Tokumoto Shoko, Miyata Yugo, Usui Kengo, Deviatiiarov Ruslan, Ohkawa Takahiro, Kondratieva Sabina, Shagimardanova Elena, Gusev Oleg, Cornette Richard, Itoh Masayoshi, Hayashizaki Yoshihide, Kikawada Takahiro
Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa 277-8562, Japan.
Institute of Agrobiological Sciences, National Institute of Agriculture and Food Research Organization (NARO), Tsukuba 305-0851, Japan.
Insects. 2020 Nov 11;11(11):781. doi: 10.3390/insects11110781.
The Pv11 cell line established from an African chironomid, , is the only cell line tolerant to complete desiccation. In Pv11 cells, a constitutive expression system for Pv11 cells was previously exploited and several reporter genes were successfully expressed. Here we report the identification of an effective minimal promoter for Pv11 cells and its application to the Tet-On inducible expression system. First, using a luciferase reporter assay, we showed that a 202 bp deletion fragment derived from the constitutively active 121-promoter functions in Pv11 cells as an appropriate minimal promoter with the Tet-On inducible expression system. The AcGFP1 ( green fluorescent protein) was also successfully expressed in Pv11 cells using the inducible system. In addition to these reporter genes, the avian myeloblastosis virus reverse transcriptase α subunit (AMV RTα), which is one of the most widely commercially available RNA-dependent DNA polymerases, was successfully expressed through the inducible expression system and its catalytic activity was verified. These results demonstrate the establishment of an inducible expression system in cells that can be preserved in the dry state and highlight a possible application to the production of large and complex proteins.
从非洲摇蚊建立的Pv11细胞系是唯一能耐受完全干燥的细胞系。在Pv11细胞中,先前已开发了一种Pv11细胞的组成型表达系统,并成功表达了几种报告基因。在此,我们报告了Pv11细胞有效最小启动子的鉴定及其在Tet-On诱导表达系统中的应用。首先,通过荧光素酶报告基因检测,我们表明,从组成型活性121-启动子衍生的202 bp缺失片段在Pv11细胞中作为Tet-On诱导表达系统的合适最小启动子发挥作用。使用诱导系统,AcGFP1(绿色荧光蛋白)也在Pv11细胞中成功表达。除了这些报告基因外,最广泛商业可用的依赖RNA的DNA聚合酶之一禽成髓细胞瘤病毒逆转录酶α亚基(AMV RTα)通过诱导表达系统成功表达,并验证了其催化活性。这些结果证明了在可干燥保存的细胞中建立了诱导表达系统,并突出了其在生产大型和复杂蛋白质方面的可能应用。