Mutagenesis analysis of the zinc-finger antiviral protein
© Wang et al; licensee BioMed Central Ltd. 2010
Received: 23 September 2009
Accepted: 13 March 2010
Published: 13 March 2010
The zinc-finger antiviral protein (ZAP) specifically inhibits the replication of certain viruses, including murine leukemia virus (MLV), by preventing the accumulation of viral mRNA in the cytoplasm. ZAP directly binds to the viral mRNA through the zinc-finger motifs and recruits the RNA exosome to degrade the target RNA. RNA helicase p72 is required for the optimal function of ZAP. In an attempt to understand the structure-function relationship of ZAP, we performed alanine scanning analysis.
A series of ZAP mutants was generated, in which three consecutive amino acids were replaced with three alanines. The mutants were analyzed for their antiviral activities against pseudotyped MLV vector. Out of the nineteen mutants analyzed, seven displayed significantly lower antiviral activities. Two mutations were in the very N-terminal domain, and five mutations were within or around the first and second zinc-finger motifs. These mutants were further analyzed for their abilities to bind to the target RNA, the exosome, and the RNA helicase p72. Mutants Nm3 and Nm63 lost the ability to bind to RNA. Mutants Nm 63 and Nm93 displayed compromised interaction with p72, while the binding of Nm133 to p72 was very modest. The interactions of all the mutants with the exosome were comparable to wild type ZAP.
The integrity of the very N-terminal domain and the first and second zinc-finger motifs appear to be required for ZAP's antiviral activity. Analyses of the mutants for their abilities to interact with the target RNA and RNA helicase p72 confirmed our previous results. The mutants that bind normally to the target RNA, the exosome, and the RNA helicase p72 may be useful tools for further understanding the mechanism underlying ZAP's antiviral activity.
Host restriction factors inhibit retrovirus infection at different steps in the retroviral life cycle by various mechanisms [1–3]. The zinc-finger antiviral protein (ZAP) was originally recovered from a screen for genes conferring resistance by cells to infection by Moloney murine leukemia virus (MLV) . In addition to MLV, ZAP was later found to inhibit the replication of Ebola virus (EBOV) and Marburg virus (MARV) , and multiple members of alphaviruses, including Sindbis virus (SINV) . The expression of ZAP does not induce a broad-spectrum antiviral state, as the replication of some viruses, including herpes simplex virus type 1 and yellow fever virus, is not affected in ZAP-expressing cells .
Analysis of the step at which ZAP inhibits MLV infection revealed that the formation and nuclear entry of the viral DNA were normal, but the viral mRNA level was significantly reduced in the cytoplasm of ZAP-expressing cells. The half-lives of the viral mRNA in the cytoplasm were about 2.5 h and 0.5 h in the control and ZAP-expressing cells, respectively, indicating that ZAP promotes the degradation of viral mRNA in the cytoplasm [4, 7].
ZAP directly binds to the target RNA and recruits the RNA processing exosome, a 3'-5' exoribonucleases complex consisting of at least nine components [7, 8], to degrade the RNA. The rat ZAP recruits the exosome through direct binding to the exosome component Rrp46. The RNA helicase p72 directly interacts with ZAP and is required for optimal function of ZAP . The sensitivity of certain viruses to the inhibitory effect of ZAP seems to be determined by the presence of the ZAP responsive element (ZRE) in the viral mRNA. The ZRE in MLV was mapped to the 3' long terminal repeat (LTR), while multiple fragments of SINV are responsive to ZAP . The sensitive sequences in EBOV and MARV were mapped to the L fragment . Among these ZREs, no obvious conserved motifs or secondary structures predicted using currently available softwares have been observed. The only common feature is that the minimum length of these ZREs is about 500 nucleotides.
