GJA5 gene (MIM no. 121013), localized at 1q21.1, encodes for the cardiac gap junction protein connexin 40. In humans, copy number variants of chromosome 1q21.1 have been associated with variable phenotypes comprising congenital heart disease (CHD), including isolated TOF. In mice, the deletion of Gja5 can cause a variety of complex CHDs, in particular of the cardiac outflow tract, corresponding to TOF in many cases. In the present study, we screened for mutations in the GJA5 gene 178 unrelated probands with isolated TOF. A heterozygous nucleotide change (c.793C>T) in exon 2 of the gene leading to the p.Pro265Ser variant at the carboxyl-terminus of the protein was found in two unrelated sporadic patients, one with classic anatomy and one with pulmonary atresia. This GJA5 missense substitution was not observed in 1568 ethnically-matched control chromosomes. Immunofluorescent staining and confocal microscopy revealed that cells expressing the mutant protein form sparse or no visible gap-junction plaques in the region of cell-cell contact. Moreover, analysis of the transfer of the gap junction permanent tracer lucifer yellow showed that cells expressing the mutant protein have a reduced rate of dye transfer compared with wild-type cells. Finally, use of a zebrafish model revealed that microinjection of the GJA5-p.Pro265Ser mutant disrupts overall morphology of the heart tube in the 37% (22/60) of embryos, compared with the 6% (4/66) of the GJA5 wild-type-injected embryos. These findings implicate GJA5 gene as a novel susceptibility gene for TOF.
Guida, V., Ferese, R., Rocchetti, M., Bonetti, M., Sarkozy, A., Cecchetti, S., et al. (2013). A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot. EUROPEAN JOURNAL OF HUMAN GENETICS, 21(1), 69-75 [10.1038/ejhg.2012.109].
|Citazione:||Guida, V., Ferese, R., Rocchetti, M., Bonetti, M., Sarkozy, A., Cecchetti, S., et al. (2013). A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot. EUROPEAN JOURNAL OF HUMAN GENETICS, 21(1), 69-75 [10.1038/ejhg.2012.109].|
|Tipo:||Articolo in rivista - Articolo scientifico|
|Carattere della pubblicazione:||Scientifica|
|Presenza di un coautore afferente ad Istituzioni straniere:||Si|
|Titolo:||A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot|
|Autori:||Guida, V; Ferese, R; Rocchetti, M; Bonetti, M; Sarkozy, A; Cecchetti, S; Gelmetti, V; Lepri, F; Copetti, M; Lamorte, G; Cristina Digilio, M; Marino, B; Zaza, A; den Hertog, J; Dallapiccola, B; De Luca, A|
|Data di pubblicazione:||gen-2013|
|Rivista:||EUROPEAN JOURNAL OF HUMAN GENETICS|
|Digital Object Identifier (DOI):||http://dx.doi.org/10.1038/ejhg.2012.109|
|Appare nelle tipologie:||01 - Articolo su rivista|