Patent Grant
8637653
1. Field of the Invention
This invention relates to a novel bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus, a viral vector advantageous for high level replication for protein expression resulting from efficient suppression of RNA silencing and also advantageous for effective virus-induced gene silencing (VIGS) when modified to incorporate weak suppression of RNA silencing, cloned from a potexvirus, Alternanthera mosaic virus (AltMV); constructs containing the required parts of the bipartite viral vectors, constructs containing the RNA-dependent RNA polymerase of AltMV infectious clones, constructs comprising the partial RdRp, TGB1, TGB2, TGB3 and CP of AltMV infectious clones, and such constructs further comprising T7 promoters, Cauliflower mosaic virus (CaMV) 35S promoters, duplicated sub-genomic RNA promoters and multiple cloning sites allowing for additional genes/sequences for expression; vectors containing exogenous T7 RNA polymerase for enhancing infectivity, variant constructs containing modifications to the efficiency of RNA silencing suppression thus enabling VIGS, a method of making a novel bipartite plant viral vector launch system comprising constructs capable of regenerating full-length infectious virus vectors advantageous for both protein expression and VIGS of exogenous genes and sequences, a method of using both the CaMV 35S promoter and the T7 promoters in the same vector making possible both DNA and RNA delivery to drive the transient expression of the infectious viral clones for efficient protein expression and VIGS, a method of ensuring early and enhanced levels of infectivity by including the addition of vectors encoding T7 RNA polymerase, and a method of manipulating the severity of infection by altering the temperature.
2. Description of the Relevant Art
Alternanthera mosaic virus (AltMV) is a potexvirus most closely related to Papaya mosaic virus, and was originally reported from a weed species, Alternanthera pungens, in Australia (Geering and Thomas. 1999. Arch. Virol. 144:577-592). AltMV has since been reported to infect various ornamental plants, including several Phlox species (Hammond et al. 2006a. Arch. Virol. 151:477-493; Hammond et al. 2006b. Acta Horticulturae 722:71-77), and Portulaca (Ciuffo and Turina. 2004. Plant Pathol. 53:515; Hammond et al. 2006a,b, supra; Baker et al. 2006. Plant Disease 90:833), Scutellaria and Crossandra (Baker et al., supra), Angelonia (Lockhart and Daughtrey. 2008. Plant Dis. 92:1473) as well as Arabidopsis and soybean (H-S. Lim and J. Hammond, unpublished). The full 6607 nt sequence of one phlox isolate, AltMV-PA, has been reported (GenBank accession no. AY863024), and has a 5′ untranslated region (UTR) of 94 nt and a 126 nt 3′ UTR excluding the poly(A) tract; there are five open reading frames which encode the RNA-dependent RNA polymerase (RdRp), the triple gene block (TGB) proteins (TGB1, TGB2, TGB3), and the coat protein (CP) (Hammond at al. 2006b, supra). Some differences in symptom expression between isolates have been reported; in Nicotiana benthamiana, AltMV-SP (from phlox) and AltMV-PA produce faint chlorotic lesions on the inoculated leaves, followed by systemic chlorotic mosaic, with some rugosity and distortion, while AltMV-Po (from portulaca) produced mild symptoms. Under low temperature conditions (<20° C.) AltMV-SP produces necrotic local lesions and severe systemic necrosis (Hammond et al. 2006a, supra) an apparent hypersensitive response. It has also been noted that two geographically distinct isolates from portulaca share several coat protein (CP) amino acid residues that distinguish them from phlox and alternanthera isolates (Hammond et al. 2006a, supra); the complete sequence of a third geographically distinct isolate from portulaca has recently become available in GenBank (FJ822136) and the CP amino acid sequence is almost identical to those of the other portulaca isolates.
The presence of multiple sequence types, or mixed infection of distinct isolates, within a single plant has been reported for several viruses of different taxonomic groups e.g. capilloviruses (Magome et al. 1997; Phytopathology 87:389-396); closteroviruses (Sentandreu et al. 2006. Arch. Virol. 151:875-894); potyviruses (Sáenz et al. 2001. Mol. Plant Microbe Interact. 14: 278-287); alfalfa mosaic virus (Hull and Plaskitt. 1970. Virology 42: 773-776), including potexviruses (e.g. Ozeki et al. 2006. Arch. Virol. 151: 2067-2075). As RNA-dependent RNA polymerase lacks a proof-reading activity, RNA virus populations tend to accumulate many minor variations around a master sequence (or multiple master sequences), and thus exist as quasispecies populations (Domingo et al. 1985. Gene 40:1-8). Variation within isolates arises by viral polymerase error at a constant rate, but many of the newly generated mutants are sequestered in virions and may not serve as replication templates (Hall et al. 2001. J. Virol. 75: 10231-10243). However, the extent of population variation is limited by selection pressure for variants that interact successfully with different host and viral proteins necessary for completion of the infection cycle (Garcia-Arenal et al. 2001. Annu. Rev. Phytopathol. 39:157-186; Schneider and Roossinck. 2001. J. Virol. 75: 6566-6571; Rico et al. 2006. J. Virol. 80: 8124-8132). In order to survive, a virus must be diverse enough to adapt rapidly to changing environments without losing fitness during passage from host to host (Liang et al. 2002. J. Virol. 76: 12320-12324). Changing environmental conditions such as temperature can affect virus RNA replication (e.g. Aldaoud et al. 1989. Intervirology 30:227-233; Kaper et al. 1995. Arch. Virol. 140: 65-74). Genetic exchange plays a role to produce population diversity in bipartite or tripartite viruses (Lin et al. 2004. J. Virol. 78:6666-6675); but recombination has also been reported within monopartite viruses such as the potyviruses (Revers et al. 1996. J. Gen. Virol. 77: 1953-1965), closteroviruses (Rubio et al. 2001. J. Virol. 75: 8054-8062), and between defective potyviral genomes delivered as RNA transcripts (Gal-On et al. 1998; J. Virol. 72:5268-5270). There is also some evidence for recombination between isolates of the potexvirus Cymbidium mosaic virus (Sherpa et al. 2007. J. Biosci. 32: 663-669; Vaughan et al. 2008. Arch. Virol. 153: 1186-1189), although others found no such evidence (Moles et al. 2007. Arch. Virol. 152: 705-715), and Malcuit et al. (2000, Virus Genes 20: 165-172) have suggested that PVX strain groups evolved through convergent evolution rather than recombination. More recently Draghici and Varrelmann (2009. J. Virol 83: 7761-7769) have demonstrated RNA recombination under high selective pressure between defective PVX genomes delivered by agroinfiltration; in this instance the defective genomes either lacked the 5′ or the 3′ viral untranslated regions (utr) such that no replication of either partial genome alone was possible. Selection may disfavor recombined strains, as a result of incompatibilities between interacting viral proteins, or between viral proteins and cis-acting viral sequences (Malcuit et al., supra). The derivation of distinct Citrus tristeza virus (CTV) lineages by evolution and/or selection from a quasispecies population aided by host passage or aphid transmission has been documented (Sentandreu et al., supra). The origin of variants from a population derived from infectious cDNA clones of Tobacco mosaic virus (Kearney et al. 1999. Arch. Virol. 144: 1513-1526; Schneider and Roossinck. 2000. J. Virol. 74:3130-3134), Cucumber mosaic virus (CMV) and Cowpea chlorotic mottle virus (Schneider and Roossinck, 2000, supra) has been documented, as has selection from a defined population of CMV variants (Li and Roossinck. 2004. J. Virol. 78:10582-10587).
