Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784812755754156032
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
work_keys_str_mv AT jensenemild engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT deichmannmarcus engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT maxin engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT vilandtrikkeu engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT schiesarogiovanni engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT rojekmarieb engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT lenggerbettina engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT eliassonline engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT ventojustinm engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT durmusogludeniz engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT hovmandsandiep engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT alabriibrahim engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT zhangjie engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT crooknathan engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts
AT jensenmichaelk engineeredcelldifferentiationandsexualreproductioninprobioticandmatingyeasts