- Open Access
Development of a gene silencing DNA vector derived from a broad host range geminivirus
© Golenberg et al; licensee BioMed Central Ltd. 2009
- Received: 05 May 2009
- Accepted: 02 July 2009
- Published: 02 July 2009
Gene silencing is proving to be a powerful tool for genetic, developmental, and physiological analyses. The use of viral induced gene silencing (VIGS) offers advantages to transgenic approaches as it can be potentially applied to non-model systems for which transgenic techniques are not readily available. However, many VIGS vectors are derived from Gemini viruses that have limited host ranges. We present a new, unipartite vector that is derived from a curtovirus that has a broad host range and will be amenable to use in many non-model systems.
The construction of a gene silencing vector derived from the geminivirus Beet curly top virus (BCTV), named pWSRi, is reported. Two versions of the vector have been developed to allow application by biolistic techniques or by agro-infiltration. We demonstrate its ability to silence nuclear genes including ribulose bisphosphate carboxylase small subunit (rbcS), transketolase, the sulfur allele of magnesium chelatase (ChlI), and two homeotic transcription factors in spinach or tomato by generating gene-specific knock-down phenotypes. Onset of phenotypes occurred 3 to 12 weeks post-inoculation, depending on the target gene, in organs that developed after the application. The vector lacks movement genes and we found no evidence for significant spread from the site of inoculation. However, viral amplification in inoculated tissue was detected and is necessary for systemic silencing, suggesting that signals generated from active viral replicons are efficiently transported within the plant.
The unique properties of the pWSRi vector, the ability to silence genes in meristem tissue, the separation of virus and silencing phenotypes, and the broad natural host range of BCTV, suggest that it will have wide utility.
- Broad Host Range
- Tungsten Particle
- Chloramphenicol Acetyl Transferase
- Viral Induce Gene Silence
- Silence Signal
Post-transcriptional gene silencing (PTGS), also known as RNA interference (RNAi) or RNA silencing, was initially described as a unique artifact of transgenic expression in petunias [1, 2], but has since been established as a widespread phenomenon in many organisms . The RNA silencing machinery is triggered by dsRNA molecules that are digested into small 21–24 nucleotide small interfering RNA (siRNA) fragments by DICER-like ribonucleases. These fragments are further processed and incorporated into the RNA induced silencing complex (RISC) which targets homologous mRNAs for degradation [4, 5]. An interesting phenomenon particularly prominent in plants is systemic spread of RNA silencing. It is in part due to this property that RNA silencing acts as an effective natural defense against plant RNA and DNA viruses.
Experimentally, RNA silencing has been utilized to produce phenocopies of knockout strains in various organisms. In Caenorhabditis elegans, exposure to solutions of dsRNA is sufficient to induce silencing of the homologous gene . Alternatively, injection of dsRNA directly into specimens or into fecund mothers of intended specimens (pRNAi – parental RNAi) can elicit the gene silencing response. In plants, gene silencing can be accomplished transiently by particle bombardment or agroinfiltration of hairpin (hp) RNA molecules or dsRNA, or of constructs expressing hpRNA. However, while these methods can result in systemic silencing of transgenes, only limited spread of the silencing signal is typically observed when endogenous genes are targeted. This limitation can be overcome by creating stable transgenes that express hpRNAs, but this approach can be time consuming and is not available in all species. Alternatively, vectors based on plant viruses that are themselves capable of systemic spread have been used to achieve systemic silencing of endogenous genes (virus-induced gene silencing; VIGS). Usually the viral vectors are designed to over-express a fragment of the target gene rather than a hpRNA. VIGS offers several advantages, including relative ease of use in intact model plants as well as in species that are not amenable to transgenic approaches [7–11]. Disadvantages can include incomplete and non-uniform silencing, virus host range restrictions, and complications in experimental interpretation resulting from virus replication and disease symptoms. An ideal virus vector would have an extremely broad host range and elicit a potent systemic silencing signal following replication in a limited number of cells.
