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usinaite1,
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1 Institute of Molecular and Cell Biology, University of Tartu, Nooruse 1, 50411 Tartu, Estonia
2 Estonian Biocentre, Riia Street 23, 51010 Tartu, Estonia
3 Institute of Biotechnology, University of Helsinki, 00014 Helsinki, Finland
Correspondence
Andres Merits
andres.merits{at}ut.ee
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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These authors contributed equally to this work. 
Present address: Protobios OÜ, Akadeemia tee 15, 12618 Tallinn, Estonia.
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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). Due to their broad host range, high levels of protein expression and small genomes, alphaviruses have been extensively exploited as models. Semliki Forest virus (SFV) is one of the best-studied alphaviruses. The SFV genome is approximately 11.5 kb long and has a 5' cap structure and 3' poly(A) sequence. It encodes four non-structural proteins (nsP1–4), involved in viral RNA synthesis, and five structural proteins. After virus entry into the cell, the genomic RNA is translated into a large, non-structural polyprotein, which is processed to form an early and subsequently a late replicase complex (Strauss & Strauss, 1994). The early replicase complex mediates synthesis of the negative-strand RNA, which, in turn, is used by the late replicase complex as template for synthesis of new genomes and subgenomic RNA for structural proteins. Structural genes are not required for replication and thus can be replaced with a polylinker and/or with foreign sequences in order to obtain SFV-based replicon vectors (Liljestrom & Garoff, 1991).
The nsP1 protein is required for alphavirus RNA replication. It has been shown that nsP1 is required for synthesis of negative-strand RNAs (Wang et al., 1991) and that nsP1 catalyses the capping reaction of viral RNAs (Ahola & Kaariainen, 1995; Wang et al., 1996). It is also the only non-structural protein to interact with membranes (Ahola et al., 1999; Salonen et al., 2003). The membrane association of nsP1 is mediated through direct interaction of the amphipathic binding peptide (BP) with anionic phospholipids (Ahola et al., 1999) and is increased by post-translational palmitoylation of between one and three cysteine residues at positions 418–420 (Laakkonen et al., 1996). It has recently been demonstrated that nsP1 can only become palmitoylated after associating with membranes via the BP (Spuul et al., 2007). The replacement of cysteines at the palmitoylation site with alanines abolishes palmitoylation of nsP1 completely, whereas the essential enzymic activities of the protein, as well as its ability to bind to cellular membranes, are not destroyed (Laakkonen et al., 1996). It has also been reported that the cysteine-to-alanine mutations did not have a significant effect on SFV viability or growth in cell culture, although SFV1PA– virus was avirulent in mice (Ahola et al., 2000).
Here, we demonstrate that substitutions or deletions at the nsP1 palmitoylation site and its surrounding sequences seriously affect the viability of SFV. The subsequent replication of the mutant viruses to high titres was found to be due to the accumulation of second-site compensatory mutations, which restored the interaction between nsP1 and nsP4 that was abolished by the primary mutations at the palmitoylation site.
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METHODS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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), and wild-type (wt) Sindbis virus (SIN) from the clone pTOTO1101 (Rice et al., 1987). A derivative of SIN with replacement of cysteine at the palmitoylation site by alanine was derived from plasmid pSIN1PA– (Ahola et al., 2000). Modified recombinant vaccinia virus Ankara expressing T7 RNA polymerase (MVA-T7) was kindly provided by Bernard Moss (NIH, Bethesda, MD, USA).
Construction of SFV mutants.
Replacement of the three cysteine residues at positions 418–420 with alanines (hereafter designated mut3A) and deletion of the three cysteine residues at positions 418–420, designated 
3, or of the RSLTCCC sequence at positions 414–420, designated 7, were performed by PCR-based mutagenesis. PCR was performed on the pTSF1 template (Peranen et al., 1993) and the DNA fragments with introduced mutations were cloned into a derivative of pSFV1 (Liljestrom & Garoff, 1991), pSFV1/d1EGFP, by exchange of the Pfl23II–SacI fragment to obtain pSFV1mut3A/d1EGFP, pSFV13/d1EGFP and pSFV17/d1EGFP. Plasmids containing full-length icDNA (pSFV4mut3A, pSFV43 and pSFV47) were created by subsequent replacement of XbaI–SpeI fragments in the corresponding replicon plasmids by structural genes from pHelper1 (Liljestrom & Garoff, 1991). The replicons and genomes with identified compensatory mutations were obtained by similar cloning procedures.
