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Human CRY1 variants associate with attention deficit/hyperactivity disorder

Authors :
I Halil Kavaklı
Arianna Goracci
Yuval Itan
Ayse Ozhan
Chiara Fallerini
Jean-Laurent Casanova
Cihan Aydin
M Ece Kars
O Emre Onat
Yiming Wu
Cem Atbaşoğlu
A. Nazli Basak
Kaya Bilguvar
Alessandra Renieri
Tayfun Ozcelik
M Allegra Trusso
Meram Can Saka
Seref Gul
Gül, Şeref
Aydın, Cihan (ORCID 0000-0003-0560-1895 & YÖK ID 214696)
Başak, Ayşe Nazlı (ORCID 0000-0001-9257-3540 & YÖK ID 1512)
Kavaklı, İbrahim Halil (ORCID 0000-0001-6624-3505 & YÖK ID 40319)
Onat, O. Emre
Kars, M. Ece
Bilguvar, Kaya
Wu, Yiming
Özhan, Ayşe
Trusso, M. Allegra
Goracci, Arianna
Fallerini, Chiara
Renieri, Alessandra
Casanova, Jean Laurent
Itan, Yuval
Atbaşoğlu, Cem E.
Saka, Meram C.
Özçelik, Tayfun
Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
Graduate School of Sciences and Engineering
College of Engineering
College of Sciences
Department of Chemical and Biological Engineering
Department of Molecular Biology and Genetics
Başak, A. N.
Source :
Journal of Clinical Investigation, J Clin Invest
Publication Year :
2020
Publisher :
American Society for Clinical Investigation, 2020.

Abstract

Attention deficit/hyperactivity disorder (ADHD) is a common and heritable phenotype frequently accompanied by insomnia, anxiety, and depression. Here, using a reverse phenotyping approach, we report heterozygous coding variations in the core circadian clock gene cryptochrome 1 in 15 unrelated multigenerational families with combined ADHD and insomnia. The variants led to functional alterations in the circadian molecular rhythms, providing a mechanistic link to the behavioral symptoms. One variant, CRY1Δ11 c.1657+3A>C, is present in approximately 1% of Europeans, therefore standing out as a diagnostic and therapeutic marker. We showed by exome sequencing in an independent cohort of patients with combined ADHD and insomnia that 8 of 62 patients and 0 of 369 controls carried CRY1Δ11. Also, we identified a variant, CRY1Δ6 c.825+1G>A, that shows reduced affinity for BMAL1/CLOCK and causes an arrhythmic phenotype. Genotype-phenotype correlation analysis revealed that this variant segregated with ADHD and delayed sleep phase disorder (DSPD) in the affected family. Finally, we found in a phenome-wide association study involving 9438 unrelated adult Europeans that CRY1Δ11 was associated with major depressive disorder, insomnia, and anxiety. These results defined a distinctive group of circadian psychiatric phenotypes that we propose to designate as "circiatric" disorders.<br />NIH Clinical and Translational Science Award (CTSA) Program; NIH; French National Research Agency (ANR) under the “Investments for the future” Program; Integrative Biology of Emerging Infectious Diseases Laboratoire d’Excellence; IEIHSEER Grant; SEAe-Host Factors Grant; PNEUMOID Project Grant; INCA/Cancéropole Ile-de-France; Turkish Academy of Sciences (TÜBA); National Center for Advancing Translational Sciences (NCAST); Rockefeller University, INSERM; HHMI, University of Paris; St. Giles Foundation; Charles Bronfman Institute for Personalized Medicine at the Icahn School of Medicine at Mount Sinai

Details

ISSN :
15588238 and 00219738
Volume :
130
Database :
OpenAIRE
Journal :
Journal of Clinical Investigation
Accession number :
edsair.doi.dedup.....c26e34969651363455b6ea63aaffd9dd
Full Text :
https://doi.org/10.1172/jci135500