- Research article
- Open Access
Heterologous expression of plant virus genes that suppress post-transcriptional gene silencing results in suppression of RNA interference in Drosophilacells
© Reavy et al; licensee BioMed Central Ltd. 2004
- Received: 22 May 2003
- Accepted: 25 August 2004
- Published: 25 August 2004
RNA interference (RNAi) in animals and post-transcriptional gene silencing (PTGS) in plants are related phenomena whose functions include the developmental regulation of gene expression and protection from transposable elements and viruses. Plant viruses respond by expressing suppressor proteins that interfere with the PTGS system.
Here we demonstrate that both transient and constitutive expression of the Tobacco etch virus HC-Pro silencing suppressor protein, which inhibits the maintenance of PTGS in plants, prevents dsRNA-induced RNAi of a lacZ gene in cultured Drosophila cells. Northern blot analysis of the RNA present in Drosophila cells showed that HC-Pro prevented degradation of lacZ RNA during RNAi but that there was accumulation of the short (23nt) RNA species associated with RNAi. A mutant HC-Pro that does not suppress PTGS in plants also does not affect RNAi in Drosophila. Similarly, the Cucumber mosaic virus 2b protein, which inhibits the systemic spread of PTGS in plants, does not suppress RNAi in Drosophila cells. In addition, we have used the Drosophila system to demonstrate that the 16K cysteine-rich protein of Tobacco rattle virus, which previously had no known function, is a silencing suppressor protein.
These results indicate that at least part of the process of RNAi in Drosophila and PTGS in plants is conserved, and that plant virus silencing suppressor proteins may be useful tools to investigate the mechanism of RNAi.
- Cucumber Mosaic Virus
- lacZ Gene
- Tobacco Rattle Virus
- Tobacco Etch Virus
- Drosophila Cell
RNA interference (RNAi) is a process in which the introduction of dsRNAs into cells leads to inactivation of expression of genes containing homologous sequences by sequence-specific degradation of mRNA (for reviews see [1, 2]). RNAi has been observed in a variety of organisms, including fruit fly, nematodes, zebrafish, mice and humans [3–7], and is mechanistically similar to post-transcriptional gene silencing (PTGS) in plants  and quelling in fungi . Genetic studies have identified a number of the proteins that are involved in these processes in Neurospora crassa [10–12], Caenorhabditis elegans [13–15] and Arabidopsis thaliana [16–18]. dsRNA has been shown to induce RNAi in cultured Drosophila cells [19–22] and biochemical studies of this system have revealed the involvement of two distinct activities; an RNA-induced silencing complex (RISC), containing both nuclease activity and RNA that carries out enzymatic degradation of target RNA , and an RNase III-like protein (Dicer) that is involved in production of short (22 nucleotide) guide RNAs from dsRNA as an early step in the RNAi process .
PTGS in plants can operate as a defence mechanism against virus infection (for reviews see [8, 23]) and numerous plant viruses encode silencing suppressors, which are thought to have developed as a response to the plant PTGS system . Plant virus-encoded silencing suppressors may target different components of the PTGS system. The HC-Pro protein, encoded by potyviruses such as Tobacco etch virus (TEV), was initially characterised as a determinant of virus movement in plants  and subsequently was shown to inhibit silencing of transgenes in transformed plants . HC-Pro antagonizes silencing in all tissues  and appears to target a step involved in the maintenance of silencing . In contrast, the 2b protein encoded by Cucumber mosaic virus (CMV), a cucumovirus, interferes with the systemic spread of the silencing signal, preventing initiation of silencing in newly emerging tissues . A survey of a small number of other different plant viruses showed that the comovirus Cowpea mosaic virus, the geminivirus African cassava mosaic virus, the potexvirus Narcissus mosaic virus, the tobamovirus TMV, the sobemovirus Rice yellow mottle virus (RYMV), the tombusvirus Tomato bushy stunt virus (TBSV) and the tobravirus Tobacco rattle virus (TRV) also were able to suppress GFP silencing . Although in this study the potexvirus PVX did not suppress silencing, using a different assay these authors showed that PVX is in fact able to prevent systemic silencing . Thus, it seems probable that many plant viruses encode proteins that allow them to evade or inhibit PTGS in certain plant species, and that different suppressor proteins target different parts of the PTGS pathway. An amenable system for studying these suppressor proteins would be an aid in determining the molecular basis of their action. Recently it has been demonstrated that an insect virus, flock house virus (FHV) encodes a protein, 2b, which acts as a suppressor of PTGS in plants . We have investigated the effects on RNAi in cultured Drosophila cells of expression of some silencing suppressors from plant viruses.
