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Open Access

Peer-reviewed

Research Article

Coordinated Function of Cellular DEAD-Box Helicases in Suppression of Viral RNA Recombination and Maintenance of Viral Genome Integrity

  • Chingkai Chuang,

    Affiliation Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, United States of America

    ⨯
  • K. Reddisiva Prasanth,

    Affiliation Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, United States of America

    ⨯
  • Peter D. Nagy

    pdnagy2@uky.edu

    Affiliation Department of Plant Pathology, University of Kentucky, Lexington, Kentucky, United States of America

    ⨯

Abstract

The intricate interactions between viruses and hosts include an evolutionary arms race and adaptation that is facilitated by the ability of RNA viruses to evolve rapidly due to high frequency mutations and genetic RNA recombination. In this paper, we show evidence that the co-opted cellular DDX3-like Ded1 DEAD-box helicase suppresses tombusviral RNA recombination in yeast model host, and the orthologous RH20 helicase functions in a similar way in plants. In vitro replication and recombination assays confirm the direct role of the ATPase function of Ded1p in suppression of viral recombination. We also present data supporting a role for Ded1 in facilitating the switch from minus- to plus-strand synthesis. Interestingly, another co-opted cellular helicase, the eIF4AIII-like AtRH2, enhances TBSV recombination in the absence of Ded1/RH20, suggesting that the coordinated actions of these helicases control viral RNA recombination events. Altogether, these helicases are the first co-opted cellular factors in the viral replicase complex that directly affect viral RNA recombination. Ded1 helicase seems to be a key factor maintaining viral genome integrity by promoting the replication of viral RNAs with correct termini, but inhibiting the replication of defective RNAs lacking correct 5’ end sequences. Altogether, a co-opted cellular DEAD-box helicase facilitates the maintenance of full-length viral genome and suppresses viral recombination, thus limiting the appearance of defective viral RNAs during replication.

Author Summary

A major force in virus evolution is the ability of viruses to recombine and change their genomes rapidly. Similar to viral replication that greatly depends on subverted cellular proteins, viral genetic recombination is also affected by host factors based on genome-wide screens with tomato bushy stunt virus (TBSV) in yeast model host. However, the roles of host factors in the viral genomic RNA recombination process remain elusive. In this paper, we show evidence, in yeast, plants and in vitro, that co-opted cellular helicases by TBSV affect viral recombination through suppressing template-switching and replication of the new recombinant viral RNAs. Based on the presented data, a new concept emerges on the roles of co-opted cellular helicases in maintaining viral genome integrity. Altogether, the hijacked cellular DEAD-box helicases are involved in maintenance of full-length viral RNA genome and suppression of viral RNA recombination, thus blocking the appearance of defective or recombinant viral RNAs during replication.

Citation: Chuang C, Prasanth KR, Nagy PD (2015) Coordinated Function of Cellular DEAD-Box Helicases in Suppression of Viral RNA Recombination and Maintenance of Viral Genome Integrity. PLoS Pathog 11(2): e1004680. https://doi.org/10.1371/journal.ppat.1004680

Editor: Aiming Wang, Agriculture and Agri-Food Canada, CANADA

Received: August 17, 2014; Accepted: January 12, 2015; Published: February 18, 2015

Copyright: © 2015 Chuang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

Data Availability: All relevant data are within the paper and its Supporting Information files.

Funding: This research was supported by the National Science Foundation (MCB-1122039) to PDN. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing interests: The authors have declared that no competing interests exist.

Introduction

RNA viruses replicate inside cells and they require many cellular factors to complete their infection cycle. The intricate interactions between viruses and hosts include evolutionary arms race and adaptation that is facilitated by the ability of RNA viruses to evolve rapidly due to high frequency mutations and genetic RNA recombination as well as reassortment of genomic components [1–3]. Interestingly, cellular and environmental factors affect viral RNA recombination, which is a process that joins two or more noncontiguous segments of the same RNA or two separate RNAs together [4,5]. Recombination could alter viral genomes by introducing insertions or duplications, combining new sequences, or leading to deletions or rearrangements. RNA recombination also functions to repair truncated or damaged viral RNA molecules [2,5–7]. Viral RNA recombination can affect virus population dynamics, contribute to virus variability, as well as function in genome repair that maintains the infectivity of RNA viruses [3,4].

Viral RNA recombination is intensively studied with Tomato bushy stunt virus (TBSV), a tombusvirus infecting plants, using yeast (Saccharomyces cerevisiae) model host. TBSV is an outstanding model for both replication and recombination studies [8–12]. Systematic genome-wide screens with TBSV have led to the identification of more than 30 host genes affecting viral RNA recombination in yeast [8,9,13–15]. Among the host factors identified is the cytosolic Xrn1p 5’-to-3’ exoribonuclease (Xrn4 in plants) that suppresses TBSV recombination [16–18]. Xrn1p was shown to rapidly degrade cellular endoribonuclease-cleaved TBSV RNAs, termed degRNAs (Fig. 1A) [16–19]. The combined effects of cellular exo- and endoribonucleases determine the accumulation of degRNAs, which are especially active in RNA recombination, and thus, these cellular factors affect the frequency of viral RNA recombination events [9,18]. An additional key cellular factor involved in TBSV recombination is Pmr1 Ca++/Mn++ pump that controls Mn++ level in the cytosol [15]. Studies revealed that the cytosolic Mn++ level could greatly affect the properties/activities of the viral replicase, including its ability to synthesize RNA and switch templates. For example, high Mn++ level (in the absence of Pmr1) leads to high frequency RNA recombination in yeast or plant cells as well as in a cell-free TBSV replication assay [15].

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Fig 1. The DDX3-like Ded1p DEAD-box helicase is a suppressor of TBSV RNA recombination.

(A) The previously defined viral RNA recombination pathway during TBSV replication. The replication-competent TBSV repRNA is cleaved by cellular endoribonucleases, such as the RNase MRP complex, followed by limited 5’ truncations by the cellular Xrn1p exoribonuclease. These processes lead to the generation of a pool of replication-competent degRNAs that serve as recombinogenic templates in template-switching events driven by the viral replicase. The sequences in recRNAs are shown schematically. (B) Depletion of Ded1p level in yeast leads to the rapid emergence of TBSV recRNAs and degRNAs. Note that doxycycline (+dox samples) leads to depletion of Ded1p expressed from the regulatable TET promoter. Replication of the TBSV DI-AU-FP repRNA (see panel A) in wt and TET::DED1 yeasts co-expressing the tombusvirus p33 and p92 replication proteins was measured by Northern blotting 24 h after initiation of TBSV replication. Note the emergence of different species of recRNAs and degRNA (see panel A) in samples with depleted Ded1p. The accumulation level of repRNA was normalized based on the ribosomal (r)RNA (bottom panel). The bottom images show the results with semi-quantitative RT-PCR, which was used to demonstrate knock-down of Ded1 mRNA levels in TET::Ded1 yeast in the presence of doxycycline. Each sample is obtained from independent yeast colonies. The experiments were repeated two-to-three times. Throughout the paper, +/- means standard deviation. (C) Measuring recRNA levels in yeast expressing wt Ded1p, ded1–95ts or ded1–199ts mutants at 23°C (permissive temperature for yeast growth) or 29°C (semi-permissive temperature). Top panel: The accumulation of TBSV DI-AU-FP repRNA, recRNAs and degRNA was measured by Northern blotting at the 24 h time point. Middle panel: The accumulation level of repRNA was normalized based on the ribosomal (r)RNA. Bottom panel: The accumulation levels of His6-p92 and His6-p33 were tested by Western blotting. Each experiment was repeated. Asterisk marks the SDS-resistant p33 homodimer. (D) Accumulation levels of degRNA and recRNAs in Ded1ts yeasts were measured by Northern blotting. The expressed TBSV template RNA was DI-RIIΔ70 degRNA, which represents a frequently isolated degRNA species lacking RI and part of RII (Panel A). See further details in panel B.

https://doi.org/10.1371/journal.ppat.1004680.g001

Tombusviruses code for two replication proteins, termed p33 and p92pol, which are translated directly from the genomic (g)RNA. p92pol RNA-dependent RNA polymerase [20,21] is produced through translational readthrough of the p33 stop codon [22–24]. The abundant p33 is an RNA chaperone that functions in RNA template selection/recruitment and in the assembly of the membrane-bound viral replicase complex (VRCs) [21,25–29].

A recent systematic screen with TBSV based on a temperature-sensitive (ts) library of yeast mutants (Prasanth and Nagy, unpublished), identified the yeast Ded1p ATP-dependent DEAD-box RNA helicase as a cellular factor affecting TBSV RNA recombination. Ded1p and ten other yeast DEAD-box proteins, which are the largest family of RNA helicases, were also identified as pro-viral factors in TBSV replication in yeast [13,30–35]. DEAD-box helicases are known to be involved in all aspects of cellular metabolism [36–38], in RNA virus replication [39–42], viral translation [43,44], and affect responses to abiotic stress and pathogen infections [45–47]. They function in RNA duplex unwinding, RNA folding, remodeling of RNA-protein complexes, and RNA clamping [48].

TBSV, which does not code for its own helicase, usurps the yeast DDX3-like Ded1p (similar to the Arabidopsis AtRH20 DEAD-box helicase), to promote (+)-strand synthesis [49]. Ded1p/AtRH20 bind to the 3’-end of the TBSV minus-strand RNA, and by locally unwinding the dsRNA replication intermediate structure [50], it renders the promoter sequence accessible to p92pol for initiation of (+)-strand RNA synthesis. Additional DEAD-box helicases, such as Dbp3p (human DDX5-like) and Fal1p (eukaryotic translation initiation factor eIF4AIII-like), which are involved in ribosome biogenesis in yeast [51–53], and the orthologous Arabidopsis RH2 and RH5 helicases bind to the 5’ proximal region in the TBSV (-)RNA [54]. This region harbors a critical replication enhancer element (REN) [55]. These co-opted cellular helicases can locally unwind the double-stranded (ds) structure within the REN of the replication intermediate and enhance (+)RNA synthesis [50,54]. Altogether, the co-opted cellular DEAD-box helicases work synergistically to enhance TBSV replication by interacting with the viral (-)RNA, dsRNA and the replication proteins within the VRCs [54].

