Placing the RPL32 Promoter Upstream of a Second Promoter Results in a Strongly Increased Number of Stably Transfected Mammalian Cell Lines That Display High Protein Expression Levels. (10th November 2010)

• Record Type: Journal Article
• Authors: Hoeksema, F.; Hamer, K.; Siep, M.; Verhees, J. A.; Otte, A. P.
• Other Names: Ohme-Takagi Masaru Academic Editor.
• Is Part Of: Biotechnology research international. Volume 2011(2011)
• Publication Date: 2010-11-10
• Subjects: Biotechnology -- Periodicals; Biotechnology; Biotechnology; Periodicals; 660.6
• DOI: 10.4061/2011/492875
• Languages: English
• ISSNs: 2090-3138

Abstract

Abstract : The use of high stringency selection systems commonly results in a strongly diminished number of stably transfected mammalian cell lines. Here we placed twelve different promoters upstream of an adjacent primary promoter and tested whether this might result in an increased number of colonies; this is in the context of a stringent selection system. We found that only the promoter of the human ribosomal protein, RPL32, induced a high number of colonies in CHO-DG44 cells. This phenomenon was observed when the RPL32 promoter was combined with the CMV, SV40, EF1- α, and the β -actin promoters. In addition, these colonies displayed high protein expression levels. The RPL32 promoter had to be functionally intact, since the deletion of a small region upstream of the transcription start site demolished its positive action. We conclude that adding the RPL32 promoter to an expression cassette in cis may be a powerful tool to augment gene expression levels.