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Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach
Human faces present crucial visual information for social interaction. Specialized brain regions are involved in the perception of faces, with the fusiform face area (FFA) a key neuronal substrate. Face processing is genetically controlled, but by which specific genes is unknown. A genome-wide appro...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410629/ https://www.ncbi.nlm.nih.gov/pubmed/22828495 http://dx.doi.org/10.1038/tp.2012.67 |
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author | Brown, A A Jensen, J Nikolova, Y S Djurovic, S Agartz, I Server, A Ferrell, R E Manuck, S B Mattingsdal, M Melle, I Hariri, A R Frigessi, A Andreassen, O A |
author_facet | Brown, A A Jensen, J Nikolova, Y S Djurovic, S Agartz, I Server, A Ferrell, R E Manuck, S B Mattingsdal, M Melle, I Hariri, A R Frigessi, A Andreassen, O A |
author_sort | Brown, A A |
collection | PubMed |
description | Human faces present crucial visual information for social interaction. Specialized brain regions are involved in the perception of faces, with the fusiform face area (FFA) a key neuronal substrate. Face processing is genetically controlled, but by which specific genes is unknown. A genome-wide approach identified common single nucleotide polymorphisms (SNPs) associated with areas of increased brain activity in response to affective facial expressions, measured with functional magnetic resonance imaging. SNPs in 20 genetic regions were linked with neural responses to negative facial expressions in a Norwegian sample (n=246), which included patients with mental illness. Three genetic regions were linked with FFA activation in a further discovery experiment using positive facial expressions and involving many of the same individuals (n=284). Two of these three regions showed significant association with right FFA activation to negative facial expressions in an independent North American replication sample of healthy Caucasians (n=85, 3q26.31, P=0.004; 20p12.3, P=0.045). The activation patterns were particularly striking for the SNP in 3q26.31, which lies in a gene TMEM212; only the FFA was activated. The specialized function of this brain region suggests that TMEM212 could contribute to the innate architecture of face processing. |
format | Online Article Text |
id | pubmed-3410629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-34106292012-08-02 Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach Brown, A A Jensen, J Nikolova, Y S Djurovic, S Agartz, I Server, A Ferrell, R E Manuck, S B Mattingsdal, M Melle, I Hariri, A R Frigessi, A Andreassen, O A Transl Psychiatry Original Article Human faces present crucial visual information for social interaction. Specialized brain regions are involved in the perception of faces, with the fusiform face area (FFA) a key neuronal substrate. Face processing is genetically controlled, but by which specific genes is unknown. A genome-wide approach identified common single nucleotide polymorphisms (SNPs) associated with areas of increased brain activity in response to affective facial expressions, measured with functional magnetic resonance imaging. SNPs in 20 genetic regions were linked with neural responses to negative facial expressions in a Norwegian sample (n=246), which included patients with mental illness. Three genetic regions were linked with FFA activation in a further discovery experiment using positive facial expressions and involving many of the same individuals (n=284). Two of these three regions showed significant association with right FFA activation to negative facial expressions in an independent North American replication sample of healthy Caucasians (n=85, 3q26.31, P=0.004; 20p12.3, P=0.045). The activation patterns were particularly striking for the SNP in 3q26.31, which lies in a gene TMEM212; only the FFA was activated. The specialized function of this brain region suggests that TMEM212 could contribute to the innate architecture of face processing. Nature Publishing Group 2012-07 2012-07-24 /pmc/articles/PMC3410629/ /pubmed/22828495 http://dx.doi.org/10.1038/tp.2012.67 Text en Copyright © 2012 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article Brown, A A Jensen, J Nikolova, Y S Djurovic, S Agartz, I Server, A Ferrell, R E Manuck, S B Mattingsdal, M Melle, I Hariri, A R Frigessi, A Andreassen, O A Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title_full | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title_fullStr | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title_full_unstemmed | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title_short | Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
title_sort | genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410629/ https://www.ncbi.nlm.nih.gov/pubmed/22828495 http://dx.doi.org/10.1038/tp.2012.67 |
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