The G38D and M163V mutations in Cx40 alter gap junction channel conductance and hemichannel activity, providing mechanistic insights into their association with atrial fibrillation.
Cx40 mutants may promote atrial arrhythmogenesis; leaves open causal role in human AF and need for targeted validation.
Mutations of Cx40 (GJA5) have been identified in people with lone chronic atrial fibrillation including G38D and M163V which were found in the same patient. We used dual whole cell patch clamp procedures to examine the transjunctional voltage (Vj) gating and channel conductance properties of these two rare mutants. Each mutant exhibited slight alterations of Vj gating properties and increased the gap junction channel conductance (γj) by 20-30 pS. While co-expression of the two mutations had similar effects on Vj gating, it synergistically increased γj by 50%. Unlike WTCx40 or M163V, G38D induced activity of a dominant 271 pS hemichannel.
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Patel et al. (2014) studied this question.
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