In the N-terminal domain of ZAP, there are four CCCH-type zinc-finger motifs. Disruption of the second or fourth finger abolished the antiviral activity of ZAP, while disruption of the first or third finger had little effect . When the N-terminal domain of the 254 amino acids of ZAP is fused to the zeocin resistance gene (NZAP-Zeo), the fusion protein displays the same antiviral activity as the full-length protein , suggesting that the N-terminal domain is the major functional domain. Indeed, the interacting regions of ZAP with the target RNA, the exosome, and the RNA helicase p72 were all mapped to this domain [7, 9, 10].
As a step to further understanding how ZAP organizes the RNA degradation machinery to degrade viral RNA, we used the alanine scanning method to explore the structure-function relationship of the N-terminal domain of ZAP.
Antiviral activity of the ZAP mutants
A series of NZAP-Zeo mutants, in which three consecutive amino-acids were substituted with three alanines, was constructed and packaged into MLV vector to transduce Rat2 cells. The transduced cells were selected in zeocin-containing medium and pooled for further analyses. Out of the 25 mutants constructed, 19 mutants rendered cells resistant to zeocin selection. However, the remaining 6 mutants failed to do so. To rule out the possibility that the mutations affected the packaging into MLV vector, these 6 constructs were also stably transfected into Rat2 cells, but none of the cells survived the selection. Why these mutants failed to render the cells resistant to zeocin remains elusive. One possibility is that the mutations interfered with the function of the zeocin resistance gene. Another possibility is that the mutations interfered with the folding of the protein, resulting in very low levels of expression.
Out of the eight mutants that displayed significantly reduced antiviral activity, seven (Nm3, 13, 63, 93, 103, 113 and 133) were further pursued. The reason that mutant Nm83 was not included was that it was expressed at a relatively low level but displayed much higher activity than Nm 63 and Nm 93, which were expressed at comparable levels. To assess whether the mutations specifically affected the antiviral activity of ZAP against MLV, the mutants with reduced activity against MLV were also assayed for their activity to inhibit the propagation of SINV. As expected, the inhibitory effect against SINV of the seven mutants was significantly impaired (Fig. 1C). In contrast, the mutants (Nm23, 53 and 153) whose antiviral activity against MLV was not affected were also active against SINV (Fig. 1C). To confirm that the mutations affected the full-length ZAP protein as NZAP-Zeo, the seven mutations were also introduced into the full-length ZAP. The proteins were expressed in 293TRex cells in a tetracycline-inducible manner and assayed for their antiviral activities against MLV-luc. As expected, all these mutants displayed very low antiviral activity compared with the wild-type ZAP (Fig. 1D).
Activities that bind the target RNA
Interaction with the RNA exosome
Interaction with p72 RNA helicase
ZAP specifically inhibits MLV replication by promoting the degradation of the viral mRNA in the cytoplasm . ZAP directly binds to the viral mRNA and recruits the RNA exosome to degrade the target RNA [7, 10]. How ZAP coordinates this process is not clear yet. Here, we used the alanine scanning method to explore the regions important for the antiviral activity of ZAP.
Summary of the ZAP mutants for their binding activities to the target RNA, the exosome, and the RNA helicase p72
The RNA binding activity of Nm3 and Nm 63 was almost depleted, while that of Nm103 was compromised (Fig. 2 and Table 1). These results suggest that the integrity of the overall structure of ZAP may be important for the protein to bind the target RNA and that there may be multiple RNA binding sites. Alternatively, these amino acids may be positioned closely in the tertiary structure such that they form an RNA binding site together. Considering that the minimum length of the ZREs so far identified is about 500 nucleotides [5, 10], the former possibility seems more plausible.
All of the seven mutants interacted with the exosome (Fig. 3 and Table 1). However, immunoprecipitation of Rrp46 failed to coprecipitate a truncated ZAP (CZAP429) (Fig. 3), indicating that the interaction between the exosome and the seven ZAP mutants was specific. The specific domain of ZAP required for exosome interaction awaits further identification.
The binding of Nm133 to the RNA helicase p72 was severely impaired, while binding of Nm63 and Nm93 was moderately reduced (Fig. 4 and Table 1). The expression levels of Nm63 and Nm93 were relatively low compared with the other mutants (Fig. 1A). We speculate that these two mutations affected the overall structure of the protein. It is possible that the region around the mutation in Nm133 is the major p72 binding domain, and changes in the protein overall structure affect the binding.
