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Published on: September 8, 2023
Myosin-Va mediates RNA distribution in primary fibroblasts from multiple organs
Verônica P Salerno1, Aldo Calliari, D William Provance
1McLaughlin Research Institute, Great Falls, Montana 59405-4900, USA.
Abstract:
Myosin-Va has been shown to have multiple functions in a variety of cell types, including a role in RNA transport in neurons. Using primary cultures of cells from organs of young dilute-lethal (Myo5a(d-l)/Myo5a(d-l)) null mutant mice and wild-type controls, we show that in some, but not all, tissues, RNA distribution is dramatically different in the homozygous null mutant cells. The dependence of RNA localization on myosin-Va correlates with the relative abundance of the brain-specific splicing pattern of the myosin-Va tail. We also show that myosin-Va is involved in RNA localization soon after synthesis, because the effects of its absence are diminished for RNAs that are more than 30 min old. Finally, we show that localization of beta-actin mRNA is significantly changed by the absence of myosin-Va. These results suggest that myosin-Va is involved in a transient transport or tethering function in the perinuclear region.
Insights
Myosin-Va protein is crucial for proper RNA distribution in certain cells, affecting RNA transport soon after synthesis. Its absence leads to altered RNA localization, particularly for beta-actin mRNA.
Area of Science:
- Cell Biology
- Molecular Biology
- Neuroscience
Background:
- Myosin-Va is a motor protein with diverse cellular functions.
- It plays a known role in RNA transport within neurons.
Purpose of the Study:
- To investigate the role of myosin-Va in RNA distribution across different tissues.
- To determine the temporal involvement of myosin-Va in RNA localization.
Main Methods:
- Utilized primary cell cultures from young dilute-lethal (Myo5a(d-l)/Myo5a(d-l)) null mutant mice and wild-type controls.
- Analyzed RNA distribution patterns in homozygous null mutant cells versus controls.
Main Results:
- Significant differences in RNA distribution were observed in some tissues of null mutant cells.
- Myosin-Va's role in RNA localization is transient, affecting newly synthesized RNAs.
- Localization of beta-actin mRNA was notably altered in the absence of myosin-Va.
Conclusions:
- Myosin-Va is implicated in the transient transport or tethering of RNA in the perinuclear region.
- The extent of RNA localization dependence on myosin-Va correlates with myosin-Va tail splicing patterns.
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