Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders

Plavc, Laura (avtor), Skubic, Cene (avtor), Dolenc-Grošelj, Leja (avtor), Rozman, Damjana (avtor)

Delayed sleep phase disorder and advanced sleep phase disorder cause disruption of the circadian clock and present with extreme morning/evening chronotype with unclear role of the genetic etiology, especially for delayed sleep phase disorder. To assess if genotyping can aid in clinical diagnosis, we examined the presence of genetic variants in circadian clock genes previously linked to both sleep disorders in Slovenian patient cohort. Based on Morning-evening questionnaire, we found 15 patients with extreme chronotypes, 13 evening and 2 morning, and 28 controls. Sanger sequencing was used to determine the presence of carefully selected candidate SNPs in regions of the CSNK1D, PER2/3 and CRY1 genes. In a patient with an extreme morning chronotype and a family history of circadian sleep disorder we identified two heterozygous missense variants in PER3 gene, c.1243C>G (NM_001377275.1 (p.Pro415Ala)) and c.1250A>G (NM_001377275.1 (p.His417Arg)). The variants were significantly linked to Advanced sleep phase disorder and were also found in proband’s father with extreme morningness. Additionally, a rare SNP was found in PER2 gene in a patient with clinical picture of Delayed sleep phase disorder. The novel variant in PER2 (NM_022817.3):c.1901–218 G>T was found in proband’s parent with eveningness, indicating an autosomal dominant inheritance. We identified a family with autosomal dominant inheritance of two PER3 heterozygous variants that can be linked to Advanced sleep phase disorder. We revealed also a rare hereditary form of Delayed sleep phase disorder with a new PER2 variant with autosomal dominant inheritance, shedding the light into the genetic causality.

• Jezik: Angleški jezik
• Ključne besede: circadian clock, genetics, PER2, sleep phase disorders, genotyping, PER3
• Vrsta gradiva: Članek v reviji
• Tipologija: 1.01 - Izvirni znanstveni članek
• Organizacija: MF - Medicinska fakulteta
• Status publikacije: Objavljeno
• Različica publikacije: Objavljena publikacija
• Leto izida: 2024
• Št. strani: Str. 757-766
• Številčenje: Vol. 41, iss. 5
• PID: 20.500.12556/RUL-158206
• UDK: 616.8
• ISSN pri članku: 0742-0528
• DOI: 10.1080/07420528.2024.2348016
• COBISS.SI-ID: 196658691
• Datum objave v RUL: 29.05.2024

PLAVC, Laura, SKUBIC, Cene, DOLENC-GROŠELJ, Leja in ROZMAN, Damjana, 2024, Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders. Chronobiology international [na spletu]. 2024. Vol. 41, no. 5, p. 757–766. [Dostopano 4 april 2025]. DOI 10.1080/07420528.2024.2348016. Pridobljeno s: https://repozitorij.uni-lj.si/IzpisGradiva.php?lang=slv&id=158206

Gradivo je del revije

• Naslov: Chronobiology international
• Skrajšan naslov: Chronobiol. int.
• Založnik: Taylor & Francis
• ISSN: 0742-0528
• COBISS.SI-ID: 27499264

Licence

• Licenca: CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
• Povezava: http://creativecommons.org/licenses/by/4.0/deed.sl
• Opis: To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.