Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gaiteri, Chris, Guilloux, Jean-Philippe, Lewis, David A., Sibille, Etienne
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
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
_version_ 1782179695956066304
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
work_keys_str_mv AT gaiterichris alteredgenesynchronysuggestsacombinedhormonemediateddysregulatedstateinmajordepression
AT guillouxjeanphilippe alteredgenesynchronysuggestsacombinedhormonemediateddysregulatedstateinmajordepression
AT lewisdavida alteredgenesynchronysuggestsacombinedhormonemediateddysregulatedstateinmajordepression
AT sibilleetienne alteredgenesynchronysuggestsacombinedhormonemediateddysregulatedstateinmajordepression