Construction of plasmids for transient expression.
The regions encoding nsP2 and nsP3 were excised from pTSF2 and pTSF3, respectively (Peranen, 1991), with appropriate restriction endonucleases. The coding sequence of SFV4 nsP4 was PCR amplified using pSP6-SFV4 as the template and primers containing appropriate restriction endonuclease sites. Fragments were cloned into pCG3F12 in frame with a bovine papillomavirus type 1 E2 protein-derived 3F12 epitope tag (Kaldalu et al., 2000). The coding sequence of nsP1 was cloned into the same expression vector without the 3F12 tag. The resulting constructs were designated pCGnsP1, pCG3F12nsP2, pCG3F12nsP3 and pCG3F12nsP4. The mut3A, 3 and 7 mutations were introduced into pCGnsP1 by subcloning and the resulting plasmids were designated pCGmut3A, pCG3 and pCG7. Compensatory mutations, together with mut3A and 3 mutations, were subcloned into the pCGmut3A and pCG3 vectors by the use of the unique restriction sites within the nsP1 sequence and the resulting clones were designated pCGmut3A/P181Q, pCGmut3A/L234F, pCGmut3A/Q357L, pCG3/M124V+A197D and pCG3/G224+T352S.
For expression of nsP1 mutant variants in HeLa cells, the pTSF1 vector (Peranen et al., 1993) was used. The mutations mut3A, 3 and 7, alone or together with corresponding compensatory mutations, were subcloned into pTSF1 from corresponding pCG vectors with EcoRV and MluI endonucleases. The resulting constructs were designated pTSFmut3A, pTSF3, pTSF7, pTSFmut3A/P181Q, pTSFmut3A/L234F, pTSFmut3A/Q357L, pTSF3/M124V+A197D and pTSF3/G224+T352S.
Construction of plasmids for bacterial expression.
The pBAT1 expression vector was used for expression of derivatives of nsP1 in Escherichia coli (Ahola et al., 1997). The nsP1 sequences carrying mut3A, 3 and 7, alone or together with compensatory mutations, were transferred to pBAT1 from the corresponding pTSF1 vectors by NcoI–HindIII fragment exchange. The resulting clones were designated pBATmut3A, pBAT3, pBAT7, pBATmut3A/P181Q, pBATmut3A/L234F, pBATmut3A/Q357L, pBAT3/M124V+A197D and pBAT3/G224+T352S.
RNA transcription and transfection.
SFV-based replicons and icDNA plasmids were linearized by SpeI digestion; pTOTO1101 based plasmids were linearized by XhoI digestion. RNAs were synthesized by SP6 RNA polymerase and used for cell transfection by electroporation as described previously (Karlsson & Liljestrom, 2003). Primary virus stocks were collected from transfected cell cultures after incubation at 37 °C for 24 h.
Virological methods.
Confluent monolayers of BHK-21 cell culture were washed with PBS, infected at an m.o.i. of 10 for 1 h at 37 °C and overlaid with complete medium. BHK-21 cells (8x106 cells) were transfected with 50 µg in vitro-synthesized RNA or infected at an m.o.i. of 10 as described above. At selected time points, 150 µl medium was sampled and virus titres in the harvested samples were determined by plaque assay.
For the infectious centre assay, 1 µg in vitro-synthesized RNA was used for electroporation of 8x106 BHK-21 cells. When needed, the amount of RNA transcripts used was increased to 10 µg. Tenfold dilutions of electroporated cells were seeded in six-well tissue-culture plates containing 1.5x106 BHK-21 cells per well. After 2 h incubation at 37 °C, cells were overlaid with 2 ml carboxymethylcellulose (CMC) containing GMEM (2 % CMC : GMEM ratio 2 : 3, final concentration FCS 1.2 %). Plaques were stained with crystal violet after 2 days incubation at 37 °C.
