| Literature DB >> 24702954 |
Saeed Al Turki1, Ashok K Manickaraj2, Catherine L Mercer3, Sebastian S Gerety4, Marc-Phillip Hitz4, Sarah Lindsay4, Lisa C A D'Alessandro2, G Jawahar Swaminathan4, Jamie Bentham5, Anne-Karin Arndt6, Jacoba Louw, Jacoba Low7, Jeroen Breckpot8, Marc Gewillig9, Bernard Thienpont8, Hashim Abdul-Khaliq10, Christine Harnack11, Kirstin Hoff12, Hans-Heiner Kramer13, Stephan Schubert14, Reiner Siebert15, Okan Toka16, Catherine Cosgrove17, Hugh Watkins17, Anneke M Lucassen3, Ita M O'Kelly3, Anthony P Salmon3, Frances A Bu'lock18, Javier Granados-Riveron19, Kerry Setchfield19, Chris Thornborough18, J David Brook19, Barbara Mulder20, Sabine Klaassen21, Shoumo Bhattacharya17, Koen Devriendt8, David F Fitzpatrick22, David I Wilson3, Seema Mital23, Matthew E Hurles24.
Abstract
Congenital heart defects (CHDs) are the most common birth defect worldwide and are a leading cause of neonatal mortality. Nonsyndromic atrioventricular septal defects (AVSDs) are an important subtype of CHDs for which the genetic architecture is poorly understood. We performed exome sequencing in 13 parent-offspring trios and 112 unrelated individuals with nonsyndromic AVSDs and identified five rare missense variants (two of which arose de novo) in the highly conserved gene NR2F2, a very significant enrichment (p = 7.7 × 10(-7)) compared to 5,194 control subjects. We identified three additional CHD-affected families with other variants in NR2F2 including a de novo balanced chromosomal translocation, a de novo substitution disrupting a splice donor site, and a 3 bp duplication that cosegregated in a multiplex family. NR2F2 encodes a pleiotropic developmental transcription factor, and decreased dosage of NR2F2 in mice has been shown to result in abnormal development of atrioventricular septa. Via luciferase assays, we showed that all six coding sequence variants observed in individuals significantly alter the activity of NR2F2 on target promoters.Entities:
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Year: 2014 PMID: 24702954 PMCID: PMC3980509 DOI: 10.1016/j.ajhg.2014.03.007
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025