The Potexvirus replicase is a single protein that contains methyltransferase, RNA helicase and RNA polymerase domains (Verchot-Lubicz et al. 2007. J. Gen. Virol. 88:1643-1655). A single amino acid change in the Pol domain of Potato virus X (PVX) or Plantago asiatica mosaic virus (PIAMV) RdRp induces systemic necrosis in N. benthamiana (Kagiwada et al. 2005. Virus. Res. 110:177-182; Ozeki et al., supra). PVX TGB1 has been reported as a suppressor of RNA silencing (Bayne et al. 2005. Plant J. 44: 471-482; Voinnet et al. 2000. Cell 103:157-167), and to block systemic spread of the silencing signal (Voinnet at al., supra). TGB1, TGB2, TGB3 and coat protein are required for movement; TGB2 and TGB3 are ER binding proteins, and TGB2 has two transmembrane domains and a central motif conserved'among potexviruses that lies in the ER lumen (Verchot-Lubicz at al., supra). PVX CP is an elicitor of the Rx resistance response, and overproduction of CP leads to Rx-mediated hypersensitive response (Bendahmane et al. 1995. Plant J. 8: 933-941; Tameling and Baulcombe. 2007. Plant Cell 19:1682-1694).
A strategy for use of RNA plant viruses as vectors was proposed by Siegel (Siegel, A. 1983. Phytopathology 73: 775) even before infectious clones of any plant viruses had been developed. According to this strategy, the rod-shaped plant viruses offered the greatest possibility as vectors, because the architecture of the particles does not place inherent limitations on the size of the insert; in contrast there are clear packaging constraints with viruses that have isometric particles. Several types of viral vectors have been developed among the rod-shaped and filamentous plant viruses, including gene replacement vectors, exemplified with Tobacco mosaic virus (TMV) by Takamatsu et al. (1987. EMBO J. 6: 307-311); gene insertion behind a duplicated subgenomic promoter from the same virus (Dawson et al. 1989. Virology 172: 285-292) or a related virus (Culver et al. 1993. Proc. Natl. Acad. Sci. USA 90: 2055-2059); translational fusions of partial or complete ORFs to either the N-terminus or C-terminus of a viral structural protein, either with or without a proteolytic cleavage site allowing processing of the fused sequence (e.g. Gopinath et al. 2000. Virology 267: 159-173), as a readthrough fusion such that both wild-type and modified viral proteins are produced (Hamamoto at al. 1993. Bio/Technology 11: 930-932); epitope display in an internal, surface-exposed loop (Porta at al. 1994. Virology 202: 949-955), functional complementation with multicomponent viruses such as Cucumber mosaic virus (Zhao et al. 2000. Arch. Virol. 145:2285-2295); functional complementation of a defective RNA by a wild-type virus (Raffo & Dawson. 1991. Virology 184: 277-289); chimeric viruses expressing a heterologous viral CP for peptide presentation or epitope display (Yusibov et al. 1997. Proc. Natl. Acad. Sci. USA 94: 5784-5788); and viral amplicons delivered from the genome of a transgenic plant (Angell & Baulcombe. 1997. EMBO J. 16: 3675-3684) or via agroinfiltration (Liu & Lomonossoff, 2002. J. Virol. Methods 105: 343-348). Mallory et al. (2002. Nat. Biotechnol. 20:622-625) reported the use of a viral suppressor of RNA silencing to overcome RNA silencing to increase expression from the viral amplicon. Knapp at al. (2005. Virology 341: 47-58) have developed a bipartite system from a defective genome of TMV lacking the CP gene, paired with a defective RNA having an internally deleted replicase gene and a functional CP gene flanked by the TMV 5′ and 3′ TMV utr. Although this bipartite form was maintained in systemic infections, systemic movement was significantly debilitated (Knapp et al. 2007. Virology 367:82-91).
Replication of defective genomes in the presence of a fully functional genome occurs in several plant viral systems; in some cases replication of a ‘defective interfering” (DI) RNA inhibits replication of the functional genome (e.g. Jones et al. 1990. Virology 176:539-545). In other cases the DI RNA may intensify symptom expression (e.g. Li et al. 1989. Proc Natl Acad Sci USA 86, 9173-9177).
A further extension of hybrid viruses, combined with complementation, has been described. Marillonet et al. (2004. Proc Natl Acad Sci USA 101: 6852-6857) and Gleba et al. (2004. Curr. Opin. Plant Biol. 7: 182-188) have developed systems in which viral functions not needed for expression can be dispensed with, and complementation used to provide equivalent functions from other sources; this has been described as the ‘deconstructed virus’ approach; expression can be optimized by elimination of functions not needed for expression. This may also aid in biocontainment, by elimination of functions contributing to vectored transmission. An efficient means of delivery of multiple separate components by agroinfiltration, combined with in planta recombination through co-expression of a recombinase, was shown to both confer high yields, and to allow greater flexibility in comparing variants of one or more system components. One or more component may be supplied as a transgene, and induction of replication and expression may be regulated by use of either a developmentally-controlled promoter, or by application of an inducer (Gleba et al. 2004, supra).
Taschner et al. (1991. Virology 181: 445-450) transformed plants with the replicase functions of Alfalfa mosaic virus (AlMV), while Mori et al (1992. J. Gen. Virol. 73: 169-172) similarly transformed plants with the replicase functions of Brome mosaic virus; Sanchez-Navarro et al. (2001. Arch. Virol. 146: 923-929) engineered RNA3 of AlMV into an expression vector using the replicase-expressing plants.
Virus-Induced Gene Silencing (VIGS) has become a significant tool for discovery of gene function in both dicotyledonous (Ratcliff of al. 2001. Plant J. 25: 237-245; Liu et al. 2002. Plant J. 31: 777-786) and monocotyledonous (Holzberg et al. 2002. Plant J. 30: 315-327) species. Although some viral vectors have been utilized for both protein expression and VIGS, including PVX (Chapman et al. 1992. Plant J. 2: 549-557; Ruiz of al. 1998, Plant Cell 10: 937-946) and Bean pod mottle virus (BPMV; Zhang & Ghabrial. 2006. Virology 344: 401-411), it is generally recognized that for high level protein expression, a virus with an effective suppressor of RNA silencing is desirable, whereas for VIGS, a less effective viral suppressor of RNA silencing is preferred (Dalmay of al. 2000. Plant Cell 12: 369-379). Indeed, it has been noted that BPMV does not effectively suppress RNA silencing, and that expression of an effective suppressor of RNA silencing in combination with BPMV vectors may be useful for enhancing foreign protein expression, which would probably need to be expressed from a co-infecting recombinant BPMV vector (Zhang and Ghabrial 2006, supra). BPMV has either weak or no suppressor of RNA silencing (Zhang and Ghabrial 2006, supra), and is more useful as a VIGS vector (Zhang et al. 2009. Mol. Plant—Microbe Interact. 22:123-131). PVX may fall into a middle group, as replication of PVX is significantly enhanced in a mixed infection with a potyvirus, as a consequence of the efficient suppression of RNA silencing provided by the potyvirus HC-Pro (Pruss et al. 1997. Plant Cell 9: 859-868), although PVX has its own suppressor of RNA silencing in TGB1 (Voinnet et al. 2000. Cell 103: 157-167).