For isolation of pseudorevertant viruses, 100 mm dishes of confluent BHK-21 cells were infected with primary stocks of the mutant viruses to obtain 20–50 plaques per plate. After 1 h incubation at 37 °C, cells were overlaid with 5 ml 0.9 % (w/v) agarose solution in GMEM and incubated for a further 2 days at 37 °C. To visualize plaques, the plates were overlaid with 3 ml 0.9 % (w/v) agarose/water solution containing 1 % (w/v) neutral red, and incubated overnight at 37 °C. Visible plaques were sampled by sterile tips and virions were eluted into GMEM. Stocks of viral clones were further amplified in BHK-21 cells.
Mapping of compensatory mutations.
Viral RNA was purified by using the NucleoSpin RNA II system (Macherey-Nagel) and used for reverse transcription by RevertAid M-MuLV reverse transcriptase (Fermentas). The non-structural region of the SFV genome was PCR-amplified using a set of 13 pairs of primers and sequenced. Amplification and sequencing were repeated for fragments containing identified mutations.
Co-immunoprecipitation.
Plasmids containing native or mutant sequences of SFV nsP1 were electroporated pairwise with plasmids pCG3F12nsP2, pCG3F12nsP3, or pCG3F12nsP4 (3 µg of each plasmid) into Cos-7 cells. Forty-eight hours post-transfection, the transfected cells were lysed in RIPA lysis buffer [50 mM Tris (pH 7.5), 400 mM NaCl, 1 mM EDTA, 1 % Igepal CA-630 (Sigma), 1 % sodium deoxycholate, 0.1 % SDS, 1 mM PMSF and EDTA-free protease inhibitor cocktail (Roche)] for 20 min on ice, incubated at –80 °C for 30 min and thawed on ice. The non-lysed fraction was removed by centrifugation at 15 000 g for 20 min. Protein concentration in cleared cell lysates was measured by Bradford assay. The amount of lysate corresponding to 1 mg total protein was incubated with nsP1-specific rabbit polyclonal antibody overnight at 4 °C. The immune complexes were precipitated with protein A–Sepharose CL-4B (Amersham Biosciences), pre-equilibrated in TNE buffer [50 mM Tris (pH 7.5), 400 mM NaCl, 1 mM EDTA]. Sepharose beads were washed four times with TNE buffer and precipitated proteins were denatured by boiling for 5 min in 50 µl Laemmli buffer. The amount of sample corresponding to 250 µg total protein was subjected to SDS-PAGE (12 % gel). Proteins were transferred to a nitrocellulose membrane, probed with the mouse 3F12 tag-specific monoclonal antibody (Kaldalu et al., 2000) and visualized by using the ECL system (Amersham Biosciences).
Immunofluorescence microscopy and palmitoylation assay.
Indirect immunofluorescence microscopy of transfected cells was carried out essentially as described by Salonen et al. (2003). Palmitoylation assay of the transiently expressed proteins was carried out as described by Spuul et al. (2007).
Expression of recombinant proteins in E. coli and guanylyltransferase (GT) assay.
E. coli strain BL21 (DE3) was transformed with the expression plasmid pBAT1 containing wt or mutant nsP1 sequences. Conditions for cell growth and recombinant protein expression have been described elsewhere (Laakkonen et al., 1994). Cells from 50 ml bacterial culture were collected at 4000 g for 10 min, resuspended in 1 ml lysis buffer [50 mM Tris/HCl (pH 8.0), 50 mM NaCl, 20 % glycerol, 0.1 % Tween 20, 1 mM DTT, 1 mM PMSF] and sonicated. The lysate was cleared by centrifugation at 15 000 g for 20 min at 4 °C, and the resulting supernatant (S15 fraction) was used for GT reaction or Western blotting. The covalent guanylyl complex formation reaction was carried out for 20 min at 30 °C in a mixture (total volume 30 µl) that contained 5 mCi (185 MBq) [
-32P]GTP (400 Ci mmol–1) in 50 mM Tris/HCl (pH 7.5), 10 mM KCl, 2 mM MgCl2, 5 mM DTT, 100 mM AdoMet (Sigma) and 5 µl sample (Ahola & Kaariainen, 1995).