Some of the most flexible VIGS systems have been developed from the geminiviruses Tobacco curly shoot virus (TbCSV), Tomato yellow leaf curl China virus (TYLCCNV) [12, 13], Tomato golden mosaic virus (TGMV) [14, 15], and Cabbage leaf curl virus (CaLCuV) . All geminiviruses encapsidate small, circular ssDNA genomes that replicate in the host cell nucleus through dsDNA intermediates. TbCSV, TYLCCNV, TGMV, and CaLCuV are members of the genus Begomovirus. TbCSV and TYLCCNV are monopartite virus, while TGMV and CaLCuV have genomes consisting of two components, DNA A and DNA B. Well studied vectors based on TGMV and CaLCuV have been shown to replicate and spread systemically in inoculated plants and to support the effective silencing of endogenous genes. In addition, they provide several advantages over RNA virus vectors. Vectors based on RNA viruses sometimes generate only transient and somewhat limited silencing of endogenous genes, most likely because the virus vector is also targeted and limited by the RNA silencing system. In contrast, geminivirus vectors are not cleared by RNA silencing (although their mRNAs are targeted) and can cause efficient and durable silencing of endogenous genes even in tissues that do not support virus replication, including the meristem [14–16]. Thus, geminiviruses appear to stimulate the production of a strong systemic silencing signal. In addition, the begomoviruses collectively have a very broad host range that includes many important crop species. Unfortunately, however, the host range of individual begomoviruses is quite narrow. For example, CaLCuV is known to infect cabbage, Arabidopsis thaliana, and Nicotiana benthamiana while TGMV is limited to a few tomato and tobacco species, and primarily to N. benthamiana [17, 18]. Other disadvantages of these begomovirus vector systems are the disease symptoms they can elicit in inoculated plants, and that both A and B genome plasmids must be co-inoculated to induce infection and silencing. Therefore cultures of helper plasmids must be maintained.
Subclass and 41 families of plants susceptible to Beet curly top virus
Construction of BCTV VIGS vectors
The two constructs were digested with XhoI and XbaI restriction enzymes following the manufacturer's protocol (Promega, Madison, WI). The digested fragments were size separated on a 1.5% agarose gel. The BCTV fragment 1338-155 and the pCR2.1:BCTV107-711 fragment were cut from the gel and extracted using a Qiagen Gel Extraction Kit (Qiagen, Valencia, CA). The fragments were ligated overnight using T4 DNA ligase at 16°C. The resultant construct, called pWSRi, was tested by a restriction digest using SacI and XbaI. Positive clones were then verified by sequencing.
A second plasmid was constructed by cloning a fragment from position 638 to position 1646. The primers used for amplification were BCTV. 638 5' AAG TGT TCG TTG TAT GAG G 3' and BCTV.1631R 5' AGT GCT GGA TAG ATT TGA C 3' (Figure 1a). The BCTV.1631R sequence was derived from the sequence found in the more aggressive accession U02311 , but was sufficiently similar to the Logan strain to allow amplification. This region includes the 3' end of the R2 gene, the entire R1 gene, and the 3' ends of the L1 and L2. The fragment was cloned into the pCR2.1 vector using TOPO TA cloning. The insert region was verified by sequencing.
The pWSRiL1- plasmid was constructed to have a G to T transversion in the start codon of the BCTV L1 gene. Two sets of primers, pWSRi.2236 (5' ATT GTG TCT CCG TTC TTG TC 3') and pWSRi.2556Rmut (5' GGA GTC CAA TT*C CTC CTA CT 3') and pWSRi.2556mut (5' AGT AGG AGG A*AT TGG ACT CC 3') and pWSRi.2836R (5' ACT CAC TAT AGG GCG AAT TG 3') were designed to amplify overlapping fragments of the pWSRi vector such that the overlapping ends would include the mutated L1 start codon (* base). The two fragments were linked together to form a 619 bp fragment by employing both as template in a PCR reaction using the outside primers. SalI and XbaI recognition sites are located internal to both primers in the fragment and are found at positions 2253 and 2825 in pWSRi. The mutated PCR fragment was then switched with the native fragment in pWSRi, by double digesting both with SalI and XbaI, gel purifying the cut plasmid and fragments, and ligating with T4 DNA ligase. The modified pWSRi plasmid was verified for the mutation by sequencing and was designated pWSRiL1-.
