Enhanced design of pCMViR-TSC plasmid vector for sustainably high cargo gene expression in mammalian cells.

ABSTRACT: The first-generation pCMViR-TSC, implemented through the promoter sandwich rule, yields 10- to 100-fold higher gene expression than the standard plasmid used with the CMV (cytomegalovirus) or CAG promoter. However, the vector's shortcomings limit its utility to transient expression only, as it is not suitable for establishing stable transformants in mammalian cells. To overcome this weakness, we here introduce the improved plasmid vector pSAKA-4B, derived from pCMViR-TSC as a second-generation chromosome-insertable vector. This vector facilitates the linear entry of the expression unit into the TTAA site of DNA universally with transposase assistance. The vector is helpful for the indefinite expression of our target gene. The new vector system is proven here to be efficient in establishing

SUBMITTER: Sakaguchi M 

PROVIDER: S-EPMC11655592 | biostudies-literature | 2024 Dec

REPOSITORIES: biostudies-literature