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Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues
The medial subnucleus of the amygdala (MeA) plays a central role in processing sensory cues required for innate behaviors. However, whether there is a link between developmental programs and the emergence of inborn behaviors remains unknown. Our previous studies revealed that the telencephalic preop...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384829/ https://www.ncbi.nlm.nih.gov/pubmed/28244870 http://dx.doi.org/10.7554/eLife.21012 |
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author | Lischinsky, Julieta E Sokolowski, Katie Li, Peijun Esumi, Shigeyuki Kamal, Yasmin Goodrich, Meredith Oboti, Livio Hammond, Timothy R Krishnamoorthy, Meera Feldman, Daniel Huntsman, Molly Liu, Judy Corbin, Joshua G |
author_facet | Lischinsky, Julieta E Sokolowski, Katie Li, Peijun Esumi, Shigeyuki Kamal, Yasmin Goodrich, Meredith Oboti, Livio Hammond, Timothy R Krishnamoorthy, Meera Feldman, Daniel Huntsman, Molly Liu, Judy Corbin, Joshua G |
author_sort | Lischinsky, Julieta E |
collection | PubMed |
description | The medial subnucleus of the amygdala (MeA) plays a central role in processing sensory cues required for innate behaviors. However, whether there is a link between developmental programs and the emergence of inborn behaviors remains unknown. Our previous studies revealed that the telencephalic preoptic area (POA) embryonic niche is a novel source of MeA destined progenitors. Here, we show that the POA is comprised of distinct progenitor pools complementarily marked by the transcription factors Dbx1 and Foxp2. As determined by molecular and electrophysiological criteria this embryonic parcellation predicts postnatal MeA inhibitory neuronal subtype identity. We further find that Dbx1-derived and Foxp2+ cells in the MeA are differentially activated in response to innate behavioral cues in a sex-specific manner. Thus, developmental transcription factor expression is predictive of MeA neuronal identity and sex-specific neuronal responses, providing a potential developmental logic for how innate behaviors could be processed by different MeA neuronal subtypes. DOI: http://dx.doi.org/10.7554/eLife.21012.001 |
format | Online Article Text |
id | pubmed-5384829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53848292017-04-10 Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues Lischinsky, Julieta E Sokolowski, Katie Li, Peijun Esumi, Shigeyuki Kamal, Yasmin Goodrich, Meredith Oboti, Livio Hammond, Timothy R Krishnamoorthy, Meera Feldman, Daniel Huntsman, Molly Liu, Judy Corbin, Joshua G eLife Neuroscience The medial subnucleus of the amygdala (MeA) plays a central role in processing sensory cues required for innate behaviors. However, whether there is a link between developmental programs and the emergence of inborn behaviors remains unknown. Our previous studies revealed that the telencephalic preoptic area (POA) embryonic niche is a novel source of MeA destined progenitors. Here, we show that the POA is comprised of distinct progenitor pools complementarily marked by the transcription factors Dbx1 and Foxp2. As determined by molecular and electrophysiological criteria this embryonic parcellation predicts postnatal MeA inhibitory neuronal subtype identity. We further find that Dbx1-derived and Foxp2+ cells in the MeA are differentially activated in response to innate behavioral cues in a sex-specific manner. Thus, developmental transcription factor expression is predictive of MeA neuronal identity and sex-specific neuronal responses, providing a potential developmental logic for how innate behaviors could be processed by different MeA neuronal subtypes. DOI: http://dx.doi.org/10.7554/eLife.21012.001 eLife Sciences Publications, Ltd 2017-03-13 /pmc/articles/PMC5384829/ /pubmed/28244870 http://dx.doi.org/10.7554/eLife.21012 Text en © 2017, Lischinsky et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Lischinsky, Julieta E Sokolowski, Katie Li, Peijun Esumi, Shigeyuki Kamal, Yasmin Goodrich, Meredith Oboti, Livio Hammond, Timothy R Krishnamoorthy, Meera Feldman, Daniel Huntsman, Molly Liu, Judy Corbin, Joshua G Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title | Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title_full | Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title_fullStr | Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title_full_unstemmed | Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title_short | Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
title_sort | embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5384829/ https://www.ncbi.nlm.nih.gov/pubmed/28244870 http://dx.doi.org/10.7554/eLife.21012 |
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