Key result
Knockdown of smyd1b in zebrafish embryos caused significant disruption of myofibril organization in both skeletal and cardiac muscles, and reduced myosin protein accumulation.
Smyd1b plays a critical role in myofibril organization and myosin folding/assembly in zebrafish cardiac and skeletal muscles.
Should not change clinical practice; leaves open Smyd1b's role in human cardiac disease pending mammalian studies.
Smyd1b is a member of the Smyd family that is specifically expressed in skeletal and cardiac muscles. Smyd1b plays a key role in thick filament assembly during myofibrillogenesis in skeletal muscles of zebrafish embryos. To better characterize Smyd1b function and its mechanism of action in myofibrillogenesis, we analyzed the effects of smyd1b knockdown on myofibrillogenesis in skeletal and cardiac muscles of zebrafish embryos. The results show that knockdown of smyd1b causes significant disruption of myofibril organization in both skeletal and cardiac muscles of zebrafish embryos. Microarray and quantitative reverse transcription-PCR analyses show that knockdown of smyd1b up-regulates heat shock protein 90 (hsp90) and unc45b gene expression. Biochemical analysis reveals that Smyd1b can be coimmunoprecipitated with heat shock protein 90 α-1 and Unc45b, two myosin chaperones expressed in muscle cells. Consistent with its potential function in myosin folding and assembly, knockdown of smyd1b significantly reduces myosin protein accumulation without affecting mRNA expression. This likely results from increased myosin degradation involving unc45b overexpression. Together these data support the idea that Smyd1b may work together with myosin chaperones to control myosin folding, degradation, and assembly into sarcomeres during myofibrillogenesis.
No takes yet. Share an insight, caveat, or question.
Li et al. (2013) studied Myofibrillogenesis / Muscle development. smyd1b knockdown vs. control morpholino was evaluated on Myofibril organization in skeletal and cardiac muscles. Knockdown of smyd1b in zebrafish embryos caused significant disruption of myofibril organization in both skeletal and cardiac muscles, and reduced myosin protein accumulation.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: