Improvement of the reverse tetracycline transactivator by single amino acid substitutions that reduce leaky target gene expression to undetectable levels

• Published in: Scientific reports Vol. 6; no. 1; p. 27697
• Main Authors: Roney, Ian J., Rudner, Adam D., Couture, Jean-François, Kærn, Mads
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 21.06.2016; Nature Publishing Group
• Subjects: 14/63; 631/337/572; 631/61/185; 96/31; 96/35; Amino Acid Substitution - genetics; Amino acids; Animals; Animals, Genetically Modified; Binding sites; Biotechnology; Biotechnology - methods; Cell Line; Cloning; Gene expression; Gene Expression Regulation - drug effects; Gene Expression Regulation - genetics; Humanities and Social Sciences; Humans; multidisciplinary; Mutation; Proteins; Science; Tetracycline - metabolism; Tetracycline - pharmacology; Trans-Activators - genetics; Trans-Activators - metabolism; Trans-Activators - pharmacology; Transcriptional Activation - drug effects; Transcriptional Activation - genetics; Yeast; Yeasts; Yeasts - genetics
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep27697

Conditional gene expression systems that enable inducible and reversible transcriptional control are essential research tools and have broad applications in biomedicine and biotechnology. The reverse tetracycline transcriptional activator is a canonical system for engineered gene expression control that enables graded and gratuitous modulation of target gene transcription in eukaryotes from yeast to human cell lines and transgenic animals. However, the system has a tendency to activate transcription even in the absence of tetracycline and this leaky target gene expression impedes its use. Here, we identify single amino-acid substitutions that greatly enhance the dynamic range of the system in yeast by reducing leaky transcription to undetectable levels while retaining high expression capacity in the presence of inducer. While the mutations increase the inducer concentration required for full induction, additional sensitivity-enhancing mutations can compensate for this effect and confer a high degree of robustness to the system. The novel transactivator variants will be useful in applications where tight and tunable regulation of gene expression is paramount.