The pWSRi vector was also transferred to a binary Ti plasmid to allow agroinfiltration. To do this, the viral sequence was tagged with a chloramphenicol acetyl transferase (CAT) gene by inserting the CAT sequence into the NotI-XhoI insertion sites in the vector. The presence of CAT facilitated transfer of the BCTV sequence because it allowed selection of positive clones. CAT (863 bp) flanked by NotI and PacI restriction sites at the 5' end, and by AscI and XhoI sites at the 3' end, was obtained by PCR from pACYC184 using the primers 5' GCG CGG CCG CTT AAT TAA CTT TTG GCG AAA ATG AG 3' and 5' GCG CTC GAG GGC GCG CCG CCA TTC ATC CGC TTA TTA TC 3'. The BCTV sequence containing CAT was excised using HindIII and XbaI and inserted into a similarly cleaved pBI121 derivative plasmid lacking the 35S-GUS-3' sequence. The resulting vector was designated pWSRiA:CAT. Other targeting sequences can be easily inserted into this base vector simply by replacing CAT and screening for chloramphenicol-sensitive colonies.
Isolation and insertion of targeting sequences
Segments of three spinach nuclear genes, rbcS, transketolase, and SpPI, were isolated by PCR and cloned into pCR4 using TOPO TA cloning. The rbcS primers were designed from the Genbank accession L76557 and were designated SprbcS.114XhoI 5' AGC TCG AGC ACC AAG AAG AAC GAT GAC A 3' and SprbcS.505RPstI 5' agc tgc agg caa tga aac tga cac a 3'. The transketolase primers were designed from the Genbank accession L76554 and were designated SpTrnktls.711XhoI 5' CTC GAG GGA AGG GAT TGC TCA GGA AG 3' and SpTrnsktls. 937RNotI 5' gcg gcc gca aag tgg gtt tgt ctg tga c 3'. The rbcS and transketolase PCR fragments were cloned into the pGEM T-easy vector using T4 DNA ligase following manufacturer's protocols (Promega, Madison, WI). The SpPI fragment was digested from a plasmid designated pSpPI, c that included the 3' end of the cDNA from position 526 to the poly-A tail (255 bp) and cloned into pBluescript SK (Stratagene, La Jolla, CA) (Genbank accession AY604515) . The inserts were then subcloned into pWSRi by double digestion with NotI and XhoI. The digested fragments were separated on a 1.5% agarose TBE gel, the appropriate DNA bands were excised, and the DNA fragments were isolated using the Qiagen Gel Extraction Kit (Qiagen, Valencia, CA). The gene fragments were individually cloned into the NotI/XhoI digested pWSRi vector using T4 DNA ligase overnight at 16°C. The orientation of the NotI/XhoI sites resulted in all three inserts being in the antisense orientation relative to R1 gene. The ligations were transformed into JM109 chemically competent cells. Transformants were screened and positive clones were verified by DNA sequencing.
pWSRi:SpAP3 was constructed by subcloning a 3' region from position 432 to 834 (403 bp) of the gene previously cloned and used for gene specific in situ hybridization studies . As in the previous construct, the appropriate fragment was size separated by electrophoresis and extracted from the gel. Ligation into the NotI/XhoI sites resulted in SpAp3 being in an antisense orientation relative to R1.
To create pWSRiA:su, a 999 bp fragment (nucleotides 250–1249) of the Arabidopsis thaliana ChlI gene was obtained from pTV:09 by PCR using the primers 5' GCG TTA ATT AAA GGC GAG ACC GGT TTA TCC 3' and 5' GCG GGC GCG CCC GGA AAC TAG AAC TCC TGA A 3'. The pTV:09 vector was kindly provided by David Baulcombe. The use of these primers placed a PacI site at the 5' end, and an AscI site at the 3' end, of the ChlI sequence. The cleaved ChlI sequence was then used to replace the CAT gene in similarly cleaved pWSRiA:CAT. The resulting construct, which contains ChlI sequence in the sense orientation relative to the viral R1 gene, was designated pWSRiA:su.
