Abstract
Orthogonal systems for heterologous protein expression as well as for the engineering of synthetic gene regulatory circuits in hosts like Saccharomyces cerevisiae depend on synthetic transcription factors (synTFs) and corresponding cis-regulatory binding sites. We have constructed and characterized a set of synTFs based on either transcription activator-like effectors or CRISPR/Cas9, and corresponding small synthetic promoters (synPs) with minimal sequence identity to the host’s endogenous promoters. The resulting collection of functional synTF/synP pairs confers very low background expression under uninduced conditions, while expression output upon induction of the various synTFs covers a wide range and reaches induction factors of up to 400. The broad spectrum of expression strengths that is achieved will be useful for various experimental setups, e.g., the transcriptional balancing of expression levels within heterologous pathways or the construction of artificial regulatory networks. Furthermore, our analyses reveal simple rules that enable the tuning of synTF expression output, thereby allowing easy modification of a given synTF/synP pair. This will make it easier for researchers to construct tailored transcriptional control systems.
Highlights
A major task in synthetic biology is the reconstruction, rewiring, and complete de novo design of transcriptional networks
To create expression plasmids for synTALE1–10, plasmid pLOGI was modified: for construction of plasmid pFM003B, the AgeI restriction site was deleted, the StuI site was replaced by PmeI and the yEGFP CDS was replaced by the SV40NLS (PKKKRKV) and the GAL4-a transactivation domain (AD) with BamHI and AgeI restriction sites in between
We investigate the use of transcription activator-like effectors (TALEs)- and dead Cas9 (dCas9)-based synthetic transcription factors (synTFs) together with small-size synthetic promoters (synPs) to drive gene expression in yeast
Summary
A major task in synthetic biology is the reconstruction, rewiring, and complete de novo design of transcriptional networks. In the study presented here, we constructed and characterized a collection of synTFs, based on dCas9 and synTALEs, along with their corresponding synPs. The library is especially designed for heterologous gene expression in the yeast S. cerevisiae.
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