Infectious clones of potexviruses including PVX (Hemenway et al. 1990. Virology 175: 365-371) have been developed and used as vectors for gene expression in plants (Chapman et al. 1992, supra) and for VIGS (Ruiz et al. 1998, supra). Separate constructs of infectious PVX clones driven by the Cauliflower mosaic virus (CaMV) 35S promoter and the bacteriophage T7 promoter have been reported (Baulcombe et al. 1995. Plant J. 7: 1045-1053). An infectious monopartite clone of PVX has been placed into a binary Agrobacterium vector under the control of the CaMV 35S promoter, and further modified with unique restriction enzymes in a Multiple Cloning Site (MCS) to allow high throughput cloning and expression of suitably constructed cDNA libraries (Takken et al. 2000. Plant J. 24: 275-283).
The bacteriophage T7 RNA polymerase (T7RNAP) is well known, and has previously been utilized from a chromosomal insertion for high-level expression of genes in bacteria (Studier & Moffatt. 1986. J Mol Biol. 189:113-130); in mammalian cells when T7RNAP was itself expressed from a recombinant vaccinia virus (Fuerst at al. 1986. Proc Natl Acad Sci USA. 83:8122-8126); and in insect cells when T7RNAP was delivered from a recombinant baculovirus (van Poelwijk et al. 1995. Biotechnology (NY). 13:261-264). The T7RNAP has also been used under the control of appropriate promoters for both tissue-specific and inducible expression in transgenic plants (Nguyen et al. 2004. Plant Biotechnol J 2, 301-310). Replication of the RNA of an insect virus was initiated (Ball. 1995. J. Virol. 69:720-727), and infectious rabies virus recovered in mammalian cells (Schnell et al. 1994. EMBO J. 13:4195-4203) using the vaccinia/T7 system. Infectious poliovirus was recovered from mammalian cells using the baculovirus/T7 system (Yap et al. 1997. Virology 231: 192-200). Reverse-genetics systems for negative-strand viruses are also often based on transcription of viral RNA by the bacteriophage T7 RNA polymerase (de Wit at al. 2007. J Gen Virol 88: 1281-1287). A hybrid baculovirus-T7 RNA polymerase system has been used for transient expression in mammalian cells (Yap et al. 1997, supra). The RNA minigenome system has been used for evaluating the functions of viral proteins and of sequences involved in viral RNA replication (Lohmann et al. 1999. Science 285: 110-113). Much of the work on the role of the 5′ and 3 UTR in viral replication has been through use of the minigenome (Dumas et al. 2007. J Virol Methods 142: 59-66; Friebe at al. 2001. J. Virol. 75: 12047-12057).
In summary, agroinfiltration, biolistic delivery of plasmid or transcripts, and mechanical inoculation of either plasmids or in vitro transcripts are the main methods for delivery of viral nucleic acids into cells. Agroinfiltration is relatively easy to apply with low cost; however, not all plant species are susceptible to agroinfiltration. In contrast, most plant species can be infected by biolistic delivery or mechanical inoculation with plasmids or in vitro transcripts, but the technique is more laborious and expensive than agroinfiltration. Each method has advantages, and disadvantages, but since most virus-based vectors are constructed with a single promoter sequence, it has not typically been possible to use both DNA and RNA delivery methods with the same vector. In addition, many plant viruses have been modified, for either protein expression or gene silencing. However, a single plant virus-based vector has been unable to effectively fulfill both functions because of the conflicting requirements for strong or weak RNA silencing suppression, respectively, for protein expression and VIGS.
Thus, there is a need for the development of alternative viral vector systems which have flexibility for modification and variation and which are applicable for effective in planta transient expression of multiple genes. We show here that the genome of representative potexviruses can be manipulated to serve as new bipartite plant viral vector launch systems for recombination in planta to regenerate full length infectious viruses, viral vectors effective for high levels of protein expression, and manipulated differently, for effective virus-induced gene silencing.
We have discovered that the genome of a potexvirus, Alternanthera mosaic virus (AltMV) can be manipulated to generate a novel bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus and that the function of such virus-based vectors can be easily changed from protein expression to virus-induced gene silencing, that they can be introduced into plants by either agroinfiltration or, in plant species recalcitrant to Agrobacterium-mediated inoculation, by mechanical inoculation of in vitro transcripts, and that T7 RNA polymerase and reverse genetic systems can be applied for developing this novel viral vector applicable to Arabidopsis and soybean in addition to Nicotiana benthamiana and a number of ornamental species.
In accordance with this discovery, it is an object of the invention to provide a novel bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus, a viral vector advantageous for high level replication for protein expression when maintaining endogenous efficient suppression of RNA silencing and for effective virus-induced gene silencing when modified for weak suppression of RNA silencing.
It is an object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: the 5′utr (untranslated region)-RdRp (RNA-dependent RNA polymerase)-3′utr construct plus the 5′utr-partial RdRp/TGB1 (Triple. Gene Block 1), TGB2, TGB3/sgPro (sub-genomic promoter)-MCS (multiple cloning site)-sgPro/CP (coat protein)-3′utr construct, wherein the T7 promoter is present in the nucleotide sequence immediately upstream of each AltMV 5′utr, and each construct is inoculated into plants, resulting in recombination in planta to regenerate full-length infectious virus, said recombination occurring within, a short overlap of a common sequence present in both constructs of the bipartite vector system (resulting from TGB1 initiating 16 nt upstream of the RdRp termination region).
It is a further object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: the 5′utr-RdRp-3′utr modified pGD cDNA construct plus the 5′utr-partial RdRp/TGB1, TGB2, TGB3/sgPro-MCS-sgPro/CP-3′utr modified pGD cDNA construct, wherein the T7 promoter is present in the nucleotide sequence immediately upstream of each AltMV 5′utr and in addition a CaMV 35S promoter is located upstream from each T7 promoter, each construct delivered by Agrobacterium-mediated inoculation, resulting in recombination in planta to regenerate full-length infectious virus.
It is an additional object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: the 5′utr-RdRp-3′utr modified pGD cDNA construct plus the 5′utr-partial RdRp/TGB1, TGB2, TGB3/sgPro-MCS-sgPro/CP-3′utr modified pGD cDNA construct, wherein the T7 promoter is present in the nucleotide sequence immediately upstream of each AltMV 5′utr, a CaMV 35S promoter is located upstream from each T7 promoter, and in addition, a construct encoding the T7 RNA polymerase (T7RNAP) is added, each construct delivered by Agrobacterium-mediated inoculation, resulting in recombination in planta to regenerate full-length infectious virus.
It is another object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr-RdRp-3′utr plus 5′utr-partial RdRp/TGB1, TGB2, TGB3/sgPro-MCS-sgPro/CP 3′utr wherein the bipartite launch system comprises chimeric constructs having anyone; or more of the substitutions R(1110)P, K(1121)R, and R(1255)K in Pol, S(1535)P in RdRp in the RdRp C-terminal region and P(88)L in TGB1.
It is a still further object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr-RdRp-3′utr plus 5′utr-partial RdRp/TGB1, 2, 3/sgPro-MCS-sgPro/CP-3′utr together with RNA transcripts for the T7 polymerase in conjunction with the 35S promoter to increase efficiency of transcription via Agrobacterium-mediated inoculation to establish infectious virus in a shorter time and with higher efficiency.
It is still another object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr RdRp-3′utr plus 5′utr-partial RdRp/TGB1, 2, 3/sgPro-MCS-sgPro/CP-3′utr wherein the nucleotide sequence encoding leucine at amino acid 88 of TGB1 is maintained resulting in a vector to be used advantageously for high level protein expression.
It is another object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr-RdRp-3′utr plus 5′utr-partial RdRp/TGB1, 2, 3/sgPro-MCS-sgPro/CP-3′utr wherein the nucleotide sequence encoding leucine at amino acid 88 of TGB1 is maintained and an additional strong suppressor of silencing, such as tombusvirus p19, is present resulting in a vector to be used advantageously for high level protein expression.