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RESULTS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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). Transfection of BHK-21 cells revealed that <1 % of cells transfected with SFV1mut3A/d1EGFP or SFV13/d1EGFP RNAs were d1EGFP-positive, whereas transfection with SFV17/d1EGFP RNA resulted in approximately 40 % of cells expressing d1EGFP. Under the same conditions, the percentage of d1EGFP-positive cells was >90 % in cultures transfected with SFV1/d1EGFP. This severe effect of mutations at the palmitoylation site on the replication ability and marker gene expression of SFV-based replicons was unexpected, as similar changes in the context of the full-length SFV genome have previously been reported not to have a serious influence on SFV viability (Ahola et al., 2000). To clarify the situation, all three mutations were transferred into pSP6-SFV4 and the infectivity of the corresponding RNA transcripts was analysed by infectious centre assay. It was found that the infectivity of SFV4mut3A and SFV43 RNAs was four orders of magnitude lower than that of SFV4 RNA, whereas the RNA infectivity of SFV47 was reduced by only about 40-fold (Fig. 1). Thus, both mut3A and 3 dramatically reduced infectivity of the corresponding transcripts, with 7 having a milder effect.
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is the accumulation of changes with a positive impact on virus replication during virus propagation. To verify this hypothesis, we compared the release of viruses from transfected BHK-21 cells with that from BHK-21 cells infected with the corresponding viruses. It was found that the growth of the SFV4mut3A, SFV43 and SFV47 in transfected cells was delayed significantly compared with that of SFV4 (Fig. 2a). The release of infectious virions was detected at 4 h post-transfection for SFV4; in contrast, the titres of the mutant viruses were below detection limits up to 6–8 h post-transfection. Consistent with previous findings, SFV47 showed the quickest growth among the mutants. The titres of SFV4 reached their maximum (109 p.f.u. ml–1) 10 h post-transfection, whereas the titres of mutated viruses were always lower and continued to grow even at 24 h post-transfection (Fig. 2a). When BHK-21 cell cultures were infected with the primary stocks of SFV4, SFV4mut3A, SFV43 or SFV47, no significant difference between the growth curves of these viruses was detected (Fig. 2b). Thus, our results support the hypothesis that some changes took place during propagation of these mutant viruses.
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). It was found that the mutation at the palmitoylation site reduced the infectivity of SIN transcripts by only about 30-fold. In growth-curve experiments, the release of infectious virions from cells transfected with transcripts from pTOTO1101 or pSIN1PA– was, in both cases, detected at 4 h post-transfection, and only a small (<1 log) reduction in the titre of SIN1PA–, compared with that of SIN, was observed between 4 and 10 h post-transfection; at later time points, no statistically significant difference between titres of these viruses was observed (data not shown). These results are consistent with the previous report that the mutation at the palmitoylation site of nsP1 has only a minor effect on the viability and replication of SIN (Ahola et al., 2000) and, accordingly, no compensatory changes are required to restore the replication of the mutant SIN genome.
Identification of putative compensatory mutations in SFV
RT-PCR and sequencing analysis confirmed the presence of original mutations at the palmitoylation site of nsP1 for all three recombinant SFV stocks. To identify the possible second-site compensatory mutations, four isolates for each mutant were plaque-purified from the primary stocks of SFV4mut3A, SFV43 and SFV47, and their non-structural regions were analysed. This analysis revealed three single mutations (P181Q, L234F and Q357L) and two double mutations (M124V+A197D and G224+T352S) in the SFV4mut3A and SFV43 clones, respectively (Table 1). All of these mutations, except G224, were single-nucleotide replacements and localized either in the methyltransferase/guanylyltransferase (MT/GT) domain (M124V, P181Q, L234F, A197D and G224) or in the C-terminal region (T352S and Q357L) of nsP1. In contrast to SFV4mut3A and SFV43, no mutations were found in the non-structural region of any plaque-purified isolate originating from SFV47.