In this work, we show evidence that Ded1p/AtRH20 helicases are strong suppressors of TBSV recombination in yeast and plants. In vitro assays show direct involvement of Ded1p in suppression of viral recombination, which requires its ATPase function. Moreover, the presented data support a new role for Ded1p in facilitating the switch from (-)-strand to (+)-strand synthesis. Interestingly, the eIF4AIII-like AtRH2 helicase enhances TBSV recombination in the absence of Ded1/AtRH20, suggesting that the coordinated action of cellular Ded1/AtRH20 and AtRH2 helicases control viral RNA recombination events. We propose a model on the role of Ded1/AtRH20 in facilitating the replication of full-length viral RNAs with intact 5’ ends while inhibiting the replication of 5’-truncated viral RNAs, thus playing a major role in maintaining the intact genome structure for TBSV.

Results

Ded1 mutants support increased level of tombusvirus RNA recombination in yeast

To characterize the role of the DDX3-like Ded1p DEAD-box RNA helicase of yeast in TBSV RNA recombination, first we utilized genetic approaches in yeast. Depletion of Ded1p resulted in ~5-fold increase in TBSV recombinant (rec)RNA accumulation (Fig. 1B, lanes 13–16). Similarly, yeast expressing either Ded1–95ts or Ded1–199ts temperature-sensitive mutants as a single source for Ded1p, led up to 5-to-10-fold increase in TBSV recRNA levels at the semi-permissive temperature (Fig. 1C, lanes 13–16 and 21–24 versus 17–20). Ded1–199ts also supported ~35-fold higher recRNA accumulation at a lower (permissive) temperature (Fig. 1C, lanes 9–12), suggesting that this particular mutant is especially suitable for viral RNA recombination studies. Ded1–199ts (G368D mutation) is known to debilitate its function in protein translation and intron splicing [56], while Ded1–95ts (T408I mutation) does not affect splicing, but maybe involved in translation and RNA decay [57]. Altogether, the above yeast genetic approaches have conclusively demonstrated that the wt Ded1p helicase is a strong suppressor of TBSV RNA recombination in yeast cells.

The most frequent recombinants in the TBSV system are generated via template-switching mechanism by the viral replicase using viral RNA templates that are cleaved by cellular endo- and exoribonucleases (schematically shown in Fig. 1A) [5,8,9,15,17,18,58]. The partially degraded (5’-truncated) viral RNA products generated by the cellular nucleases are called degRNAs, which serve as templates for viral RNA recombination (Fig. 1A) [8,9]. Interestingly, the amounts of degRNAs also increased by ~3-to-10-fold, suggesting their efficient generation and replication in Ded1ts mutant yeasts (Fig. 1C) or in yeast with depleted Ded1p (Fig. 1B). Interestingly, the degRNAs are superior templates for high frequency recombination when expressed in yeast cells in the presence of the viral p33/p92pol replication proteins (Fig. 1D) [8,9]. Both Ded1–95ts and Ded1–199ts supported 3-to-8-fold higher recRNA accumulation from the DI-RIIΔ70 degRNA template than the wt Ded1p did in yeast (Fig. 1D). These data further supported the suppressor function of Ded1p in TBSV recRNA accumulation in yeast.

The surprisingly robust accumulation of the 5’-truncated degRNAs in both ded1–95ts and ded1–199ts yeasts expressing the full-length DI-AU-FP repRNA (Fig. 1C) was likely due to enhanced efficiency of their replication, because expression of the representative DI-RIIΔ70 degRNA accumulated to high level (up to ~5-fold increase) in ded1–95ts and ded1–199ts yeast strains in comparison with the wt yeast (Fig. 1D). These findings indicate an unexpected role of Ded1p in suppressing the replication of the 5’-truncated degRNAs. This is in contrast with the pro-viral role of Ded1p in enhancing the accumulation of TBSV DI-72 repRNA, which carries the authentic 5’ end sequence (see also below) [49,54].

Ded1 mutants support increased level of (-)RNA products from TBSV recRNAs and degRNAs in yeast

Testing the accumulation of (+) versus the (-)RNA products revealed ~9-fold increased (-)recRNA production in case of ded1–199ts yeast at semi-permissive temperature in comparison with wt yeast (Fig. 2A). Interestingly, similar to the high level of (-)recRNAs, accumulation of truncated (-)degRNAs was also increased by ~4-fold, while the amount of full-length (-)repRNA changed only slightly (DI-AU-FP repRNA, Fig. 2A) in ded1–199ts yeast. Altogether, (-)recRNAs accumulated to ~3-fold higher level than the full-length DI-AU-FP (-)repRNA in ded1–199ts yeast (Fig. 2A). On the contrary, the DI-AU-FP repRNA was the most prevalent (+)RNA product, while the (+)recRNAs and (+)degRNA products accumulated to 3-to-7-fold lesser amounts than the (+)repRNA in ded1–199ts yeast (Fig. 2A).

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Fig 2. Increased level of TBSV minus-strand synthesis on recRNAs and degRNAs in yeast expressing ded1–199ts mutant.

(A) Top and bottom panels: Northern blot analysis of (+) and (-)RNA levels, respectively, in wt and ded1–199ts yeast.The ratios of the most abundant recRNAs versus repRNA (DI-AU-FP) and degRNA versus repRNA were calculated. See further details in Fig. 1. Note that viral RNA recombination is a chance event depending on many factors and when the first recombination event occurs, thus influencing the outcome. Quantitation is based on multiple repeats (different yeast streaks) in each experiment, and despite the different numbers on recRNAs, both Figure 1 and 2 show the same trend. (B) Top panel: In vitro RNA binding assay with purified wt Ded1p and mutants. The assay contained the 32P-labeled DI-72 (-)repRNA (~0.1 pmol) plus increasing amount of MBP, MBP-Ded1, MBP-Ded1–95 or MBP-Ded1–199 (all were used in 40, 80 and 160 nM). The free or Ded1p-bound ssRNA was separated on nondenaturing 5% acrylamide gels. Bottom panel: The MBP-affinity purified MBP-Ded1 and mutants are analyzed on a SDS-PAGE gel.

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Since ded1–95ts and ded1–199ts mutations are present within the RNA binding domain of the Ded1p helicase [56], we have tested if the mutants show altered viral RNA binding characteristic when compared with the wt Ded1p. The EMSA assay with DI-72(-) RNA template revealed that the purified ded1–95ts and ded1–199ts mutants bound to the viral (-)RNA with up to 25-fold reduced efficiency in vitro (Fig. 2B). The low efficiency in viral (-)RNA binding by these Ded1p mutants could be the reason for these mutants supporting the increased rate of viral recombination, high level of degRNA accumulation and reduction in viral (+)-strand synthesis (see Discussion).

In comparison with the results obtained via ded1–95ts and ded1–199ts mutants, we observed a similar trend with increased accumulation of (-)recRNA and (-)degRNA products obtained with the recombinogenic DI-AU-FP repRNA, when yeast expressed Ded1p at a reduced level (+doxycycline treatment, Fig. 3A-B). Altogether, these data revealed that Ded1p is important in regulation of (+) versus (-)RNA products and this regulation depends on the presence of the authentic 5’ end sequence from TBSV (+)repRNA.

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Fig 3. Ded1p depletion leads to increased level of TBSV minus-strand synthesis on recRNAs and degRNAs in yeast.

(A) Top and bottom panels: Northern blot analysis of (+) and (-)RNA levels, respectively, in TET::DED1 yeast after depletion of Ded1p level (+dox samples) or normal Ded1p level (-dox, no doxycyclin added).The ratios of the most abundant recRNAs versus repRNA (DI-AU-FP) and degRNA versus repRNA were calculated. See further details in Fig. 1. (B) Similar to panel A, except TET::DED1 yeast was grown at 23°C. (C) Similar to panel A, except DI-72 repRNA was expressed in TET::DED1 yeast for TBSV recombination studies. Note that DI-72 repRNA is a much better template than the longer DI-AU-FP repRNA. Also, the recRNAs are larger than DI-72 repRNA, as indicated by arrowheads.

https://doi.org/10.1371/journal.ppat.1004680.g003

To confirm the importance of co-opted Ded1p in viral RNA replication and recombination, we also tested the accumulation of various Δ+) and (-)RNA products with the efficient DI-72 repRNA, which replicates to the highest level among all TBSV RNAs in yeast and plants cells [59,60]. As expected based on previous publications [49,61], depletion of Ded1p by doxycycline in TET::DED1 yeast, reduced the accumulation of DI-72 (+)repRNAs by ~4-fold, while the accumulation of new (+)recRNAs and (+)degRNA products was below the detection limit (top image in Fig. 3C, lanes 3–4 and 7–8). Interestingly, however, (-)recRNA and (-)degRNA products, which were almost as abundant as the full-length DI-72 (-)repRNA, were detected in yeasts with depleted Ded1p level (bottom image in Fig. 3C, lanes 3–4 and 7–8). The corresponding (-)recRNA and (-)degRNA products were below detection limit in yeasts expressing Ded1p to high level (bottom image in Fig. 3C, lanes 1–2 and 5–6). Altogether, these results demonstrate that Ded1p plays a critical role in suppression of the formation and accumulation of recRNA and degRNA products during minus-strand synthesis.

Ded1 suppresses the formation of recRNAs and the replication of the 5’-truncated degRNAs in vitro

To dissect the inhibitory function of Ded1p in recRNA formation and degRNA replication, first we used an in vitro assay with isolated yeast membranes [62]. The yeast membrane fraction contains the tombusvirus replicase in complex with the viral RNAs, thus facilitating studies on the viral RNAs functionally associated with the replicase. Denaturing PAGE analysis of the in vitro replicase products revealed that both recRNAs and degRNAs were actively replicated by the tombusvirus replicase derived from ded1–199ts yeast (~13-to-21-fold higher level than in wt replicase), while these RNAs were barely detectable in the replicase from wt yeast (Fig. 4A). In addition, ded1–199ts replicase supported ~6-to-7-fold higher level of (-)recRNAs and (-)degRNAs in comparison with slightly reduced DI-AU-FP (-)repRNA carrying the authentic 5’ end sequence in vitro (Fig. 4B). The (+)recRNAs and (+)degRNAs accumulated to 3-fold higher level in ded1–199ts yeast than the corresponding RNAs in wt yeast, but (+)recRNAs and (+)degRNAs were ~12-fold less abundant than the DI-AU-FP (+)repRNA in vitro (Fig. 4B-C). Thus, similar to the situation in yeast cells, wt Ded1p suppressed in vitro (-)-strand synthesis with the recRNAs and degRNAs, but not with DI-AU-FP repRNA carrying the authentic 5’ end sequence.

