Intronic positioning maximizes co-expression and co-amplification of nonselectable heterologous genes

J. M. Abrams, S. M. Thorpe, R. T. Schimke

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

The overproduction of heterologous gene products in mammalian cells is often a prerequisite for studies of protein structure, function, and therapeutic efficacy. We report that recombinant fusion of a nonselectable reporter template into the intronic sequences of an amplifiable minigene gives dramatically enhanced co-expression efficiency in stable, primary transformants. Further incremental selective pressure for marker gene amplification results in the rapid acquisition of very high expression levels from the intronically positioned reporter. Nested within a constitutively expressing gene, these templates can be independently regulated at moderate gene dosage levels. Intronic positioning may therefore be of general utility for a variety of recombinant studies.

Original languageEnglish (US)
Pages (from-to)14016-14021
Number of pages6
JournalJournal of Biological Chemistry
Volume264
Issue number24
StatePublished - 1989

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Amplification
Genes
Gene Dosage
Gene Amplification
Fusion reactions
Cells
Proteins
Therapeutics

ASJC Scopus subject areas

  • Biochemistry

Cite this

Intronic positioning maximizes co-expression and co-amplification of nonselectable heterologous genes. / Abrams, J. M.; Thorpe, S. M.; Schimke, R. T.

In: Journal of Biological Chemistry, Vol. 264, No. 24, 1989, p. 14016-14021.

Research output: Contribution to journalArticle

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