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Neuropeptide precursor VGF is genetically associated with social anhedonia and underrepresented in the brain of major mental illness: its downregulation by DISC1

Ramos Amigo, Adriana; Rodríguez-Seoane, C.; Rosa Benito, Isaac; Trossbach, S. V.; Ortega-Alonso, A.; Tomppo, L.; Ekelund, J.; Veijola, J.; Järvelin, M. R.; Alonso Lorenzo, Jana; Veiga García, Sonia; Sawa, A.; Hennah, W.; García Alonso, Ángel; Korth, C.; Rodríguez Requena, Jesús
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URI: http://hdl.handle.net/20.500.11940/5977
PMID: 24934694
DOI: 10.1093/hmg/ddu303
ISSN: 0964-6906
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Texto completo disponible por cortesía de Hum Mol Genet . 2014 Nov 15;23(22):5859-65. doi: 10.1093/hmg/ddu303. Epub 2014 Jun 16. (336.2Kb)
Fecha de publicación
2014
Título de revista
HUMAN MOLECULAR GENETICS
Tipo de contenido
Artigo
MeSH
Anhedonia | Brain | Cohort Studies | Down-Regulation | Humans | Mental Disorders | Nerve Growth Factors | Nerve Tissue Proteins | Neurons | Pedigree | Polymorphism, Single Nucleotide
Resumen
In a large Scottish pedigree, disruption of the gene coding for DISC1 clearly segregates with major depression, schizophrenia and related mental conditions. Thus, study of DISC1 may provide a clue to understand the biology of major mental illness. A neuropeptide precursor VGF has potent antidepressant effects and has been reportedly associated with bipolar disorder. Here we show that DISC1 knockdown leads to a reduction of VGF, in neurons. VGF is also downregulated in the cortices from sporadic cases with major mental disease. A positive correlation of VGF single-nucleotide polymorphisms (SNPs) with social anhedonia was also observed. We now propose that VGF participates in a common pathophysiology of major mental disease.

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