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Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts
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 deca...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582028/ https://www.ncbi.nlm.nih.gov/pubmed/36261657 http://dx.doi.org/10.1038/s41467-022-33961-y |
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author | Jensen, Emil D. Deichmann, Marcus Ma, Xin Vilandt, Rikke U. Schiesaro, Giovanni Rojek, Marie B. Lengger, Bettina Eliasson, Line Vento, Justin M. Durmusoglu, Deniz Hovmand, Sandie P. Al’Abri, Ibrahim Zhang, Jie Crook, Nathan Jensen, Michael K. |
author_facet | Jensen, Emil D. Deichmann, Marcus Ma, Xin Vilandt, Rikke U. Schiesaro, Giovanni Rojek, Marie B. Lengger, Bettina Eliasson, Line Vento, Justin M. Durmusoglu, Deniz Hovmand, Sandie P. Al’Abri, Ibrahim Zhang, Jie Crook, Nathan Jensen, Michael K. |
author_sort | Jensen, Emil D. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9582028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95820282022-10-21 Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts Jensen, Emil D. Deichmann, Marcus Ma, Xin Vilandt, Rikke U. Schiesaro, Giovanni Rojek, Marie B. Lengger, Bettina Eliasson, Line Vento, Justin M. Durmusoglu, Deniz Hovmand, Sandie P. Al’Abri, Ibrahim Zhang, Jie Crook, Nathan Jensen, Michael K. Nat Commun Article 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. Nature Publishing Group UK 2022-10-19 /pmc/articles/PMC9582028/ /pubmed/36261657 http://dx.doi.org/10.1038/s41467-022-33961-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jensen, Emil D. Deichmann, Marcus Ma, Xin Vilandt, Rikke U. Schiesaro, Giovanni Rojek, Marie B. Lengger, Bettina Eliasson, Line Vento, Justin M. Durmusoglu, Deniz Hovmand, Sandie P. Al’Abri, Ibrahim Zhang, Jie Crook, Nathan Jensen, Michael K. Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title | Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title_full | Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title_fullStr | Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title_full_unstemmed | Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title_short | Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
title_sort | engineered cell differentiation and sexual reproduction in probiotic and mating yeasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582028/ https://www.ncbi.nlm.nih.gov/pubmed/36261657 http://dx.doi.org/10.1038/s41467-022-33961-y |
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