INVESTIGADORES
BOUZAT Cecilia Beatriz
congresos y reuniones científicas
Título:
Molecular Function of Heteromeric Nicotinic Receptors Containing the α7 Subunit and its Duplicated Form
Autor/es:
LASALA M; CORRADI J; BRUZZONE, ARIANA; ESANDI MC; BOUZAT C
Lugar:
Mar del Plata
Reunión:
Congreso; Congreso Anual de la Sociedad Argentina de Investigación en Neurociencias; 2017
Resumen:
The α7 nicotinic receptor subunit gene, CHRNA7, codes for a subunit that forms the homomeric α7 receptor, which is involved in learning and memory. Exons 5-10 of CHRNA7 were duplicated and fused to the FAM7A gene, given rise to the CHRFAM7A gene. The product of the resulting chimeric gene, dupα7, is a truncated subunit that lacks part of the ACh binding site. We here combined cell expression, confocal microscopy, western blot, and electrophysiological recordings in HEK cells to understand the functional role of the dupα7 subunit. We found that cells transfected with dupα7 cDNA express the dupα7 protein but show neither surface binding of an α7 specific antagonist nor agonist-elicited currents. To determine if dupα7 co-assembles into functional receptors with α7, we used an α7 subunit carrying mutations in determinants of conductance (α7LC) as a reporter of receptor stoichiometry. Co-expression of α7LC with dupα7 or the reverse combination, α7 with dupα7LC, allowed detection of single-channel openings elicited by ACh, indicating that α7 and dupα7 subunits co-assemble into functional heteromeric receptors. The analysis revealed that a minimum of two α7 subunits is required for forming functional receptors and that activation of the heteromeric receptors occurs through the α7/α7 interface. Our results contribute to the understanding of the functional significance of the partial duplication of the α7 gene.