Erved in polyQ disorders [42]. As what we show in Figure 5, SUMO-1 modification of mutant-type ataxin-3 increased the early apoptosis rate of the neurons, indicating that SUMOylation might enhance the stability of mutant-type ataxin3, thus increase its cytotoxicity, however the concrete mechanism still needs intensive study in future. In conclusion, our study demonstrated that SUMOylation on K166, the first described residue of SUMO-1 modification of ataxin-3, partially increased the stability of mutant-type ataxin-3, and the rate of apoptosis arisen from the cytotoxicity of the modified protein. Those support the hypothesis that SUMO-1 modification has a toxic effect on mutant-type ataxin-3 and participates in the pathogenesis of SCA3/MJD. Further studies in Drosophila models should be done to confirm these findings.The Effect of SUMOylation on Ataxin-Figure 4. SUMO-1 modification partially increased ataxin-3-68Q stability. HEK293 cells were transfected with GFP-ataxin-3 or GFP-ataxin3K166R. Immunoblotting analysis showed difference between the soluble (S) and insoluble (I) ataxin-3 in 20Q and 68Q with or without K166 (A). At 48 h after transfection, both aggregates formation cells and its immunoflurescence density were quantified. Bromopyruvic acid chemical information plasmid groups: 1. GFP-ataxin-3-20Q; 2. GFP-ataxin-3-20QK166R; 3. GFP-ataxin-3-68Q; 4. GFP-ataxin-3-68QK166R. Statistical significance was assessed with a one-way ANOVA. The amount of aggregates formation cells: 1 and 3: P,0.05 (*); 1 and 2: P.0.05 (**); 3 and 4: P.0.05 (***) (B). Immunoflurescence density of aggregates: 1 and 3: P,0.05 (*); 1 and 2: P.0.05 (**); 3 and 4: P.0.05 (***) (C). At 24 h after transfection, cells were treated with CHX (100 mg/ml) to prevent protein synthesis. Cells were harvested at 0, 1, 3, 7, 15 h after CHX treatment, subject to 12 SDS-PAGE, and analyzed by immunoblotting with anti-GFP antibody (D). doi:10.1371/journal.pone.0054214.gMaterials and Tramiprosate site methods Plasmid constructionPlasmids for myc-ataxin-3 and SUMO-1 in pcDNA3.1-mycHis(-)B (Invitrogen) have been described previously [32]. Ataxin3K8R, ataxin-3K166R, and ataxin-3K206R were all generated by sitedirected mutagenesis using long primers and overlap methods with primers M1/M2, M3/M4, M5/M6, respectively. GFP-ataxin-3 and GFP-ataxin-3K166R were constructed by subcloning the PCR product amplified using primers M1/M2 with pcDNA3.1-mycHis(-) B-ataxin-3 into pEGFP-N1 (Invitrogen) at SalI/BamHI sitesrespectively. The p36FLAG-myc-CMV-24-SUMO-1 plasmid was kindly provided by Professor Wang Guanghui. All constructs were confirmed by sequencing. Primers used in this study are shown in Table 1.Cell culture and transfectionHEK293 cells were cultured overnight in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco) supplemented with 10 fetal bovine serum (FBS) (Gibco) and antibiotics penicillin/streptomycin at 37uC under 5 CO2, and then transfected with expressing plasmids using LipofectamineTM 2000 reagent (Invitrogen)The Effect of SUMOylation on Ataxin-Figure 5. Early apoptosis rate in HEK293 cells. Plasmid Groups: 1. pcDNA3.1-myc-His(-)B; 2. pcDNA3.1-myc-His(-)B-ataxin-3-20Q; 3. pcDNA3.1myc-His(-)B-ataxin-3-20QK166R; 4. pcDNA3.1-myc-His(-)B-ataxin-3-68Q; 5. pcDNA3.1-myc-His(-)B-ataxin-3-68QK166R. Statistical significance was assessed with a one-way ANOVA: 2 and 4: P,0.05 (*); 2 and 3 P.0.05 (**); 4 and 5: P,0.05 (***). doi:10.1371/journal.pone.0054214.gaccording to the manufacturer’s protocol in DMEM without FBS. The same volume of