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野猪基质附着区域增强了转染到HEK293T细胞中的PiggyBac系统的表达。

Sus scrofa matrix attachment region enhances expression of the PiggyBac system transfected into HEK293T cells.

作者信息

Wang Xin-Jian, Wang Jiang, Wang Yue-Ying, Guo Yu-Jie, Chu Bei-Bei, Yang Guo-Yu

机构信息

Key Laboratory of Animal Biochemistry and Nutrition, Ministry of Agriculture, Henan Agricultural University, Zhengzhou, Henan, China.

College of Animal Husbandary and Veterinary Science, Henan Agricultural University, Wenhua Road 95, Zhengzhou, 450002, People's Republic of China.

出版信息

Biotechnol Lett. 2016 Jun;38(6):949-58. doi: 10.1007/s10529-016-2074-7. Epub 2016 Mar 10.

Abstract

OBJECTIVES

To determine the effects of the Sus scrofa matrix attachment region (SusMAR) on transgene expression in HEK293T cells.

RESULTS

Three expression vectors with the MAR at different sites in the PiggyBac (PB) transposon vector backbone were compared: two MARs flanking the β-galactosidase (β-gal) expression cassette, and one at the upstream or downstream site. Bos taurus MAR (BosMAR) and a β-gal expression cassette without MARs were the positive and negative controls, respectively. Compared to the control, β-gal activity of all SusMAR and BosMAR vectors was significantly improved in the presence of PB transposase (PBase). However, only the downstream SusMAR and upstream BosMAR vectors showed increased expression in the absence of PBase. Expression was significantly increased in all vectors with the PBase group compared to those without the PBase group. Gene copy numbers were not increased compared to the negative control.

CONCLUSIONS

SusMAR enhanced recombinant gene expression levels and stability in HEK293T cells, was not increase transgene copy number. These results could facilitate the development of vectors for stable production of therapeutic proteins.

摘要

目的

确定猪基质附着区(SusMAR)对人胚肾293T细胞(HEK293T)中转基因表达的影响。

结果

比较了在PiggyBac(PB)转座子载体骨架中不同位点带有MAR的三种表达载体:两个MAR位于β-半乳糖苷酶(β-gal)表达盒两侧,一个位于上游或下游位点。牛基质附着区(BosMAR)和无MAR的β-gal表达盒分别作为阳性和阴性对照。与对照相比,在存在PB转座酶(PBase)的情况下,所有SusMAR和BosMAR载体的β-gal活性均显著提高(PBase)。然而,只有下游SusMAR和上游BosMAR载体在不存在PBase的情况下表达增加。与无PBase组相比,PBase组所有载体的表达均显著增加。与阴性对照相比,基因拷贝数没有增加。

结论

SusMAR提高了HEK293T细胞中重组基因的表达水平和稳定性,并未增加转基因拷贝数。这些结果有助于开发用于稳定生产治疗性蛋白质的载体。

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