Effects of transient expression of the TEV HC-Pro and CMV 2b proteins on RNAi in Drosophilacells
Effects of plant virus gene silencing suppressors on RNAi in Drosophila cells.
% cells stained *
82.86 ± 9.12
pMT/V5-His/lacZ + dsRNA
17.70 ± 4.25
pMT/V5-His/lacZ + dsRNA + pMT-HC-Pro
45.78 ± 4.89
pMT/V5-His/lacZ + dsRNA + pMT-HC-Pro-K
14.62 ± 2.81
pMT/V5-His/lacZ + dsRNA + pMT-2b
11.13 ± 1.58
pMT/V5-His/lacZ + dsRNA + pMT-16K
47.25 ± 3.4
42.04 ± 3.07
pMT/V5-His/lacZ + dsRNA
31.70 ± 2.46
40.67 ± 2.36
pMT/V5-His/lacZ + dsRNA
6.50 ± 1.2
41.16 ± 2.36
pMT/V5-His/lacZ + dsRNA
9.17 ± 2.56
RNAi in stable cell lines expressing TEV HC-Pro or CMV 2b
Similar results were obtained when the DS2-2b cells were grown in the presence of CuSO4 to induce expression of the virus protein before transfection with pMT/V5-His/lacZ and dsRNA, indicating that the CMV 2b protein could suppress neither the initiation nor the maintenance of the dsRNA-induced silencing in the Drosophila cells.
Identification of silencing suppression in Drosophilacells by another plant virus protein
We were interested to determine if the Drosophila cell system could be used as a screen for RNAi suppression effects caused by other virus proteins. We chose to examine the potential RNAi suppression activity of a protein from the tobravirus TRV. This virus is able to suppress transgene silencing in plants  but the specific viral protein responsible for this activity has not been identified. TRV, like the other tobraviruses has a bipartite, positive strand RNA genome , however, the larger RNA (RNA1) can infect plants systemically in the absence of RNA2 to produce what is known as an NM-infection. This occurs frequently in particular cultivars of potato and is often associated with increased symptom severity. Clearly, therefore, RNA1 encodes all the functions necessary for virus multiplication including, possibly, suppression of PTGS/host defence. The one protein encoded by RNA1 without an assigned function is a 16K cysteine-rich protein which was, thus, investigated as a candidate silencing suppressor protein.
One characteristic of plant virus silencing suppressor proteins is often significant enhancement of disease symptoms when they are over-expressed from a viral vector . Similar results were obtained from preliminary experiments showing that expression of the TRV 16K gene from a PVX vector did increase the severity of symptoms in infected plants. Inoculation of Nicotiana benthamiana plants with PVX alone initially induced vein chlorosis and systemic leaf curling, although the plants continued to grow. Inoculation with PVX carrying the 16K gene caused similar initial symptoms but led to tip necrosis and death of the plants .
The TRV 16K protein was expressed in Drosophila cells after transfection of cells with the expression plasmid pMT-16K, and the 16K protein could be detected by western blotting when the cells were induced with CuSO4 (Fig 2, lane 4) but not when cells were not induced (Fig 2, lane 3). A stably-transformed cell line (DS2-16k) containing pMT-16k behaved in a similar way (Fig 2, lanes 7, 8). No cross-reacting protein was detected in non-transfected cells (Fig 2, lanes 1,2). Co-transfection of pMT/V5-His/lacZ with dsRNA and pMT-16K resulted in ~47% of transfected cells staining blue (Table 1) compared to ~18% when transfected with pMT/V5-His/lacZ and dsRNA. The 16K protein therefore partially suppressed RNAi in Drosophila cells.
Detection of lacZgene transcripts
Detection of siRNAs
Suppression of RNAi in Drosophila cells by some plant virus proteins indicates that at least part of the processes of RNAi and PTGS is conserved between plants and Drosophila. TEV HC-Pro is one of a family of proteins that suppress PTGS in plants and the CMV 2b protein has a similar ability . These proteins are thought to target different components of the PTGS system, as the CMV 2b protein interferes with the spread of a silencing signal after initial induction of silencing, thus, preventing silencing from initiating in newly emerging leaves. The potyvirus HC-Pro protein, however, interferes with the maintenance of silencing in all tissues [26, 27]. These differences were reflected in the Drosophila cell system where HC-Pro could suppress RNAi but the 2b gene apparently was ineffective. As there is no spread of a silencing signal in cultured Drosophila cells, the failure of the CMV 2b protein to act in this system is not unexpected. It was also significant that a mutant version of HC-Pro (K) that is defective in suppression of gene silencing  but is effective in proteolytic cleavage  was also unable to suppress RNAi in Drosophila cells. This strongly supports the idea that the TEV HC-Pro protein targets the same component of the plant PTGS system and the Drosophila RNAi system. Our demonstration that the TRV 16K protein also is able to interfere with RNAi in Drosophila cells, leads us to suggest that many other plant virus silencing suppressor proteins are likely to be functional in this system.
