Age-dependent expression changes of circadian system-related genes reveal a potentially conserved link to aging.


Journal

Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617

Informations de publication

Date de publication:
19 12 2021
Historique:
received: 16 03 2021
accepted: 01 12 2021
pubmed: 20 12 2021
medline: 1 2 2022
entrez: 19 12 2021
Statut: ppublish

Résumé

The circadian clock system influences the biology of life by establishing circadian rhythms in organisms, tissues, and cells, thus regulating essential biological processes based on the day/night cycle. Circadian rhythms change over a lifetime due to maturation and aging, and disturbances in the control of the circadian system are associated with several age-related pathologies. However, the impact of chronobiology and the circadian system on healthy organ and tissue aging remains largely unknown. Whether aging-related changes of the circadian system's regulation follow a conserved pattern across different species and tissues, hence representing a common driving force of aging, is unclear. Based on a cross-sectional transcriptome analysis covering 329 RNA-Seq libraries, we provide indications that the circadian system is subjected to aging-related gene alterations shared between evolutionarily distinct species, such as

Identifiants

pubmed: 34923482
pii: 203788
doi: 10.18632/aging.203788
pmc: PMC8751596
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

25694-25716

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Auteurs

Emanuel Barth (E)

Bioinformatics/High Throughput Analysis, Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena, Jena, Germany.

Akash Srivastava (A)

Bioinformatics/High Throughput Analysis, Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena, Jena, Germany.
FLI Leibniz Institute for Age Research, Jena, Germany.
Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Diane Wengerodt (D)

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Milan Stojiljkovic (M)

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Hubertus Axer (H)

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Otto W Witte (OW)

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Alexandra Kretz (A)

Hans Berger Department of Neurology, Jena University Hospital, Jena, Germany.

Manja Marz (M)

Bioinformatics/High Throughput Analysis, Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena, Jena, Germany.
FLI Leibniz Institute for Age Research, Jena, Germany.
German Center for Integrative Biodiversity Research (iDiv), Halle-Jena-Leipzig, Germany.
European Virus Bioinformatics Center (EVBC), Jena, Germany.

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