It is an additional object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr RdRp-3′utr plus 5′utr-partial RdRp/TGB1,2,3/sgPro-MCS/CP 3′utr wherein the nucleotide sequence encoding amino acid 88 of TGB1 is modified resulting in the amino acid substitution of proline for leucine and thereby converting TGB1 of AltMV from an effective silencing suppressor to a weak suppressor of RNA silencing, resulting in the AltMV vector to be used advantageously for virus-induced gene silencing (VIGS).
It is a still another object of the invention to provide recombinant nucleotide sequences comprising the bipartite launch system: 5′utr-RdRp-3′utr plus 5′utr-partial RdRp/TGB1, 2,3/sgPro-MCS-sgPro/CP-3′utr wherein the nucleotide sequence of TGB1 is modified to reflect a single or dual amino acid substitution, L->P or LL->P thereby converting TGB1 of AltMV and other Flexiviridae members from effective silencing suppressors to weak suppressors of RNA silencing thus resulting in variants of the same vector to be used for high level protein expression or for virus-induced gene silencing, respectively and wherein the Flexiviridae members of the genus Potexvirus having equivalent single amino acid changes in a comparable region of TGB1 are Potato virus X (PVX), or dual amino changes in PIAMV-NMV, the Nandina mosaic virus isolate of Plantago asiatica mosaic virus.
It is a still further object of the invention to provide constructs and vectors which comprise the nucleotide sequences of the two parts of the bipartite launch system.
It is another object of the invention to provide a host cell comprising the vector containing the constructs comprising the bipartite launch system of Alternanthera mosaic virus (AltMV) and other members of the Flexiviridae.
It is an additional object of the invention to provide RdRp as a transgene without 5′ and 3′ UTR to serve as a biocontainment system preventing the formation of infectious virus.
It is another object of the invention to provide a method of using the nucleotide sequences of a bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus, viral vectors advantageous for high level replication for protein expression when efficient suppression of RNA silencing is maintained and operably linked with the promoters of the bipartite system, capable of driving expression of a gene in a plant cell.
It is another object of the invention to provide a method of using the nucleotide sequences of a bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus, viral vectors advantageous for effective virus-induced gene silencing when incorporating weak suppression of RNA silencing, operably linked with the promoters of the bipartite system, capable of driving expression of a gene in a plant cell.
It is still another object of the invention to provide a method of manipulating the nucleotide sequences of a bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus and to obtain viral vectors to affect efficiency of silencing suppression thus converting TGB1 of AltMV and other Flexiviridae from effective silencing suppressors to weak suppressors of RNA silencing resulting in a variant infectious virus or vector to be used for high level protein expression or incorporating weak suppression of RNA silencing resulting in a variant infectious virus or vector to be used for effective virus-induced gene silencing.
It is yet another object of the invention to provide plants, plant cells, and plant parts, and plant seeds which have been infected by the bipartite plant viral vector launch system of the invention.
It is an additional object of the invention to provide a method of attenuating severe symptoms by manipulating levels of protein expression by substitution of domains in TGB1, and RdRp (including the Pol domain).
It is an additional object of the invention to provide a method of reducing symptom expression and ablating necrosis without affecting replication efficiency and protein expression by substituting the CP of AltMV-Po for CP of AltMV-SP.
It is another object of the invention to provide a method of increasing replication and levels of protein expression by growing the plants at temperatures lower than 25° C.
It is still another object of the invention to provide a method of using the nucleotide sequences of a bipartite plant viral vector launch system for recombination in planta to regenerate full-length infectious virus vectors advantageous for high level protein expression of multiple genes and sequences by maintaining the original TGB1 sequence and efficiency of silencing suppression of AltMV and other Flexiviridae.
It is another object of the invention to provide a method of increasing expression still more by manipulating the system by adding additional suppressors of silencing, by adding constructs encoding T7 RNA polymerase, and by altering the temperature.
It is an additional object of the invention to provide a method of using the nucleotide sequences of a bipartite plant viral vector launch system for recombination in planta to regenerate full-length variant infectious virus vectors advantageous for effective virus-induced gene silencing when the TGB1 sequence of AltMV and other Flexiviridae has been modified to a weak suppressor of RNA silencing.
Other objects and advantages of this invention will become readily apparent from the ensuing description.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the U.S. Patent and Trademark Office upon request and payment of the necessary fee.
This invention concerns the creation of multiple, biologically distinct, infectious clones derived from AltMV-SP, from which we had previously obtained a partial sequence (Hammond et al., 2006b, supra), and the use of these clones and chimeric derivatives to identify some of the determinants contributing to symptom expression and replication efficiency of AltMV. These infectious clones were then developed into a viral vector system of considerable flexibility, with variants optimized for high level protein expression, or optimized for induction of Virus-Induced Gene Silencing (VIGS). The vector system was modified such that the initial full length vector constructs were suitable for delivery by either agroinfiltration (based on the CaMV 35S promoter) or in vitro RNA transcripts (based on the T7 promoter) from the same plasmid. Co-agro-infiltration of the bipartite constructs with constructs carrying the T7 RNA polymerase and the Tomato bushy stunt virus (TBSV) p19 genes significantly enhanced infection, and reduced the time to symptom expression. A further modification was to create a bipartite vector delivery system, separating the replicase (RdRp) from the movement and encapsidation functions (Triple Gene Block, TGB; and CP), allowing easier insertion of a Gene of Interest, and the potential for high throughput cloning. Co-agro-infiltration of the bipartite constructs with constructs carrying the T7 RNA polymerase and the TBSV p19 genes resulted in high efficiency of infection resulting from precise recombination of the bipartite transcripts in planta to regenerate a full length AltMV genome. While in vitro T7 transcripts, and agroinfiltration of constructs driven by the CaMV 35S or other promoters have commonly been used to initiate infections from cloned plant viruses, we are not aware of any previous utilization of transient in vivo transcription from the T7RNAP in planta; in most applications the T7 polymerase is supplied from a stably transformed chromosomal location.
The RdRp P01 domain, TGB1, and CP were all shown to contribute to symptom expression, and both the P01 domain and TGB1 appear to significantly affect replication efficiency. Unlike some other potexviruses, AltMV was not found to uniformly induce hypersensitive response; however, hypersensitive response was observed primarily at low temperature with variants that replicate with high efficiency, and correlated with particular amino acid residues. In contrast to the on-going emergence of variation and subsequent selection reported in some other systems, we report the stable co-existence of two dominant sequence types within isolate AltMV-SP over a period of several years and multiple passages in Nicotiana benthamiana following the original isolation from Phlox stolonifera. We relate this to modulation of both replication and symptoms when both sequence variants are present, and avoidance of hypersensitive response (Lim et al. 2010. J. Gen Virol 91: 277-287).
