Data of at least two 4EGI-1 site independent experiments are shown. Error bars: standard error of triplicated samples. Statistical analyses were conducted with an unpaired t test, with values of p,0.05 considered statistically significant. *p,0.05, **p,0.005. doi:10.1371/journal.pone.0053578.gproinflammatory cytokine induction downstream of RIG-I signaling [31]. To explore the involvement of CARD9 in IPS1 mediated signaling, we knocked down CARD9 in a stable HeLa clone expressing FK-IPS and examined its effect on the activation of IFN-b and IL-6 genes (Figure S7). Although IFN-b gene induction by Eliglustat web oligomerization was little affected by reducing CARD9, IL-6 gene activation was significantly attenuated. Considering the result that IL-6 gene activation is more dependent on TBM1/2 (Figure 3C, 3D), it is tempting to speculate that TBM1/2 preferentially promote NF-kB activation, whereas TBM3 has a primary role of IRF-3/7 activation.Our results support a model that CARD of IPS-1 receives signaling from RLR via CARD-CARD interaction to initiate oligomerization through mitochondrial dynamism; however, CARD of IPS-1 alone is not sufficient to trigger downstream signaling. 25331948 On the other hand, TBMs are essential for further signaling by the recruitment of TRAF3 and 6, which is initiated by molecular oligomerization. Consistent with this model, we observed that artificial oligomerization of IPS-1 induced recruitment of TRAF6 into the NP-40-insoluble fraction (Figure S6). Thus, IPS-1 receives and transmitssignaling through the functions of CARD and the TRAF motif, respectively.Materials and Methods Plasmid Constructsp-55C1BLuc, p-55A2Luc, p-125Luc, pRLtk, pEF-Bos-FLAGRIG-I CARD and pEF-Bos-FLAG-IPS-1 plasmids have been described [11,32]. Expression plasmids of FKBP36v (oligomerization peptide), pC4M-Fv2E, and pC4Fv1E were obtained from ARIAD (ARGENT Regulated Homodimerization kit). We reconstructed the vector, pC4Fv3E, which contains 3 tandem repeats of FKBP36v [18]. To construct IPS-1 fused three tandem FKBP, we amplified the IPS-1 sequence by PCR and inserted it into the SpeI site of pC4Fv3E. Site-directed FK-fused IPS-1 mutants (FK-IPS E457D, FK-IPS 400?40 E457D) were constructed using a KOD-Plus mutagenesis kit (TOYOBO, Japan). Nucleotide sequences for these constructs were confirmed with the BigDye DNA sequencing kit (Applied Biosystems). Expression vectors encording Flag-MAVS and Flag-mini-MAVS were obtained from Dr. Zhijian J. Chen.Delimitation of Critical Domain in IPS-Figure 4. Essential role of TBM3 in signaling. A. Schematic representation of FK-IPS fusion proteins. Asterisks represent the point mutation. B, C. HeLa cells stably expressing indicated FK-IPS mutants were mock treated or treated with AP20187 for 3 h. Cellular RNA were extracted and analyzed for IFN-b (B) or IL-6 (C) mRNA by qPCR. D . IPS-12/2 MEFs were transiently transfected with the luciferase reporter plasmid, p-55C1BLuc (for IRF, D, F) or p-55A2Luc (for NF-kB, E, G), together with indicated FK-IPS-1 fusion constructs. For TBM3 mutants, substituted amino acids are shown as red letters (F, G). Cells were treated with or without AP20187 for 6 h. Relative luciferase activities were determined as described in the Materials and Methods. A representative result of at least two independent experiments is shown. Error bars: standard error of triplicated samples. doi:10.1371/journal.pone.0053578.gCell, DNA Transfection, and Preparation of Cell ExtractsHeLa, 293T cells [32,33] and Mouse embryoni.Data of at least two independent experiments are shown. Error bars: standard error of triplicated samples. Statistical analyses were conducted with an unpaired t test, with values of p,0.05 considered statistically significant. *p,0.05, **p,0.005. doi:10.1371/journal.pone.0053578.gproinflammatory cytokine induction downstream of RIG-I signaling [31]. To explore the involvement of CARD9 in IPS1 mediated signaling, we knocked down CARD9 in a stable HeLa clone expressing FK-IPS and examined its effect on the activation of IFN-b and IL-6 genes (Figure S7). Although IFN-b gene induction by oligomerization was little affected by reducing CARD9, IL-6 gene activation was significantly attenuated. Considering the result that IL-6 gene activation is more dependent on TBM1/2 (Figure 3C, 3D), it is tempting to speculate that TBM1/2 preferentially promote NF-kB activation, whereas TBM3 has a primary role of IRF-3/7 activation.Our results support a model that CARD of IPS-1 receives signaling from RLR via CARD-CARD interaction to initiate oligomerization through mitochondrial dynamism; however, CARD of IPS-1 alone is not sufficient to trigger downstream signaling. 25331948 On the other hand, TBMs are essential for further signaling by the recruitment of TRAF3 and 6, which is initiated by molecular oligomerization. Consistent with this model, we observed that artificial oligomerization of IPS-1 induced recruitment of TRAF6 into the NP-40-insoluble fraction (Figure S6). Thus, IPS-1 receives and transmitssignaling through the functions of CARD and the TRAF motif, respectively.Materials and Methods Plasmid Constructsp-55C1BLuc, p-55A2Luc, p-125Luc, pRLtk, pEF-Bos-FLAGRIG-I CARD and pEF-Bos-FLAG-IPS-1 plasmids have been described [11,32]. Expression plasmids of FKBP36v (oligomerization peptide), pC4M-Fv2E, and pC4Fv1E were obtained from ARIAD (ARGENT Regulated Homodimerization kit). We reconstructed the vector, pC4Fv3E, which contains 3 tandem repeats of FKBP36v [18]. To construct IPS-1 fused three tandem FKBP, we amplified the IPS-1 sequence by PCR and inserted it into the SpeI site of pC4Fv3E. Site-directed FK-fused IPS-1 mutants (FK-IPS E457D, FK-IPS 400?40 E457D) were constructed using a KOD-Plus mutagenesis kit (TOYOBO, Japan). Nucleotide sequences for these constructs were confirmed with the BigDye DNA sequencing kit (Applied Biosystems). Expression vectors encording Flag-MAVS and Flag-mini-MAVS were obtained from Dr. Zhijian J. Chen.Delimitation of Critical Domain in IPS-Figure 4. Essential role of TBM3 in signaling. A. Schematic representation of FK-IPS fusion proteins. Asterisks represent the point mutation. B, C. HeLa cells stably expressing indicated FK-IPS mutants were mock treated or treated with AP20187 for 3 h. Cellular RNA were extracted and analyzed for IFN-b (B) or IL-6 (C) mRNA by qPCR. D . IPS-12/2 MEFs were transiently transfected with the luciferase reporter plasmid, p-55C1BLuc (for IRF, D, F) or p-55A2Luc (for NF-kB, E, G), together with indicated FK-IPS-1 fusion constructs. For TBM3 mutants, substituted amino acids are shown as red letters (F, G). Cells were treated with or without AP20187 for 6 h. Relative luciferase activities were determined as described in the Materials and Methods. A representative result of at least two independent experiments is shown. Error bars: standard error of triplicated samples. doi:10.1371/journal.pone.0053578.gCell, DNA Transfection, and Preparation of Cell ExtractsHeLa, 293T cells [32,33] and Mouse embryoni.