Biolistic bombardment of plants
Silencing of rbcS and transketolase
Plants silenced after treatment
a. Initial Trials
1. no DNA (mock)
0 of 6 plants
0 of 6 plants
0 of 6 plants
4. pWSRi + pBCTV.R1
0 of 6 plants
6 of 6 plants
6. pWSRi:rbcS + pBCTV.R1
6 of 6 plants
6 of 6 plants
8. pWSRi:transketolase + pBCTV.R1
6 of 6 plants
b. Secondary Trials
12 strong to moderate
5 medium to light
1 no response
12 strong to moderate
3 no response
Plants were also treated by an alternative biolistic protocol using the Helios Gene Gun (Bio-Rad, Hercules, CA). In this protocol, 50 μl of plasmids were mixed with 20 mg of sterilized tungsten powder. The slurry was mixed well and spread on a microscope slide to allow the water to evaporate. The tungsten was then funneled into PVP-coated tubing for bullet preparation. Bullets were fired from the Helios Gene Gun at 90 psi of helium at a distance of 1–3 cm.
Agroinfiltration of tomato
Tomato plants (Solanum lycopersicum cv. Rutgers) were grown in a growth chamber at 24°C under a 14 hour light cycle. Agroinfiltration was carried out as previously described (Wang et al., 2005) Briefly, the pWSRiA:CAT and pWSRiA:ChlI vectors were transformed into Agrobacterium tumefaciens strain C51c. Cultures were grown overnight at 30° in medium containing 20 μM acetosyringone, and resuspended to OD600 = 1 in 10 mM MES buffer containing 10 mM MgCl2 and 20 μM acetosyringone. Cells were allowed to stand in the buffer for 3 hours prior to infiltration onto the underside of cotyledons and leaves of tomato seedlings (two to four leaf stage) using a 1 ml syringe lacking a needle.
Primer design for PCR assay of viral infection and vector transport
Total nucleic acids were extracted from whole spinach leaves that demonstrated bleaching following earlier pWSRi:SprbcS treatment using a standard CTAB DNA extraction protocol. SprbcS.114XhoI and SprbcS.505RPstI primers were used as positive controls on both leaf and plasmid DNAs. SprbcS.505R and pWSRi.1338R (5' TTA GTA TTA TCC GTA TTA TCA CTC GAG CAG CCT 3') primers were used to assay the presence of pWSRi:rbcS DNA. pWSRi.1338R directly flanks the XhoI insertion site in the pWSRiplasmid and so can be used with an insertion sequence specific primer to verify the presence of the cloned insertion sequence within pWSRi. To detect evidence of recombination and transposition of viral sequences of the pWSRi vector constructs, we designed two new primers, BCTV. 3007 (5' CAA CTC TCA TAA GGG CCA TC 3') and BCTV.177R (5' GGG GCC CAC TAA CTT TAC TT 3'). The two primers are located in the L and R fragments of the pWSRi vector and are separated by the pCR2.1 plasmid sequences. In subsequent trials in which pWSRiL1- replication was tested, we used pWSRi.2236 (5' ATT GTG TCT CCG TTC TTG TC 3') and pWSRi.2556R (5' GGA GTC CAA TAC CTC CTA CT 3'). These primers are in the L region and can amplify both pWSRi and pWSRiL1-.
Quantification of mRNA knockdown by quantitative RT-PCR
Total RNA was extracted from leaves of pWSRiA:ChlI and pWSRiA:CAT treated plants four weeks after agroinfiltration using Trizol following the manufacturer's protocol. Concentration of the total RNA was estimated by spectrophotometry. Five ul of each RNA extract was mixed with 2 ul 100 uM random hexamers, 1 ul RNase Inhibitors and nuclease free water to a volume of 20 ul. The samples were heated to 70°C for five minutes and then placed on ice. A master mix consisting of 10 ul M-MLV RT 5× Buffer, 2.5 ul 10 mM dNTP, 15.5 ul water, and 2 ul M-MLV Reverse Transcriptase was added to each sample. The samples were left at room temperature for 10 minutes and then incubated at 55°C for an additional 50 minutes. One ul RNase H was then added and the samples were incubated at 37°C for 20 minutes.
