Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.

Abstract

Recently, GATA4 and NKX2.5 were reported as the disease genes of atrial septal defect (ASD) but the relationship between the locations of their mutations and phenotypes is not clear. We analyzed GATA4 and NKX2.5 mutations in 16 familial ASD cases, including four probands with atrioventricular conduction disturbance (AV block) and two with pulmonary stenosis (PS), by PCR and direct sequencing, and examined their phenotypes clinically. Five mutations, including two GATA4 and three NKX2.5 mutations, were identified in 31.3% of the probands with ASD, and three of them were novel. The two GATA4 mutations in the probands without AV block were S52F and E359Xfs (c.1075delG) that was reported previously, and three NKX2.5 mutations in the probands with AV block were A88Xfs (c.262delG), R190C, and T178M. Additionally, we observed some remarkable phenotypes, i.e., dextrocardia with E359Xfs (c.1075delG) and cribriform type ASD with R190C, both of which are expected to be clues for further investigations. Furthermore, progressive, most severe AV block was closely related with a missense mutation in a homeodomain or with a nonsense/frame-shift mutation of NKX2.5 for which classification has not been clearly proposed. This pinpoints essential sites of NKX2.5 in the development of the conduction system.

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@article{HirayamaYamada2005PhenotypesWG, title={Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.}, author={Kayoko Hirayama-Yamada and Mitsuhiro Kamisago and Kaoru Akimoto and Hiroyuki Aotsuka and Yoshihide Nakamura and Hideshi Tomita and Michiko Furutani and Shin-ichiro Imamura and Atsuyoshi Takao and Makoto Nakazawa and Rumiko Matsuoka}, journal={American journal of medical genetics. Part A}, year={2005}, volume={135 1}, pages={47-52} }