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A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice

Males and females use distinct brain circuits to cope with similar challenges. Using RNA sequencing of ribosome-bound mRNA from hippocampal CA3 neurons, we found remarkable sex differences and discovered that female mice displayed greater gene expression activation after acute stress than males. Str...

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Autores principales: Marrocco, Jordan, Petty, Gordon H., Ríos, Mariel B., Gray, Jason D., Kogan, Joshua F., Waters, Elizabeth M., Schmidt, Eric F., Lee, Francis S., McEwen, Bruce S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634406/
https://www.ncbi.nlm.nih.gov/pubmed/28993643
http://dx.doi.org/10.1038/s41467-017-01014-4
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author Marrocco, Jordan
Petty, Gordon H.
Ríos, Mariel B.
Gray, Jason D.
Kogan, Joshua F.
Waters, Elizabeth M.
Schmidt, Eric F.
Lee, Francis S.
McEwen, Bruce S.
author_facet Marrocco, Jordan
Petty, Gordon H.
Ríos, Mariel B.
Gray, Jason D.
Kogan, Joshua F.
Waters, Elizabeth M.
Schmidt, Eric F.
Lee, Francis S.
McEwen, Bruce S.
author_sort Marrocco, Jordan
collection PubMed
description Males and females use distinct brain circuits to cope with similar challenges. Using RNA sequencing of ribosome-bound mRNA from hippocampal CA3 neurons, we found remarkable sex differences and discovered that female mice displayed greater gene expression activation after acute stress than males. Stress-sensitive BDNF Val66Met mice of both sexes show a pre-stressed translational phenotype in which the same genes that are activated without applied stress are also induced in wild-type mice by an acute stressor. Behaviourally, only heterozygous BDNF Val66Met females exhibit spatial memory impairment, regardless of acute stress. Interestingly, this effect is not observed in ovariectomized heterozygous BDNF Val66Met females, suggesting that circulating ovarian hormones induce cognitive impairment in Met carriers. Cognitive deficits are not observed in males of either genotype. Thus, in a brain region not normally associated with sex differences, this work sheds light on ways that genes, environment and sex interact to affect the transcriptome’s response to a stressor.
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spelling pubmed-56344062017-10-12 A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice Marrocco, Jordan Petty, Gordon H. Ríos, Mariel B. Gray, Jason D. Kogan, Joshua F. Waters, Elizabeth M. Schmidt, Eric F. Lee, Francis S. McEwen, Bruce S. Nat Commun Article Males and females use distinct brain circuits to cope with similar challenges. Using RNA sequencing of ribosome-bound mRNA from hippocampal CA3 neurons, we found remarkable sex differences and discovered that female mice displayed greater gene expression activation after acute stress than males. Stress-sensitive BDNF Val66Met mice of both sexes show a pre-stressed translational phenotype in which the same genes that are activated without applied stress are also induced in wild-type mice by an acute stressor. Behaviourally, only heterozygous BDNF Val66Met females exhibit spatial memory impairment, regardless of acute stress. Interestingly, this effect is not observed in ovariectomized heterozygous BDNF Val66Met females, suggesting that circulating ovarian hormones induce cognitive impairment in Met carriers. Cognitive deficits are not observed in males of either genotype. Thus, in a brain region not normally associated with sex differences, this work sheds light on ways that genes, environment and sex interact to affect the transcriptome’s response to a stressor. Nature Publishing Group UK 2017-10-09 /pmc/articles/PMC5634406/ /pubmed/28993643 http://dx.doi.org/10.1038/s41467-017-01014-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Marrocco, Jordan
Petty, Gordon H.
Ríos, Mariel B.
Gray, Jason D.
Kogan, Joshua F.
Waters, Elizabeth M.
Schmidt, Eric F.
Lee, Francis S.
McEwen, Bruce S.
A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title_full A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title_fullStr A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title_full_unstemmed A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title_short A sexually dimorphic pre-stressed translational signature in CA3 pyramidal neurons of BDNF Val66Met mice
title_sort sexually dimorphic pre-stressed translational signature in ca3 pyramidal neurons of bdnf val66met mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634406/
https://www.ncbi.nlm.nih.gov/pubmed/28993643
http://dx.doi.org/10.1038/s41467-017-01014-4
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