Ssat1a regulatory pattern that suggests the 332,389 region of ssat1b

Ssat1a regulatory pattern that suggests the 332,389 region of ssat1b alone is not sufficient to inhibit the background protein translation (Figure 4B). Further, ssat1bab, which contains the 332,374 nucleotide region of ssat1a and the remainder of ssat1b, behaved like ssat1b. These results, which are summarized in table 1, indicateThree Zebrafish ssat1 GenesFigure 4. Translational regulation Dimethylenastron site inside the ORF of zebrafish family of Ssat1 proteins. (A) HEK 293T cells were transiently transfected with the plasmid encoding myc-tagged full-length human SSAT1, zebrafish Ssat1a, Ssat1b, or Ssat1c. After incubation for 12 h, transfected cells were treated with 10 mM DENSPM, 20 mM MG132, or vehicle for 24 h. (B) HEK 293T cells were transiently transfected with the plasmid encoding myctagged zebrafish Ssat1 chimeric enzymes (detail in Materials and Methods). After incubation for 12 h, transfected cells were treated with vehicle (lane 1 and 3) or 10 mM DENSPM (lane 2 and 4) for 24 h. Cell lysates (5 mg total protein in each lane) were prepared and the protein content of Ssat1 and bactin in each sample was detected by western blotting with anti-myc and anti-b-actin antibody. doi:10.1371/journal.pone.0054017.gthat both the 59 and 39 regions of ssat1b are important for translational regulation inside the ORF.The Stability of Zebrafish Ssat1 ProteinsBy increasing the transfected plasmid by 2-fold 26001275 and protein loading by 10-fold, the expression of zebrafish Ssat1b and Ssat1c in cells cultured in normal medium could be observed by western blotting. We used these conditions to observe protein stability inside cells. After adding cycloheximine to the culture medium, translation of Ssat1 was stopped and the protein was subsequently turned over. As shown in Figure 4A, the Ssat1b protein was quickly turned over after translation was stopped (Fig. 5A, lanes 3?). Protein degradation was mediated by proteasome, since the addition of MG132 prevented degradation (Fig. 5A, lane 2). In addition, the presence of spermidine improved the stability of Ssat1b up to 6 hr (Fig. 5A, lanes 6?). On the other hand, Ssat1a and Ssat1c were more stable and no obvious protein degradation occurred within 6 h (Fig. 5). The 10 ssat1a and ssat1b chimeric genes were also applied to identify the critical regions responsible for rapid degradation(Fig. 2B). Our results indicated that none of the chimeric proteins, which contain the C-terminal regions of Ssat1a, turned over rapidly without spermidine treatment, such as Ssat1b467a, Ssat1b332a, and Ssat1aba shown here (Fig. 5B, lanes 1?). Moreover, the chimeric proteins, which contain the C-terminal regions of Ssat1b, did not undergo rapid degradation without spermidine treatment, unless they contain more than 70 residues from the Ssat1b C-terminal region, such as Ssat1a332b (Fig. 5B, lanes 4?) or Ssat1a248b (data not shown). The results, which are summarized in Table 1, indicated the last 70 residues of Ssat1b are important for the regulation of protein stability.The Enzyme Activities of Zebrafish SsatThe kinetic studies indicated all 3 Ssat1 isoenzymes were bioactive and could use both spermidine and spermine as substrates. However, the substrate preference of these isoenzymes was different. Ssat1b had similar Km values for spermidine and spermine, while Ssat1a had a KS 176 biological activity smaller Km toward spermidine and Ssat1c had a smaller Km for spermine (Table 2). Ssat1a and Ssatb had a better kcat/Km value for spermidine than that for spermine,Table 1. Trans.Ssat1a regulatory pattern that suggests the 332,389 region of ssat1b alone is not sufficient to inhibit the background protein translation (Figure 4B). Further, ssat1bab, which contains the 332,374 nucleotide region of ssat1a and the remainder of ssat1b, behaved like ssat1b. These results, which are summarized in table 1, indicateThree Zebrafish ssat1 GenesFigure 4. Translational regulation inside the ORF of zebrafish family of Ssat1 proteins. (A) HEK 293T cells were transiently transfected with the plasmid encoding myc-tagged full-length human SSAT1, zebrafish Ssat1a, Ssat1b, or Ssat1c. After incubation for 12 h, transfected cells were treated with 10 mM DENSPM, 20 mM MG132, or vehicle for 24 h. (B) HEK 293T cells were transiently transfected with the plasmid encoding myctagged zebrafish Ssat1 chimeric enzymes (detail in Materials and Methods). After incubation for 12 h, transfected cells were treated with vehicle (lane 1 and 3) or 10 mM DENSPM (lane 2 and 4) for 24 h. Cell lysates (5 mg total protein in each lane) were prepared and the protein content of Ssat1 and bactin in each sample was detected by western blotting with anti-myc and anti-b-actin antibody. doi:10.1371/journal.pone.0054017.gthat both the 59 and 39 regions of ssat1b are important for translational regulation inside the ORF.The Stability of Zebrafish Ssat1 ProteinsBy increasing the transfected plasmid by 2-fold 26001275 and protein loading by 10-fold, the expression of zebrafish Ssat1b and Ssat1c in cells cultured in normal medium could be observed by western blotting. We used these conditions to observe protein stability inside cells. After adding cycloheximine to the culture medium, translation of Ssat1 was stopped and the protein was subsequently turned over. As shown in Figure 4A, the Ssat1b protein was quickly turned over after translation was stopped (Fig. 5A, lanes 3?). Protein degradation was mediated by proteasome, since the addition of MG132 prevented degradation (Fig. 5A, lane 2). In addition, the presence of spermidine improved the stability of Ssat1b up to 6 hr (Fig. 5A, lanes 6?). On the other hand, Ssat1a and Ssat1c were more stable and no obvious protein degradation occurred within 6 h (Fig. 5). The 10 ssat1a and ssat1b chimeric genes were also applied to identify the critical regions responsible for rapid degradation(Fig. 2B). Our results indicated that none of the chimeric proteins, which contain the C-terminal regions of Ssat1a, turned over rapidly without spermidine treatment, such as Ssat1b467a, Ssat1b332a, and Ssat1aba shown here (Fig. 5B, lanes 1?). Moreover, the chimeric proteins, which contain the C-terminal regions of Ssat1b, did not undergo rapid degradation without spermidine treatment, unless they contain more than 70 residues from the Ssat1b C-terminal region, such as Ssat1a332b (Fig. 5B, lanes 4?) or Ssat1a248b (data not shown). The results, which are summarized in Table 1, indicated the last 70 residues of Ssat1b are important for the regulation of protein stability.The Enzyme Activities of Zebrafish SsatThe kinetic studies indicated all 3 Ssat1 isoenzymes were bioactive and could use both spermidine and spermine as substrates. However, the substrate preference of these isoenzymes was different. Ssat1b had similar Km values for spermidine and spermine, while Ssat1a had a smaller Km toward spermidine and Ssat1c had a smaller Km for spermine (Table 2). Ssat1a and Ssatb had a better kcat/Km value for spermidine than that for spermine,Table 1. Trans.