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Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq
Sleep deprivation is a global health problem adversely affecting health as well as causing decrements in learning and performance. Sleep deprivation induces significant changes in gene transcription in many brain regions, with the hippocampus particularly susceptible to acute sleep deprivation. Howe...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713217/ https://www.ncbi.nlm.nih.gov/pubmed/33272296 http://dx.doi.org/10.1186/s13041-020-00702-5 |
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author | Lyons, Lisa C. Chatterjee, Snehajyoti Vanrobaeys, Yann Gaine, Marie E. Abel, Ted |
author_facet | Lyons, Lisa C. Chatterjee, Snehajyoti Vanrobaeys, Yann Gaine, Marie E. Abel, Ted |
author_sort | Lyons, Lisa C. |
collection | PubMed |
description | Sleep deprivation is a global health problem adversely affecting health as well as causing decrements in learning and performance. Sleep deprivation induces significant changes in gene transcription in many brain regions, with the hippocampus particularly susceptible to acute sleep deprivation. However, less is known about the impacts of sleep deprivation on post-transcriptional gene regulation. To identify the effects of sleep deprivation on the translatome, we took advantage of the RiboTag mouse line to express HA-labeled Rpl22 in CaMKIIα neurons to selectively isolate and sequence mRNA transcripts associated with ribosomes in excitatory neurons. We found 198 differentially expressed genes in the ribosome-associated mRNA subset after sleep deprivation. In comparison with previously published data on gene expression in the hippocampus after sleep deprivation, we found that the subset of genes affected by sleep deprivation was considerably different in the translatome compared with the transcriptome, with only 49 genes regulated similarly. Interestingly, we found 478 genes differentially regulated by sleep deprivation in the transcriptome that were not significantly regulated in the translatome of excitatory neurons. Conversely, there were 149 genes differentially regulated by sleep deprivation in the translatome but not in the whole transcriptome. Pathway analysis revealed differences in the biological functions of genes exclusively regulated in the transcriptome or translatome, with protein deacetylase activity and small GTPase binding regulated in the transcriptome and unfolded protein binding, kinase inhibitor activity, neurotransmitter receptors and circadian rhythms regulated in the translatome. These results indicate that sleep deprivation induces significant changes affecting the pool of actively translated mRNAs. [Image: see text] |
format | Online Article Text |
id | pubmed-7713217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77132172020-12-03 Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq Lyons, Lisa C. Chatterjee, Snehajyoti Vanrobaeys, Yann Gaine, Marie E. Abel, Ted Mol Brain Research Sleep deprivation is a global health problem adversely affecting health as well as causing decrements in learning and performance. Sleep deprivation induces significant changes in gene transcription in many brain regions, with the hippocampus particularly susceptible to acute sleep deprivation. However, less is known about the impacts of sleep deprivation on post-transcriptional gene regulation. To identify the effects of sleep deprivation on the translatome, we took advantage of the RiboTag mouse line to express HA-labeled Rpl22 in CaMKIIα neurons to selectively isolate and sequence mRNA transcripts associated with ribosomes in excitatory neurons. We found 198 differentially expressed genes in the ribosome-associated mRNA subset after sleep deprivation. In comparison with previously published data on gene expression in the hippocampus after sleep deprivation, we found that the subset of genes affected by sleep deprivation was considerably different in the translatome compared with the transcriptome, with only 49 genes regulated similarly. Interestingly, we found 478 genes differentially regulated by sleep deprivation in the transcriptome that were not significantly regulated in the translatome of excitatory neurons. Conversely, there were 149 genes differentially regulated by sleep deprivation in the translatome but not in the whole transcriptome. Pathway analysis revealed differences in the biological functions of genes exclusively regulated in the transcriptome or translatome, with protein deacetylase activity and small GTPase binding regulated in the transcriptome and unfolded protein binding, kinase inhibitor activity, neurotransmitter receptors and circadian rhythms regulated in the translatome. These results indicate that sleep deprivation induces significant changes affecting the pool of actively translated mRNAs. [Image: see text] BioMed Central 2020-12-03 /pmc/articles/PMC7713217/ /pubmed/33272296 http://dx.doi.org/10.1186/s13041-020-00702-5 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lyons, Lisa C. Chatterjee, Snehajyoti Vanrobaeys, Yann Gaine, Marie E. Abel, Ted Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title | Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title_full | Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title_fullStr | Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title_full_unstemmed | Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title_short | Translational changes induced by acute sleep deprivation uncovered by TRAP-Seq |
title_sort | translational changes induced by acute sleep deprivation uncovered by trap-seq |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713217/ https://www.ncbi.nlm.nih.gov/pubmed/33272296 http://dx.doi.org/10.1186/s13041-020-00702-5 |
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