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Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations
Research shows that brain circuits controlling vital physiological processes are closely linked with endogenous time-keeping systems. In this study, we aimed to examine oscillatory gene expression patterns of well-characterized neuronal circuits by reanalyzing publicly available transcriptomic data...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518731/ https://www.ncbi.nlm.nih.gov/pubmed/37752952 http://dx.doi.org/10.1016/j.isci.2023.107810 |
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author | Lee, Justine Chen, Siwei Monfared, Roudabeh Vakil Derdeyn, Pieter Leong, Kenneth Chang, Tiffany Beier, Kevin Baldi, Pierre Alachkar, Amal |
author_facet | Lee, Justine Chen, Siwei Monfared, Roudabeh Vakil Derdeyn, Pieter Leong, Kenneth Chang, Tiffany Beier, Kevin Baldi, Pierre Alachkar, Amal |
author_sort | Lee, Justine |
collection | PubMed |
description | Research shows that brain circuits controlling vital physiological processes are closely linked with endogenous time-keeping systems. In this study, we aimed to examine oscillatory gene expression patterns of well-characterized neuronal circuits by reanalyzing publicly available transcriptomic data from a spatiotemporal gene expression atlas of a non-human primate. Unexpectedly, brain structures known for regulating circadian processes (e.g., hypothalamic nuclei) did not exhibit robust cycling expression. In contrast, basal ganglia nuclei, not typically associated with circadian physiology, displayed the most dynamic cycling behavior of its genes marked by sharp temporally defined expression peaks. Intriguingly, the mammillary bodies, considered hypothalamic nuclei, exhibited gene expression patterns resembling the basal ganglia, prompting reevaluation of their classification. Our results emphasize the potential for high throughput circadian gene expression analysis to deepen our understanding of the functional synchronization across brain structures that influence physiological processes and resulting complex behaviors. |
format | Online Article Text |
id | pubmed-10518731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-105187312023-09-26 Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations Lee, Justine Chen, Siwei Monfared, Roudabeh Vakil Derdeyn, Pieter Leong, Kenneth Chang, Tiffany Beier, Kevin Baldi, Pierre Alachkar, Amal iScience Article Research shows that brain circuits controlling vital physiological processes are closely linked with endogenous time-keeping systems. In this study, we aimed to examine oscillatory gene expression patterns of well-characterized neuronal circuits by reanalyzing publicly available transcriptomic data from a spatiotemporal gene expression atlas of a non-human primate. Unexpectedly, brain structures known for regulating circadian processes (e.g., hypothalamic nuclei) did not exhibit robust cycling expression. In contrast, basal ganglia nuclei, not typically associated with circadian physiology, displayed the most dynamic cycling behavior of its genes marked by sharp temporally defined expression peaks. Intriguingly, the mammillary bodies, considered hypothalamic nuclei, exhibited gene expression patterns resembling the basal ganglia, prompting reevaluation of their classification. Our results emphasize the potential for high throughput circadian gene expression analysis to deepen our understanding of the functional synchronization across brain structures that influence physiological processes and resulting complex behaviors. Elsevier 2023-09-01 /pmc/articles/PMC10518731/ /pubmed/37752952 http://dx.doi.org/10.1016/j.isci.2023.107810 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Lee, Justine Chen, Siwei Monfared, Roudabeh Vakil Derdeyn, Pieter Leong, Kenneth Chang, Tiffany Beier, Kevin Baldi, Pierre Alachkar, Amal Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title | Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title_full | Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title_fullStr | Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title_full_unstemmed | Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title_short | Reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
title_sort | reanalysis of primate brain circadian transcriptomics reveals connectivity-related oscillations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518731/ https://www.ncbi.nlm.nih.gov/pubmed/37752952 http://dx.doi.org/10.1016/j.isci.2023.107810 |
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