Differential expression of tropomyosin during segmental heart development in Mexican axolotl

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Abstract
The Mexican axolotl, Ambystoma mexicanum, serves as an intriguing model to investigate myofibril organization and heart development in vertebrates. The axolotl has a homozygous recessive cardiac lethal gene “c” which causes a failure of ventricular myofibril formation and contraction. However, the conus of the heart beats, and has organized myofibrils. Tropomyosin (TM), an essential component of the thin filament, has three known striated muscle isoforms (TPM1α, TPM1κ, and TPM4α) in axolotl hearts. However, it is not known whether there are differential expression patterns of these tropomyosin isoforms in various segments of the heart. Also, it is not understood whether these isoforms contribute to myofibril formation in a segment‐specific manner. In this study, we have utilized anti‐sense oligonucleotides to separately knockdown post‐transcriptional expression of TPM1α and TPM4α. We then evaluated the organization of myofibrils in the conus and ventricle of normal and cardiac mutant hearts using immunohistochemical techniques. We determined that the TPM1α isoform, a product of the TPM1 gene, was essential for myofibrillogenesis in the conus, whereas TPM4α, the striated muscle isoform of the TPM4 gene, was essential for myofibrillogenesis in the ventricle. Our results support the segmental theory of vertebrate heart development. J. Cell. Biochem. 99: 952–965, 2006.

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