| Literature DB >> 29923154 |
Amélie Pinard1,2, Nathalie Eudes1, Julia Mitchell1,3, Fanny Bajolle4,5, Maude Grelet1, Joséphine Okoronkwo4,5, Damien Bonnet4,5, Gwenaelle Collod-Béroud1, Stéphane Zaffran6,7.
Abstract
Ventricular septal defect (VSD) including outlet VSD of double outlet right ventricle (DORV) and perimembranous VSD are among the most common congenital heart diseases found at birth. HOXB1 encodes a homeodomain transcription factor essential for normal cardiac outflow tract development. The aim of the present study was to investigate the possible genetic effect of sequence variations in HOXB1 on VSD. The coding regions and splice junctions of the HOXB1 gene were sequenced in 57 unrelated VSD patients. As a result, a homozygous c.74_82dup (p.Pro28delinsHisSerAlaPro) variant was identified in one individual with DORV. We also identified five previously reported polymorphisms (rs35114525, rs12946855, rs14534040, rs12939811, and rs7207109) in 18 patients (12 DORV and 6 perimembranous VSD). Our study did not show any pathogenic alterations in the coding region of HOXB1 among patients with VSD. To our knowledge this is the first study investigating the role of HOXB1 in nonsyndromic VSD, which provide more insight on the etiology of this disease.Entities:
Keywords: Congenital heart disease; Genetics; HOXB1; Variant; Ventricular septal defect
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Year: 2018 PMID: 29923154 DOI: 10.1007/s11033-018-4212-x
Source DB: PubMed Journal: Mol Biol Rep ISSN: 0301-4851 Impact factor: 2.316