The aliquots of each sample were then diluted in nuclease free water based on the original concentrations of total RNA such that the cDNAs from 2.5 ng RNA were diluted to a final volume of 50 ul. 2× master sybr green PCR mixes minus the template and primers for nine 20 ul PCR reactions were prepared for each sample. Eighteen ul (2 ul per reaction) of the diluted cDNAs were then added to the master mixes and mixed. This batch mixing assured that each control and experimental PCR reaction would have the same concentration of cDNA within each sample trial. The reaction volumes were then divided into two tubes (4 reactions each), and 8 ul of 2.5 uM forward and reverse primer pairs were added. For the experimental reactions, two primers were designed from the Solanum lycopersicum sequence BT012789 to produce a 394 bp product (LeChelatase.630 5'-TGG GAC AAT CGA CAT TGA GA-3' and LeChelatase.1023R 5'-TTC TTG CTC CCC CTT GTA TG-3'). Ambion QuantumRNA Universal 18S primers were mixed in a 4:6 ratio with the 18S competimers and used for the internal control reactions. The expected PCR product would be 324 bp in length. The two master mixes (Mg-Chelatase and 18S) were then aliquoted into three replicate wells each on a 96 well plate, with the three replicates staggered over the plate. Thus each cDNA sample was measured in three replicates for each of the Mg Chelatase (su) and 18S control primer pairs. The PCR temperature settings were 94°C for 10 minutes followed by 40 cycles of 94°C 15 seconds, 60°C 15 seconds, and 72°C 45 seconds, and reactions were run and the data collected on a Stratagene Mx3000P. Mean threshold cycles for the Mg-Chelatase (su) and 18S were calculated for each sample. The delta CT (Threshold cycleChelatase -Threshold cycle18S) was calculated from the means and the delta CT variances were calculated by summing the individual CT variances as there should be no covariance of the sample errors.
Construction and description of pWSRi
A plasmid vector was constructed by cloning two fragments of BCTV into a bacterial plasmid vector (pCR 2.1; Invitrogen). The first fragment included the viral R3 gene and the 5' portions of the R2 and R1 genes. R1 (also known as V1) directs synthesis of the capsid protein and R2 (V2) encodes a protein required for the efficient accumulation of viral ssDNA. Both R1 and R3 (V3) are required for spread of the virus in the infected plant [27, 28]. Nonsense mutations were introduced into the already truncated R2 and R1 genes. The R2 open reading frame is truncated by 12 amino acids, while the R1 gene encodes only 19 amino acids. These mutations are intended to prevent virion production and viral movement within the plant. The second fragment included a 3' fragment of R1, the intact L1, L2, L3, and L4 genes, as well as the viral origin of replication encompassing the conserved hairpin loop structure . L1 (also known as C1 or Rep) is the only viral gene required for replication. L3 (C3) encodes the replication enhancer (REn), and L2 (C2) specifies a protein that is important for pathogenesis and has silencing suppressor activity. The L4 gene also specifies a pathogenicity factor [21, 27, 30–34]. An overlapping region between the two viral fragments was included to allow intramolecular recombination. Thus a fully replication-competent, but truncated BCTV genome (the viral vector) is released from the plasmid vector following recombination in plant cells . However, the absence of R2 function minimizes the accumulation of viral ssDNA and the absence of R1 (capsid protein and movement factor) precludes virion production and virus spread.
Further modifications were designed to place the insertion site for targeting sequences and to prevent translation of spurious fusion proteins. The NotI-XhoI insertion sites for targeting sequences were introduced 14 bp downstream of the introduced R1 stop codon and 64 bp before the R1 natural stop codon to retain mRNA processing signals. Thus the targeting sequence should be transcribed as part of the rightward transcription unit that includes the R1 gene . The natural stop codon of the L3 gene is on the opposite strand and is 92 bp from the XhoI cloning site. Because of the stop codons in the R1, R2, and L3 reading frames, no fusion proteins should be produced. However, placement of the Not1-XhoI insertion sites near the termini of two converging transcription units should favor transcription of complementary RNAs containing the targeting sequence. The completed plasmid was designated pWSRi. A map of the plasmid is shown in Figure 1b and sequences in the vicinity of the targeting sequence insertion site are given in Figure 1c.