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Fig 4. Suppression of TBSV recRNA accumulation by Ded1p in in vitro replication assays.

(A) The membrane-enriched fraction (MEF) was isolated from wt or ded1–199ts yeast expressing the tombusvirus p33 and p92 replication proteins in combination with the DI-AU-FP repRNA, followed by in vitro tombusvirus replication assay. The denaturing PAGE analysis shows the emergence of recRNAs and degRNA as indicated. (B–C) Northern blot analysis of the polarity of the TBSV RNAs synthesized in the MEF assay (see panel A, except the assay was done with nonlabeled ribonucleotides) using 32P-labeled probes to detect (-)-strands and (+)-strands, respectively. The ratios between various TBSV RNAs were calculated as in Fig. 2. (D) Scheme of the yeast cell-free (CFE) assay for TBSV replication. Note that the assembly of the TBSV replicase takes place in the CFE using recombinant viral components as shown. The TBSV p33 and p92 replication proteins and Ded1p and its mutants (D1 is inactive, D11 has enhanced ATPase activity) were purified from E. coli. (E) Reduced replication of the full-length DI-72 repRNA in TET::DED1 yeast CFEs with high or depleted levels of Ded1p (see Fig. 1). (F-G) Denaturing PAGE analysis of the effect of Ded1p and its mutants on the replication of the full-length recombinogenic DI-AU-FP and the 5’-truncated DI-RIIΔ70 degRNA, respectively, in the CFE assay. The experiments were repeated twice.

https://doi.org/10.1371/journal.ppat.1004680.g004

The second assay was based on a cell-free extract (CFE) from yeast with depleted Ded1p that was used to assemble the tombusvirus replicase in vitro using purified recombinant p33/p92pol and (+)repRNAs (Fig. 4D) [49]. The CFE supports a complete replication cycle resulting in both (-) and (+)-stranded repRNA products [29]. As expected, Ded1p facilitates the production of (+)repRNAs carrying the authentic 5’ end sequence [Fig. 4E, lanes 3–4, see reduced DI-72 repRNA accumulation in CFE with depleted Ded1p (+dox)] [49]. Similarly, addition of the purified recombinant wt Ded1p to the CFE programmed with DI-AU-FP (+)repRNA, which carries the authentic 5’ end sequence, led to a ~50% increase in repRNA accumulation (Fig. 4F, lane 2), while the ATPase-deficient D1 mutant of Ded1p [49,63] could not stimulate repRNA replication in vitro (Fig. 4F, lane 3). On the contrary, addition of the purified recombinant wt Ded1p or D11 mutant with increased ATPase activity [63] to the CFE with the 5’-truncated DI-RIIΔ70 degRNA, led to ~40–50% decrease in degRNA accumulation (Fig. 4G, lanes 2 and 4 versus lane 1), while D1 mutant did not affect the replication of DI-RIIΔ70 degRNA in the CFE (lane 3). Based on these data from CFE assays, we conclude that Ded1p inhibits the replication of recRNAs or degRNAs missing the authentic 5’ end sequence likely through blocking the (-)-strand synthesis on these RNA templates.

Ded1p helicase promotes the release of the p92 RdRp protein from the template RNA in vitro

Based on known features of DEAD-box helicases in remodeling protein-RNA complexes [48,64], we reasoned that Ded1p might be involved in releasing the p92 RdRp protein from the (+)RNA template at the end of (-)-strand synthesis, thus decreasing the chance for template-switching events (see Discussion). To test this model, we developed an in vitro assay with a soluble form of p92, called p92-Δ167N, which can specifically use TBSV-derived (+)RNA template for RNA synthesis in vitro in the presence of biotynylated UTP and other ribonucleotides as shown schematically in Fig. 5A [21]. The biotynylated viral dsRNA form was then captured via streptavidin beads (Fig. 5B). We then added purified Ded1p to the beads to facilitate the putative release of the p92-Δ167N RdRp from the captured dsRNA product. The amount of dsRNA-bound versus released p92-Δ167N was measured by Western blotting (Fig. 5B-C). These experiments revealed that three-times more p92-Δ167N was released from the viral dsRNA product when purified wt Ded1p was included in the assay (Fig. 5C, lanes 4 versus 1).

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Fig 5. Ded1p DEAD-box helicase promotes the release of the viral RNA from the p92 RdRp in vitro.

(A) Scheme of the in vitro assay to produce biotinylated RNA bound to TBSV RdRp. We used an in vitro activated purified p92 derivative (called p92-Δ167N), which can specifically use TBSV-derived (+)RNA template for RNA synthesis in vitro for 3’terminal extension on the added template RNA as shown schematically [21]. (B) The scheme shows the in vitro RdRp reaction consisting of p92-Δ167N RdRp and soluble fraction of yeast CFE (with depleted endogenous Ded1p due to the use of TET::Ded1 yeast) to activate the RdRp function. The activated RdRp then introduces biotin-labeled UTP to the template, allowing for the capture of the RNA product (a hairpin-like dsRNA) associated with p92-Δ167N RdRp on streptavidin-coated agarose beads. Then the addition of purified Ded1p might facilitate the release of the p92-Δ167N RdRp from the RNA. (C) The amounts of eluted versus bound p92-Δ167N RdRp was measured by Western blotting (see images). The eluate contains the released p92-Δ167N RdRp from the streptavidin beads, while the SDS fraction contains p92-Δ167N RdRp that was left on the beads after Ded1p treatment. (D) EMSA assay with p92-Δ167N RdRp in the presence of Ded1p helicase. The 32P-labeled RNA probe was RI(+), which is bound by both p92-Δ167N RdRp and Ded1p in vitro. The RNA probe and the first added protein (indicated at the top) was allowed to form an RNP complex, followed by the addition of the second protein 15 min latter. We used 0.4 μg of affinity-purified MBP-p92-Δ167N RdRp and 1.0 and 2.0 μg of affinity-purified GST-Ded1p or GST. Lanes 10–11 contain samples with both proteins added to the 32P-labeled RNA probe at the same time. The bound 32P-labeled RNA probe was quantitated. Note that the diffused band (“smear”) likely represent the released RNA probe from the RNP complex (see the enhanced images at the bottom) only under the given conditions. The higher values with Ded1p (lanes 14–15) are likely due to the better RNA-binding by Ded1p then p92-Δ167N (lane 3).

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In another assay, we used EMSA with MBP-p92-Δ167N and purified GST-Ded1p based on 32P-labeled RI(+) RNA as a probe. Both MBP-p92-Δ167N and GST-Ded1p bind to the probe when applied alone (Fig. 5D, lanes 3 and 14, respectively). However, when we added p92-Δ167N first to the probe, followed 15 min latter by addition of GST-Ded1p, then the release of the probe was detectable in the form of diffused label (“smear”) (Fig. 5D, lanes 4–5 versus 6–7 with purified GST as a control). Interestingly, the release of the probe was dependent on the presence of ATP, suggesting that Ded1p requires ATP for this function (Fig. 5D, lanes 8–9 versus 4–5). The diffused label was also observed when Ded1p was added first to the RNA, followed by p92-Δ167N (Fig. 5D, lanes 12–13), suggesting that Ded1p and p92-Δ167N likely form a complex that releases the viral RNA.

Ded1 suppresses recombination and the replication of the 5’-truncated degRNAs independent of Xrn1p 5’-to-3’ exoribonuclease in yeast

To establish the function of Ded1p during TBSV replication and RNA recombination, we examined if Ded1p affects these processes via controlling Xrn1p 5’-to-3’ exoribonuclease, which is a key enzyme in TBSV RNA stability and for suppression of TBSV RNA recombination in yeast [5,16–18,65]. For these studies, we expressed a 5’-truncated repRNA (DI-ΔRI, Fig. 6A), which goes through further 5’-truncations (up to ~70 nt, where RII(+)-SL hairpin structure stops the nuclease activity) in the presence of Xrn1p in wt yeast (Fig. 6A), while this truncation process is weak in xrn1Δ yeast (Fig. 6B) [65]. DI-ΔRI RNA did not accumulate in ded1–199ts yeast, similar to wt yeast (Fig. 6B, lanes 13–16 and 1–4), while DI-(RI accumulated to high level in xrn1Δ yeast (Fig. 6B, lanes 5–8). Also, the profile of recRNAs accumulating in ded1–199ts yeast was similar to that in wt yeast and different from that in xrn1Δ yeast (Fig. 6B). Thus, it seems that ded1p mutation does not affect TBSV RNA recombination and degRNA accumulation via inhibition of the Xrn1p activity. This conclusion was further supported by RNA stability experiments that showed comparable half-life for degRNA in ded1–95ts and ded1–199ts yeasts to the wt yeast (Fig. 6C).

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Fig 6. Suppression of viral RNA recombination by Ded1 helicase is independent of the Xrn1 pathway.

