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Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex

G-protein–coupled signal transduction mediates most cellular responses to hormones and neurotransmitters; this signaling system transduces a large variety of extracellular stimuli into neurons and is the most widely used mechanism for cell communication at the synaptic level. The heterotrimeric G-pr...

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Autores principales: Chavarría-Siles, Iván, Rijpkema, Mark, Lips, Esther, Arias-Vasquez, Alejandro, Verhage, Matthijs, Franke, Barbara, Fernández, Guillén, Posthuma, Danielle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615342/
https://www.ncbi.nlm.nih.gov/pubmed/22510535
http://dx.doi.org/10.1093/cercor/bhs061
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author Chavarría-Siles, Iván
Rijpkema, Mark
Lips, Esther
Arias-Vasquez, Alejandro
Verhage, Matthijs
Franke, Barbara
Fernández, Guillén
Posthuma, Danielle
author_facet Chavarría-Siles, Iván
Rijpkema, Mark
Lips, Esther
Arias-Vasquez, Alejandro
Verhage, Matthijs
Franke, Barbara
Fernández, Guillén
Posthuma, Danielle
author_sort Chavarría-Siles, Iván
collection PubMed
description G-protein–coupled signal transduction mediates most cellular responses to hormones and neurotransmitters; this signaling system transduces a large variety of extracellular stimuli into neurons and is the most widely used mechanism for cell communication at the synaptic level. The heterotrimeric G-proteins have been well established as key regulators of neuronal growth, differentiation, and function. More recently, the heterotrimeric G-protein genes group was associated with general cognitive ability. Although heterotrimeric G-proteins are linked to both cognitive ability aond neuron signaling, it is unknown whether heterotrimeric G-proteins are also important for brain structure. We tested for association between local cerebral gray matter volume and the heterotrimeric G-protein genes group in 294 subjects; a replication analysis was performed in an independent sample of 238 subjects. Voxel-based morphometry revealed a strong replicated association between 2 genes encoding heterotrimeric G-proteins with specific local increase in medial frontal cortex volume, an area known to be involved in cognitive control and negative affect. This finding suggests that heterotrimeric G-proteins might modulate medial frontal cortex gray matter volume. The differences in gray matter volume due to variations in genes encoding G-proteins may be explained by the role of G-proteins in prenatal and postnatal neocortex development.
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spelling pubmed-36153422013-04-03 Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex Chavarría-Siles, Iván Rijpkema, Mark Lips, Esther Arias-Vasquez, Alejandro Verhage, Matthijs Franke, Barbara Fernández, Guillén Posthuma, Danielle Cereb Cortex Articles G-protein–coupled signal transduction mediates most cellular responses to hormones and neurotransmitters; this signaling system transduces a large variety of extracellular stimuli into neurons and is the most widely used mechanism for cell communication at the synaptic level. The heterotrimeric G-proteins have been well established as key regulators of neuronal growth, differentiation, and function. More recently, the heterotrimeric G-protein genes group was associated with general cognitive ability. Although heterotrimeric G-proteins are linked to both cognitive ability aond neuron signaling, it is unknown whether heterotrimeric G-proteins are also important for brain structure. We tested for association between local cerebral gray matter volume and the heterotrimeric G-protein genes group in 294 subjects; a replication analysis was performed in an independent sample of 238 subjects. Voxel-based morphometry revealed a strong replicated association between 2 genes encoding heterotrimeric G-proteins with specific local increase in medial frontal cortex volume, an area known to be involved in cognitive control and negative affect. This finding suggests that heterotrimeric G-proteins might modulate medial frontal cortex gray matter volume. The differences in gray matter volume due to variations in genes encoding G-proteins may be explained by the role of G-proteins in prenatal and postnatal neocortex development. Oxford University Press 2013-05 2012-04-17 /pmc/articles/PMC3615342/ /pubmed/22510535 http://dx.doi.org/10.1093/cercor/bhs061 Text en © The Authors 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Chavarría-Siles, Iván
Rijpkema, Mark
Lips, Esther
Arias-Vasquez, Alejandro
Verhage, Matthijs
Franke, Barbara
Fernández, Guillén
Posthuma, Danielle
Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title_full Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title_fullStr Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title_full_unstemmed Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title_short Genes Encoding Heterotrimeric G-proteins Are Associated with Gray Matter Volume Variations in the Medial Frontal Cortex
title_sort genes encoding heterotrimeric g-proteins are associated with gray matter volume variations in the medial frontal cortex
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615342/
https://www.ncbi.nlm.nih.gov/pubmed/22510535
http://dx.doi.org/10.1093/cercor/bhs061
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