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Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver
In eukaryotes, RNA is synthesised in the nucleus, spliced, and exported to the cytoplasm where it is translated and finally degraded. Any of these steps could be subject to temporal regulation during the circadian cycle, resulting in daily fluctuations of RNA accumulation and affecting the distribut...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377612/ https://www.ncbi.nlm.nih.gov/pubmed/35921362 http://dx.doi.org/10.1371/journal.pgen.1009903 |
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author | Hurni, Clémence Weger, Benjamin D. Gobet, Cédric Naef, Felix |
author_facet | Hurni, Clémence Weger, Benjamin D. Gobet, Cédric Naef, Felix |
author_sort | Hurni, Clémence |
collection | PubMed |
description | In eukaryotes, RNA is synthesised in the nucleus, spliced, and exported to the cytoplasm where it is translated and finally degraded. Any of these steps could be subject to temporal regulation during the circadian cycle, resulting in daily fluctuations of RNA accumulation and affecting the distribution of transcripts in different subcellular compartments. Our study analysed the nuclear and cytoplasmic, poly(A) and total transcriptomes of mouse livers collected over the course of a day. These data provide a genome-wide temporal inventory of enrichment in subcellular RNA, and revealed specific signatures of splicing, nuclear export and cytoplasmic mRNA stability related to transcript and gene lengths. Combined with a mathematical model describing rhythmic RNA profiles, we could test the rhythmicity of export rates and cytoplasmic degradation rates of approximately 1400 genes. With nuclear export times usually much shorter than cytoplasmic half-lives, we found that nuclear export contributes to the modulation and generation of rhythmic profiles of 10% of the cycling nuclear mRNAs. This study contributes to a better understanding of the dynamic regulation of the transcriptome during the day-night cycle. |
format | Online Article Text |
id | pubmed-9377612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-93776122022-08-16 Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver Hurni, Clémence Weger, Benjamin D. Gobet, Cédric Naef, Felix PLoS Genet Research Article In eukaryotes, RNA is synthesised in the nucleus, spliced, and exported to the cytoplasm where it is translated and finally degraded. Any of these steps could be subject to temporal regulation during the circadian cycle, resulting in daily fluctuations of RNA accumulation and affecting the distribution of transcripts in different subcellular compartments. Our study analysed the nuclear and cytoplasmic, poly(A) and total transcriptomes of mouse livers collected over the course of a day. These data provide a genome-wide temporal inventory of enrichment in subcellular RNA, and revealed specific signatures of splicing, nuclear export and cytoplasmic mRNA stability related to transcript and gene lengths. Combined with a mathematical model describing rhythmic RNA profiles, we could test the rhythmicity of export rates and cytoplasmic degradation rates of approximately 1400 genes. With nuclear export times usually much shorter than cytoplasmic half-lives, we found that nuclear export contributes to the modulation and generation of rhythmic profiles of 10% of the cycling nuclear mRNAs. This study contributes to a better understanding of the dynamic regulation of the transcriptome during the day-night cycle. Public Library of Science 2022-08-03 /pmc/articles/PMC9377612/ /pubmed/35921362 http://dx.doi.org/10.1371/journal.pgen.1009903 Text en © 2022 Hurni 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 Hurni, Clémence Weger, Benjamin D. Gobet, Cédric Naef, Felix Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title | Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title_full | Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title_fullStr | Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title_full_unstemmed | Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title_short | Comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
title_sort | comprehensive analysis of the circadian nuclear and cytoplasmic transcriptome in mouse liver |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9377612/ https://www.ncbi.nlm.nih.gov/pubmed/35921362 http://dx.doi.org/10.1371/journal.pgen.1009903 |
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