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首页> 外文期刊>Cytotechnology >Cetyltriethylammonium bromide stimulating transcription of Bombyx mori nucleopolyhedrovirus gp64 gene promoter mediated by viral factors
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Cetyltriethylammonium bromide stimulating transcription of Bombyx mori nucleopolyhedrovirus gp64 gene promoter mediated by viral factors

机译:十六烷基三乙基溴化铵刺激病毒因子介导的家蚕核多角体病毒gp64基因启动子的转录

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摘要

To characterize the effects of cetyltriethylammonium bromide (CTAB) on the transcription of gp64 promoter from Bombyx mori nucleopolyhedrovirus (BmNPV), the plasmid pBmgp64Luc used in transient expression assay system was constructed by using the luciferase gene as a reporter under the control of BmNPV gp64 promoter. When the Bombyx mori cells (Bm-N) were transfected with the pBmgp64Luc, different treatments were undertaken. We found that the transient expression activity of luciferase could not be augmented directly by CTAB treatment alone, but could be enhanced more than 2 times by BmNPV treatment alone at a multiplicity of infection (MOI) of 0.5. Through co-treatment with 0.1 μg ml?1 of CTAB and BmNPV at a MOI of 0.5, the enzymatic activity increased 5.21 times. We presumed that the stimulation of transcription of BmNPV gp64 promoter by CTAB was mediated by viral factors from BmNPV. In addition, the time curves of luciferase activity in cells transfected with pBmgp64Luc and transactivated by virus were observed.
机译:为了表征十六烷基三乙基溴化铵(CTAB)对家蚕核多角体病毒(BmNPV)的gp64启动子转录的影响,在BmNPV gp64启动子的控制下,以荧光素酶基因为报告基因,构建了瞬时表达测定系统中使用的质粒pBmgp64Luc。 。当用pBmgp64Luc转染家蚕细胞(Bm-N)时,进行了不同的处理。我们发现,单独使用CTAB处理无法直接增强荧光素酶的瞬时表达活性,而在感染复数(MOI)为0.5的情况下,单独进行BmNPV处理可以使荧光素酶的瞬时表达活性提高2倍以上。通过以0.5的MOI与0.1μg/ ml的CTAB和BmNPV共同处理,酶活性增加了5.21倍。我们假定CTAB刺激BmNPV gp64启动子的转录是由BmNPV的病毒因子介导的。另外,观察到用pBmgp64Luc转染并被病毒反激活的细胞中荧光素酶活性的时间曲线。

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