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Inter-layer and inter-subject variability of diurnal gene expression in human skin
The skin is the largest human organ with a circadian clock that regulates its function. Although circadian rhythms in specific functions are known, rhythms in the proximal clock output, gene expression, in human skin have not been thoroughly explored. This work reports 24 h gene expression rhythms i...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803873/ https://www.ncbi.nlm.nih.gov/pubmed/36601580 http://dx.doi.org/10.1093/nargab/lqac097 |
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author | del Olmo, Marta Spörl, Florian Korge, Sandra Jürchott, Karsten Felten, Matthias Grudziecki, Astrid de Zeeuw, Jan Nowozin, Claudia Reuter, Hendrik Blatt, Thomas Herzel, Hanspeter Kunz, Dieter Kramer, Achim Ananthasubramaniam, Bharath |
author_facet | del Olmo, Marta Spörl, Florian Korge, Sandra Jürchott, Karsten Felten, Matthias Grudziecki, Astrid de Zeeuw, Jan Nowozin, Claudia Reuter, Hendrik Blatt, Thomas Herzel, Hanspeter Kunz, Dieter Kramer, Achim Ananthasubramaniam, Bharath |
author_sort | del Olmo, Marta |
collection | PubMed |
description | The skin is the largest human organ with a circadian clock that regulates its function. Although circadian rhythms in specific functions are known, rhythms in the proximal clock output, gene expression, in human skin have not been thoroughly explored. This work reports 24 h gene expression rhythms in two skin layers, epidermis and dermis, in a cohort of young, healthy adults, who maintained natural, regular sleep-wake schedules. 10% of the expressed genes showed such diurnal rhythms at the population level, of which only a third differed between the two layers. Amplitude and phases of diurnal gene expression varied more across subjects than layers, with amplitude being more variable than phases. Expression amplitudes in the epidermis were larger and more subject-variable, while they were smaller and more consistent in the dermis. Core clock gene expression was similar across layers at the population-level, but were heterogeneous in their variability across subjects. We also identified small sets of biomarkers for internal clock phase in each layer, which consisted of layer-specific non-core clock genes. This work provides a valuable resource to advance our understanding of human skin and presents a novel methodology to quantify sources of variability in human circadian rhythms. |
format | Online Article Text |
id | pubmed-9803873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98038732023-01-03 Inter-layer and inter-subject variability of diurnal gene expression in human skin del Olmo, Marta Spörl, Florian Korge, Sandra Jürchott, Karsten Felten, Matthias Grudziecki, Astrid de Zeeuw, Jan Nowozin, Claudia Reuter, Hendrik Blatt, Thomas Herzel, Hanspeter Kunz, Dieter Kramer, Achim Ananthasubramaniam, Bharath NAR Genom Bioinform Standard Article The skin is the largest human organ with a circadian clock that regulates its function. Although circadian rhythms in specific functions are known, rhythms in the proximal clock output, gene expression, in human skin have not been thoroughly explored. This work reports 24 h gene expression rhythms in two skin layers, epidermis and dermis, in a cohort of young, healthy adults, who maintained natural, regular sleep-wake schedules. 10% of the expressed genes showed such diurnal rhythms at the population level, of which only a third differed between the two layers. Amplitude and phases of diurnal gene expression varied more across subjects than layers, with amplitude being more variable than phases. Expression amplitudes in the epidermis were larger and more subject-variable, while they were smaller and more consistent in the dermis. Core clock gene expression was similar across layers at the population-level, but were heterogeneous in their variability across subjects. We also identified small sets of biomarkers for internal clock phase in each layer, which consisted of layer-specific non-core clock genes. This work provides a valuable resource to advance our understanding of human skin and presents a novel methodology to quantify sources of variability in human circadian rhythms. Oxford University Press 2022-12-31 /pmc/articles/PMC9803873/ /pubmed/36601580 http://dx.doi.org/10.1093/nargab/lqac097 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of NAR Genomics and Bioinformatics. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Standard Article del Olmo, Marta Spörl, Florian Korge, Sandra Jürchott, Karsten Felten, Matthias Grudziecki, Astrid de Zeeuw, Jan Nowozin, Claudia Reuter, Hendrik Blatt, Thomas Herzel, Hanspeter Kunz, Dieter Kramer, Achim Ananthasubramaniam, Bharath Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title | Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title_full | Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title_fullStr | Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title_full_unstemmed | Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title_short | Inter-layer and inter-subject variability of diurnal gene expression in human skin |
title_sort | inter-layer and inter-subject variability of diurnal gene expression in human skin |
topic | Standard Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803873/ https://www.ncbi.nlm.nih.gov/pubmed/36601580 http://dx.doi.org/10.1093/nargab/lqac097 |
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