Key result
Mice lacking the GJA1-20k isoform died suddenly at 2 to 4 weeks of age with severely abnormal electrocardiograms and reduced gap junctions due to degradation of poorly trafficked Cx43.
Why the study?
GJA1-20k was identified as an auxiliary subunit for Cx43 trafficking in heterologous systems, but its role in Cx43 maintenance and ventricular arrhythmias in vivo remained to be determined.
The internally translated GJA1-20k isoform is critical for Cx43 gap junction trafficking and preventing its degradation, and its absence leads to severe ventricular arrhythmias and sudden cardiac death.
GJA1-20k may improve Cx43 trafficking in failing hearts; leaves open whether isoform targeting reduces arrhythmias in patients.
Connexin-43 (Cx43) gap junctions provide intercellular coupling, which ensures rapid action potential propagation and synchronized heart contraction. Alterations in Cx43 localization and reductions in gap junction coupling occur in failing hearts, contributing to ventricular arrhythmias and sudden cardiac death. Recent reports have found that an internally translated Cx43 isoform, GJA1-20k, is an auxiliary subunit for the trafficking of Cx43 in heterologous expression systems. Here, we have created a mouse model by using CRISPR technology to mutate a single internal translation initiation site in Cx43 (M213L mutation), which generates full-length Cx43, but not GJA1-20k. We found that GJA1M213L/M213L mice had severely abnormal electrocardiograms despite preserved contractile function, reduced total Cx43, and reduced gap junctions, and they died suddenly at 2 to 4 weeks of age. Heterozygous GJA1M213L/WT mice survived to adulthood with increased ventricular ectopy. Biochemical experiments indicated that cytoplasmic Cx43 had a half-life that was 50% shorter than membrane-associated Cx43. Without GJA1-20k, poorly trafficked Cx43 was degraded. The data support that GJA1-20k, an endogenous entity translated independently of Cx43, is critical for Cx43 gap junction trafficking, maintenance of Cx43 protein, and normal electrical function of the mammalian heart.
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Xiao et al. (2020) studied Ventricular arrhythmias and sudden cardiac death (Animal model) (n=70). GJA1-M213L mutation (loss of GJA1-20k) vs. Wild-type (WT) mice was evaluated on Survival and cardiac electrical function. Mice lacking the GJA1-20k isoform died suddenly at 2 to 4 weeks of age with severely abnormal electrocardiograms and reduced gap junctions due to degradation of poorly trafficked Cx43.
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