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33 (M124V+A197D and G224+T352S) and their effects were analysed as for the original mutants. It was found that the introduction of these mutations increased the infectivity of in vitro-synthesized RNAs to a level comparable with that of SFV4 RNA (Table 1
). Thus, the identified mutations did rescue the infectivity of SFV harbouring mut3A or 3 mutations.
Changes identified in SFV43 isolates were double mutations (M124V+A197D and G224+T352S). When they were introduced separately into pSFV43, the subsequent analysis revealed that only one mutation from each pair (A197D and G224, respectively) provided a compensatory effect, whereas the other was functionally neutral (Table 1).
In order to demonstrate that compensatory mutations are also responsible for the differences between primary and secondary growth curves (Fig. 2), similar growth curves for two recombinants, SFV4mut3A-P181Q and SFV43-G224+T352S, were constructed. It was found that, unlike SFV4mut3A and SFV43, the growth of SFV4mut3A-P181Q and SFV43-G224+T352S in transfected BHK-21 cells had no delay in virion release, although their accumulation was slightly slower than that of SFV4 (Fig. 3a). When BHK-21 cells were infected with the primary viral stocks of SFV4mut3A-P181Q and SFV43-G224+T352S, no differences from SFV4 were detected (Fig. 3b).
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). Thus, the identified compensatory mutations are almost-neutral mutations in the SFV4 background.
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3 or 7 deletions and analysed as described above. The results indicated that the L234F was able to compensate defects caused by the 3 mutation (Table 2). In contrast, the L234F mutation decreased the infectivity of full-length RNA of SFV47 by approximately 20-fold (Table 2). Based on these results, it can be suggested that the consequences of mut3A and 3 have a rather similar effect on nsP1 and can therefore be compensated by the same mutation(s). In contrast, the 7 mutation has a different effect.
Enzymic activities and palmitoylation of mutant forms of nsP1
It has been reported that the CCC to AAA (418–420) mutation has a relatively minor effect on the enzymic activities of recombinant nsP1 (Laakkonen et al., 1996). To find out whether that is the case for nsP1s harbouring mut3A, 3 and 7 mutations or compensatory mutations together with mut3A and 3 mutations, proteins were expressed in E. coli and their GT activities were assayed. As is evident from the data presented in Fig. 4(a), the GT activity of recombinant proteins with mut3A, 3 and 7 was very similar to that of wt nsP1 and all recombinant proteins with compensatory mutations had GT activity as well. As the GT activity of nsP1 is completely dependent on its MT activity (Ahola & Kaariainen, 1995), the data indicate that the analysed proteins should possess MT activity as well. Thus, it can be concluded that defects (if any) in enzymic activities of mutant nsP1s could not represent the main reason for the very low infectivity of mut3A and 3 constructs.
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), the data presented above clearly indicate that all recombinant nsP1s must be membrane-bound. This finding is consistent with the model that the primary binding of nsP1 to the membranes is mediated by the BP and that only then is it strengthened by covalent palmitoylation (Spuul et al., 2007). All three mutations analysed in this study were expected to abolish palmitoylation of nsP1. The reversion of original mutations was never observed in this study, indicating strongly that palmitoylation of nsP1 was not restored. This hypothesis was verified directly by expression of mutant nsP1s by use of the MVA-T7 system in HeLa cells and the labelling of recombinant proteins with [9,10(n)-3H]palmitic acid. This experiment revealed that only wt nsP1 was palmitoylated (Fig. 4b), confirming that mut3A, 3 and 7 did indeed abolish palmitoylation and that the compensatory mutations did not restore that function.
