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Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts

Emil D. Jensen (), Marcus Deichmann, Xin Ma, Rikke U. Vilandt, Giovanni Schiesaro, Marie B. Rojek, Bettina Lengger, Line Eliasson, Justin M. Vento, Deniz Durmusoglu, Sandie P. Hovmand, Ibrahim Al’Abri, Jie Zhang, Nathan Crook and Michael K. Jensen ()
Additional contact information
Emil D. Jensen: Technical University of Denmark, Kgs
Marcus Deichmann: Technical University of Denmark, Kgs
Xin Ma: Technical University of Denmark, Kgs
Rikke U. Vilandt: Technical University of Denmark, Kgs
Giovanni Schiesaro: Technical University of Denmark, Kgs
Marie B. Rojek: Technical University of Denmark, Kgs
Bettina Lengger: Technical University of Denmark, Kgs
Line Eliasson: Technical University of Denmark, Kgs
Justin M. Vento: North Carolina State University
Deniz Durmusoglu: North Carolina State University
Sandie P. Hovmand: Technical University of Denmark, Kgs
Ibrahim Al’Abri: North Carolina State University
Jie Zhang: Technical University of Denmark, Kgs
Nathan Crook: North Carolina State University
Michael K. Jensen: Technical University of Denmark, Kgs

Nature Communications, 2022, vol. 13, issue 1, 1-15

Abstract: Abstract G protein-coupled receptors (GPCRs) enable cells to sense environmental cues and are indispensable for coordinating vital processes including quorum sensing, proliferation, and sexual reproduction. GPCRs comprise the largest class of cell surface receptors in eukaryotes, and for more than three decades the pheromone-induced mating pathway in baker’s yeast Saccharomyces cerevisiae has served as a model for studying heterologous GPCRs (hGPCRs). Here we report transcriptome profiles following mating pathway activation in native and hGPCR-signaling yeast and use a model-guided approach to correlate gene expression to morphological changes. From this we demonstrate mating between haploid cells armed with hGPCRs and endogenous biosynthesis of their cognate ligands. Furthermore, we devise a ligand-free screening strategy for hGPCR compatibility with the yeast mating pathway and enable hGPCR-signaling in the probiotic yeast Saccharomyces boulardii. Combined, our findings enable new means to study mating, hGPCR-signaling, and cell-cell communication in a model eukaryote and yeast probiotics.

Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33961-y

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DOI: 10.1038/s41467-022-33961-y

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