We have created four infectious clones from AltMV-SP (
There were significant differences in the level of replication of the four infectious AltMV clones at 25° C., with 3-7>4-7>3-1>4-1, whether measured by QPCR of the CP or RdRp (
In order to determine which sequences might be present in the original isolate AltMV-SP, we amplified the region across the MluI site from an AltMV-SP infection initiated from frozen tissue, that had been stored about three years and multiple passages in N. benthamiana prior to the creation of the infectious clones. The amplified fragment included nucleotide positions that differ between the two clones of each region making up the infectious clones. The two dominant sequences recovered from this experiment corresponded to AltMV 4-7 (SEQ ID NO:1; severe) and AltMV 3-1 (SEQ ID NO:2; mild), in an 11:2 ratio. Two additional sequence types were recovered, sharing a A residue upstream of the MluI site where each of the infectious clones has a G, and a T residue where the infectious clones have either T or C; at a position downstream of the Mlu I site, one of these additional sequences has an A, and the other a G, residues that also differentiate 3′ clones 1 and 7 (
To further examine the stability of co-infection of 4-7 and 3-1, and to examine the effects of temperature on virus replication, each isolate was inoculated singly, or in mixed infection, in parallel with original isolate AltMV-SP. Groups of plants were grown at 25° C., and separately at 15° C. Co-inoculation of 4-7 and 3-1 produced symptoms indistinguishable from AltMV-SP. Q-RTPCR showed that RNA accumulation of [3-1+4-7] was indistinguishable from 3-1 alone or from AltMV-SP at either 15° C. or 25° C.; accumulation of 4-7 alone was significantly higher. In each case accumulation was >4-fold higher at 15° C. than at 25° C. (
The ability of AltMV 3-1 and 4-7 sequences to coexist was evaluated by labeling AltMV 3-1 with eGFP, and 4-7 with DsRed. When the two marked viruses were co-inoculated to N. benthamiana, approximately equal areas of GFP and DsRed expression were observed in the earliest systemically infected leaves, at 10 dpi. However, at 30 dpi, the uppermost infected leaves of plants grown at 25° C. showed approximately 10 times as large an area of DsRed as of GFP, with many co-infected cells (
Taken together, the ratios of the 4-7:3-1 in both the original AltMV-SP and mixed infections of the DsRed- and GFP-labeled clones, and the moderation of symptoms in the mixed infection compared to AltMV 4-7 alone, suggest that the mixed infection is maintained because the symptom amelioration is beneficial to survival of the host, and thus also to long-term propagation of the more severe sequence type represented by clone AltMV 4-7.
The influence of temperature on the ratio of 4-7[DsRed] to 3-1[eGFP] is interesting, and presumably results at least in part from the increased severity of all sequence types at lower temperature. Presumably at lower temperature there is less difference in the effects of the two sequence types on the host, and therefore AltMV 4-7 loses some of its competitive advantage.
It is noteworthy that the most severe symptoms observed were induced by AltMV 3-7, and the mildest symptom by 4-1, sequence combinations that were not detected among the PCR products from the central region of the original AltMV-SP genome (
It has been observed previously in chimeric infectious clones of the potyvirus Potato virus A that one chimera induced a symptom phenotype distinct from either parental isolate, while a second would not infect potato systemically, suggesting that different parts of the genome function coordinately (Paalme et al. 2004. J. Gen. Virol. 85: 739-747). Although AltMV 3-7 and 4-1 are stable in single infections, it is possible that they are less fit in a mixed population. Indeed, in a mixed infection of 4-1:eGFP and 3-7:DsRed, 4-1:eGFP was barely detectable at 10 dpi, and not at all in upper leaves at 30 dpi (
The presence of two distinct sequence types (quasispecies clouds) in AltMV-SP could be explained either by co-infection, or by sequence divergence over many seasons in the phlox host, as phlox is a vegetatively propagated crop. Biological variants have been isolated from various citrus species infected with Citrus tristeza virus by either vectored transmission or host passage (e.g. Sentandreu et al., supra), and also from another potexvirus, PIAMV. Two biologically distinct sub-isolates (Li1 and Li6) were obtained from a lily isolate of PIAMV (Ozeki et al., supra); lily is also a vegetatively propagated crop. PIAMV sub-isolate Li1 caused a systemic hypersensitive response-like necrosis in N. benthamiana, whereas Li6 caused an asymptomatic infection; PIAMV RdRp amino acid (aa) 1154 was shown to contribute to the necrotic symptoms by substitution in infectious clones, although necrotic symptoms were not correlated with viral accumulation (Ozeki et al., supra). However, in contrast to the nine aa differences over the full genomes of Li1 and Li6 (seven in RdRp, one in TGB1, and one in TGB3; Ozeki et al., supra), AltMV 4-7 and AltMV 3-1 differ by 49 aa in RdRp, one in TGB1, and none in TGB2, TGB3, or CP. In further work, it was shown that PIAMV has high divergence within the RdRp, with seven Japanese isolates from lily and primrose sharing only 82-85% aa sequence identity with a Russian Plantago isolate and a US Nandina isolate (Komatsu of al. 2008. Arch. Virol. 153: 193-198); closer inspection shows that only 15 aa residues differ between the six Japanese lily isolates (all derived from a single plant), while 41 further positions differentiate the lily isolates from the primrose isolate, and a total of 303 aa positions differ when the RdRp sequences of all nine isolates are aligned (data not shown). The 49 aa differences between the RdRps of AltMV 3-1 and 4-7, derived from the same plant, show these isolates to be considerably more divergent that the PIAMV isolates obtained from a single lily plant.
It has previously been observed that a single amino acid in the polymerase domain of the RdRp of both PVX and PIAMV contributes to necrotic symptoms in N. benthamiana (Kagiwada et al., supra; Ozeki at al., supra). However, in both of these cases the levels of replication of necrotic and non-necrotic point mutants were similar, as measured by CP accumulation. In the case of AltMV, exchange of the Pol domain, with its three aa differences, is correlated with increased replication as well as necrosis; the increase in replication levels observed at 15° C. in all isolates is also correlated with necrosis (
Substitution of TGB1, with a single amino acid change, also affected symptom expression. Whereas AltMV 4-1 was essentially symptomless, substitution of TGB1 [L(88)] in 4-1 L resulted in mosaic symptoms by 20 dpi, and substitution of both Pol and TGB1 (4-1PRKL) resulted in necrosis by 10 dpi with continued severe symptoms (
The CP gene of AltMV was identified as a third contributor to symptom expression, and the elicitor of necrosis, in four types of experiment. Although there were no differences between the CP genes of infectious clones 4-7 and 3-1, we had available clones of the 3′ region of AltMV-Po, which differs in nine amino acid positions from AltMV-SP (Hammond of al., 2006a,b). Substitution of the AltMV-Po CP (SEQ ID NO:5) into AltMV 3-7 resulted in amelioration of symptom expression including a lack of necrosis, at both 25° C. and 15° C. (
The PVX CP has been reported as a trigger of the hypersensitive reaction (Verchot-Lubicz et al., supra), and when expressed at high levels under control of the 35S promoter, induced hypersensitive response (Bendahmane et al., 2000. Plant J. 21: 73-81). Our results suggest that AltMV-SP CP is a determinant of necrosis and hypersensitive response at low temperature, and in the isolates that accumulate to the highest levels, also at 25° C. (
