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An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice

Adults of many species will care for young offspring that are not their own, a phenomenon called alloparenting. However, in many cases, nonparental adults must be sensitized by repeated or extended exposures to newborns before they will robustly display parental-like behaviors. To capture neurogenom...

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Autores principales: Seward, Christopher H., Saul, Michael C., Troy, Joseph M., Dibaeinia, Payam, Zhang, Huimin, Sinha, Saurabh, Stubbs, Lisa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863255/
https://www.ncbi.nlm.nih.gov/pubmed/35192674
http://dx.doi.org/10.1371/journal.pone.0263632
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author Seward, Christopher H.
Saul, Michael C.
Troy, Joseph M.
Dibaeinia, Payam
Zhang, Huimin
Sinha, Saurabh
Stubbs, Lisa J.
author_facet Seward, Christopher H.
Saul, Michael C.
Troy, Joseph M.
Dibaeinia, Payam
Zhang, Huimin
Sinha, Saurabh
Stubbs, Lisa J.
author_sort Seward, Christopher H.
collection PubMed
description Adults of many species will care for young offspring that are not their own, a phenomenon called alloparenting. However, in many cases, nonparental adults must be sensitized by repeated or extended exposures to newborns before they will robustly display parental-like behaviors. To capture neurogenomic events underlying the transition to active parental caring behaviors, we analyzed brain gene expression and chromatin profiles of virgin female mice co-housed with pregnant dams during pregnancy and after birth. After an initial display of antagonistic behaviors and a surge of defense-related gene expression, we observed a dramatic shift in the chromatin landscape specifically in amygdala of the pup-exposed virgin females compared to females co-housed with mother before birth, accompanied by a dampening of anxiety-related gene expression. This epigenetic shift coincided with hypothalamic expression of the oxytocin gene and the emergence of behaviors and gene expression patterns classically associated with maternal care. The results outline a neurogenomic program associated with dramatic behavioral changes and suggest molecular networks relevant to human postpartum mental health.
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spelling pubmed-88632552022-02-23 An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice Seward, Christopher H. Saul, Michael C. Troy, Joseph M. Dibaeinia, Payam Zhang, Huimin Sinha, Saurabh Stubbs, Lisa J. PLoS One Research Article Adults of many species will care for young offspring that are not their own, a phenomenon called alloparenting. However, in many cases, nonparental adults must be sensitized by repeated or extended exposures to newborns before they will robustly display parental-like behaviors. To capture neurogenomic events underlying the transition to active parental caring behaviors, we analyzed brain gene expression and chromatin profiles of virgin female mice co-housed with pregnant dams during pregnancy and after birth. After an initial display of antagonistic behaviors and a surge of defense-related gene expression, we observed a dramatic shift in the chromatin landscape specifically in amygdala of the pup-exposed virgin females compared to females co-housed with mother before birth, accompanied by a dampening of anxiety-related gene expression. This epigenetic shift coincided with hypothalamic expression of the oxytocin gene and the emergence of behaviors and gene expression patterns classically associated with maternal care. The results outline a neurogenomic program associated with dramatic behavioral changes and suggest molecular networks relevant to human postpartum mental health. Public Library of Science 2022-02-22 /pmc/articles/PMC8863255/ /pubmed/35192674 http://dx.doi.org/10.1371/journal.pone.0263632 Text en © 2022 Seward et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Seward, Christopher H.
Saul, Michael C.
Troy, Joseph M.
Dibaeinia, Payam
Zhang, Huimin
Sinha, Saurabh
Stubbs, Lisa J.
An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title_full An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title_fullStr An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title_full_unstemmed An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title_short An epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
title_sort epigenomic shift in amygdala marks the transition to maternal behaviors in alloparenting virgin female mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8863255/
https://www.ncbi.nlm.nih.gov/pubmed/35192674
http://dx.doi.org/10.1371/journal.pone.0263632
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