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Cell Cycle Quiescence can Suppress Transcription from an Ecdysone Receptor–Based Inducible Promoter in Mammalian Cells
Author(s) -
Sabine Wallbaum,
Nicole Grau,
Anja Schmid,
Katharina Frick,
Antje Neeb,
Jonathan P. Sleeman
Publication year - 2009
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000113121
Subject(s) - biology , reporter gene , ecdysone receptor , gene expression , microbiology and biotechnology , gene , cell cycle , transcription (linguistics) , transcription factor , regulation of gene expression , promoter , 3t3 cells , cell culture , ecdysone , nuclear receptor , transfection , genetics , linguistics , philosophy
Inducible gene expression is a powerful tool for basic research, gene therapy and biotechnology, whose utility depends in part on consistent levels of induction regardless of metabolic status or physiological context. Here we examined the inducibility of the ecdysone receptor-based RheoSwitch mammalian inducible expression system in proliferating cells and in cell cycle-arrested cells. We found that both contact inhibition and growth arrest subsequent to serum deprivation dramatically reduced the levels of induction of reporter genes that could be achieved in 3T3 fibroblasts but in not NMuMG mammary epithelial cells. These data have implications for the use of the RheoSwitch system in inducible gene expression applications.

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