TY - JOUR
T1 - Cross-talk and decision making in MAP kinase pathways
AU - McClean, Megan N.
AU - Mody, Areez
AU - Broach, James R.
AU - Ramanathan, Sharad
N1 - Funding Information:
We thank J. Weiner, P. Houston, K. Thorn, K. Duevel, L. Schneper, E. Xu and P. Hersen for help with experiments, R. Tsien and E. Winters for reagents, A. Sengupta, A. Murray and M. Tyers for helpful discussions and A. Regev, L. Garwin, K. Vestrepen, P. Swain, E. O’Shea, I. Nachman, N. Barkai and A. Amon for comments on the manuscript. This work was supported by grants from the NIH (J.R.B.), GRPW fellowship, Lucent Technologies (M.N.M.), Keck Futures Initiative (S.R.) and the FAS Center for Systems Biology (S.R. and M.N.M.). Requests for materials should be addressed to S.R. ([email protected]).
PY - 2007/3
Y1 - 2007/3
N2 - Cells must respond specifically to different environmental stimuli in order to survive. The signal transduction pathways involved in sensing these stimuli often share the same or homologous proteins. Despite potential cross-wiring, cells show specificity of response. We show, through modeling, that the physiological response of such pathways exposed to simultaneous and temporally ordered inputs can demonstrate system-level mechanisms by which pathways achieve specificity. We apply these results to the hyperosmolar and pheromone mitogen-activated protein (MAP) kinase pathways in the yeast Saccharomyces cerevisiae. These two pathways specifically sense osmolar and pheromone signals, despite sharing a MAPKKK, Ste11, and having homologous MAPKs (Fus3 and Hog1). We show that in a single cell, the pathways are bistable over a range of inputs, and the cell responds to only one stimulus even when exposed to both. Our results imply that these pathways achieve specificity by filtering out spurious cross-talk through mutual inhibition. The variability between cells allows for heterogeneity of the decisions.
AB - Cells must respond specifically to different environmental stimuli in order to survive. The signal transduction pathways involved in sensing these stimuli often share the same or homologous proteins. Despite potential cross-wiring, cells show specificity of response. We show, through modeling, that the physiological response of such pathways exposed to simultaneous and temporally ordered inputs can demonstrate system-level mechanisms by which pathways achieve specificity. We apply these results to the hyperosmolar and pheromone mitogen-activated protein (MAP) kinase pathways in the yeast Saccharomyces cerevisiae. These two pathways specifically sense osmolar and pheromone signals, despite sharing a MAPKKK, Ste11, and having homologous MAPKs (Fus3 and Hog1). We show that in a single cell, the pathways are bistable over a range of inputs, and the cell responds to only one stimulus even when exposed to both. Our results imply that these pathways achieve specificity by filtering out spurious cross-talk through mutual inhibition. The variability between cells allows for heterogeneity of the decisions.
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U2 - 10.1038/ng1957
DO - 10.1038/ng1957
M3 - Article
C2 - 17259986
AN - SCOPUS:33847324364
SN - 1061-4036
VL - 39
SP - 409
EP - 414
JO - Nature Genetics
JF - Nature Genetics
IS - 3
ER -