SiRNAs were detected in our cell lines expressing HC-Pro and the TRV 16K protein even though suppression of silencing was observed. This is not totally unexpected for a number of possible reasons. Firstly, suppression of RNAi is partial in our cultures indicating that some RNAi, and presumably siRNA production, does occur in some of the cells. We have observed with cells expressing the lacZ gene alone that there is considerable variation in the amount of staining of individual cells indicating differences in the amount of gene expression in individual cells. There is no reason to suppose that this variability in gene expression is limited to the lacZ gene and it is possible that low levels of the suppressors may fail to inhibit silencing in some of the cells within a culture. Secondly, the experimental protocol requires a time delay between transfection of the cells with the lacZ plasmid and dsRNA before induction of expression of the suppressor proteins in order to allow the cells to recover from the transfection procedure. Some production of siRNAs from the dsRNA may possibly occur in cells during this lag period before the suppressors are induced. For these reasons the usefulness of the Drosophila RNAi system for studying the mechanisms of action of plant virus suppressor proteins may be limited.
Mutants of Arabidopsis that are impaired in PTGS have an increased susceptibility to CMV, showing that PTGS can operate as a defensive system that targets viruses . Plant virus-encoded silencing suppressors are thought to have developed as a response to this defensive aspect of the plant PTGS system, and subsequent studies have shown that, as would be expected, a wide variety of plant viruses encode silencing suppressors . The suppressors encoded by these viruses are unrelated in amino acid sequence, and are likely to act at different points in the silencing process, making them ideal probes to investigate the silencing machinery. We anticipate that using different suppressors from a wide range of viruses may permit a detailed examination of the biochemical process of RNAi in Drosophila and possibly other organisms as well as allowing detailed characterisation of the mode of action of the virus suppressor proteins. Furthermore, it is becoming apparent that RNAi or PTGS may play a role in processes other than defence against foreign RNAs. Transformation of plants with TEV HC-Pro or rgs-CaM, a plant-encoded PTGS-suppressor protein related to calmodulin, interrupted normal development and led to the formation of differentiated tumours at the stem/root junction . The Arabidopsis gene CARPEL FACTORY is related to Drosophila Dicer and is involved in plant development and fertility , and the EGO-1 gene of C. elegans also appears to have a role in both RNAi and germ-line development 15]. Components of the RNAi mechanism including a homolog of Dicer are also involved in synthesis of short temporal RNAs that regulate developmental timing in C. elegans [40–42]. Intervention with plant virus silencing suppressors may therefore have significant utility in determining the involvement of RNAi in development and differentiation in plants and animals, and possibly in manipulating these processes.
These results indicate that at least part of the process of RNAi in Drosophila and PTGS in plants is conserved, and that plant virus silencing suppressor proteins may be useful tools to investigate the mechanism of RNAi.
A region (nucleotides 1055–2449) of the TEV genome containing the HC-Pro sequence was amplified by reverse transcription – polymerase chain reaction (RT-PCR) using as a template RNA from an infected plant, and primers HC-Pro-1 (5'-CCGGTACCATGAGCGACAAATCAATCTCTGAGGC-3') and HC-Pro-2 (5'-GGCTCGAGCTACACATCTCGGTTCATCCCTCC-3'). The primers add an ATG codon to the start of the open reading frame and the HC-Pro gene was cloned as a KpnI-XhoI fragment into pMT/V5-HisA (Invitrogen) to produce plasmid pMT-HC-Pro. The same primers were also used to clone a mutant HC-Pro gene (TEV-K; ) from transgenic plants to produce plasmid pMT-HC-Pro/K. The 2b gene was amplified from RNA2 of CMV isolate Fny using primers 392 (5'-GAACCATGGAATTGAACGTAGGTGC) and 393 (5'-GGGTACCTCAGAAAGCACCTTCCGCC) and cloned into pGemT (Promega) before subcloning into pMT-V5-HisA. The TRV 16K gene was amplified from RNA1 of TRV isolate PpK20 using primers 433 (5'-TCATCATGACGTGTGTACTCAAGGG-3') and 434 (5'-AAGGTACCATCAAAAAGCAAACG-3') to insert BspHI and KpnI sites upstream and downstream, respectively, of the gene. The PCR product was cloned into pMT/V5-HisA to produce plasmid pMT-16K. The nucleotide sequences of the cloned PCR inserts were confirmed by sequencing.