To test whether the viral capsid protein is necessary for or can enhance silencing activity, possibly by supporting at least limited virus spread, a second plasmid was constructed by cloning a segment of BCTV from position 638 to position 1649 into pCR2.1. This putative helper plasmid was designed to express the complete R1 capsid-encoding gene and was designated pBCTV.R1.
Silencing of endogenous nuclear genes encoding photosynthetic enzymes in spinach
Subsequent trials were performed without the pBCTV.R1 plasmid (Table 2b). Three sets of 6 plants were treated on different occasions with pWSRi:trnkls. In total, 12 of the 18 plants showed strong to moderate bleaching, three plants displayed no bleaching, and three plants died after treatment most likely due to the trauma of the biolistic treatment. Three additional sets of 6 plants were treated with pWSRi:rbcS. Twelve plants developed strong to medium bleaching, five plants displayed moderate bleaching, and one plant showed no response.
In treatments with pWSRi:rbcS and pWSRi:trnktl, bleaching first appeared on the newest leaves and later in older leaves until most leaves above the inoculation site were affected. In older leaves, progressive bleaching could sometimes be seen beginning at the petiole and spreading into the leaf blade and distally along the midrib, until most or all of the leaf was affected (Figure 2c). Following treatments with pWSRi, pWSRi:rbcS, and pWSRi:trnktls there was no evidence of BCTV disease symptoms which include upwardly rolled leaf margins, deformation and curling of younger leaves, vein swelling, and stunting. Wild-type BCTV is normally restricted to the phloem and, by design, the movement-defective BCTV vector is unable to spread from the site of inoculation. The absence of disease symptoms is consistent with this expectation. Thus the observation of bleaching throughout the leaf blade, including mesophyll tissues, indicated that silencing of rbcS and transketolase was due to systemic propagation of durable and/or distally amplified signals initiated from the locally confined virus vector.
Silencing of genes expressed in the floral meristem
To confirm that silencing signals were systemically propagated from the BCTV vector, we asked whether it could be used to silence genes in meristematic tissue, from which geminiviruses are normally excluded. We first tested fragments from the spinach B class floral identity genes PISTILLATA (SpPI) and APETALA3 (SpAP3) in pWSRi . According to the angiosperm ABC model, B class genes are necessary for the development of petals and stamens . However, normal dioecious spinach plants have only male or female flowers. Further, in spinach flowers petals are completely absent in both sexes, and the stamen whorl is additionally absent in female flowers. Thus in spinach, PI and AP3 function is required and these genes are expressed only in male flowers .
Silencing with pWSRi:floral homeotic gene constructs
12 normal females
14 males with mixed floral organs
7 normal females
1 normal male
10 males with mixed floral organs
Similar results were obtained following inoculation with pWSRi:SpAP3. Flowers exhibiting a range of phenotypes, including mixed male and female characteristics (Figure 3d), were observed only in male plants and not in female plants (Table 3). Thus the effects of inoculation with pWSRi:SpPI and pWSRi:SpAP3 were entirely consistent with the known functions of these B class genes and with their patterns of expression in spinach .
In summary, we observed specific and predictable phenotypic effects following inoculation of spinach plants with pWSRi constructs targeting Calvin cycle enzyme-coding genes as well as different B class floral identity genes. This allowed us to conclude that the pWSRi vector can be used to generate durable systemic silencing signals effective against endogenous genes of different types and expressed in different tissues, in absence of virus disease symptoms.
Viral DNA replication, but not virus spread, is required for silencing
We asked whether non-replicating BCTV can sponsor silencing of an endogenous gene by constructing a pWSRiL1-:SpPI plasmids containing the identical SpPI insert previously shown to be effective when used in pWSRi:SpPI. The replication-defective pWSRiL1-:SpPI plasmid was inoculated to 12 plants. Five plants developed as normal females and seven plants developed as normal males. There were no transformed organs or modified flowers on any plants. We concluded that virus replication in inoculated cells is necessary to generate an effective systemic silencing signal, and that significant spread to non-inoculated cells is not required.
