A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene

Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like p...

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Published inMolecular psychiatry Vol. 18; no. 2; pp. 255 - 263
Main Authors Papassotiropoulos, A, Stefanova, E, Vogler, C, Gschwind, L, Ackermann, S, Spalek, K, Rasch, B, Heck, A, Aerni, A, Hanser, E, Demougin, P, Huynh, K-D, Luechinger, R, Klarhöfer, M, Novakovic, I, Kostic, V, Boesiger, P, Scheffler, K, de Quervain, D J-F
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.02.2013
Nature Publishing Group
Subjects
Online AccessGet full text
ISSN1359-4184
1476-5578
1476-5578
DOI10.1038/mp.2011.148

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Abstract Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 ( CTNNBL1 ) was significantly ( P =7 × 10 −8 ) associated with verbal memory performance in a cognitively healthy cohort from Switzerland ( n =1073) and was replicated in a second cohort from Serbia ( n =524; P =0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
AbstractList Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 ( CTNNBL1 ) was significantly ( P =7 × 10 −8 ) associated with verbal memory performance in a cognitively healthy cohort from Switzerland ( n =1073) and was replicated in a second cohort from Serbia ( n =524; P =0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genomewide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P =7 x [10.sup.-8] associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n =1073) and was replicated in a second cohort from Serbia (n = 524; P =0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory. Molecular Psychiatry (2013) 18, 255-263; doi: 10.1038/mp.2011.148; published online 22 November 2011 Keywords: beta-catenin-like; fMRI; GWAS; memory 961 -0.05 ±0.03 564 -0.04 ± 0.04 397 -0.07 ± 0.04 434 -0.14 ± 0.06
Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genomewide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P =7 x [10.sup.-8] associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n =1073) and was replicated in a second cohort from Serbia (n = 524; P =0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P=7 × 10(-8)) associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n=1073) and was replicated in a second cohort from Serbia (n=524; P=0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P=7 10 super(-8)) associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n=1073) and was replicated in a second cohort from Serbia (n=524; P=0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P=7 × 10(-8)) associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n=1073) and was replicated in a second cohort from Serbia (n=524; P=0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a dense genome-wide screen to identify episodic memory-related gene variants. A genomic locus encoding the brain-expressed beta-catenin-like protein 1 (CTNNBL1) was significantly (P=7 × 10(-8)) associated with verbal memory performance in a cognitively healthy cohort from Switzerland (n=1073) and was replicated in a second cohort from Serbia (n=524; P=0.003). Gene expression studies showed CTNNBL1 genotype-dependent differences in beta-catenin-like protein 1 mRNA levels in the human cortex. Functional magnetic resonance imaging in 322 subjects detected CTNNBL1 genotype-dependent differences in memory-related brain activations. Converging evidence from independent experiments and different methodological approaches suggests a role for CTNNBL1 in human memory.
Audience Academic
Author Kostic, V
Novakovic, I
Luechinger, R
Ackermann, S
Scheffler, K
Stefanova, E
Aerni, A
de Quervain, D J-F
Papassotiropoulos, A
Vogler, C
Gschwind, L
Spalek, K
Huynh, K-D
Heck, A
Demougin, P
Rasch, B
Hanser, E
Klarhöfer, M
Boesiger, P
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Issue 2
Keywords fMRI
beta-catenin-like
GWAS
memory
Language English
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Snippet Unbiased genome-wide screens combined with imaging data on brain function may identify novel molecular pathways related to human cognition. Here we performed a...
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SubjectTerms 631/378/1595
631/378/2583
692/700/1421/65
Apoptosis Regulatory Proteins - genetics
Apoptosis Regulatory Proteins - metabolism
Behavioral Sciences
Biological Psychology
Brain - blood supply
Brain - physiology
Cognition & reasoning
Cohort Studies
Female
Gene expression
Gene Expression - genetics
Genetic aspects
Genetic testing
Genetic variation
Genome-Wide Association Study
Genomes
Genotype
Genotype & phenotype
Humans
Image Processing, Computer-Assisted
Magnetic Resonance Imaging
Male
Medical imaging
Medicine
Medicine & Public Health
Memory
Memory - physiology
Neuroimaging
Neurosciences
Nuclear Proteins - genetics
Nuclear Proteins - metabolism
Original
original-article
Oxygen - blood
Pharmacotherapy
Polymorphism, Single Nucleotide - genetics
Proteins
Psychiatry
Psychological aspects
RNA, Messenger - metabolism
Serbia
Switzerland
University students
Verbal Learning - physiology
Young adults
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Title A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene
URI https://link.springer.com/article/10.1038/mp.2011.148
https://www.ncbi.nlm.nih.gov/pubmed/22105620
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https://pubmed.ncbi.nlm.nih.gov/PMC3554877
Volume 18
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