id paper:paper_19450877_v6_n272_p_Baltanas
record_format dspace
spelling paper:paper_19450877_v6_n272_p_Baltanas2023-06-08T16:32:30Z Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway Baltanás, Rodrigo Bush, Alan Couto, Alicia Susana Durrieu, Lucia Colman Lerner, Alejandro Ariel glycerol mitogen activated protein kinase mitogen activated protein kinase kinase 1 pheromone protein protein Slt2 unclassified drug adaptation article cell structure cell wall cellular stress response controlled study homeostasis hyperosmotic stress morphogenesis negative feedback nonhuman osmoadaptation osmolarity priority journal steady state turnover time yeast cell Cell Wall MAP Kinase Signaling System Membrane Proteins Mitogen-Activated Protein Kinases Osmosis Pheromones Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins Environmental and internal conditions expose cells to a multiplicity of stimuli whose consequences are difficult to predict. We investigate the response to mating pheromone of yeast cells adapted to high osmolarity. Events downstream of pheromone binding involve two mitogen-activated protein kinase (MAPK) cascades: the pheromone response (PR) and the cell wall integrity (CWI) response. Although the PR MAPK pathway shares components with a third MAPK pathway, the high osmolarity (HOG) response, each one is normally only activated by its cognate stimulus, a phenomenon called insulation. We found that in cells adapted to high osmolarity, PR activated the HOG pathway in a pheromone- and osmolarity-dependent manner. Activation of HOG by the PR was not due to loss of insulation, but rather a response to a reduction in internal osmolarity, which resulted from an increase in glycerol release caused by the PR. By analyzing single-cell time courses, we found that stimulation of HOG occurred in discrete bursts that coincided with the "shmooing" morphogenetic process. Activation required the polarisome, the CWI MAPK Slt2, and the aquaglyceroporin Fps1. HOG activation resulted in high glycerol turnover, which improved adaptability to rapid changes in osmolarity. Our work shows how a differentiation signal can recruit a second, unrelated sensory pathway to fine-tune yeast response in a complex environment. Fil:Baltanás, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Bush, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Couto, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Durrieu, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Colman-Lerner, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19450877_v6_n272_p_Baltanas http://hdl.handle.net/20.500.12110/paper_19450877_v6_n272_p_Baltanas
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic glycerol
mitogen activated protein kinase
mitogen activated protein kinase kinase 1
pheromone
protein
protein Slt2
unclassified drug
adaptation
article
cell structure
cell wall
cellular stress response
controlled study
homeostasis
hyperosmotic stress
morphogenesis
negative feedback
nonhuman
osmoadaptation
osmolarity
priority journal
steady state
turnover time
yeast cell
Cell Wall
MAP Kinase Signaling System
Membrane Proteins
Mitogen-Activated Protein Kinases
Osmosis
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
spellingShingle glycerol
mitogen activated protein kinase
mitogen activated protein kinase kinase 1
pheromone
protein
protein Slt2
unclassified drug
adaptation
article
cell structure
cell wall
cellular stress response
controlled study
homeostasis
hyperosmotic stress
morphogenesis
negative feedback
nonhuman
osmoadaptation
osmolarity
priority journal
steady state
turnover time
yeast cell
Cell Wall
MAP Kinase Signaling System
Membrane Proteins
Mitogen-Activated Protein Kinases
Osmosis
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Baltanás, Rodrigo
Bush, Alan
Couto, Alicia Susana
Durrieu, Lucia
Colman Lerner, Alejandro Ariel
Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
topic_facet glycerol
mitogen activated protein kinase
mitogen activated protein kinase kinase 1
pheromone
protein
protein Slt2
unclassified drug
adaptation
article
cell structure
cell wall
cellular stress response
controlled study
homeostasis
hyperosmotic stress
morphogenesis
negative feedback
nonhuman
osmoadaptation
osmolarity
priority journal
steady state
turnover time
yeast cell
Cell Wall
MAP Kinase Signaling System
Membrane Proteins
Mitogen-Activated Protein Kinases
Osmosis
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
description Environmental and internal conditions expose cells to a multiplicity of stimuli whose consequences are difficult to predict. We investigate the response to mating pheromone of yeast cells adapted to high osmolarity. Events downstream of pheromone binding involve two mitogen-activated protein kinase (MAPK) cascades: the pheromone response (PR) and the cell wall integrity (CWI) response. Although the PR MAPK pathway shares components with a third MAPK pathway, the high osmolarity (HOG) response, each one is normally only activated by its cognate stimulus, a phenomenon called insulation. We found that in cells adapted to high osmolarity, PR activated the HOG pathway in a pheromone- and osmolarity-dependent manner. Activation of HOG by the PR was not due to loss of insulation, but rather a response to a reduction in internal osmolarity, which resulted from an increase in glycerol release caused by the PR. By analyzing single-cell time courses, we found that stimulation of HOG occurred in discrete bursts that coincided with the "shmooing" morphogenetic process. Activation required the polarisome, the CWI MAPK Slt2, and the aquaglyceroporin Fps1. HOG activation resulted in high glycerol turnover, which improved adaptability to rapid changes in osmolarity. Our work shows how a differentiation signal can recruit a second, unrelated sensory pathway to fine-tune yeast response in a complex environment.
author Baltanás, Rodrigo
Bush, Alan
Couto, Alicia Susana
Durrieu, Lucia
Colman Lerner, Alejandro Ariel
author_facet Baltanás, Rodrigo
Bush, Alan
Couto, Alicia Susana
Durrieu, Lucia
Colman Lerner, Alejandro Ariel
author_sort Baltanás, Rodrigo
title Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
title_short Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
title_full Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
title_fullStr Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
title_full_unstemmed Pheromone-induced morphogenesis improves osmoadaptation capacity by activating the HOG MAPK pathway
title_sort pheromone-induced morphogenesis improves osmoadaptation capacity by activating the hog mapk pathway
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_19450877_v6_n272_p_Baltanas
http://hdl.handle.net/20.500.12110/paper_19450877_v6_n272_p_Baltanas
work_keys_str_mv AT baltanasrodrigo pheromoneinducedmorphogenesisimprovesosmoadaptationcapacitybyactivatingthehogmapkpathway
AT bushalan pheromoneinducedmorphogenesisimprovesosmoadaptationcapacitybyactivatingthehogmapkpathway
AT coutoaliciasusana pheromoneinducedmorphogenesisimprovesosmoadaptationcapacitybyactivatingthehogmapkpathway
AT durrieulucia pheromoneinducedmorphogenesisimprovesosmoadaptationcapacitybyactivatingthehogmapkpathway
AT colmanlerneralejandroariel pheromoneinducedmorphogenesisimprovesosmoadaptationcapacitybyactivatingthehogmapkpathway
_version_ 1768543581143826432