Silencing of an endogenous nuclear gene in tomato
To further test the utility of the BCTV-based vector, and to determine if agroinfiltration might be used as an alternative delivery method, a binary Ti plasmid-based version of the vector (pWSRiA) was constructed and tested in tomato (Solanum lycopersicum). A targeting sequence directed against a 1 kb fragment of the sulfur allele (su) of magnesium chelatase from Arabidopsis thaliana was inserted to create pWSRiA:su. Comparison of homologous gene sequences from Arabidopsis and solanaceous species suggested that there was sufficient sequence identity to support at least partial silencing. As the ChlI allele is required for the synthesis of chlorophyll, loss of function results in leaf bleaching. A vector containing an irrelevant chloramphenicol acetyltransferase targeting sequence (pWSRiA:CAT) served as a negative control.
Silencing of Magnesium chelatase (su): Bleaching response in treated tomato plants by trial.
Plants silenced after treatment
Silencing of Magnesium chelatase (su): Quantification of Magnesium chelatase (su) mRNA in three pWSRiA:ChlI versus control treatment
Mean ct Mg
Chelatase ± s.e.
Mean ct 18S ± s.e.
Delta ct ± 98% confidence limit
Relative Mg chelatase mRNA (2Delta-Delta ct)
26.96 ± 0.05
27.34 ± 0.08
-0.38 ± 0.10
24.67 ± 0.06
25.72 ± 0.06
-1.06 ± 0.10
24.39 ± 0.08
25.64 ± 0.05
-1.61 ± 0.11
25.26 ± .010
27.92 ± 0.17
-2.66 ± 0.22
Although agroinfiltration is generally not an efficient method of gene delivery in tomato, these results allow us to conclude that pWSRi-based vectors can be effectively delivered by this method. This is likely due to the fact that the viral vector, once released from the plasmid vector, is highly amplified in inoculated cells.
Penetrance and expressivity are target gene dependent
Throughout the trials, we noticed that the proportion of treated plants that demonstrated a gene-specific altered phenotype (comparable to penetrance) and the degree to which individual plants had altered phenotypes (comparable to expressivity) differed among the various target gene constructs. Silencing of floral organ identity transcription factors appeared to occur more frequently and with more consistent phenotypic effects than silencing of photosynthetic genes. We suspect that the level of gene expression and the longer half-life of the enzymatic proteins compared to the transcription factors may affect the level of penetrance and explain the somewhat less robust silencing observed in plants where rbcS, transketolase, or ChlI was targeted. Additionally, we have noted anecdotally that penetrance was lower at lower temperatures, as has been previously reported for other VIGS systems .
In all treatments, the silencing phenotypes varied spatially and temporally over the plant. For example, bleaching observed in pWSRiA:ChlI treated tomato plants appeared variegated, and in pWSRi:rbcS treated spinach plants, bleaching was often detected starting at the base of the leaf and spreading into the blade and along the midrib in late developing leaves (Figure 2C and Figure 6). In all cases, we observed the phenotypic changes first in organs that were not inoculated directly with the plasmid, and indeed had not developed at the time of application of the plasmid. Therefore the silencing signal must be transported to newly developing sink organs. We infer that the varied spatial and temporal appearance of the silencing effect reflects the time that the silencing signal (siRNA) takes to move systemically through the plant and the point of development of the affected meristem or organ when the signal arrives.
In conclusion, we report the development of a silencing vector derived from the geminivirus BCTV and show that it is effective when used to target housekeeping genes or genes encoding transcription factors expressed in floral meristems. Replication, but not spread, of the virus vector is required for silencing, and we speculate that active BCTV replicons elicit strong and durable silencing signals that spread systemically and are efficiently amplified at distal sites by host silencing machinery. Regardless of mechanism, this separation of virus and target gene phenotypes, coupled with the extremely broad host range of BCTV and the flexibility in means of application, suggests that pWSRi-based vectors will prove to be useful probes of gene function in a wide variety of plant species.
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