Circadian clock gene polymorphisms implicated in human pathologies

dc.contributor.authorJanoski, Jesse R.en
dc.contributor.authorAiello, Ignacioen
dc.contributor.authorLundberg, Clayton W.en
dc.contributor.authorFinkielstein, Carla V.en
dc.date.accessioned2025-02-04T20:43:31Zen
dc.date.available2025-02-04T20:43:31Zen
dc.date.issued2024-06-12en
dc.description.abstractCircadian rhythms, ~24 h cycles of physiological and behavioral processes, can be synchronized by external signals (e.g., light) and persist even in their absence. Consequently, dysregulation of circadian rhythms adversely affects the well-being of the organism. This timekeeping system is generated and sustained by a genetically encoded endogenous mechanism composed of interlocking transcriptional/translational feedback loops that generate rhythmic expression of core clock genes. Genome-wide association studies (GWAS) and forward genetic studies show that SNPs in clock genes influence gene regulation and correlate with the risk of developing various conditions. We discuss genetic variations in core clock genes that are associated with various phenotypes, their implications for human health, and stress the need for thorough studies in this domain of circadian regulation.en
dc.description.versionPublished versionen
dc.format.extentPages 834-852en
dc.format.extent19 page(s)en
dc.format.mimetypeapplication/pdfen
dc.identifier.doihttps://doi.org/10.1016/j.tig.2024.05.006en
dc.identifier.eissn1362-4555en
dc.identifier.issn0168-9525en
dc.identifier.issue10en
dc.identifier.orcidFinkielstein, Carla [0000-0002-8417-4643]en
dc.identifier.otherS0168-9525(24)00110-0 (PII)en
dc.identifier.pmid38871615en
dc.identifier.urihttps://hdl.handle.net/10919/124493en
dc.identifier.volume40en
dc.language.isoenen
dc.publisherCell Pressen
dc.relation.urihttps://www.ncbi.nlm.nih.gov/pubmed/38871615en
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectcircadian medicineen
dc.subjectcircadian rhythmen
dc.subjectclock genesen
dc.subjectgenetic variationsen
dc.subjectgenome-wide associationen
dc.subjectpolymorphismen
dc.subject.meshHumansen
dc.subject.meshGene Expression Regulationen
dc.subject.meshCircadian Rhythmen
dc.subject.meshPolymorphism, Single Nucleotideen
dc.subject.meshGenome-Wide Association Studyen
dc.subject.meshCLOCK Proteinsen
dc.subject.meshCircadian Clocksen
dc.titleCircadian clock gene polymorphisms implicated in human pathologiesen
dc.title.serialTrends in Geneticsen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten
dc.type.otherJournalen
dcterms.dateAccepted2024-05-14en
pubs.organisational-groupVirginia Techen
pubs.organisational-groupVirginia Tech/Scienceen
pubs.organisational-groupVirginia Tech/Science/Biological Sciencesen
pubs.organisational-groupVirginia Tech/Faculty of Health Sciencesen
pubs.organisational-groupVirginia Tech/All T&R Facultyen
pubs.organisational-groupVirginia Tech/Science/COS T&R Facultyen
pubs.organisational-groupVirginia Tech/VT Carilion School of Medicineen
pubs.organisational-groupVirginia Tech/VT Carilion School of Medicine/Surgeryen
pubs.organisational-groupVirginia Tech/VT Carilion School of Medicine/Psychiatry and Behavioral Medicineen
pubs.organisational-groupVirginia Tech/VT Carilion School of Medicine/Psychiatry and Behavioral Medicine/Secondary Appointment-Psychiatry and Behavioral Medicineen
pubs.organisational-groupVirginia Tech/VT Carilion School of Medicine/Surgery/Secondary Appointment-Surgeryen

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
TIG_2024.pdf
Size:
1.8 MB
Format:
Adobe Portable Document Format
Description:
Published version
License bundle
Now showing 1 - 1 of 1
Name:
license.txt
Size:
1.5 KB
Format:
Plain Text
Description: