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Circadian regulation of the Drosophila astrocyte transcriptome

Recent studies have demonstrated that astrocytes cooperate with neurons of the brain to mediate circadian control of many rhythmic processes including locomotor activity and sleep. Transcriptional profiling studies have described the overall rhythmic landscape of the brain, but few have employed app...

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Detalles Bibliográficos
Autores principales: You, Samantha, Yu, Alder M., Roberts, Mary A., Joseph, Ivanna J., Jackson, F. Rob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483315/
https://www.ncbi.nlm.nih.gov/pubmed/34543266
http://dx.doi.org/10.1371/journal.pgen.1009790
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author You, Samantha
Yu, Alder M.
Roberts, Mary A.
Joseph, Ivanna J.
Jackson, F. Rob
author_facet You, Samantha
Yu, Alder M.
Roberts, Mary A.
Joseph, Ivanna J.
Jackson, F. Rob
author_sort You, Samantha
collection PubMed
description Recent studies have demonstrated that astrocytes cooperate with neurons of the brain to mediate circadian control of many rhythmic processes including locomotor activity and sleep. Transcriptional profiling studies have described the overall rhythmic landscape of the brain, but few have employed approaches that reveal heterogeneous, cell-type specific rhythms of the brain. Using cell-specific isolation of ribosome-bound RNAs in Drosophila, we constructed the first circadian “translatome” for astrocytes. This analysis identified 293 “cycling genes” in astrocytes, most with mammalian orthologs. A subsequent behavioral genetic screen identified a number of genes whose expression is required in astrocytes for normal sleep behavior. In particular, we show that certain genes known to regulate fly innate immune responses are also required for normal sleep patterns.
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spelling pubmed-84833152021-10-01 Circadian regulation of the Drosophila astrocyte transcriptome You, Samantha Yu, Alder M. Roberts, Mary A. Joseph, Ivanna J. Jackson, F. Rob PLoS Genet Research Article Recent studies have demonstrated that astrocytes cooperate with neurons of the brain to mediate circadian control of many rhythmic processes including locomotor activity and sleep. Transcriptional profiling studies have described the overall rhythmic landscape of the brain, but few have employed approaches that reveal heterogeneous, cell-type specific rhythms of the brain. Using cell-specific isolation of ribosome-bound RNAs in Drosophila, we constructed the first circadian “translatome” for astrocytes. This analysis identified 293 “cycling genes” in astrocytes, most with mammalian orthologs. A subsequent behavioral genetic screen identified a number of genes whose expression is required in astrocytes for normal sleep behavior. In particular, we show that certain genes known to regulate fly innate immune responses are also required for normal sleep patterns. Public Library of Science 2021-09-20 /pmc/articles/PMC8483315/ /pubmed/34543266 http://dx.doi.org/10.1371/journal.pgen.1009790 Text en © 2021 You 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
You, Samantha
Yu, Alder M.
Roberts, Mary A.
Joseph, Ivanna J.
Jackson, F. Rob
Circadian regulation of the Drosophila astrocyte transcriptome
title Circadian regulation of the Drosophila astrocyte transcriptome
title_full Circadian regulation of the Drosophila astrocyte transcriptome
title_fullStr Circadian regulation of the Drosophila astrocyte transcriptome
title_full_unstemmed Circadian regulation of the Drosophila astrocyte transcriptome
title_short Circadian regulation of the Drosophila astrocyte transcriptome
title_sort circadian regulation of the drosophila astrocyte transcriptome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8483315/
https://www.ncbi.nlm.nih.gov/pubmed/34543266
http://dx.doi.org/10.1371/journal.pgen.1009790
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