A new blood DNA methylation signature for Koolen-de Vries syndrome : Classification of missense KANSL1 variants and comparison to fibroblast cells
Awamleh, Zain (Hospital for Sick Children (Toronto, Canadà))
Choufani, Sanaa (Hospital for Sick Children (Toronto, Canadà))
Wu, Wendy (Hospital for Sick Children (Toronto, Canadà))
Rots, Dmitrijs (Radboud University Medical Center)
Dingemans, Alexander J.M. (Radboud University Medical Center)
Nadif Kasri, Nael (Radboud University Medical Center)
Boronat, Susana (Institut de Recerca Sant Pau)
Ibañez-Mico, Salvador (Hospital Universitario Virgen de la Arrixaca (Múrcia))
Cuesta Herraiz, Laura (Hospital de Manises (València))
Ferrer, Irene (Consorcio Hospital General de Valencia)
Martínez Carrascal, Antonio (Hospital de Requena)
Pérez-Jurado, Luis Alberto (Universitat Pompeu Fabra)
Aznar Lain, Gemma (Universitat Pompeu Fabra)
Ortigoza-Escobar, Juan Dario (Institut de Recerca Sant Joan de Déu)
de Vries, Bert B.A. (Hospital for Sick Children (Toronto, Canadà))
Koolen, David A. (Hospital for Sick Children (Toronto, Canadà))
Weksberg, Rosanna (Hospital for Sick Children (Toronto, Canadà))

Data:	2024
Resum:	Pathogenic variants in KANSL1 and 17q21. 31 microdeletions are causative of Koolen-de Vries syndrome (KdVS), a neurodevelopmental syndrome with characteristic facial dysmorphia. Our previous work has shown that syndromic conditions caused by pathogenic variants in epigenetic regulatory genes have identifiable patterns of DNA methylation (DNAm) change: DNAm signatures or episignatures. Given the role of KANSL1 in histone acetylation, we tested whether variants underlying KdVS are associated with a DNAm signature. We profiled whole-blood DNAm for 13 individuals with KANSL1 variants, four individuals with 17q21. 31 microdeletions, and 21 typically developing individuals, using Illumina's Infinium EPIC array. In this study, we identified a robust DNAm signature of 456 significant CpG sites in 8 individuals with KdVS, a pattern independently validated in an additional 7 individuals with KdVS. We also demonstrate the diagnostic utility of the signature and classify two KANSL1 VUS as well as four variants in individuals with atypical clinical presentation. Lastly, we investigated tissue-specific DNAm changes in fibroblast cells from individuals with KdVS. Collectively, our findings contribute to the understanding of the epigenetic landscape related to KdVS and aid in the diagnosis and classification of variants in this structurally complex genomic region.
Nota:	Altres ajuts: This work was supported by a Canadian Institutes of Health Research (CIHR) grants to RW (PJT-178315) and the Ontario Brain Institute (Province of Ontario Neurodevelopmental Disorders (POND) network (IDS11-02)) grants to RW.
Drets:	Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.
Llengua:	Anglès
Document:	Article ; recerca ; Versió publicada
Matèria:	Abnormalities, Multiple ; Chromosome 17q21.31 Deletion Syndrome ; Chromosome Deletion ; Chromosomes, Human, Pair 17 ; DNA Methylation ; Genes, Regulator ; Humans ; Intellectual Disability
Publicat a:	European Journal of Human Genetics, Vol. 32 Núm. 3 (march 2024) , p. 324-332, ISSN 1476-5438

DOI: 10.1038/s41431-024-01538-6
PMID: 38282074

9 p, 2.2 MB

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