(A) Schematic representation of the previously characterized Xrn1-driven TBSV RNA recombination pathway in yeast. Plasmid-driven expression of the DI-(RI in the presence of p33/p92 replication proteins leads to partial 5’ truncations by the cellular Xrn1p 5’-to-3’ exoribonuclease generating DI-RIIΔ70-like degRNAs as shown. DI-RIIΔ70-like degRNAs then participate in RNA recombination as shown. (B) Recombination profile of DI-(RI RNA in xrn1Δ, met22Δ (as a control) and in ded1–199 yeasts. The original expressed DI-(RI degRNA, DI-RIIΔ70-like degRNAs and recRNAs are depicted with arrowheads and arrows, respectively. Note that the recRNA profile is dramatically different in xrn1Δ yeast when compared to ded1–199 yeast. (C) Half-like of DI-RIIΔ70 degRNA in WT, ded1–95 and ded1–199 yeasts. Note that yeast did not express p33/p92 proteins.

https://doi.org/10.1371/journal.ppat.1004680.g006

AtRH2 DEAD-box helicase promotes the formation of recRNAs and the replication of the 5’-truncated degRNAs in yeast

Because TBSV replication is known to depend on two types of cellular DEAD-box helicases, namely the DDX3-like Ded1p/AtRH20 that bind to the 3’end of the (-)RNA and the eIF4AIII-like Fal1p/AtRH2 helicases that bind to a 5’ proximal enhancer element in the (-)RNA (Fig. 7A) [49,54], we also tested the effect of expression of AtRH2 on TBSV recombination in yeast. We observed up to ~12-fold enhanced level of TBSV RNA recombination in wt and 26-fold increase in ded1–199ts yeasts expressing AtRH2 (Fig. 7B, lanes 5–6, 17–18 and 11–12, 23–24). In contrast, expression of AtRH20 helicase (Fig. 7C), which is a Ded1p ortholog, suppressed recRNA accumulation in both wt and ded1–199ts yeasts (Fig. 7B). Thus, different co-opted cellular helicases have opposite effects on TBSV recombination in yeast.

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Fig 7. Opposite effects of subverted cellular DEAD-box helicases on TBSV recombination in yeast and in the CFE assay.

(A) TBSV co-opt two groups of cellular helicases that become part of the VRCs: the DDX3-like Ded1/AtRH20 and the eIF4AIII-like AtRH2. These helicases bind to different cis-acting replication elements present at the 3’ and 5’ ends of the viral (-)RNA as shown. Note that RI(-) carries the promoter for (+)-strand synthesis, while the RIII(-) is a replication enhancer element (REN). (B) Over-expression of AtRH2 enhances recRNAs and degRNA accumulation, while over-expression of AtRH20 decreases the occurrence of these RNAs in wt or ded1–199ts yeasts. The Northern blot analysis was done as in Fig. 1. (C) Western blot analysis to detect the expression level of His6-tagged cellular helicases and the His6-tagged viral replication proteins in the WT and ded1–199ts yeasts. Asterisk marks the SDS-resistant p33 dimer. (D) The scheme of the CFE-based TBSV replication assay. Note that the level of Ded1p was depleted in TET::DED1 yeast prior to CFE isolation. (E) Denaturing PAGE analysis of the accumulation of 5’-truncated DI-RIIΔ70 degRNA used as the original template in the CFE assay and the in vitro generated recRNA. See further details in Fig. 3.

https://doi.org/10.1371/journal.ppat.1004680.g007

To test if AtRH2 has direct function in TBSV recombination, we used the CFE-based TBSV replication assay prepared from yeast with depleted Ded1p (Fig. 7D). Interestingly, the addition of purified recombinant AtRH2 increased the replication of the 5’-truncated DI-RIIΔ70 degRNA by ~2-fold and RNA recombination also by ~2-fold (Fig. 7E, lanes 3–4 versus 1–2). However, the stimulatory effect of AtRH2 on RNA recombination is neutralized by the addition of purified recombinant Ded1p helicase (Fig. 7E, lanes 5–6), suggesting that AtRH2 only promotes formation of recRNAs and the replication of the 5’-truncated degRNAs when Ded1p helicase is depleted. In other words, Ded1p helicase seems to be the dominant factor with its recombination suppressor activity.

Opposite roles of AtRH2 and AtRH20 plant helicases in viral RNA recombination and the replication of the 5’-truncated degRNAs in plants

To confirm the roles of the above cellular helicases in TBSV RNA recombination in plants, we over-expressed AtRH2 and AtRH20 in Nicotiana benthamiana plants also expressing DI-AU-FP repRNA in the presence of Cucumber necrosis virus (CNV), a closely related tombusvirus that serves as a helper virus for the TBSV repRNA. The helper tombusvirus provides the p33 and p92 replication proteins in trans for the replication of repRNA and the de novo generated recRNAs in this system. We found that the Ded1p ortholog AtRH20 suppressed TBSV recRNA accumulation by ~2-fold, while AtRH2 increased recRNAs by ~2-fold (Fig. 8A). These data indicate that the different co-opted cellular helicases have opposite effects on TBSV recombination in plants. Over-expression of AtRH20 also suppressed the accumulation of the 5’-truncated DI-RIΔ degRNA and the further truncated degRNAs, ultimately resulting in ~3-fold less recRNA accumulation than in control plants (Fig. 8B, lanes 4–6 versus 1–3). Based on these results, we suggest that the roles of the two cellular helicases in plants are comparable to the functions of these helicases in vitro in the CFE assay and in yeast.

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Fig 8. Opposite effects of subverted cellular DEAD-box helicases on TBSV recombination in plants.

(A) Over-expression of AtRH2 or AtRH20 was done in N. benthamiana leaves by agroinfiltration. The same leaves were agro-infiltrated to co-express CNV helper virus and the DI-AU-FP repRNA from the 35S promoter. The control samples were obtained from leaves not expressing AtRH2 or AtRH20 proteins (lanes 5–8). Total RNA was extracted from leaves 4 days after agroinfiltration. The accumulation of repRNA, recRNAs and degRNA in N. benthamiana leaves was measured by Northern blotting (top panel), see Fig. 1 for details. The ribosomal RNA (rRNA) was used as a loading control and shown in agarose gel stained with ethidium-bromide (bottom panel). (B) Over-expression of AtRH20 inhibits recRNA formation from the degRNAs. AtRH20 was over-expressed in N. benthamiana leaves by agroinfiltration. The same leaves were co-agro-infiltrated to co-express CNV p33 and p92 replication proteins and the DI-RIΔ degRNA from the 35S promoter. The control samples were obtained from leaves not expressing AtRH20 protein (lanes 1–3). See further details in panel A.

https://doi.org/10.1371/journal.ppat.1004680.g008

Discussion

Viral RNA recombination and the generation of defective viral RNA molecules are thought to be chance events that take place during viral RNA replication. It is possible that RNA viruses regulate these unique processes to guarantee the efficient replication of the full-length viral RNA and to reduce the competition of various viral RNAs for viral- and host factors. Accordingly, the role of viral replicase proteins in viral RNA recombination and defective RNA generation has been documented before [4,66–71]. However, based on systematic genome-wide screens performed with TBSV in yeast surrogate host [8,9], a new concept on the key roles of cellular factors in viral RNA recombination and defective RNA generation is emerging [5,15–18,58,65]. Among such cellular factors are DEAD-box helicases as demonstrated in this paper.

DDX3-like Ded1 DEAD-box helicase is a strong suppressor of tombusvirus RNA recombination in yeast

This work based on genetic approaches with Ded1p ts mutants or depletion of Ded1p in yeast and in vitro approaches with cell-free replication of TBSV RNAs strongly supports a TBSV recombination suppressor activity of the co-opted Ded1p cellular helicase. Since the ATPase-deficient D1 mutant of Ded1p does not have recombination suppressor activity in vitro (Fig. 4), it seems that Ded1p helicase has a direct inhibitory function in TBSV RNA recombination. The AtRH20 helicase, a plant ortholog of Ded1p, also has similar recombination suppressor activity in yeast and in plants. Importantly, the recombination suppressor activity of Ded1p is independent of the recombination suppressor activity of the previously characterized Xrn1p 5’-to-3’ exoribonuclease, which acts by efficiently removing degRNAs and recRNAs generated during TBSV replication (Fig. 6) [16–18,65]. Altogether, Ded1p helicase is the first co-opted cellular factor in the viral replicase complex that has been shown to directly affect viral (+)RNA recombination.

A novel role of Ded1 in maintaining genome integrity and in suppression of the replication of recRNAs and the 5’-truncated degRNAs

A previously demonstrated function of co-opted Ded1p helicase is to locally unwind the double-stranded RNA replication product after the (-) RNA synthesis is completed on the (+)RNA template (Fig. 9A) [49,50,54]. Ded1p then facilitates the loading of the viral replicase onto the 3’ end of the (-)-stranded RNA portion of the dsRNA intermediate with the assistance of the co-opted cellular glyceraldehyde-3-phosphate dehydrogenase (GAPDH) [49,50,54]. Thus, ultimately, Ded1p promotes the asymmetrical (i.e., excess) production of new (+)-strand RNAs by allowing the selective use of the (-)RNA in the dsRNA intermediate template.

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Fig 9. Models showing the functions of subverted cellular DEAD-box helicases in TBSV replication and viral RNA recombination.

(A) We propose that the DDX3-like Ded1/AtRH20 helicase facilitates the release of the pausing viral RdRp (shown as p92) at the end of the template, leading to switch from (-)-strand synthesis to (+)-strand synthesis. The previously defined additional functions of Ded1p and the eIF4AIII-like AtRH2 helicase is to open the dsRNA at the promoter region (cPR plus promoter proximal replication enhancer, PPE REN, indicated by rectangles) and the RIII(-)replication enhancer, as shown schematically [49,54,61]. Also shown is the long-range RNA-RNA interaction between the RIII(-) REN and the cPR region, which is proposed to help repeated use of the (-)RNA of the dsRNA as template for (+)RNA synthesis. The hairpin structure indicates the critical RII(+)-SL sequence required for the p33 replication protein-driven recruitment of the viral (+)RNA into replication. The RI(+) and the complementary RI(-) RNA sequences bound by Ded1p are shown with wide bars. (B) Our model suggests that Ded1/AtRH20 suppresses viral RNA recombination by facilitating the release of the pausing p92 at the end of degRNA recombinogenic template (created by cellular nucleases as shown). This activity of Ded1p results in suppression of RNA recombination (template-switching by p92), see the boxed portion of the model. Depletion of Ded1p or when Ded1p is mutated (ded1–199ts), p92 could stay on the degRNA template that likely promotes template-switching to a new (+)degRNA as shown as acceptor degRNA or to the 3’ end of the same (+)degRNA. On the other hand, in the absence of Ded1p, the eIF4AIII-like AtRH2 helicase could facilitate (-)RNA synthesis by opening up the dsRNA intermediate of degRNA that might lead to re-loading p92 RdRp to the 3’end of the (+)-strand for a new round of (-)degRNA synthesis. Similar activity by AtRH2 on degRNA might also facilitate template-switching by p92 RdRp for more efficient recombination. Altogether, these models take into account the co-ordinated actions of the two groups of subverted cellular helicases during replication and recombination.

https://doi.org/10.1371/journal.ppat.1004680.g009

However, this work also reveals a new role of Ded1p in inhibition of (-)-strand synthesis, especially with those RNA templates that lack authentic 5’ sequences, such as degRNAs and recRNAs (Figs. 2–3). Interestingly, the amount of (-)recRNAs and (-)degRNAs far exceeds the DI-AU-FP (-)repRNA in Ded1p deficient yeast or in vitro when Ded1p mutant is present, while the (+)repRNA is more abundant than (+)recRNAs or (+)degRNAs (Figs. 2–3). In case of the highly efficient DI-72 repRNA, the (-)recRNAs and (-)degRNAs are only detected when Ded1p is depleted (Fig. 3). Thus, one major function of the co-opted wt Ded1p is to promote the efficient replication of only the full-length viral RNAs, while suppressing the replication of 5’-truncated viral RNAs, lacking critical cis-acting elements. This novel function of Ded1p in maintenance of genome integrity seems to be manifested during (-)-strand synthesis.

