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Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression
Coordinated gene transcript levels across tissues (denoted “gene synchrony”) reflect converging influences of genetic, biochemical and environmental factors; hence they are informative of the biological state of an individual. So could brain gene synchrony also integrate the multiple factors engaged...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848620/ https://www.ncbi.nlm.nih.gov/pubmed/20376317 http://dx.doi.org/10.1371/journal.pone.0009970 |
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author | Gaiteri, Chris Guilloux, Jean-Philippe Lewis, David A. Sibille, Etienne |
author_facet | Gaiteri, Chris Guilloux, Jean-Philippe Lewis, David A. Sibille, Etienne |
author_sort | Gaiteri, Chris |
collection | PubMed |
description | Coordinated gene transcript levels across tissues (denoted “gene synchrony”) reflect converging influences of genetic, biochemical and environmental factors; hence they are informative of the biological state of an individual. So could brain gene synchrony also integrate the multiple factors engaged in neuropsychiatric disorders and reveal underlying pathologies? Using bootstrapped Pearson correlation for transcript levels for the same genes across distinct brain areas, we report robust gene transcript synchrony between the amygdala and cingulate cortex in the human postmortem brain of normal control subjects (n = 14; Control/Permutated data, p<0.000001). Coordinated expression was confirmed across distinct prefrontal cortex areas in a separate cohort (n = 19 subjects) and affected different gene sets, potentially reflecting regional network- and function-dependent transcriptional programs. Genewise regional transcript coordination was independent of age-related changes and array technical parameters. Robust shifts in amygdala-cingulate gene synchrony were observed in subjects with major depressive disorder (MDD, denoted here “depression”) (n = 14; MDD/Permutated data, p<0.000001), significantly affecting between 100 and 250 individual genes (10–30% false discovery rate). Biological networks and signal transduction pathways corresponding to the identified gene set suggested putative dysregulated functions for several hormone-type factors previously implicated in depression (insulin, interleukin-1, thyroid hormone, estradiol and glucocorticoids; p<0.01 for association with depression-related networks). In summary, we showed that coordinated gene expression across brain areas may represent a novel molecular probe for brain structure/function that is sensitive to disease condition, suggesting the presence of a distinct and integrated hormone-mediated corticolimbic homeostatic, although maladaptive and pathological, state in major depression. |
format | Text |
id | pubmed-2848620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-28486202010-04-07 Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression Gaiteri, Chris Guilloux, Jean-Philippe Lewis, David A. Sibille, Etienne PLoS One Research Article Coordinated gene transcript levels across tissues (denoted “gene synchrony”) reflect converging influences of genetic, biochemical and environmental factors; hence they are informative of the biological state of an individual. So could brain gene synchrony also integrate the multiple factors engaged in neuropsychiatric disorders and reveal underlying pathologies? Using bootstrapped Pearson correlation for transcript levels for the same genes across distinct brain areas, we report robust gene transcript synchrony between the amygdala and cingulate cortex in the human postmortem brain of normal control subjects (n = 14; Control/Permutated data, p<0.000001). Coordinated expression was confirmed across distinct prefrontal cortex areas in a separate cohort (n = 19 subjects) and affected different gene sets, potentially reflecting regional network- and function-dependent transcriptional programs. Genewise regional transcript coordination was independent of age-related changes and array technical parameters. Robust shifts in amygdala-cingulate gene synchrony were observed in subjects with major depressive disorder (MDD, denoted here “depression”) (n = 14; MDD/Permutated data, p<0.000001), significantly affecting between 100 and 250 individual genes (10–30% false discovery rate). Biological networks and signal transduction pathways corresponding to the identified gene set suggested putative dysregulated functions for several hormone-type factors previously implicated in depression (insulin, interleukin-1, thyroid hormone, estradiol and glucocorticoids; p<0.01 for association with depression-related networks). In summary, we showed that coordinated gene expression across brain areas may represent a novel molecular probe for brain structure/function that is sensitive to disease condition, suggesting the presence of a distinct and integrated hormone-mediated corticolimbic homeostatic, although maladaptive and pathological, state in major depression. Public Library of Science 2010-04-01 /pmc/articles/PMC2848620/ /pubmed/20376317 http://dx.doi.org/10.1371/journal.pone.0009970 Text en Gaiteri et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Gaiteri, Chris Guilloux, Jean-Philippe Lewis, David A. Sibille, Etienne Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title | Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title_full | Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title_fullStr | Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title_full_unstemmed | Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title_short | Altered Gene Synchrony Suggests a Combined Hormone-Mediated Dysregulated State in Major Depression |
title_sort | altered gene synchrony suggests a combined hormone-mediated dysregulated state in major depression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848620/ https://www.ncbi.nlm.nih.gov/pubmed/20376317 http://dx.doi.org/10.1371/journal.pone.0009970 |
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