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Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development
Early life stress (ELS) has been shown to have a significant impact on typical brain development and the manifestation of psychological disorders through epigenetic modifications that alter gene expression. Line1, a retrotransposon associated with genetic diversity, has been linked with various psyc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878767/ https://www.ncbi.nlm.nih.gov/pubmed/33574362 http://dx.doi.org/10.1038/s41598-021-82953-3 |
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author | Cuarenta, Amelia Kigar, Stacey L. Henion, Ian C. Chang, Liza Bakshi, Vaishali P. Auger, Anthony P. |
author_facet | Cuarenta, Amelia Kigar, Stacey L. Henion, Ian C. Chang, Liza Bakshi, Vaishali P. Auger, Anthony P. |
author_sort | Cuarenta, Amelia |
collection | PubMed |
description | Early life stress (ELS) has been shown to have a significant impact on typical brain development and the manifestation of psychological disorders through epigenetic modifications that alter gene expression. Line1, a retrotransposon associated with genetic diversity, has been linked with various psychological disorders that are associated with ELS. Our previous work demonstrated altered Line1 DNA copy number in the neonatal period following stressful experiences; we therefore chose to investigate whether early life stress altered Line1 retrotransposition persists into the juvenile period of development. Our study uses a neonatal predator odor exposure (POE) paradigm to model ELS in rats. We examined Line1 using qPCR to assess Line1 expression levels and DNA copy number in the male and female juvenile amygdala, hippocampus and prefrontal cortex—areas chosen for their association with affective disorders and stress. We report a sex difference in Line1 levels within the juvenile amygdala. We also find that ELS significantly increases Line1 DNA copy number within the juvenile amygdala which correlates with reduced juvenile social play levels, suggesting the possibility that Line1 may influence juvenile social development. |
format | Online Article Text |
id | pubmed-7878767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78787672021-02-12 Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development Cuarenta, Amelia Kigar, Stacey L. Henion, Ian C. Chang, Liza Bakshi, Vaishali P. Auger, Anthony P. Sci Rep Article Early life stress (ELS) has been shown to have a significant impact on typical brain development and the manifestation of psychological disorders through epigenetic modifications that alter gene expression. Line1, a retrotransposon associated with genetic diversity, has been linked with various psychological disorders that are associated with ELS. Our previous work demonstrated altered Line1 DNA copy number in the neonatal period following stressful experiences; we therefore chose to investigate whether early life stress altered Line1 retrotransposition persists into the juvenile period of development. Our study uses a neonatal predator odor exposure (POE) paradigm to model ELS in rats. We examined Line1 using qPCR to assess Line1 expression levels and DNA copy number in the male and female juvenile amygdala, hippocampus and prefrontal cortex—areas chosen for their association with affective disorders and stress. We report a sex difference in Line1 levels within the juvenile amygdala. We also find that ELS significantly increases Line1 DNA copy number within the juvenile amygdala which correlates with reduced juvenile social play levels, suggesting the possibility that Line1 may influence juvenile social development. Nature Publishing Group UK 2021-02-11 /pmc/articles/PMC7878767/ /pubmed/33574362 http://dx.doi.org/10.1038/s41598-021-82953-3 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cuarenta, Amelia Kigar, Stacey L. Henion, Ian C. Chang, Liza Bakshi, Vaishali P. Auger, Anthony P. Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title | Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title_full | Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title_fullStr | Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title_full_unstemmed | Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title_short | Early life stress during the neonatal period alters social play and Line1 during the juvenile stage of development |
title_sort | early life stress during the neonatal period alters social play and line1 during the juvenile stage of development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7878767/ https://www.ncbi.nlm.nih.gov/pubmed/33574362 http://dx.doi.org/10.1038/s41598-021-82953-3 |
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