cDNA corresponding to ~500 bp of the 5' end of the lacZ gene was amplified using pcDNA3.1/HisB/lacZ (Invitrogen) as a template and primers lacZ-1 (5'- TAATACGACTCACTATAGGGAGACCCAAGCTGGCTAGC-3') and lacZ-2 (5'- TAATACGACTCACTATAGGGCAAACGGCGGATTGACCG-3'). Both primers contain T7 RNA polymerase promoter sequences (shown underlined). The PCR product was used to direct synthesis of dsRNA using T7 RNA polymerase (Invitrogen) after which the DNA template was removed by DNase digestion.
Cell culture and transfection
DS2 cells, DES expression medium and the lacZ expression plasmid pMT/V5-His/lacZ were supplied as part of the Drosophila Expression System (Invitrogen) and cells were grown according to the manufacturer's instructions. Cells were grown in 60 mm dishes and transfected by calcium phosphate co-precipitation with various mixtures of 10 μg each of pMT/V5-His/lacZ and the suppressor expression plasmid DNAs and 5 μg dsRNA. In control transfections, 10 μg of an empty expression plasmid (pMT/V5-HisB) replaced the suppressor expression plasmid. After transfection the cells were washed twice in DES medium and grown for eight hours before expression of proteins was induced by addition of CuSO4 to a final concentration of 500 μM. Stably transformed lines expressing the HC-Pro, 2b or a6k genes were established by co-transfection of cells with pMT-HC-Pro or pMT-2b and pCo-Hygro (Invitrogen) followed by selection of transformed cells in medium containing hygromycin. Cells were stained 48 hrs after transfection to detect lacZ gene expression using a β-Gal Staining Kit (Invitrogen). Four randomly selected fields of view each containing ~100 cells were selected in each of duplicate plates and the number of cells staining blue was counted.
Cell lysates were analysed by polyacrylamide gel electrophoresis and separated proteins were transferred to nitocellulose using a carbonate buffer . The blots were probed with an anti-CMV 2b  or anti 16K antibody  followed by a goat anti-rabbit alkaline phosphatase conjugate. Blots were developed using SigmaFast NBT/BCIP substrate (Sigma, Poole, UK).
Northern blot analysis of RNA from Drosophilacells
RNA was extracted from Drosophila cells using TriPure Isolation Reagent (Boehringer). Samples of RNA were separated by electrophoresis on formaldehyde/agarose gels, transferred to nylon membrane and probed with digoxigenin-labelled DNA probes corresponding to ~500nts at the 5' end of the lacZ gene or to the HC-Pro cDNA described above, as appropriate and essentially as described . The probes were made by PCR using primers lacZ-3 (5'- GGAGACCCAAGCTGGCTAGC-3') and lacZ-4 (5'- GGCAAACGGCGGATTGACCG-3') for the lacZ probe, and HC-Pro-1 and HC-Pro-2 for the HC-Pro probe. Digoxigenin-labeled RNA Molecular Weight Marker II (Roche Molecular Biochemicals) was run as a size marker.
For detection of short (~23nt) RNA species total RNA preparations from Drosophila cell cultures were fractionated by chromatography using sepharose CL-2B agarose (Sigma) in Micro Bio-Spin columns (Bio Rad), following the manufacturers instructions. ~20 μg of the short RNA species were separated by electrophoresis in a 15% polyacrylamide gel containing 7 M Urea and electroblotted as described by Llave et al. . After electrophoresis the gel was stained with ethidium bromide and photographed under ultra-violet light before the RNA species were transferred to Hybond N+ membrane (Amersham) by electroblotting. For the detection of siRNAs, a digoxigenin-labelled RNA probe complementary to the 5' region of the lacZ gene as described above was synthesised from a PCR fragment containing the gene fragment downstream of a T7 RNA polymerase promoter, and hybridised to the blots according to the manufacturer instructions (Roche Diagnostics). Induction and detection of siRNAs to GFP or to 35S promoter sequences in agroinfiltrated plant tissue was performed as described by Canto et al. .
We thank Hugh Barker for useful discussions and help with photography of cells. We thank Vicki Vance for providing us with TEV HC-Pro mutant K. SCRI is grant-aided by the Scottish Executive Rural affairs Department.
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