DMEM.Erved in polyQ disorders [42]. As what we show in Figure 5, SUMO-1 modification of mutant-type ataxin-3 increased the early apoptosis rate of the neurons, indicating that SUMOylation might enhance the stability of mutant-type ataxin3, thus increase its cytotoxicity, however the concrete mechanism still needs intensive study in future. In conclusion, our study demonstrated that SUMOylation on K166, the first described residue of SUMO-1 modification of ataxin-3, partially increased the stability of mutant-type ataxin-3, and the rate of apoptosis arisen from the cytotoxicity of the modified protein. Those support the hypothesis that SUMO-1 modification has a toxic effect on mutant-type ataxin-3 and participates in the pathogenesis of SCA3/MJD. Further studies in Drosophila models should be done to confirm these findings.The Effect of SUMOylation on Ataxin-Figure 4. SUMO-1 modification partially increased ataxin-3-68Q stability. HEK293 cells were transfected with GFP-ataxin-3 or GFP-ataxin3K166R. Immunoblotting analysis showed difference between the soluble (S) and insoluble (I) ataxin-3 in 20Q and 68Q with or without K166 (A). At 48 h after transfection, both aggregates formation cells and its immunoflurescence density were quantified. Plasmid groups: 1. GFP-ataxin-3-20Q; 2. GFP-ataxin-3-20QK166R; 3. GFP-ataxin-3-68Q; 4. GFP-ataxin-3-68QK166R. Statistical significance was assessed with a one-way ANOVA. The amount of aggregates formation cells: 1 and 3: P,0.05 (*); 1 and 2: P.0.05 (**); 3 and 4: P.0.05 (***) (B). Immunoflurescence density of aggregates: 1 and 3: P,0.05 (*); 1 and 2: P.0.05 (**); 3 and 4: P.0.05 (***) (C). At 24 h after transfection, cells were treated with CHX (100 mg/ml) to prevent protein synthesis. Cells were harvested at 0, 1, 3, 7, 15 h after CHX treatment, subject to 12 SDS-PAGE, and analyzed by immunoblotting with anti-GFP antibody (D). doi:10.1371/journal.pone.0054214.gMaterials and Methods Plasmid constructionPlasmids for myc-ataxin-3 and SUMO-1 in pcDNA3.1-mycHis(-)B (Invitrogen) have been described previously [32]. Ataxin3K8R, ataxin-3K166R, and ataxin-3K206R were all generated by sitedirected mutagenesis using long primers and overlap methods with primers M1/M2, M3/M4, M5/M6, respectively. GFP-ataxin-3 and GFP-ataxin-3K166R were constructed by subcloning the PCR product amplified using primers M1/M2 with pcDNA3.1-mycHis(-) B-ataxin-3 into pEGFP-N1 (Invitrogen) at SalI/BamHI sitesrespectively. The p36FLAG-myc-CMV-24-SUMO-1 plasmid was kindly provided by Professor Wang Guanghui. All constructs were confirmed by sequencing. Primers used in this study are shown in Table 1.Cell culture and transfectionHEK293 cells were cultured overnight in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco) supplemented with 10 fetal bovine serum (FBS) (Gibco) and antibiotics penicillin/streptomycin at 37uC under 5 CO2, and then transfected with expressing plasmids using LipofectamineTM 2000 reagent (Invitrogen)The Effect of SUMOylation on Ataxin-Figure 5. Early apoptosis rate in HEK293 cells. Plasmid Groups: 1. pcDNA3.1-myc-His(-)B; 2. pcDNA3.1-myc-His(-)B-ataxin-3-20Q; 3. pcDNA3.1myc-His(-)B-ataxin-3-20QK166R; 4. pcDNA3.1-myc-His(-)B-ataxin-3-68Q; 5. pcDNA3.1-myc-His(-)B-ataxin-3-68QK166R. Statistical significance was assessed with a one-way ANOVA: 2 and 4: P,0.05 (*); 2 and 3 P.0.05 (**); 4 and 5: P,0.05 (***). doi:10.1371/journal.pone.0054214.gaccording to the manufacturer’s protocol in DMEM without FBS. The same volume of DMEM.
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