The effect of the [L(88)P] difference in TGB1 was further examined through co-agroinfiltration of each variant with smGFP in N. benthamiana, and comparison with AltMV TGB2, TGB3, and CP, as well as the well-characterized suppressors of RNA silencing HC-Pro and TBSV p19. The TGB1 from AltMV 3-7 (L88) shows obvious suppression of GFP silencing comparable to p19 and HC-Pro (
We have demonstrated that AltMV TGB1L88 is an effective suppressor of RNA silencing, whereas TGB1P88 has significantly weaker silencing suppression activity; we have also shown that TGB1L88 and TGB1P88 interact to interfere with silencing suppression (Lim et al., 2010 supra). In order to better understand these differences, we examined the subcellular localization of GFP:TGB1L88 and GFP:TGB1P88 following agroinfiltration of pGDG-TGB1L88 and pGDG-TGB1P88 constructs in N. benthamiana. Single expression of GFP:TGB1L88 or GFP:TGB1P88 differed in nuclear localization; GFP:TGB1L88 was observed largely as discrete aggregates inside the nucleus (presumed to be the nucleolus), as demonstrated by reduced DAPI staining in the area of GFP accumulation (
Further evidence for the inhibition of RNA silencing suppression was obtained by over-expression of either TGB1L88 or TGB1P88 as added genes from AltMV infectious clone 4-7 (
Mild infectious clone 3-1, which has TGB1P88 in the genomic position, normally produces mild mosaic (Lim et al., 2010 supra). Over-expression of TGB1P88 as an added gene (
Multiple conserved motifs have been identified within the TGB1 proteins of potexviruses and hordeiviruses, and the C-terminal region of PVX TGB1 has been shown dispensable for ATPase activity (Morosov et al., 1999). Conserved domains I, IA, II, III, IV, V, and VI of AltMV TGB1 were compared with those of PVX (
The subcellular localization of each TGB1 NTPase/helicase domain mutant was then examined by agroinfiltration of GFP:TGB1 fusions (pGDG-TGB1X) to observe nuclear and cell wall localization. The GFP:TGB1G88 mutant localized at the nuclear periphery and at the cell wall, where it was retained following plasmolysis (
Necrosis was observed in multiple combinations of CMV isolates and the satellite RNA D-CARNA 5 at 24° C., while necrosis was significantly reduced or absent with some strains, but increased with another at 32° C.; the necrosis was primarily dependent upon increased levels of viral replication (Kaper et al., supra). The effect of temperature on silencing suppressors and plant defense mechanisms has been noted previously (Chellappan et al. 2005. Plant Physiol. 138: 1828-1841; Qu et al. 2005. J. Virol. 79: 15209-15217; Jovel et al. 2007. J. Virol. 81: 12285-12297; Siddiqui et al. 2008. J. Gen. Virol. 89: 1502-1508). The increased symptom severity of all clones at 15° C. compared to 25° C. is presumably due to more effective suppression of RNA silencing (or reduced ability of the plant to activate silencing), as demonstrated by the very marked increase in replication of AltMV 4-1 at the lower temperature (
Cumulatively, these results suggest that necrotic symptom expression of AltMV is strongly influenced by three viral gene products, the RdRp, TGB1, and CP, with CP acting as the elicitor of necrosis. Although we were able to demonstrate significant differences due to the Pol domain of the RdRp, it is clear that the 45 aa differences in the upstream region (differences between 5′ RdRp clones 3 and 4) also exert a significant effect, as clones 3-7 and 3-1 each replicated to a higher level than the equivalent clones with the clone 4 RdRp domain. It is clear that both the Pol domain and TGB1 also contribute significantly to replication efficiency.
The ability of T7 RNA polymerase to direct gene expression in trans from a co-infiltrated binary plasmid was evaluated by co-infiltrating N. benthamiana leaves with pCAM-T7RNAP with pGD-T7eGFP and pGD-PFGe7T, respectively containing eGFP coding sequences inserted in sense and antisense orientations relative to the CaMV 35S and bacteriophage T7 promoters. Infiltration without pCAM-T7RNAP served as a control (
We next demonstrated that constructs of the full length viral clones containing both the CaMV 35S and the T7 promoters were infectious. Each full-length AltMV cDNA including the fused T7 promoter was cloned into the pGD binary vector with the 17 RNA polymerase terminator sequence downstream of AltMV to produce pGD-AltMV (3-7, 4-7, 3-1, and 4-1) (
aCoinfiltrated with T7 polymerase and p19
bInfiltrated with p19 without T7 polymerase
cXbal cut linearized pGD-AltMV transcribed in vitro
dNumber of plants developing systemic symptoms
eNumber of plants inoculated
fDays post inoculation
Direct mechanical inoculation of N. benthamiana with pGD-AltMV 3-7 plasmid DNA did not result in infection under conditions that yielded infection with in vitro RNA transcripts from the same vector construct.
Since Tobacco rattle virus and PVX expression vectors were stable with a duplicated homologous subgenomic promoter (Ratcliff et al., 2001; Chapman et al., 1992), we inserted a copy of the AltMV CP-subgenomic promoter region upstream of the MCS containing eGFP as described (Lim et al, 2010, supra). In N. benthamiana and A. thaliana plants inoculated with AltMV 3-7-eGFP (TGB1L88) or AltMV 3-1-eGFP (TGB1P88), expression of eGFP was detected by LCSM in systemically infected leaves at 10 dpi (data not shown). At 30 dpi eGFP fluorescence was detected in styles, and petals of N. benthamiana (
AltMV eGFP expression also was detected in Arabidopsis plants systemically infected with AltMV 3-7-eGFP, including seed pods (
To test the ability of the RdRp region to support replication in trans using agroinfiltration, we separated the RdRp (with non-viral 5′- and 3′UTR) and 5TGB123-eGFP-CP3 (with AltMV 5′- and 3′-UTR), and inserted each into the pGD vector (
Nicotiana benthamiana was co-infiltrated with pGD-5RdRp3 (
We were interested in whether a bipartite vector could be generated that would maintain the separation of the genome functions. The initial 3′ region construct (pGD-5TGB123-CP3C) consisted of an in-frame translational fusion of N- and C-terminal domains of RdRp, which overlaps TGB1. Two features of this construct were important; it has previously been demonstrated that accumulation of a defective RNA of ClYMV required maintenance of the fusion ORF (White et al., 1992), and although the minimal origin of assembly of PapMV was shown to occur within the 5′ 38-47 nt (Sit et al., 1994), the initiation complexes observed by Abouhaidar & Bancroft (1978) encapsidated about 200 nt.
We created two additional 3′ region constructs; pGD-5TGB123-CP3A (
No infection was observed with [pGD-5RdRp3+pGD-5TGB123-CP3A] either with or without pCAM-T7RNAP (Table 4). Within 20 dpi, systemic symptoms were detected from [pGD-5RdRp3+pGD-5TGB123-CP3B] plus pCAM-T7RNAP, but no symptoms were detected in the absence of pCAM-T7RNAP (Table 4). When each combination was co-infiltrated with pCAM-T7RNAP, [pGD-5RdRp3+pGD-5TGB123-CP3C] produced a much higher incidence of symptomatic plants than with [pGD-5RdRp3+pGD-5TGB123-CP3B] (Table 4).
a3′ construct coinfiltrated with pGD-5RdRp3, pCAM-T7RNAP and pGD-p19
b3′ construct coinfiltrated with pGD-5RdRp3 and pGD-p19
cNumber of plants developing systemic symptoms
dNumber of N. benthamiana infiltrated
eNot applicable
fDays post inoculation
No plants of N. benthamiana inoculated with in vitro RNA transcripts of any combination of pGD-5RdRp3 and the various pGD-5TGB123-CP3 variants developed infection.
Because the full-length pGD-AItMV construct was about 13 Kb, there were no enzyme sites that could be used to directly insert foreign sequences. Thus, as shown in
Expression of eGFP from an infection initiated using the binary launch system was readily detected through four passages in N. benthamiana by mechanical inoculation of sap from systemically infected tissues, by confocal microscopy; following the fifth passage, faint expression of eGFP could be detected in initially infected leaves, but not in upper leaves showing typical AltMV symptoms.