Nm13 and Nm113 bound to the target RNA, the exosome, and p72 normally, suggesting that other mechanisms exist for their reduced antiviral activity. In mammalian cells mRNA degradation is a highly complex process [20, 21]. General mRNA degradation starts from deadenylation. The deadenylated mRNA is degraded 3'-5 by the RNA processing exosome. The mRNA is also decapped by the decapping enzyme complex and then degraded 5'-3 by the exoribonuclease XrnI. Co-factors, such as the RNA helicase p72 for ZAP , are involved. Furthermore, the activity of trans-acting factor is usually regulated by cellular factors. The properties of Nm13 and Nm113 suggest that other cellular factors may exist that interact with ZAP and are involved in ZAP-mediated RNA degradation.
A mechanism independent of the interaction of ZAP with the target RNA, exosome, or p72 may theoretically also exist. A mutant ZAP that failed to interact with the target RNA, the exosome, or p72, but still retained the antiviral activity would imply the existence of such a mechanism. To explore this possibility, we analyzed the mutants Nm23, 53 and 153, which displayed comparable antiviral activity as wild-type ZAP, for their interaction with the target RNA, the exosome, and p72. These mutants interacted with the target RNA, the exosome, and p72 similarly as the wild-type ZAP (Additional file 1). Further investigation should be needed to explore whether a mechanism exists independent of the interaction of ZAP with the target RNA, exosome or p72.
We identified seven mutants of ZAP whose antiviral activity was significantly reduced. Five mutants displayed reduced binding to the target RNA or the RNA helicase p72, confirming our previous results. The other two mutants may be useful tools for further understanding the mechanism for ZAP-mediated RNA degradation.
The plasmids pBabe-NZAP-Zeo and pNZAP-Zeo-myc have been described previously [4, 22]. pBabe-NZAP-Zeo-myc expresses myc-tagged rat NZAP-Zeo. To generate pBabe-NZAP-Zeo-myc, the EcoRI-ClaI fragment of pBabe-NZAP-Zeo was replaced with EcoRI-BamHI and BamHI-ClaI PCR-derived fragments. The EcoRI-BamHI fragment, which covers the sequence encoding NZAP was PCR-amplified from pNZAP-Zeo-myc using forward primer NZ-SP bearing an EcoRI site and reverse primer Bam-AP bearing a silent mutation to create a BamHI site. The BamHI-ClaI fragment, which covers the sequence encoding Zeo-myc was PCR amplified from pNZAP-Zeo-myc using forward primer Bam-SP bearing a silent mutation to create a BamHI site, and reverse primer NZ-AP bearing a ClaI site.
To generate the alanine substitution mutant, in which three consecutive amino-acids of every ten amino-acids were substituted with three alanines, the EcoRI-ClaI fragment of pBabe-NZAP-Zeo-myc was replaced with EcoRI-NotI and NotI -ClaI PCR-derived fragments. The sequence comprising the NotI site and an additional nucleotide encodes three consecutive alanines. The EcoRI-NotI fragment was PCR amplified from pBabe-NZAP-Zeo-myc using forward primer NZ-SP and reverse primer bearing a NotI site. The NotI -ClaI fragment was PCR amplified from pBabe-NZAP-Zeo-myc using forward primer bearing a NotI site and reverse primer NZ-AP. The sequences of the primers are listed below, with the restriction sites in bold.
