
Visual cortical surface area varies two- to threefold between human individuals, is highly heritable, and has been correlated with visual acuity and visual perception. However, it is still largely unknown what specific genetic and environmental factors contribute to normal variation in the area of visual cortex. To identify SNPs associated with the proportional surface area of visual cortex, we performed a genome-wide association study followed by replication in two independent cohorts. We identified one SNP (rs6116869) that replicated in both cohorts and had genome-wide significant association (P(combined) = 3.2 × 10(-8)). Furthermore, a metaanalysis of imputed SNPs in this genomic region identified a more significantly associated SNP (rs238295; P = 6.5 × 10(-9)) that was in strong linkage disequilibrium with rs6116869. These SNPs are located within 4 kb of the 5' UTR of GPCPD1, glycerophosphocholine phosphodiesterase GDE1 homolog (Saccharomyces cerevisiae), which in humans, is more highly expressed in occipital cortex compared with the remainder of cortex than 99.9% of genes genome-wide. Based on these findings, we conclude that this common genetic variation contributes to the proportional area of human visual cortex. We suggest that identifying genes that contribute to normal cortical architecture provides a first step to understanding genetic mechanisms that underlie visual perception.
Source
Bakken TE et al. Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Proc Natl Acad Sci U S A. 2012 Mar 6;109(10):3985-90. doi: 10.1073/pnas.1105829109. Epub 2012 Feb 16. PubMed PMID: 22343285; PubMed Central PMCID: PMC3309762. Link to article on publisher's site
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Notes
Full author list omitted for brevity. For the full list of authors, see article appendix. David Kennedy, Jean Frazier and Lauren Yakutis are authors for the Pediatric Imaging, Neurocognition, and Genetics Study.