Ded1p-driven suppression of replication of degRNAs might be critical in cells loaded with cytosolic ribonucleases that likely generate many truncated viral RNAs. These defective RNAs could likely compete with the full-length viral RNAs for viral- and host factors, thus leading to reduced viral replication. However, the co-opted cellular Ded1p helicase facilitates proper replication of TBSV RNAs and protects TBSV from competition by defective viral genomes. Since Ded1p inhibits the replication of recRNAs or degRNAs lacking the authentic 5’ end sequence through blocking the (-)-strand synthesis on these RNA templates, lesser amount of defective viral dsRNAs could accumulate. The reduced amount of dsRNA is an advantage for the virus, because dsRNAs could efficiently trigger antiviral responses, such as RNAi (or RNA silencing in plants) [72–74].

The co-opted eIF4AIII-like AtRH2 helicase facilitates viral RNA recombination and promotes the replication of the 5’-truncated viral RNAs

Another surprising finding in this study is the stimulatory effect of a second group of co-opted cellular DEAD-box helicases on TBSV RNA recombination. Accordingly, over-expression of the eIF4AIII-like AtRH2 in yeast or plant cells led to increased level of recRNA accumulation (Figs. 7–8).

The AtRH2 helicase binds to the 5’ proximal region of the viral (-)RNA, which harbors the RIII(-) REN, resulting in localized unwinding of the dsRNA replication intermediate [50,54]. Although this unwinding process is important for the replication of the full-length TBSV RNA, it seems that it only works “properly” for TBSV replication when Ded1p/AtRH20 helicase is also present in the replicase complex. Based on these observations, the emerging concept is that the coordinated action of these two co-opted cellular helicases is required for efficient replication of the full-length viral RNA. If Ded1p is missing or the eIF4AIII-like AtRH2 is present in excess amount within the replicase complex, then the frequency of viral RNA recombination increases and replication of 5’-truncated viral degRNAs becomes more efficient. Therefore, these conditions favor the rapid evolution of TBSV, which could be advantageous under some circumstances, but disadvantageous when the wt TBSV is the best-adapted to the host/environment.

Model for the co-opted cellular helicases in TBSV replication, viral RNA recombination and maintenance of viral genome integrity

Previous works revealed roles for Ded1p/AtRH20 and AtRH2 DEAD-box helicases during TBSV (+)-strand synthesis [49,54], which was based on local unwinding of the dsRNA replication intermediate to facilitate initiation of (+)-strand synthesis by the viral replicase (Fig. 9A). However, this work unearthed a novel function for Ded1p helicase by showing an increased level of (-)RNA production from recRNAs and degRNAs in yeast expressing mutant Ded1p or with depleted level of Ded1p. To explain these findings, we propose that Ded1p helicase facilitates the displacement of the viral p92 RdRp protein from the dsRNA product at the end of (-)-strand synthesis, as shown schematically in Fig. 9A. In case of the full-length viral RNA, the localized unwinding of the “left side” of the dsRNA then promotes the association of the p92 RdRp with the 3’ cis-acting elements in the (-)RNA portion of dsRNA, followed by (+)-strand synthesis via strand-displacement mechanism as shown before [50]. Thus, basically, Ded1p/AtRH20 helicases could promote the switch from (-)- to (+)-strand synthesis.

In case of the 5’-truncated RNAs, Ded1p/AtRH20 helicases could likely displace the p92 RdRp from the 5’ end of the degRNAs (Fig. 9B). Displacement of p92 RdRp from the template would likely inhibit template-switching events during (-)-strand synthesis. Accordingly, in vitro assays support this model by providing evidence that Ded1p promotes dissociation of p92 RdRp from the viral RNA (Fig. 5). Moreover, Ded1p helicase might not be able to open the ds degRNA to facilitate initiation of (+)-strand synthesis due to the absence of RI(-) sequence (i.e. Ded1p binding sequence) in the (-)degRNA [49]. Indeed, all degRNAs identified lack the authentic 3’ end viral sequences in the (-)RNA [15,18,65]. Based on these, we propose that Ded1p helicase suppresses the use of 5’-truncated degRNAs in (+)-strand synthesis. Overall, the p92 displacement ability of Ded1p likely inhibits template-switching RNA recombination and the replication of recRNAs (Fig. 9B).

However, when Ded1p is depleted or mutant Ded1p is present, then p92 RdRp protein will not be efficiently displaced from the dsRNA [after finishing (-)RNA synthesis on the (+)RNA template], and this condition then facilitates template-switching-based RNA recombination (Fig. 9B). In addition, the replication of degRNAs and recRNAs is also increased in the absence of functional Ded1p, likely due to the presence of AtRH2 type helicase in the VRCs, which facilitates unwinding of the “right-side” of the dsRNA template, thus promoting re-initiation on the plus-strands of dsRNA templates to generate new minus-strands (Fig. 9B). AtRH2 cannot facilitate re-initiation on the (+)RNA when Ded1/AtRH20 is present due to the recruitment of p92 to the (-) 3’-end sequences by Ded1p, long-range RNA-RNA interactions and additional cellular factors, such as GAPDH, as described earlier [54]. Altogether, the above events could explain the increased level of (-)RNAs from degRNAs and recRNAs in yeast either expressing mutant Ded1p or with depleted Ded1p.

Overall, the novel function of the DDX3-like Ded1p/RH20 helicases is the down-regulation/inhibition of (-)RNA synthesis by promoting the efficient switch from (-)RNA to (+)RNA synthesis. Interestingly, this feature requires the authentic viral 3’ end sequences on the (-)RNA, suggesting similarities between telomeres and viral RNA synthesis in protection of the ends of linear nucleic acids [75,76]. Those viral RNAs lacking the authentic terminal sequences could replicate less efficiently in the presence of Ded1p/AtRH20 helicases, suggesting that TBSV recruits a cellular helicase to protect and promote the replication of the full-length viral RNAs, while suppressing the accumulation of recRNAs and degRNAs during viral infections. Therefore, based on this work, a new concept emerges on the roles of co-opted cellular helicases in maintaining viral genome integrity.

Materials and Methods

Yeast strains and expression plasmids

The yeast (Saccharomyces cerevisiae) strain BY4741 (MATa his3(1 leu2(0 met15Δ0 ura3(0), R1158 and TET::DED1 (yTHC library) were obtained from Open Biosystems. The temperature-sensitive (ts) yeast strains ded1–95ts and ded1–199ts were of generous gift from C. Boone (U. Toronto).

The yeast expression plasmids LpGAD-His92 (containing CNV p92pol gene behind the CUP1 promoter, LEU2 selection), and HpHisGBK-His33/DI-AU-FP (co-expressing p33 from the CUP1 promoter and DI-AU-FP repRNA from GAL1 promoter, HIS3 selection), HpHisGBK-HFHis33/DI-72 (co-expressing p33 from the CUP1 promoter and DI-72 repRNA from GAL1 promoter, HIS3 selection), UpGBK-His33/DI-AU-FP (co-expressing p33 from the ADH1 promoter and DI-AU-FP repRNA from GAL1 promoter, URA3 selection) have been previously described [8]. Plasmid HpGBK-His33/DI-RIIΔ70 was made by PCR-amplification of DI-72RIIΔ70 with primers #1546 (CCGCGAATTCACGGATTAGAAGCCGCCGAGCGGGT) and #1069 (CCGGTCGAGCTCTACCAGGTAATATACCACAACGTGTGT). The PCR product was restriction digested with EcoRI and SacI and ligated into the plasmid HpGBK-His33/DI-72 to replace the full-length DI-72 fragment.

The E. coli expression plasmids pMAL-Ded1, pMAL-D1, pMAL-D11 and pMAL-RH2 were prepared previously [49,54]. To prepare plasmids for expression of MBP-tagged Ded1p ts mutants, genomic DNA of ded1–95 or ded1–199 strains were used as templates in PCR with primers #3956 (CCAGCTGCAGTCACCACCAAGAAGAGTTG) and #3957 (CCAGGAATTCATGGCTGAACTGAGCGAACAAG). The PCR products were cloned into pMalc-2x vector at EcoRI and PstI sites. For GST-Ded1p expression, pMAL-Ded1 was used as a template in PCR with primers #4308 (TGGAACTTGGAATTGTTTACACCTTAGTCTGTTGACTTAA) and #4309 (CCAGCTCGAGTCACCACCAAGAAGAGTTG). The PCR products were cloned into pGEX-his-RE vector at SpeI and XhoI site.

The plant expression plasmids pGD-RH2, pGD-RH20, pGD-CNV and pGD-DI-AU-FP were described previously [54,65]. To obtain plasmids HpGBK-His-RH20 and HpGBK-His-RH2, the plasmids pMAL-RH20 or pMAL-RH2 [54,61], respectively, were used as templates in PCR with primers #4315 (CCAGGGATCCATGAGTGCATCATGGGCAG) and #4316 (CCAGCTGCAGCTAATCCCAAGCACTGGTC) for RH20; and #4816 (CCAGGGATCCATGGCGACAGCGAATCCTGG) and #5117 (CCAGCTGCAGTTAGATAAGATCAGCTACATTC) for RH2 open reading frames. The PCR products were cloned into HpGBK-His vector at BamHI and PstI sites.