We further demonstrated that the critical substitution of Proline for Leucine at AltMV TGB1 residue 88, with its effects on efficacy of RNA silencing suppression, can be duplicated at the equivalent residues of other potexvirus TGB1 proteins. Leu residues equivalent to AltMV TGB1 residue 88 were identified by alignment of multiple potexvirus TGB1 amino acid sequences (
PVX TGB1P86 was observed to accumulate around the periphery of the nucleus and into the cytoplasm, whereas PVX TGB1L86 yielded discrete aggregates within the nucleus (
NMV TGB1P86/P89 and NMV TGB1L86/L89 were separately over-expressed from mild infectious clone AltMV 4-1 (AltMV TGB1P88;
A new infectious clone of PVX, under the control of the T7 promoter, was produced in the TOPO vector (TOPO-PVX), and in vitro transcripts were shown to be infectious on N. benthamiana. The PVX genome, including the T7 promoter, was then transferred to pGD-T7ttr. The resulting clone, pGD-PVX, was infectious by both in vivo transcription following agroinfiltration in the presence of pCAM-T7RNAP, or from in vitro transcripts (data not shown), as previously demonstrated with pGD-AltMV variants. The PVX TGB1P86 was substituted into pGD-PVX, and WT (TGB1L86) and mutant (TGB1P86) clones were agroinoculated separately to N. benthamiana. Symptoms of the WT (TGB1L86) were typical mosaic, whereas the TGB1P86 mutant induced significantly milder mottle symptoms, and western blotting of equivalent leaf extracts with PVX-specific antibodies revealed a significantly lower amount of coat protein, consistent with lower levels of replication (
In a preferred embodiment of the present invention, a host cell containing the nucleotide sequences of the invention is a bacterial cell, in particular, an Agrobacterium tumefaciens cell.
For both direct gene transfer and Agrobacterium-mediated transfer, transformation is usually (but not necessarily) undertaken with a selectable marker which may provide resistance to an antibiotic (kanamycin, hygromycin or methatrexate) or a herbicide (sulfonylurea, imidazolinone, or basta). The choice of selectable marker is not, however, critical to the invention.
As used herein, the terms “nucleic acid molecule”, “nucleic acid sequence”, “polynucleotide”, “polynucleotide sequence”, “nucleic acid fragment”, “isolated nucleic acid fragment” are used interchangeably herein. These terms encompass nucleotide sequences and the like. A polynucleotide may be a polymer of RNA or DNA that is single- or double-stranded and that optionally contains synthetic, non-natural or altered nucleotide bases. A polynucleotide in the form of a polymer of DNA may be comprised of one or more segments of cDNA, genomic DNA, synthetic DNA, or mixtures thereof.
The term “isolated” polynucleotide refers to a polynucleotide that is substantially free from other nucleic acid sequences, such as other chromosomal and extrachromosomal DNA and RNA, that normally accompany or interact with it as found in its naturally occurring environment. However, isolated polynucleotides may contain polynucleotide sequences which may have originally existed as extrachromosomal DNA but exist as a nucleotide insertion within the isolated polynucleotide. Isolated polynucleotides may be purified from a host cell in which they naturally occur. Conventional nucleic acid purification methods known to skilled artisans may be used to obtain isolated polynucleotides. The term also embraces recombinant polynucleotides and chemically synthesized polynucleotides.
As used herein, “recombinant” refers to a nucleic acid molecule which has been obtained by manipulation of genetic material using restriction enzymes, ligases, and similar genetic engineering techniques as described by, for example, Sambrook et al. 1989. Molecular Cloning: A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. or DNA Cloning: A Practical Approach, Vol. I and II (Ed. D. N. Glover), IRL Press, Oxford, 1985. “Recombinant,” as used herein, does not refer to naturally occurring genetic recombinations.
As used herein, the term “chimeric” refers to two or more DNA molecules which are derived from different sources, strains, or species, which do not recombine under natural conditions, or to two or more DNA molecules from the same species, which are linked in a manner that does not occur in the native genome. A “construct” or “chimeric gene construct” refers to a nucleic acid sequence encoding a protein, operably linked to a promoter and/or other regulatory sequences.
As used herein, the term “express” or “expression” is defined to mean transcription alone. “Altered levels” or “altered expression” refers to the production of gene product(s) in transgenic organisms in amounts or proportions that differ from that of normal or non-transformed organisms.
As used herein, the terms “encoding”, “coding”, or “encoded” when used in the context of a specified nucleic acid mean that the nucleic acid comprises the requisite information to guide translation of the nucleotide sequence into a specified protein. The information by which a protein is encoded is specified by the use of codons. A nucleic acid encoding a protein may comprise non-translated sequences (e.g., introns) within translated regions of the nucleic acid or may lack such intervening non-translated sequences (e.g., as in cDNA).
The term “operably linked” refers to the association of two or more nucleic acid fragments on a single nucleic acid fragment so that the function of one is affected by the other. For example, a promoter is operably linked with a coding sequence when it is capable of affecting the expression of that coding sequence (i.e., that the coding sequence is under the transcriptional control of the promoter). Coding sequences can be operably linked to regulatory sequences in sense or antisense orientation.
“Regulatory sequences” refer to nucleotide sequences located upstream (5′ non-coding sequences), within, or downstream (3′ non-coding sequences) of a coding sequence, and which influence the transcription, RNA processing or stability, or translation of the associated coding sequence. Regulatory sequences here may include promoters: T7 promoter, CaMV 35S promoter and sub-genomic promoters (two, on either side of the MCS), translation leader sequences, introns, and polyadenylation recognition sequences.
“Promoter” refers to a nucleotide sequence capable of controlling the expression of a coding sequence or functional RNA. In general, a coding sequence is located 3′ to a promoter sequence. The promoter sequence consists of proximal and more distal upstream elements, the latter elements often referred to as enhancers. Accordingly, an “enhancer” is a nucleotide sequence that can stimulate promoter activity and may be an innate element of the promoter or a heterologous element inserted to enhance the level or tissue-specificity of a promoter. Promoters may be derived in their entirety from a native gene, or be composed of different elements derived from different promoters found in nature, or even comprise synthetic nucleotide segments. One exemplification here is the native AltMV coat protein sub-genomic promoter which has been duplicated and is positioned on each side of MCS; however, sub-genomic promoters from other viruses can be used. It is understood by those skilled in the art that different promoters may direct the expression of a gene in different tissues or cell types, or at different stages of development, or in response to different environmental conditions. Promoters that cause a nucleic acid fragment to be expressed in most cell types at most times are commonly referred to as “constitutive promoters”. New promoters of various types useful in plant cells are constantly being discovered; numerous examples may be found in the compilation by Okamuro and Goldberg. 1989. Biochemistry of Plants 15:1-82. It is further recognized that since in most cases the exact boundaries of regulatory sequences have not been completely defined, nucleic acid fragments of different lengths may have identical promoter activity.
The “translation leader sequence” refers to a nucleotide sequence located between the promoter sequence of a gene and the coding sequence. The translation leader sequence is present in the fully processed mRNA upstream of the translation start sequence. The translation leader sequence may affect processing of the primary transcript to mRNA, mRNA stability or translation efficiency.
The “3′ non-coding sequences” refer to nucleotide sequences located downstream of a coding sequence and include polyadenylation recognition sequences and other sequences encoding regulatory signals capable of affecting mRNA processing or gene expression. The polyadenylation signal is usually characterized by affecting the addition of polyadenylic acid tracts to the 3′ end of the mRNA precursor.
