De novo copy number variants associated with intellectual disability have a paternal origin and age bias

Jayne Y. Hehir-Kwa, Benjamín Rodríguez-Santiago, Lisenka E. Vissers, Nicole de Leeuw, Rolph Pfundt, Jan K. Buitelaar, Luis A. Pérez-Jurado, Joris A. Veltman

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

84 Citaten (Scopus)

Samenvatting

Background: De novo mutations and structural rearrangements are a common cause of intellectual disability (ID) and other disorders with reduced or null reproductive fitness. Insight into the genomic and environmental factors predisposing to the generation of these de novo events is therefore of significant clinical importance. Methods: This study used information from single nucleotide polymorphism microarrays to determine the parent-of-origin of 118 rare de novo copy number variations (CNVs) detected in a cohort of 3443 patients with ID. Results: The large majority of these CNVs (76%, p=1.14×310 -8) originated on the paternal allele. This paternal bias was independent of CNV length and CNV type. Interestingly, the paternal bias was less pronounced for CNVs flanked by segmental duplications (64%), suggesting that molecular mechanisms involved in the formation of rare de novo CNVs may be dependent on the parent-of-origin. In addition, a significantly increased paternal age was only observed for those CNVs which were not flanked by segmental duplications (p=0.02). Conclusion This indicates that rare de novo CNVs are increasingly being generated with advanced paternal age by replication based mechanisms during spermatogenesis. Conclusion: This indicates that rare de novo CNVs are increasingly eing generated with advanced paternal age by replication based mechanisms during spermatogenesis.

Originele taal-2Engels
Pagina's (van-tot)776-778
Aantal pagina's3
TijdschriftJournal of Medical Genetics
Volume48
Nummer van het tijdschrift11
DOI's
StatusGepubliceerd - nov. 2011
Extern gepubliceerdJa

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