Yeast transformation and cultivation

Yeast strains were co-transformed with plasmids by using the lithium acetate/ssDNA/polyethylene glycol method, and transformants were selected by complementation of auxotrophic markers [77]. For TBSV recombination assay in BY4741, ded1–95ts, ded1–199ts, R1158 and TET::DED1, yeast strains were co-transformed with LpGAD-His92 and HpGBK-His33/DI-AU-FP, HpGBK-His33/DI-RIIΔ70 or HpHisGBK-HFHis33/DI-72. The transformed BY4741, ded1–95ts, and ded1–199ts strains were pre-grown at 23°C overnight in SC-LH- (synthetic complete media without histidine and leucine) media with 2% galactose. Then, 50 μM CuSO4 was added to the yeast cultures to launch virus replication and recombination. Yeast was grown at either 23°C or 29°C for 24 h before sample collection for analysis. The transformed R1158 and TET::DED1 strains were pre-grown at 29°C overnight in SC-ULH- (synthetic complete media without uracil, histidine and leucine) media with 2% galactose containing 10 μg/ml doxycycline. Then, 50 μM CuSO4 was added to the yeast cultures to launch virus replication and recombination at 23°C or 29°C for 24 h.

In the complementation study, BY4741 and ded1–199ts strains were co-transformed with LpGAD-His92, UpGBK-His33/DI-AU-FP and the indicated plasmids (HpGBK-HisRH20 or HpGBK-HisRH2) expressing one of the host helicases. The transformed yeast strains were pre-grown at 23°C overnight in SC-ULH- media with 2% galactose, followed by the addition of 50 μM CuSO4 and culturing at 23°C or 29°C for 24 h.

For viral RNA stability assay, BY4741 ded1–95ts, and ded1–199ts strains were transformed with UpYC-DI-RIIΔ70 [18]. The transformed yeast strains were grown at 23°C in SC-U- media with 2% galactose. After 24 h, the cultures were re-suspended in SC-U- media with 2% glucose and grown at 23°C or 29°C. The samples were collected at given time points mentioned in figure legend.

To observe the TBSV DI-(RI RNA recombination profile in BY4741, (Xrn1, (Met22, and ded1–199ts yeast strains, they were co-transformed with HpGBK-His33, LpGAD-His92 and pYC2-DI-(RI. The transformed cultures were inoculated on to ULH-/glucose media and grown at 23°C for 12 hrs. Yeast cultures were collected by centrifugation and dissolved in ULH-/galactose media supplemented with 50 μM CuSO4. Cultures were grown at 23°C for two days before sample collection for RNA analysis.

Tombusvirus RNA analysis

TBSV RNA recombination was analyzed using total RNA extracted from yeast and plants. Standard RNA extraction and Northern blot analysis was performed as described in previous publication [78]. To detect TBSV (+)RNA or (-)RNA, we prepared 32P-labeled DI-72RIII/IV probe with in vitro T7-based transcription using PCR-amplified DNA obtained on HpGBK-His33/Gal1-DI-72 template with primers #22 (GTAATACGACTCACTATAGGGCTGCATTTCTGCAATGTTCC)/ #1165 (AGCGAGTAAGACAGACTCTTCA) for (+)RNA detection; and primers #18 (GTAATACGACTCACTATAGGAGAAAGCGAGTAAGACAG) / #1190 (GGGCTGCATTTCTGCAATG) for (-)RNA detection.

Typhoon FLA 9500 system (GE) and ImageQuant TL software were used to detect and quantify the bands in the gels. The repRNA and degRNA bands were identified based on molecular markers, while the recRNAs were identified based on previously characterized recRNAs [15,16,58,65]. Only the bands representing the major recRNAs (which are pointed at in figures) were quantified. All these RNAs were normalized based on ribosomal RNA level in all samples.

Recombinant protein purification from E coli

Recombinant MBP-tagged helicase proteins and MBP-tagged TBSV p33 and p92 replication proteins or MBP-p92Δ167N were expressed in E coli and purified as published before [49]. Briefly, the expression plasmids were transformed into E. coli strain BL21 (DE3) CodonPlus. Protein expression was induced by isopropyl-β-D-thiogalactopyranoside (IPTG) at 16°C for 8 h. After collection of the cultures by centrifugation at 4000 xg for 5 min, the cells were re-suspended and broken in reduced-salt column buffer (25 mM NaCl, 30 mM HEPES-KOH pH 7.4, 1 mM EDTA, 10 mM β-mercaptoethanol). The lysate was centrifuged at 14,000 rpm for 10 min to remove cell debris. Then, the supernatant was incubated with amylose resin (NEB) at 4°C for 1 h. After washing the resin with 50 ml reduced-salt column buffer (without β-mercaptoethanol), the recombinant proteins were eluted in maltose buffer (column buffer containing 0.18% (W/V) maltose).

In vitro replication assay using yeast membrane-enriched fractions

The membrane-enriched fraction (MEF) was obtained as published previously [62,78]. Briefly, yeast strains were transformed and grown as described above for TBSV recombination in yeast. Yeast cultures were collected and processed to obtain the MEFs containing the in vivo-assembled replicase complexes as previously described [78]. Each membrane fraction preparation was adjusted based on the relative amounts of His6-tagged p33 and comparable amounts of replicase (based on p33) from each preparation were used in the subsequent in vitro replicase assay. The replicase assay was performed as described [62,78]. Briefly, the in vitro assay (50 μl) contained 10 μl of the normalized MEF preparations, 10 mM DTT, 50 mM Tris-Cl pH 8.0, 10 mM MgCl2, 0.1 U RNase inhibitor, 1 mM ATP, 1 mM CTP, 1 mM GTP and 0.1 μl of α32P-UTP (3000 Ci/mmol). Reaction mixtures were incubated at 25°C for 3h, followed by phenol/chloroform extraction and isopropanol/ammonium acetate (10:1) precipitation. 32P-labeled RNA products were analyzed in 5% acrylamide/8 M urea gels. To detect the membrane associated RNA, membrane preparations that contained comparable amounts of replicase were used to extract the viral RNA by standard phenol/chloroform extraction and isopropanol/ammonium acetate (10:1) precipitation. Then, the RNAs were analyzed by Northern blotting with (+) or (-) RNA specific probes.

Yeast cell free extract (CFE) based in vitro replication assay

CFEs from BY4741 and TET::DED1 treated with 10 μg/ml doxycycline were prepared as described earlier [29,62] and adjusted to contain comparable amounts of total protein. The in vitro CFE-based assays were performed in 20 μl total volume containing 1 μl of adjusted CFE, 0.5 μg DI-72 (+), DI-RIIΔ70 (+) or DI-AU-FP (+)RNA transcripts (separately), 0.5 μg purified MBP-p33, 0.5 μg purified MBP-p92pol (both recombinant proteins were purified from E. coli) [79], 30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 5 mM magnesium acetate, 0.13 M sorbitol, 0.4 μl actinomycin D (5 mg/ml), 2 μl of 150 mM creatine phosphate, 0.2 μl of 10 mg/ml creatine kinase, 0.2 μl of RNase inhibitor, 0.2 μl of 1 M dithiothreitol (DTT), 2 μl of 10 mM ATP, CTP, and GTP and 0.25 mM UTP and 0.1 μl of 32P-UTP. 0.3 μg of MBP-Ded1, MBP-D1 or MBP-D11, respectively, was added to the assay to test their activities during viral RNA synthesis. Reaction mixtures were incubated for 3 h at 25°C, followed by phenol/chloroform extraction and isopropanol/ammonium acetate (10:1) precipitation. 32P-labeled RNA products were analyzed in 5% acrylamide/8 M urea gels [62].

Gel mobility shift assay

The 32P-labeled full-length DI-72 (-)RNA and the RI(+) RNA were generated as described [79]. Ded1p and ts mutants were incubated with 5 ng of 32P-labeled DI-72(-) RNA probe in a binding buffer (50 mM Tris-HCl [pH 8.2], 10 mM MgCl2, 1 mM EDTA, 10% glycerol, 200 ng of yeast tRNA [Sigma], and 2 U of RNase inhibitor [Ambion]) at 25°C for 15 min. After the binding, the samples were analyzed by 5% nondenaturing PAGE performed at 200 V for 1 h in a cold room. To test the template release activity, briefly, 32P-labeled RI(+)RNA probe was incubated with p92-Δ167N at 25°C for 15 min, followed by adding affinity-purified GST-Ded1p to the reaction with or without 1 mM ATP, then the reaction was incubated at 25°C for 30 min. In addition, probe was also incubated with proteins in a different order mentioned in figure legend.

Biotinylation and template release assay

First, p92-Δ167N RdRp assay was used to produce the biotin-labeled partial dsRNA product [21]. Briefly, the in vitro RdRp reaction was performed in 20 μl total volume containing 1 μl of adjusted CFE (soluble fraction only), 0.5 μg DI-mini (+)RNA transcript [21], 0.5 μg affinity-purified MBP-p92-Δ167N, 30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 5 mM magnesium acetate, 0.13 M sorbitol, 0.2 μl actinomycin D (5 mg/ml), 2 μl of 150 mM creatine phosphate, 0.2 μl of 10 mg/ml creatine kinase, 0.2 μl of RNase inhibitor, 0.2 μl of 1 M dithiothreitol (DTT), 2 μl of 10 mM ATP, CTP, and GTP and 0.1 mM UTP and 0.1 μl of biotin-UTP. Reaction mixture was incubated at 25°C for 30 min. Note that we combined 10 separate in vitro reactions in the subsequent experiment. After incubation, the free, unincorporated biotin-UTP was removed by Sepharose G-25 column. Then, 200 μl of in vitro RdRp reaction mixture were incubated with Strepavidin-beads (MagneSphere Magnetic Separation Products, Promega) at 25°C for 10 min to capture the biotin-labeled RNA and the RNA-bound p92-Δ167N RdRp as well. Then, we washed the beads once with 0.1% SSC buffer, followed by incubation of the beads with GST-Ded1p or GST (as a control) in RdRp buffer (10 mM DTT, 50 mM Tris–Cl pH 8.0, 10 mM MgCl2) with 1 mM ATP at 25°C for 10 min to elute (release) the p92-Δ167N RdRp from the streptavidin-bound RNA. Then, we collected and precipitated the eluted proteins with 10% TCA. The precipitated proteins (eluate fraction in Fig. 5C) were dissolved in 30 μl SDS buffer. We also recovered the p92-Δ167N RdRp from the streptavidin-bound RNA by boiling the beads in 30 μl SDS buffer for 5 min (SDS fraction in Fig. 5C). All the protein samples were analyzed by Western blotting method with anti-MBP antibody to detect the amount of p92-Δ167N RdRp in the obtained samples.