Subcellular localization of mutant forms of nsP1
The analysis of the subcellular localization of mutant nsP1s in transfected HeLa cells by the MVA-T7 system revealed that, as expected, the wt nsP1 was localized almost exclusively at the plasma membrane and caused extensive induction of filopodium-like extensions (Fig. 5a). In contrast, nsP1-mut3A and nsP1-3 localized both on the plasma membrane and in the cytoplasm of transfected cells and caused no (or very little) formation of filopodium-like extensions (Fig. 5b, c). Expression of nsP1-7 also did not result in formation of filopodium-like extensions but, in contrast to nsP1-mut3 and nsP1-3, the nsP1-7 localized mostly at the plasma membrane of transfected cells (Fig. 5d). Addition of the compensatory mutations to nsP1-mut3 and nsP1-3 always resulted in more extensive plasma-membrane localization of the recombinant proteins (Fig. 5e–i); this phenomenon is clearest in the cases of nsP1-mut3A-Q357L (Fig. 5g) and nsP1-3-M124V+A197D (Fig. 5h). With the notable exception of nsP1-mut3A-L234F (Fig. 5f), all of the recombinant proteins with compensatory mutations also induced the formation of filopodium-like extensions, although these structures were always less prominent than those induced by wt nsP1. Thus, the effects of compensatory mutations on the formation of filopodium-like extensions differ from each other. However, it should be noted that all viruses with compensatory mutations in their genome (but not SFV4-7) caused the formation of filopodium-like extensions on the plasma membrane of infected BHK-21 cells, indicating that this phenomenon may depend on the mode of nsP1 expression and/or on the host cell type.
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). To determine the effects of mut3A, 3 and 7 on interactions of nsP1 with other non-structural proteins, nsP1, nsP1-mut3A, nsP1-3 and nsP1-7 were expressed pairwise with nsP2, nsP3 or nsP4 in Cos-7 cells and complexes were immunoprecipitated under native conditions with the anti-nsP1 antibody. The results of this experiment failed to reveal any difference between wt and mutated nsP1 regarding their interactions with nsP2 and nsP3, which were negative and positive, respectively (data not shown). However, in contrast to wt nsP1 and nsP1-7, nsP1-mut3A and nsP1-3 failed to interact with nsP4 (Fig. 6). Importantly, it was also demonstrated that the introduction of the compensatory mutations P181Q, L234F or Q357L into nsP1-mut3A and mutations M124V+A197D or G224+T352S into nsP1-3 restored their interaction with nsP4 (Fig. 6). These findings suggest the possibility that one of the reasons for the low infectivity of SFV4mut3A and SFV43 was the lack or significant debilitation of interaction between nsP1 and nsP4 and that the compensation occurred through its restoration.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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). In this work, we have shown that the replacement of these cysteines by alanines or their deletion was detrimental to recombinant RNA infectivity, whilst the more extended deletion comprising residues 414–420 caused a less dramatic effect. It appeared that the accumulation of SFV4mut3A and SFV43 to high titres in the second-passage virus stock was due to the appearance of compensatory mutations either in the MT/GT domain or in the C-terminal part of nsP1. None of the compensatory mutations found in this study restored the palmitoylation of recombinant proteins, confirming that the palmitoylation of nsP1 is not strictly required for SFV replication (Ahola et al., 2000). The discrepancy between the results described above and those reported previously is likely to be due to the heterogeneous nature of the mutant virus stock used in the earlier study.
The rapid accumulation of compensatory mutations requires very low initial infectivity of the original mutant RNA. In this case, the infection will start from a small fraction of transfected cells, followed by the release of virus and de novo infection of initially uninfected cells, thus providing conditions for the selection of mutations with a positive impact on virus growth. No compensatory mutation in the non-structural region of plaque-purified isolates of SFV47 was identified in this study; the sufficiently high infectivity of SFV47 prevented the takeover of the original genotype by pseudo-revertants during single-cycle infection. The change of the single cysteine to alanine at the palmitoylation site of SIN nsP1 had only a very mild effect on virus multiplication in transfected cells. The changes were even smaller than those observed for SFV47 and, therefore, as for SFV47, no compensatory changes are required for SIN1PA–. It is tempting to speculate that the mild effect in the case of SIN may be due to the smaller change in the protein (only one cysteine residue is mutated); however, the results obtained for SFV47 indicate that there is no direct correlation between the size of the mutated region and the corresponding phenotypic change.
