Abstract
The systemic RNA interference defective-1 (SID-1) can transport double-stranded RNA (dsRNA) into cytosol across the cytoplasmic membrane. We report here that ectopic expression of Caenorhabditis elegans SID-1 allows BmN4 cells to import extracellular plasmid dsDNA into cells via the direct soaking method. Interestingly, BmN4-SID1 cells incorporate dsRNA and plasmid DNA simultaneously. Furthermore, the ectopic SID-1 allows us to establish a stably transformed cell line by the simple soaking method. Our results provide an alternative method for silkworm gene function analysis with low cost and low cell toxicity.
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The cost of publication was supported in part by the Research Grant for Young Investigators of Faculty of Agriculture, Kyushu University.
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Xu, J., Yoshimura, K., Mon, H. et al. Establishment of Caenorhabditis elegans SID-1-Dependent DNA Delivery System in Cultured Silkworm Cells. Mol Biotechnol 56, 193–198 (2014). https://doi.org/10.1007/s12033-013-9694-0
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DOI: https://doi.org/10.1007/s12033-013-9694-0