Tombusvirus recombination in Nicotiana benthamiana

Cultures of Agrobacterium tumefaciens C58C1 strain carrying pGD-RH2 or pGD-RH20 were used for transient expression of Arabidopsis thaliana RH2 and RH20 [54,61]. N. benthamiana plants were infiltrated with A. tumefaciens carrying pGD-RH2 (OD600 = 0.3) or pGD-RH20 (OD600 = 0.3) together with pGD-CNV (OD600 = 0.3) and pGD-DI-AU-FP (OD600 = 0.3) to launch tombusvirus replication and induce RNA recombination. Leaf infiltration with A. tumefaciens carrying “empty” pGD plasmid was used as a control. We also performed agroinfiltration with pGD-p33 + pGD-p92+ pGD-DI-ΔRI at a final concentration of 0.3 (OD600). Three and four days after agro-infiltration, samples from the agro-infiltrated leaves were collected from the agroinfiltrated leaves. Total RNA was extracted and Northern blot analysis was performed as previously described [16].

Acknowledgments

We thank Drs. Judit Pogany and Nick Kovalev for comments on the manuscript. Ded1 mutants are the generous gift of Dr. N.K. Tanner (Centre Médical Universitaire, Geneva, Switzerland).

Author Contributions

Conceived and designed the experiments: CC KRP PDN. Performed the experiments: CC KRP. Analyzed the data: CC KRP PDN. Contributed reagents/materials/analysis tools: CC KRP. Wrote the paper: CC KRP PDN.