pcDNA4/TO/myc-ZAP was previously described as pZAP-myc . Zm3, Zm13, Zm23, Zm53, Zm63, Zm93, Zm103, Zm113, Zm133 and Zm153 express myc-tagged full-length ZAP containing the alanine substitutions corresponding to those in Nm3, Nm13, Nm23, Nm53, Nm63, Nm93, Nm103, Nm113, Nm133 and Nm153, respectively. To generate Zm3, the PCR fragment amplified with Z-SP/Mid-AP as primers and Nm3 as template was digested with BamHI and NheI and used to replace the BamHI-NheI fragment of pcDNA4/TO/myc-ZAP. The same strategy was employed to generate Zm13, Zm23, Zm53, Zm63, Zm93, Zm103 and Zm113. To generate Zm133, the PCR fragment generated using Nm133 as template and Z-SP/Mid-RP as primers, and the PCR fragment using pcDNA4/TO/myc-ZAP as template and Mid-SP/Z-AP as primers were mixed and amplified using PCR primers Z-SP and Z-AP. The resulting BamHI-EcoRI fragment was used to replace the BamHI-EcoRI fragment of pcDNA4/TO/myc-ZAP. The same strategy was employed to generate Zm153.
pcDNA4/TO/myc-CZAP429 expresses myc-tagged CZAP429(amino acids 429-776 of ZAP). To generate pcDNA4/TO/myc-CZAP429, a ZAP fragment was amplified by using forward primer CZAP429SP bearing a BamHI site and reverse primer CZAP429AP bearing a NotI site and was used to replace the BamHI-NotI fragment of pcDNA4TO/myc-ZAP.
All the cells were maintained in DMEM supplemented with10% FBS. Transfection was performed using Fugene 6 (Roche Diagnostics) according to the manufacturer's instruction. Rat2-HA-Zeo and Rat2-NZAP-Zeo cells have been described previously . The pBabe-NZAP-Zeo-myc based constructs expressing NZAP-Zeo-myc mutants were packaged into MLV vector to transduce Rat2 cells. The cells were selected with zeocin (100 μg/ml), and zeocin-resistant cells were pooled for further analyses.
MLV-luc has been previously reported . To evaluate the antiviral activities of the NZAP-Zeo-myc mutants, cells were seeded in 35 mm dishes and infected with MLV-luc on the next day. Infection was conducted for 3 h followed by replacement of the infection medium with fresh medium. 48 hours later, the cells were lysed and luciferase activities were measured. Fold inhibition was calculated as the luciferase activity in the Rat2-HA-Zeo control cells divided by the luciferase activity in the cells expressing the NZAP-Zeo-myc mutants.
The methods for SINV infection and titration have been previously described . Briefly, cells were seeded at 7 × 105 in six-well dishes the day prior to infection. The next day, the cells were infected with the Toto1101 virus (MOI of 1) for 1 h. The titer of the stock was determined on BHK21 cells. After infection, the cells were washed twice with medium, and 2 ml of fresh medium was added. At 48 h post infection, the supernatants were collected and titrated in duplicate wells using permissive BHK21 cells.
293TRex and 293TRex-ZAP cell lines have been described previously . To generate 293TRex cell lines expressing the ZAP mutants in a tetracycline-inducible manner, pcDNA4/TO/myc-ZAP mutants were stably transfected into 293TRex cells and selected in zeocin-containing medium. Zeocin resistant cells were pooled and used for further analyses.
In vitro RNA binding assay
The method has been described previously .
Cells were lysed in lysis buffer B (30 mM Hepes pH7.6, 100 mM NaCl, 0.5% NP-40 and protease inhibitors cocktail) on ice for 10 minutes, and the lysates were clarified by centrifugation at 4°C for 10 minutes at 13000 rpm. The supernatant was mixed with proteinG plus-agarose (Santa Cruz Biotechnology) and the antibody, and incubated at 4°C for 2 h. The resins were then washed 3 times with lysis buffer B, and the bound proteins were detected by Western blotting.
Pull down assay
GST fusion proteins were immobilized on glutathione Sepharose 4B and then incubated with the lysate of the cells expressing the NZAP-Zeo-myc mutants in the presence of RNase A (100 μg/ml) for 2 h at 4°C. The resin was washed three times with PBS, and then analyzed by SDS-PAGE and Western blotting.
We thank Xuemin Guo for helpful technical support. This work was supported in part by Grants (to GG) from National Science Foundation (30470092 and 30530020) and Ministry of Science and Technology (973 Program 2006CB504302) of China.
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