1. Academic Validation
  2. SEMPER: Stoichiometric expression of mRNA polycistrons by eukaryotic ribosomes for compact, ratio-tunable multi-gene expression

SEMPER: Stoichiometric expression of mRNA polycistrons by eukaryotic ribosomes for compact, ratio-tunable multi-gene expression

  • Cell Syst. 2024 Jul 17;15(7):597-609.e4. doi: 10.1016/j.cels.2024.06.001.
Mengtong Duan 1 Ishaan Dev 2 Andrew Lu 3 Goar Ayrapetyan 2 Mei Yi You 1 Mikhail G Shapiro 4
Affiliations

Affiliations

  • 1 Division of Biology and Biological Engineering, Caltech, Pasadena, CA 91125, USA.
  • 2 Division of Chemistry and Chemical Engineering, Caltech, Pasadena, CA 91125, USA.
  • 3 Division of Biology and Biological Engineering, Caltech, Pasadena, CA 91125, USA; UCLA-Caltech Medical Scientist Training Program, UCLA, Los Angeles, CA 90095, USA.
  • 4 Division of Chemistry and Chemical Engineering, Caltech, Pasadena, CA 91125, USA; Andrew and Peggy Cherng Department of Medical Engineering, Caltech, Pasadena, CA 91125, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA. Electronic address: mikhail@caltech.edu.
Abstract

Here, we present a method for expressing multiple open reading frames (ORFs) from single transcripts using the leaky scanning model of translation initiation. In this approach termed "stoichiometric expression of mRNA polycistrons by eukaryotic ribosomes" (SEMPER), adjacent ORFs are translated from a single mRNA at tunable ratios determined by their order in the sequence and the strength of their translation initiation sites. We validate this approach by expressing up to three fluorescent proteins from one plasmid in two different cell lines. We then use it to encode a stoichiometrically tuned polycistronic construct encoding gas vesicle acoustic reporter genes that enables efficient formation of the multi-protein complex while minimizing cellular toxicity. We also demonstrate that SEMPER enables polycistronic expression of recombinant monoclonal Antibodies from plasmid DNA and of two fluorescent proteins from single mRNAs made through in vitro transcription. Finally, we provide a probabilistic model to elucidate the mechanisms underlying SEMPER. A record of this paper's transparent peer review process is included in the supplemental information.

Keywords

Monte Carlo; acoustic reporter; circuit; eukaryotes; gas vesicle; gene expression; in vitro transcription; mRNA; mammalian cell; monoclonal antibodies; polycistronic; ratio; synthetic biology; toxicity; tunable.

Figures
Products