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Cytoplasmic FMR1-Interacting Protein 2 Is a Major Genetic Factor Underlying Binge Eating.
- Source :
-
Biological psychiatry [Biol Psychiatry] 2017 May 01; Vol. 81 (9), pp. 757-769. Date of Electronic Publication: 2016 Oct 25. - Publication Year :
- 2017
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Abstract
- Background: Eating disorders are lethal and heritable; however, the underlying genetic factors are unknown. Binge eating is a highly heritable trait associated with eating disorders that is comorbid with mood and substance use disorders. Therefore, understanding its genetic basis will inform therapeutic development that could improve several comorbid neuropsychiatric conditions.<br />Methods: We assessed binge eating in closely related C57BL/6 mouse substrains and in an F <subscript>2</subscript> cross to identify quantitative trait loci associated with binge eating. We used gene targeting to validate candidate genetic factors. Finally, we used transcriptome analysis of the striatum via messenger RNA sequencing to identify the premorbid transcriptome and the binge-induced transcriptome to inform molecular mechanisms mediating binge eating susceptibility and establishment.<br />Results: C57BL/6NJ but not C57BL/6J mice showed rapid and robust escalation in palatable food consumption. We mapped a single genome-wide significant quantitative trait locus on chromosome 11 (logarithm of the odds = 7.4) to a missense mutation in cytoplasmic FMR1-interacting protein 2 (Cyfip2). We validated Cyfip2 as a major genetic factor underlying binge eating in heterozygous knockout mice on a C57BL/6N background that showed reduced binge eating toward a wild-type C57BL/6J-like level. Transcriptome analysis of premorbid genetic risk identified the enrichment terms morphine addiction and retrograde endocannabinoid signaling, whereas binge eating resulted in the downregulation of a gene set enriched for decreased myelination, oligodendrocyte differentiation, and expression.<br />Conclusions: We identified Cyfip2 as a major significant genetic factor underlying binge eating and provide a behavioral paradigm for future genome-wide association studies in populations with increased genetic complexity.<br /> (Copyright © 2016 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Adaptor Proteins, Signal Transducing
Animals
Binge-Eating Disorder metabolism
Bulimia genetics
Bulimia metabolism
Compulsive Behavior genetics
Compulsive Behavior metabolism
Corpus Striatum metabolism
Female
Male
Mice, Inbred C57BL
Mice, Knockout
Mutation, Missense
Quantitative Trait Loci
Transcriptome
Binge-Eating Disorder genetics
Nerve Tissue Proteins genetics
Nerve Tissue Proteins physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1873-2402
- Volume :
- 81
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Biological psychiatry
- Publication Type :
- Academic Journal
- Accession number :
- 27914629
- Full Text :
- https://doi.org/10.1016/j.biopsych.2016.10.021