Tivate the Pbs2p then activate the HOG pathway under osmotic

Tivate the Pbs2p then activate the HOG pathway under osmotic stress [5,11,23]. They work functionally redundant to some extent [2,35,36]. However, the three MAPKKKs have different order Eliglustat activation patterns. To study the activation patterns of the three MAPKKKs, we constructed the double mutant strains: ssk2Dssk22D, MedChemExpress I-BRD9 ste11Dssk2D and ste11Dssk22D and analyzed the phosphorylation of Hog1punder various levels of stress. Results of our experiments are presented in Figure 5. In the ssk2Dssk22D mutant that completely relies on Ste11p for Hog1p activation, the phosphorylation of Hog1p was weakly detected under 0.2 M sorbitol and exhibited a slower maximum response to the severe osmotic stress (1.0 M sorbitol) than the response of the wild type strain (Figure 5A). Under severe osmotic shock (1.0 M sorbitol), the phosphorylation of Hog1p peaked within 5 min in wild type strain (Figure 1B). In the ssk2Dssk22D mutant, Hog1p phosphorylation peaked at about 10 min under 1.0 M sorbitol. Cells lacking STE11 and SSK2 (ste11Dssk2D mutant) did not respond to low osmolarity (up to 0.4 M sorbitol), and displayed much slower response at each osmolarity (Generally the peak fallsAlternative Activation of Ssk2p in Osmotic StressFigure 5. Three MAPKKKs involved in HOG pathway have different properties. A. Hog1p phosphorylation pattern of ssk2Dssk22D mutant. B. Hog1p phosphorylation pattern of ssk22Dste11D mutant. C. Hog1p phosphorylation pattern of ssk2Dste11D mutant. D. Hog1p phosphorylation pattern of ste11Dssk22Dssk2 D(1?40). E. Scheme of HOG pathway. doi:10.1371/journal.pone.0054867.gat the 30 minutes point after osmotic shock ), and showed a much lower maximum response than the response of the wild type and other double mutants (Figure 5C). In the ste11Dssk2D mutant, Hog1p phosphorylation peaked at 30 min under 0.8 M and 1.0 M sorbitol.In the ste11Dssk22D mutant which has a functional Ssk2p, cells responded as fast as wild type cells, with the maximum response that was similar to that of the wild type. But the duration of the response of the ste11Dssk22D mutant under severe osmotic stress (0.8 M?.0M sorbitol) was shorter than that of the ssk2Dssk22DAlternative Activation of Ssk2p in Osmotic StressAlternative Activation of Ssk2p in Osmotic StressFigure 6. Ssk2p plays essential role in salt tolerance. A. The osmosensitivity phenotype of the S. cerevisiae HOG pathway mutants under KCL stress. B. The sodium-resistance phenotype of the S. cerevisiae HOG pathway mutants under various concentrations of NaCL. C. The lithium-sensitivity phenotype of the S. cerevisiae HOG pathway mutants under lithium stress. D. The truncated Ssk2 missing the amino acids 177,240aa caused reduced salt resistance of the ste11Dssk22D cells. E. The osmosensitivity phenotype of the S. cerevisiae HOG pathway mutants under sorbitol stress. F. The phenotype of Ssk2 D(177,239) cells is similar to that of the Ssk2D(1,240) cells. doi:10.1371/journal.pone.0054867.gmutant and wild type strain (Figure 5B). However, as we discussed above, there are at least two inputs into the Ssk2p: Ssk1p and the X factor (Figure 5E). Therefore, the activation of Hog1p by Ssk2p should be divided into two parts. Pattern of Hog1p’s activation by the X factor can be considered similar to that of the mutant ste11Dssk1Dssk22D (Figure 2A). To test the activation pattern of Ssk1p, we transformed the mutant Ssk2p lacking the segment of amino acids 1,240 into the triple mutant ste11Dssk2Dssk22D. Phosphorylation of Hog1p was detec.Tivate the Pbs2p then activate the HOG pathway under osmotic stress [5,11,23]. They work functionally redundant to some extent [2,35,36]. However, the three MAPKKKs have different activation patterns. To study the activation patterns of the three MAPKKKs, we constructed the double mutant strains: ssk2Dssk22D, ste11Dssk2D and ste11Dssk22D and analyzed the phosphorylation of Hog1punder various levels of stress. Results of our experiments are presented in Figure 5. In the ssk2Dssk22D mutant that completely relies on Ste11p for Hog1p activation, the phosphorylation of Hog1p was weakly detected under 0.2 M sorbitol and exhibited a slower maximum response to the severe osmotic stress (1.0 M sorbitol) than the response of the wild type strain (Figure 5A). Under severe osmotic shock (1.0 M sorbitol), the phosphorylation of Hog1p peaked within 5 min in wild type strain (Figure 1B). In the ssk2Dssk22D mutant, Hog1p phosphorylation peaked at about 10 min under 1.0 M sorbitol. Cells lacking STE11 and SSK2 (ste11Dssk2D mutant) did not respond to low osmolarity (up to 0.4 M sorbitol), and displayed much slower response at each osmolarity (Generally the peak fallsAlternative Activation of Ssk2p in Osmotic StressFigure 5. Three MAPKKKs involved in HOG pathway have different properties. A. Hog1p phosphorylation pattern of ssk2Dssk22D mutant. B. Hog1p phosphorylation pattern of ssk22Dste11D mutant. C. Hog1p phosphorylation pattern of ssk2Dste11D mutant. D. Hog1p phosphorylation pattern of ste11Dssk22Dssk2 D(1?40). E. Scheme of HOG pathway. doi:10.1371/journal.pone.0054867.gat the 30 minutes point after osmotic shock ), and showed a much lower maximum response than the response of the wild type and other double mutants (Figure 5C). In the ste11Dssk2D mutant, Hog1p phosphorylation peaked at 30 min under 0.8 M and 1.0 M sorbitol.In the ste11Dssk22D mutant which has a functional Ssk2p, cells responded as fast as wild type cells, with the maximum response that was similar to that of the wild type. But the duration of the response of the ste11Dssk22D mutant under severe osmotic stress (0.8 M?.0M sorbitol) was shorter than that of the ssk2Dssk22DAlternative Activation of Ssk2p in Osmotic StressAlternative Activation of Ssk2p in Osmotic StressFigure 6. Ssk2p plays essential role in salt tolerance. A. The osmosensitivity phenotype of the S. cerevisiae HOG pathway mutants under KCL stress. B. The sodium-resistance phenotype of the S. cerevisiae HOG pathway mutants under various concentrations of NaCL. C. The lithium-sensitivity phenotype of the S. cerevisiae HOG pathway mutants under lithium stress. D. The truncated Ssk2 missing the amino acids 177,240aa caused reduced salt resistance of the ste11Dssk22D cells. E. The osmosensitivity phenotype of the S. cerevisiae HOG pathway mutants under sorbitol stress. F. The phenotype of Ssk2 D(177,239) cells is similar to that of the Ssk2D(1,240) cells. doi:10.1371/journal.pone.0054867.gmutant and wild type strain (Figure 5B). However, as we discussed above, there are at least two inputs into the Ssk2p: Ssk1p and the X factor (Figure 5E). Therefore, the activation of Hog1p by Ssk2p should be divided into two parts. Pattern of Hog1p’s activation by the X factor can be considered similar to that of the mutant ste11Dssk1Dssk22D (Figure 2A). To test the activation pattern of Ssk1p, we transformed the mutant Ssk2p lacking the segment of amino acids 1,240 into the triple mutant ste11Dssk2Dssk22D. Phosphorylation of Hog1p was detec.