References

  1. 1. Worobey M, Holmes EC (1999) Evolutionary aspects of recombination in RNA viruses. J Gen Virol 80 (Pt 10): 2535–2543. pmid:10573145
  2. 2. Scheel TK, Galli A, Li YP, Mikkelsen LS, Gottwein JM, et al. (2013) Productive homologous and non-homologous recombination of hepatitis C virus in cell culture. PLoS Pathog 9: e1003228. pmid:23555245
  3. 3. Roossinck MJ (2003) Plant RNA virus evolution. Curr Opin Microbiol 6: 406–409. pmid:12941413
  4. 4. Nagy PD, Simon AE (1997) New insights into the mechanisms of RNA recombination. Virology 235: 1–9. pmid:9300032
  5. 5. Nagy PD (2011) The roles of host factors in tombusvirus RNA recombination. Adv Virus Res 81: 63–84. pmid:22094079
  6. 6. Rao AL, Hall TC (1993) Recombination and polymerase error facilitate restoration of infectivity in brome mosaic virus. J Virol 67: 969–979. pmid:8419651
  7. 7. Nagy PD, Carpenter CD, Simon AE (1997) A novel 3′-end repair mechanism in an RNA virus. Proc Natl Acad Sci U S A 94: 1113–1118. pmid:9037015
  8. 8. Serviene E, Jiang Y, Cheng CP, Baker J, Nagy PD (2006) Screening of the yeast yTHC collection identifies essential host factors affecting tombusvirus RNA recombination. J Virol 80: 1231–1241. pmid:16415000
  9. 9. Serviene E, Shapka N, Cheng CP, Panavas T, Phuangrat B, et al. (2005) Genome-wide screen identifies host genes affecting viral RNA recombination. Proc Natl Acad Sci U S A 102: 10545–10550. pmid:16027361
  10. 10. Nagy PD, Pogany J (2012) The dependence of viral RNA replication on co-opted host factors. Nature Reviews Microbiology 10: 137–149. pmid:22183253
  11. 11. Nagy PD, Barajas D, Pogany J (2012) Host factors with regulatory roles in tombusvirus replication. Curr Opin Virol 2: 685–692.
  12. 12. Nagy PD, Pogany J (2010) Global genomics and proteomics approaches to identify host factors as targets to induce resistance against Tomato bushy stunt virus. Adv Virus Res 76: 123–177. pmid:20965073
  13. 13. Li Z, Barajas D, Panavas T, Herbst DA, Nagy PD (2008) Cdc34p Ubiquitin-Conjugating Enzyme Is a Component of the Tombusvirus Replicase Complex and Ubiquitinates p33 Replication Protein. J Virol 82: 6911–6926. pmid:18463149
  14. 14. Jaag HM, Stork J, Nagy PD (2007) Host transcription factor Rpb11p affects tombusvirus replication and recombination via regulating the accumulation of viral replication proteins. Virology 368: 388–404. pmid:17689583
  15. 15. Jaag HM, Pogany J, Nagy PD (2010) A host Ca2+/Mn2+ ion pump is a factor in the emergence of viral RNA recombinants. Cell Host Microbe 7: 74–81. pmid:20114029
  16. 16. Jaag HM, Nagy PD (2009) Silencing of Nicotiana benthamiana Xrn4p exoribonuclease promotes tombusvirus RNA accumulation and recombination. Virology 386: 344–352. pmid:19232421
  17. 17. Cheng CP, Jaag HM, Jonczyk M, Serviene E, Nagy PD (2007) Expression of the Arabidopsis Xrn4p 5′-3′ exoribonuclease facilitates degradation of tombusvirus RNA and promotes rapid emergence of viral variants in plants. Virology 368: 238–248. pmid:17688902
  18. 18. Cheng CP, Serviene E, Nagy PD (2006) Suppression of viral RNA recombination by a host exoribonuclease. J Virol 80: 2631–2640. pmid:16501073
  19. 19. Jiang Y, Cheng CP, Serviene E, Shapka N, Nagy PD (2010) Repair of lost 5′ terminal sequences in tombusviruses: Rapid recovery of promoter- and enhancer-like sequences in recombinant RNAs. Virology 404: 96–105. pmid:20537671
  20. 20. Panaviene Z, Panavas T, Nagy PD (2005) Role of an internal and two 3′-terminal RNA elements in assembly of tombusvirus replicase. J Virol 79: 10608–10618. pmid:16051853
  21. 21. Pogany J, Nagy PD (2012) p33-Independent Activation of a Truncated p92 RNA-Dependent RNA Polymerase of Tomato Bushy Stunt Virus in Yeast Cell-Free Extract. J Virol 86: 12025–12038. pmid:22933278
  22. 22. Panaviene Z, Baker JM, Nagy PD (2003) The overlapping RNA-binding domains of p33 and p92 replicase proteins are essential for tombusvirus replication. Virology 308: 191–205. pmid:12706102
  23. 23. Oster SK, Wu B, White KA (1998) Uncoupled expression of p33 and p92 permits amplification of tomato bushy stunt virus RNAs. J Virol 72: 5845–5851. pmid:9621045
  24. 24. Scholthof KB, Scholthof HB, Jackson AO (1995) The tomato bushy stunt virus replicase proteins are coordinately expressed and membrane associated. Virology 208: 365–369. pmid:11831721
  25. 25. Monkewich S, Lin HX, Fabian MR, Xu W, Na H, et al. (2005) The p92 polymerase coding region contains an internal RNA element required at an early step in Tombusvirus genome replication. J Virol 79: 4848–4858. pmid:15795270
  26. 26. Panavas T, Hawkins CM, Panaviene Z, Nagy PD (2005) The role of the p33:p33/p92 interaction domain in RNA replication and intracellular localization of p33 and p92 proteins of Cucumber necrosis tombusvirus. Virology.
  27. 27. Pogany J, White KA, Nagy PD (2005) Specific binding of tombusvirus replication protein p33 to an internal replication element in the viral RNA is essential for replication. J Virol 79: 4859–4869. pmid:15795271
  28. 28. Stork J, Kovalev N, Sasvari Z, Nagy PD (2011) RNA chaperone activity of the tombusviral p33 replication protein facilitates initiation of RNA synthesis by the viral RdRp in vitro. Virology 409: 338–347. pmid:21071052
  29. 29. Pogany J, Stork J, Li Z, Nagy PD (2008) In vitro assembly of the Tomato bushy stunt virus replicase requires the host Heat shock protein 70. Proc Natl Acad Sci U S A 105: 19956–19961. pmid:19060219
  30. 30. Shah Nawaz-Ul-Rehman M, Reddisiva Prasanth K, Baker J, Nagy PD (2013) Yeast screens for host factors in positive-strand RNA virus replication based on a library of temperature-sensitive mutants. Methods 59: 207–216. pmid:23147170
  31. 31. Shah Nawaz-Ul-Rehman M, Martinez-Ochoa N, Pascal H, Sasvari Z, Herbst C, et al. (2012) Proteome-wide overexpression of host proteins for identification of factors affecting tombusvirus RNA replication: an inhibitory role of protein kinase C. J Virol 86: 9384–9395. pmid:22718827
  32. 32. Mendu V, Chiu M, Barajas D, Li Z, Nagy PD (2010) Cpr1 cyclophilin and Ess1 parvulin prolyl isomerases interact with the tombusvirus replication protein and inhibit viral replication in yeast model host. Virology 406: 342–351. pmid:20709345
  33. 33. Li Z, Pogany J, Panavas T, Xu K, Esposito AM, et al. (2009) Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor. Virology 385: 245–260. pmid:19131084
  34. 34. Jiang Y, Serviene E, Gal J, Panavas T, Nagy PD (2006) Identification of essential host factors affecting tombusvirus RNA replication based on the yeast Tet promoters Hughes Collection. J Virol 80: 7394–7404. pmid:16840320
  35. 35. Panavas T, Serviene E, Brasher J, Nagy PD (2005) Yeast genome-wide screen reveals dissimilar sets of host genes affecting replication of RNA viruses. Proc Natl Acad Sci U S A 102: 7326–7331. pmid:15883361
  36. 36. Linder P, Lasko P (2006) Bent out of shape: RNA unwinding by the DEAD-box helicase Vasa. Cell 125: 219–221. pmid:16630807
  37. 37. Cordin O, Banroques J, Tanner NK, Linder P (2006) The DEAD-box protein family of RNA helicases. Gene 367: 17–37. pmid:16337753
  38. 38. Linder P (2008) mRNA export: RNP remodeling by DEAD-box proteins. Curr Biol 18: R297–299. pmid:18397738
  39. 39. Ranji A, Boris-Lawrie K (2010) RNA helicases: emerging roles in viral replication and the host innate response. RNA Biol 7: 775–787. pmid:21173576
  40. 40. Huang TS, Wei T, Laliberte JF, Wang A (2010) A host RNA helicase-like protein, AtRH8, interacts with the potyviral genome-linked protein, VPg, associates with the virus accumulation complex, and is essential for infection. Plant Physiol 152: 255–266. pmid:19880609
  41. 41. Garbelli A, Radi M, Falchi F, Beermann S, Zanoli S, et al. (2011) Targeting the human DEAD-box polypeptide 3 (DDX3) RNA helicase as a novel strategy to inhibit viral replication. Curr Med Chem 18: 3015–3027. pmid:21651478
  42. 42. Upadya MH, Aweya JJ, Tan YJ (2014) Understanding the interaction of hepatitis C virus with host DEAD-box RNA helicases. World J Gastroenterol 20: 2913–2926. pmid:24659882
  43. 43. Noueiry AO, Chen J, Ahlquist P (2000) A mutant allele of essential, general translation initiation factor DED1 selectively inhibits translation of a viral mRNA. Proc Natl Acad Sci U S A 97: 12985–12990. pmid:11069307
  44. 44. Bolinger C, Sharma A, Singh D, Yu L, Boris-Lawrie K (2010) RNA helicase A modulates translation of HIV-1 and infectivity of progeny virions. Nucleic Acids Res 38: 1686–1696. pmid:20007598
  45. 45. Umate P, Tuteja R, Tuteja N (2010) Genome-wide analysis of helicase gene family from rice and Arabidopsis: a comparison with yeast and human. Plant Mol Biol 73: 449–465. pmid:20383562
  46. 46. Kant P, Kant S, Gordon M, Shaked R, Barak S (2007) STRESS RESPONSE SUPPRESSOR1 and STRESS RESPONSE SUPPRESSOR2, two DEAD-box RNA helicases that attenuate Arabidopsis responses to multiple abiotic stresses. Plant Physiol 145: 814–830. pmid:17556511
  47. 47. Dalmay T, Horsefield R, Braunstein TH, Baulcombe DC (2001) SDE3 encodes an RNA helicase required for post-transcriptional gene silencing in Arabidopsis. EMBO J 20: 2069–2078. pmid:11296239
  48. 48. Jankowsky E (2011) RNA helicases at work: binding and rearranging. Trends Biochem Sci 36: 19–29. pmid:20813532
  49. 49. Kovalev N, Pogany J, Nagy PD (2012) A Co-Opted DEAD-Box RNA Helicase Enhances Tombusvirus Plus-Strand Synthesis. PLoS Pathog 8: e1002537. pmid:22359508
  50. 50. Kovalev N, Pogany J, Nagy PD (2014) Template role of double-stranded RNA in tombusvirus replication. J Virol 88: 5638–5651. pmid:24600009
  51. 51. Weaver PL, Sun C, Chang TH (1997) Dbp3p, a putative RNA helicase in Saccharomyces cerevisiae, is required for efficient pre-rRNA processing predominantly at site A3. Mol Cell Biol 17: 1354–1365. pmid:9032262
  52. 52. Garcia I, Albring MJ, Uhlenbeck OC (2012) Duplex destabilization by four ribosomal DEAD-box proteins. Biochemistry 51: 10109–10118. pmid:23153376
  53. 53. Alexandrov A, Colognori D, Steitz JA (2011) Human eIF4AIII interacts with an eIF4G-like partner, NOM1, revealing an evolutionarily conserved function outside the exon junction complex. Genes Dev 25: 1078–1090. pmid:21576267
  54. 54. Kovalev N, Nagy PD (2014) The Expanding Functions of Cellular Helicases: The Tombusvirus RNA Replication Enhancer Co-opts the Plant eIF4AIII-Like AtRH2 and the DDX5-Like AtRH5 DEAD-Box RNA Helicases to Promote Viral Asymmetric RNA Replication. PLoS Pathog 10: e1004051. pmid:24743583
  55. 55. Panavas T, Nagy PD (2005) Mechanism of stimulation of plus-strand synthesis by an RNA replication enhancer in a tombusvirus. J Virol 79: 9777–9785. pmid:16014939
  56. 56. Chuang RY, Weaver PL, Liu Z, Chang TH (1997) Requirement of the DEAD-Box protein ded1p for messenger RNA translation. Science 275: 1468–1471. pmid:9045610
  57. 57. Burckin T, Nagel R, Mandel-Gutfreund Y, Shiue L, Clark TA, et al. (2005) Exploring functional relationships between components of the gene expression machinery. Nat Struct Mol Biol 12: 175–182. pmid:15702072
  58. 58. Jaag HM, Lu Q, Schmitt ME, Nagy PD (2011) Role of RNase MRP in viral RNA degradation and RNA recombination. J Virol 85: 243–253. pmid:20962095
  59. 59. White KA, Nagy PD (2004) Advances in the molecular biology of tombusviruses: gene expression, genome replication, and recombination. Prog Nucleic Acid Res Mol Biol 78: 187–226. pmid:15210331
  60. 60. Panavas T, Nagy PD (2003) Yeast as a model host to study replication and recombination of defective interfering RNA of Tomato bushy stunt virus. Virology 314: 315–325. pmid:14517084
  61. 61. Kovalev N, Barajas D, Nagy PD (2012) Similar roles for yeast Dbp2 and Arabidopsis RH20 DEAD-box RNA helicases to Ded1 helicase in tombusvirus plus-strand synthesis. Virology 432: 470–484. pmid:22832121
  62. 62. Pogany J, Nagy PD (2008) Authentic replication and recombination of Tomato bushy stunt virus RNA in a cell-free extract from yeast. J Virol 82: 5967–5980. pmid:18417594
  63. 63. Banroques J, Doere M, Dreyfus M, Linder P, Tanner NK (2010) Motif III in superfamily 2 “helicases” helps convert the binding energy of ATP into a high-affinity RNA binding site in the yeast DEAD-box protein Ded1. J Mol Biol 396: 949–966. pmid:20026132
  64. 64. Linder P, Jankowsky E (2011) From unwinding to clamping—the DEAD box RNA helicase family. Nat Rev Mol Cell Biol 12: 505–516. pmid:21779027
  65. 65. Jaag HM, Nagy PD (2010) The combined effect of environmental and host factors on the emergence of viral RNA recombinants. PLoS Pathog 6: e1001156. pmid:20975943
  66. 66. Cheng CP, Panavas T, Luo G, Nagy PD (2005) Heterologous RNA replication enhancer stimulates in vitro RNA synthesis and template-switching by the carmovirus, but not by the tombusvirus, RNA-dependent RNA polymerase: implication for modular evolution of RNA viruses. Virology 341: 107–121. pmid:16083933
  67. 67. Panaviene Z, Nagy PD (2003) Mutations in the RNA-binding domains of tombusvirus replicase proteins affect RNA recombination in vivo. Virology 317: 359–372. pmid:14698673
  68. 68. Cheng CP, Nagy PD (2003) Mechanism of RNA recombination in carmo- and tombusviruses: evidence for template switching by the RNA-dependent RNA polymerase in vitro. J Virol 77: 12033–12047. pmid:14581540
  69. 69. Figlerowicz M, Nagy PD, Tang N, Kao CC, Bujarski JJ (1998) Mutations in the N terminus of the brome mosaic virus polymerase affect genetic RNA-RNA recombination. J Virol 72: 9192–9200. pmid:9765466
  70. 70. Nagy PD, Dzianott A, Ahlquist P, Bujarski JJ (1995) Mutations in the helicase-like domain of protein 1a alter the sites of RNA-RNA recombination in brome mosaic virus. J Virol 69: 2547–2556. pmid:7884905
  71. 71. Kim MJ, Kao C (2001) Factors regulating template switch in vitro by viral RNA-dependent RNA polymerases: implications for RNA-RNA recombination. Proc Natl Acad Sci U S A 98: 4972–4977. pmid:11309487
  72. 72. Ding SW (2010) RNA-based antiviral immunity. Nat Rev Immunol 10: 632–644. pmid:20706278
  73. 73. Pumplin N, Voinnet O (2013) RNA silencing suppression by plant pathogens: defence, counter-defence and counter-counter-defence. Nat Rev Microbiol 11: 745–760. pmid:24129510
  74. 74. Szittya G, Burgyan J (2013) RNA interference-mediated intrinsic antiviral immunity in plants. Curr Top Microbiol Immunol 371: 153–181. pmid:23686235
  75. 75. Gunes C, Rudolph KL (2013) The role of telomeres in stem cells and cancer. Cell 152: 390–393. pmid:23374336
  76. 76. Nandakumar J, Cech TR (2013) Finding the end: recruitment of telomerase to telomeres. Nat Rev Mol Cell Biol 14: 69–82. pmid:23299958
  77. 77. Chuang C, Barajas D, Qin J, Nagy PD (2014) Inactivation of the Host Lipin Gene Accelerates RNA Virus Replication through Viral Exploitation of the Expanded Endoplasmic Reticulum Membrane. PLoS Pathog 10: e1003944. pmid:24586157
  78. 78. Barajas D, Li Z, Nagy PD (2009) The Nedd4-type Rsp5p ubiquitin ligase inhibits tombusvirus replication by regulating degradation of the p92 replication protein and decreasing the activity of the tombusvirus replicase. J Virol 83: 11751–11764. pmid:19759160
  79. 79. Rajendran KS, Nagy PD (2003) Characterization of the RNA-binding domains in the replicase proteins of tomato bushy stunt virus. J Virol 77: 9244–9258. pmid:12915540