Cargando…
Endogenous circadian time genes expressions in the liver of mice under constant darkness
BACKGROUND: The circadian rhythms regulate physiological functions and metabolism. Circadian Time (CT) is a unit to quantify the rhythm of endogenous circadian clock, independent of light influence. To understand the gene expression changes throughout CT, C57BL/6 J mice were maintained under constan...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066782/ https://www.ncbi.nlm.nih.gov/pubmed/32160860 http://dx.doi.org/10.1186/s12864-020-6639-4 |
_version_ | 1783505309864558592 |
---|---|
author | Li, Huan Zhang, Shiyao Zhang, Wenxiang Chen, Siyu Rabearivony, Anjara Shi, Yujie Liu, Jie Corton, Christopher J. Liu, Chang |
author_facet | Li, Huan Zhang, Shiyao Zhang, Wenxiang Chen, Siyu Rabearivony, Anjara Shi, Yujie Liu, Jie Corton, Christopher J. Liu, Chang |
author_sort | Li, Huan |
collection | PubMed |
description | BACKGROUND: The circadian rhythms regulate physiological functions and metabolism. Circadian Time (CT) is a unit to quantify the rhythm of endogenous circadian clock, independent of light influence. To understand the gene expression changes throughout CT, C57BL/6 J mice were maintained under constant darkness (DD) for 6 weeks, and the liver samples were collected starting at 9:00 AM (CT1), and every 4 h in a 24-h cycle (CT5, CT9, CT13, CT17 and CT21). Total RNA was extracted and subjected to RNA-Seq data (deposited as GSE 133342, L-DD). To compare gene oscillation pattern under normal light-dark condition (LD, GSE114400) and short time (2 days) dark-dark condition (S-DD, GSE70497), these data were retried from GEO database, and the trimmed mean of M-values normalization was used to normalize the three RNA-seq data followed by MetaCycle analysis. RESULTS: Approximate 12.1% of the genes under L-DD exhibited significant rhythmically expression. The top 5 biological processes enriched in L-DD oscillation genes were mRNA processing, aromatic compound catabolic process, mitochondrion organization, heterocycle catabolic process and cellular nitrogen compound mitotic catabolic process. The endogenous circadian rhythms of clock genes, P450 genes and lipid metabolism genes under L-DD were further compared with LD and S-DD. The oscillation patterns were similar but the period and amplitude of those oscillation genes were slightly altered. RT-qPCR confirmed the selected RNA sequence findings. CONCLUSIONS: This is the first study to profile oscillation gene expressions under L-DD. Our data indicate that clock genes, P450 genes and lipid metabolism genes expressed rhythmically under L-DD. Light was not the necessary factor for persisting circadian rhythm but influenced the period and amplitude of oscillation genes. |
format | Online Article Text |
id | pubmed-7066782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70667822020-03-18 Endogenous circadian time genes expressions in the liver of mice under constant darkness Li, Huan Zhang, Shiyao Zhang, Wenxiang Chen, Siyu Rabearivony, Anjara Shi, Yujie Liu, Jie Corton, Christopher J. Liu, Chang BMC Genomics Research Article BACKGROUND: The circadian rhythms regulate physiological functions and metabolism. Circadian Time (CT) is a unit to quantify the rhythm of endogenous circadian clock, independent of light influence. To understand the gene expression changes throughout CT, C57BL/6 J mice were maintained under constant darkness (DD) for 6 weeks, and the liver samples were collected starting at 9:00 AM (CT1), and every 4 h in a 24-h cycle (CT5, CT9, CT13, CT17 and CT21). Total RNA was extracted and subjected to RNA-Seq data (deposited as GSE 133342, L-DD). To compare gene oscillation pattern under normal light-dark condition (LD, GSE114400) and short time (2 days) dark-dark condition (S-DD, GSE70497), these data were retried from GEO database, and the trimmed mean of M-values normalization was used to normalize the three RNA-seq data followed by MetaCycle analysis. RESULTS: Approximate 12.1% of the genes under L-DD exhibited significant rhythmically expression. The top 5 biological processes enriched in L-DD oscillation genes were mRNA processing, aromatic compound catabolic process, mitochondrion organization, heterocycle catabolic process and cellular nitrogen compound mitotic catabolic process. The endogenous circadian rhythms of clock genes, P450 genes and lipid metabolism genes under L-DD were further compared with LD and S-DD. The oscillation patterns were similar but the period and amplitude of those oscillation genes were slightly altered. RT-qPCR confirmed the selected RNA sequence findings. CONCLUSIONS: This is the first study to profile oscillation gene expressions under L-DD. Our data indicate that clock genes, P450 genes and lipid metabolism genes expressed rhythmically under L-DD. Light was not the necessary factor for persisting circadian rhythm but influenced the period and amplitude of oscillation genes. BioMed Central 2020-03-12 /pmc/articles/PMC7066782/ /pubmed/32160860 http://dx.doi.org/10.1186/s12864-020-6639-4 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 Article Li, Huan Zhang, Shiyao Zhang, Wenxiang Chen, Siyu Rabearivony, Anjara Shi, Yujie Liu, Jie Corton, Christopher J. Liu, Chang Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title | Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title_full | Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title_fullStr | Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title_full_unstemmed | Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title_short | Endogenous circadian time genes expressions in the liver of mice under constant darkness |
title_sort | endogenous circadian time genes expressions in the liver of mice under constant darkness |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066782/ https://www.ncbi.nlm.nih.gov/pubmed/32160860 http://dx.doi.org/10.1186/s12864-020-6639-4 |
work_keys_str_mv | AT lihuan endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT zhangshiyao endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT zhangwenxiang endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT chensiyu endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT rabearivonyanjara endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT shiyujie endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT liujie endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT cortonchristopherj endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness AT liuchang endogenouscircadiantimegenesexpressionsintheliverofmiceunderconstantdarkness |