Division of Applied Biology, Faculty of Textile Science and Technology, Shinshu University, Ueda, Nagano, 386-8567, Japan.
Mol Biol Rep. 2010 Apr;37(4):1815-21. doi: 10.1007/s11033-009-9615-2. Epub 2009 Jul 25.
Spider dragline silk is a unique fibrous protein with a combination of tensile strength and elasticity, but the isolation of large amounts of silk from spiders is not feasible. In this study, we generated germline-transgenic silkworms (Bombyx mori) that spun cocoons containing recombinant spider silk. A piggyBac-based transformation vector was constructed that carried spider dragline silk (MaSp1) cDNA driven by the sericin 1 promoter. Silkworm eggs were injected with the vector, producing transgenic silkworms displaying DsRed fluorescence in their eyes. Genotyping analysis confirmed the integration of the MaSp1 gene into the genome of the transgenic silkworms, and silk protein analysis revealed its expression and secretion in the cocoon. Compared with wild-type silk, the recombinant silk displayed a higher tensile strength and elasticity. The results indicate the potential for producing recombinant spider silk in transgenic B. mori.
蜘蛛牵引丝是一种具有高强度和弹性的独特纤维蛋白,但从蜘蛛中大量分离出丝是不可行的。在这项研究中,我们生成了能吐含有重组蜘蛛丝茧的转基因组蚕(Bombyx mori)。我们构建了一个基于 PiggyBac 的转化载体,该载体携带丝氨酸 1 启动子驱动的蜘蛛牵引丝(MaSp1)cDNA。我们用该载体注射蚕卵,产生了在眼睛中显示 DsRed 荧光的转基因蚕。基因分型分析证实了 MaSp1 基因已整合到转基因组蚕的基因组中,并且丝蛋白分析表明其在茧中表达和分泌。与野生型丝相比,重组丝显示出更高的拉伸强度和弹性。结果表明,在转基因组蚕中生产重组蜘蛛丝具有潜力。