Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Biol Pharm Bull. 2012;35(9):1534-8. doi: 10.1248/bpb.b12-00329.
A positive feedback system, using GAL4-vp16 (a fusion protein of yeast GAL4 and herpes simplex virus vp16) as an activator and firefly luciferase as a reporter, maintained luciferase expression for 7 d in mice. However, the luciferase expression decreased after 7 d, and this phenomenon could be caused by immunoreactions against these exogenous proteins. This hypothesis was examined by the following three strategies, designed to avoid the putative immunoreactions: (i) use of the endogenous secreted alkaline phosphatase (SEAP) protein as a reporter, (ii) replacement of vp16 with endogenous transcription factors, and (iii) insertion of the target sequence of microRNA expressed in cells of hematopoietic origin, to suppress GAL4-vp16 expression in antigen-presenting cells. The results obtained in this study suggested that silencing would be induced by mechanism(s) besides immunoreactions against reporter and activator proteins.
采用 GAL4-vp16(酵母 GAL4 和单纯疱疹病毒 vp16 的融合蛋白)作为激活剂,萤火虫荧光素酶作为报告基因的正反馈系统,可在小鼠中维持 7 天的荧光素酶表达。然而,7 天后荧光素酶表达下降,这种现象可能是由于对外源蛋白的免疫反应引起的。通过以下三种策略来检验这一假说,旨在避免潜在的免疫反应:(i)使用内源性分泌型碱性磷酸酶(SEAP)蛋白作为报告基因,(ii)用内源性转录因子替代 vp16,(iii)插入在造血细胞中表达的 microRNA 的靶序列,以抑制抗原呈递细胞中 GAL4-vp16 的表达。本研究的结果表明,沉默是由除了针对报告基因和激活蛋白的免疫反应之外的机制诱导的。