It is evident from our data that the lack of nsP1 palmitoylation is not the main reason for the low infectivity of SFV4mut3A and SFV43. Similarly, this defect cannot be attributed to defects in GT/MT activities, as the corresponding recombinant proteins were enzymically active. In addition, although most of the identified compensatory mutations were located within the MT/GT domain of nsP1, none of them caused a significant increase in enzymic activity of the corresponding recombinant protein (Fig. 4a).
Direct interactions of nsP1 with nsP3 and nsP4 have been shown previously in co-immunoprecipitation experiments (Salonen et al., 2003). The importance of interactions between nsP1 and the N terminus of nsP4 for the recognition of the promoter for minus-strand RNA synthesis has been revealed in SIN replication (Shirako et al., 2000). Another genetic study also supported nsP1–nsP4 interaction (Fata et al., 2002). Here, we demonstrated that mutations mut3A and 3 destroyed or debilitated the interaction between nsP1 and nsP4, possibly resulting in defect(s) in the assembly of the replication complex. Interestingly, the 7 mutation did not preclude the interaction of nsP1 with nsP4. A possible explanation could be that the conformational changes in the nsP1 three-dimensional structure, caused on the one hand by mut3A or 3 mutations and on the other hand by 7 mutation, are different. This conclusion is supported by the finding that compensatory mutation L234F, identified from an SFV4mut3A isolate, could compensate 3, but was deleterious for 7.
The presence of enzymic activity and plasma-membrane localization indicate that the lack of palmitoylation does not prevent the membrane binding of the corresponding mutant nsP1s. However, some changes in subcellular localization of nsP1 were observed for both nsP1-mut3A and nsP1-3: they are less abundant at the plasma membrane and partially localized in the cytoplasm of transfected cells. As the third mutant protein, nsP1-7, as well as proteins with compensatory mutations, had more extensive plasma-membrane localization (Fig. 5), it can be speculated that the defect in membrane association and/or subcellular targeting may be another mechanism underlying the low infectivity of these recombinant viruses. Indeed, if mut3A and 3 were to result only in defects in the interaction between nsP1 and nsP4, it would be logical to assume that compensatory mutations could take place in either of the proteins. However, we were unable to find any mutations in the nsP4 region either in the plaque-purified viruses described above or in a larger number of isolates, purified and analysed specifically for this purpose (data not shown). The most likely explanation for this is that mut3A or 3 led to multiple defects in the localization and functions of nsP1 and only changes in the same protein can compensate for these defects.
Mutations preventing the palmitoylation of nsP1 are reported to prevent the formation of filopodium-like extensions in infected or transfected cells (Ahola et al., 2000; Laakkonen et al., 1998). The biological significance of filopodium formation is not known but, nevertheless, it represents a notable characteristic of SFV infection. Therefore, it is interesting to note that HeLa cells transiently expressing nsP1-mut3A-P181Q, nsP1-mut3A-Q357L, nsP1-3-M124V+A197D and nsP1-3-G224+T352S did have filopodium-like extensions on the plasma membrane, indicating that nsP1 palmitoylation is not strictly required for the formation of these structures. In contrast to other compensatory mutations, the L234F change did not restore the formation of filopodium-like extensions; therefore, it is possible that these mutants can be used for studies of the functional significance of this poorly understood phenomenon. However, it should be mentioned that, in BHK-21 cells infected with the corresponding viruses, the morphological differences were much less prominent, indicating possible significance of the expression mode (infection versus transient expression), presence or absence of other non-structural proteins and/or host cell type for this phenomenon.
Taken together, our results support the idea that palmitoylation of nsP1 as such is not required for efficient replication, nor does it determine the interaction between nsP1 and nsP4 or the initial plasma-membrane localization of nsP1. Instead, it is more likely that the effects of mutations can be attributed to conformational changes caused by the deletions/substitutions at the palmitoylation site.
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ACKNOWLEDGEMENTS |
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REFERENCES |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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Received 21 January 2007;
accepted 2 March 2007.
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), SFV4mut3A (
), SFV4
) and SFV4
) in 8x106 BHK-21 cells upon (a) transfection with 50 µg in vitro-synthesized RNAs or (b) infection at an m.o.i. of 10. Data from one of two reproducible experiments are shown.
