Key result
Plakophilin 2 knockdown disrupts heart development, causing bradycardia, cardiac oedema, and desmosome breakdown.
Why the study?
Mutations in the human plakophilin 2 gene cause arrhythmogenic right ventricular cardiomyopathy, but the effects of plakophilin 2 loss on heart development are not fully understood.
Answers are grounded in this paper and cite their sources.
Zebrafish PKP2 knockdown phenotypes require mammalian validation; leaves open translational relevance to human ARVC.
The desmosomal armadillo protein plakophilin 2 is the only plakophilin expressed in the heart, and mutations in the human plakophilin 2 gene result in arrhythmogenic right ventricular cardiomyopathy. To investigate loss of function, we knocked down plakophilin 2 by morpholino microinjection in zebrafish. This resulted in decreased heart rate, cardiac oedema, blood pooling, a failure of the heart to pattern correctly and a twisted tail. Co-injection of plakophilin 2 mRNA rescued the morphant phenotype, indicating the specificity of the knockdown. Desmosome numbers were decreased in morphant hearts and the plaque and midline structures of the desmosomes in the intercalated discs were disrupted when examined by electron microscopy. cmlc2 and vmhc expression at 48 hours post-fertilization (hpf) showed incomplete looping of the heart in morphant embryos by whole mount in situ hybridization, and bmp4 expression was expanded into the ventricle. The domain of expression of the heart marker nkx2.5 at 24 hpf was expanded. At the 18 somite stage, expression of the cardiogenic gene lefty2 was abolished in the left cardiac field, with concomitant increases in bmp4, spaw and lefty1 expression, likely resulting in the looping defects. These results indicate that plakophilin 2 has both structural and signalling roles in zebrafish heart development.
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Moriarty et al. (2012) studied Heart development / Arrhythmogenic right ventricular cardiomyopathy model. Plakophilin 2 knockdown by morpholino microinjection was evaluated on Heart development, structural changes, and gene expression. Knockdown of plakophilin 2 in zebrafish resulted in decreased heart rate, cardiac oedema, looping defects, and disrupted desmosomes, indicating structural and signalling roles in heart development.
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