“RNA transcript” refers to the product resulting from RNA polymerase-catalyzed transcription of a DNA sequence. When the RNA transcript is a perfect complementary copy of the DNA sequence, it is referred to as the primary transcript or it may be an RNA sequence derived from posttranscriptional processing of the primary transcript and is referred to as the mature RNA. “Messenger RNA (mRNA)” refers to the RNA that is without introns and that can be translated into polypeptides by the cell. “cDNA” refers to a DNA that is complementary to and derived from an mRNA template. The cDNA can be single-stranded or converted to double stranded form using, for example, the Klenow fragment of DNA polymerase I. “Sense” RNA refers to an RNA transcript that includes the mRNA and so can be translated into a polypeptide by the cell. “Antisense”, when used in the context of a particular nucleotide sequence, refers to the complementary strand of the reference transcription product. “Antisense RNA” refers to an RNA transcript that is complementary to all or part of a target primary transcript or mRNA and that blocks the expression of a target gene. The complementarity of an antisense RNA may be with any part of the specific nucleotide sequence, i.e., at the 5′ non-coding sequence, 3′ non-coding sequence, introns, or the coding sequence. “Functional RNA” refers to sense RNA, antisense RNA, ribozyme RNA, or other RNA that may not be translated but yet has an effect on cellular processes.
“Transformation” refers to the transfer of a nucleic acid fragment into the genome of a host organism, resulting in genetically stable inheritance. Host organisms containing the transformed nucleic acid fragments are referred to as “transgenic” organisms. Examples of methods of plant transformation include Agrobacterium-mediated transformation (De Blaere et al. 1987. Meth. Enzymol. 143:277) and particle-accelerated or “gene gun” transformation technology (Klein et al. 1987. Nature (London) 327:70-73; U.S. Pat. No. 4,945,050, incorporated herein by reference). Additional transformation methods are disclosed below. Thus, isolated polynucleotides of the present invention can be incorporated into recombinant constructs, typically DNA constructs, capable of introduction into and replication in a host cell. Such a construct can be a vector that includes a replication system and sequences that are capable of transcription and translation of a polypeptide-encoding sequence in a given host cell. A number of vectors suitable for stable transfection of plant cells or for the establishment of transgenic plants have been described in, e.g., Pouwels et al. 1985. Supp. 1987. Cloning Vectors: A Laboratory Manual; Weissbach and Weissbach. 1989. Methods for Plant Molecular Biology, Academic Press, New York; and Flevin at al. 1990. Plant Molecular Biology Manual, Kluwer Academic Publishers, Boston. Typically, plant expression vectors include, for example, one or more cloned plant genes under the transcriptional control of 5′ and 3′ regulatory sequences and a dominant selectable marker. Such plant expression vectors also can contain a promoter regulatory region (e.g., a regulatory region controlling inducible or constitutive, environmentally- or developmentally-regulated, or cell- or tissue-specific expression), a transcription initiation start site, a ribosome binding site, an RNA processing signal, a transcription termination site, and/or a polyadenylation signal.
A “protein” or “polypeptide” is a chain of amino acids arranged in a specific order determined by the coding sequence in a polynucleotide encoding the polypeptide. Each protein or polypeptide has a unique function.
The term “substantially pure” as used herein refers to a polypeptide that is substantially free of other proteins, lipids, carbohydrates or other materials with which it is naturally associated. One skilled in the art can purify proteins using standard techniques for protein purification. The purity of the polypeptide can also be determined by amino-terminal amino acid sequence analysis.
The invention includes functional polypeptides and functional fragments thereof, as well as mutants and variants having the same biological function or activity. As used herein, the terms “functional fragment”, “mutant” and “variant” refers to a polypeptide which possesses biological function or activity identified through a defined functional assay and associated with a particular biologic, morphologic, or phenotypic alteration in the cell. Functional fragments, for example, can vary in size from a polypeptide fragment as small as an epitope capable of binding an antibody molecule, to a large polypeptide capable of participating in the characteristic induction or programming of phenotypic changes within a cell.
A heterologous coding sequence refers to coding sequences which encode peptides or proteins, unrelated to, or, other than, the polypeptides provided above and which are not intrinsically found in the position provided in the chimeric gene construct.
Genes encoding the AltMV and Flexiviridae viral proteins and enzymes of the bipartite vector as well as proteins and enzymes included in the multiple cloning site can be cloned using a variety of techniques according to the invention. The simplest procedure for the cloning of such genes requires the cloning of complementary DNA from viral genomic RNA, or of genomic DNA from an organism identified as producing said protein(s), and the transfer of the cloned DNA on a suitable plasmid or vector to a host organism which does not produce the protein, followed by the identification of transformed hosts to which the ability to produce the protein has been conferred. The transforming protein function-conferring DNA can be cleaved into smaller fragments and the smallest which maintains the protein function-conferring ability can be further characterized. Techniques suitable for cloning by homology include standard library screening by DNA hybridization or polymerase chain reaction (PCR) amplification using primers derived from conserved sequences. As defined herein, two DNA sequences are substantially homologous when at least 80% (preferably at least 85% and most preferably 90%) of the nucleotides match over the defined length of the sequence using algorithms such as CLUSTAL or PILEUP. Sequences that are substantially homologous can be identified in a Southern hybridization experiment under stringent conditions as is known in the art. See, for example, Sambrook et al., supra. Sambrook et al. describe highly stringent conditions as a hybridization temperature 5-10° C. below the Tm of a perfectly matched target and probe; thus, sequences that are “substantially homologous” would hybridize under such conditions.
As used herein, “substantially similar” refers to nucleic acid fragments wherein changes in one or more nucleotide bases results in substitution of one or more amino acids, but do not affect the functional properties of the polypeptide encoded by the nucleotide sequence. “Substantially similar” also refers to modifications of the nucleic acid fragments of the instant invention such as deletion or insertion of nucleotides that do not substantially affect the functional properties of the resulting transcript. It is therefore understood that the invention encompasses more than the specific exemplary nucleotide or amino acid sequences and includes functional equivalents thereof. Alterations in a nucleic acid fragment that result in the production of a chemically equivalent amino acid at a given site, but do not affect the functional properties of the encoded polypeptide, are well known in the art. Thus, a codon for the amino acid alanine, a hydrophobic amino acid, may be substituted by a codon encoding another less hydrophobic residue, such as glycine, or a more hydrophobic residue, such as valine, leucine, or isoleucine. Similarly, changes which result in substitution of one negatively charged residue for another, such as aspartic acid for glutamic acid, or one positively charged residue for another, such as lysine for arginine, can also be expected to produce a functionally equivalent product. Nucleotide changes which result in alteration of the N-terminal and C-terminal portions of the polypeptide molecule would also not be expected to alter the activity of the polypeptide. Each of the proposed modifications is well within the routine skill in the art, as is determination of retention of biological activity of the encoded products. A method of selecting an isolated polynucleotide that affects the level of expression of a polypeptide in a virus or in a host cell (eukaryotic, such as plant, yeast, fungi, or algae; prokaryotic, such as bacteria) may comprise the steps of: constructing an isolated polynucleotide of the present invention or an isolated chimeric gene of the present invention; introducing the isolated polynucleotide or the isolated chimeric gene into a host cell; measuring the level of a polypeptide in the host cell containing the isolated polynucleotide; and comparing the level of a polypeptide in the host cell containing the isolated polynucleotide with the level of a polypeptide in a host cell that does not contain the isolated polynucleotide.
Moreover, substantially similar nucleic acid fragments may also be characterized by their ability to hybridize. Estimates of such homology are provided by either DNA-DNA or DNA-RNA hybridization under conditions of stringency as is well understood by those skilled in the art (1985. Nucleic Acid Hybridization, Hames and Higgins, Eds., IRL Press, Oxford, U.K.). Stringency conditions can be adjusted to screen for moderately similar fragments, such as homologous sequences from distantly related organisms, to highly similar fragments, such as genes that duplicate functional enzymes from closely related organisms.
Thus, isolated sequences that encode AltMV polypeptides and which hybridize under stringent conditions to the sequences disclosed herein, or to fragments thereof, are encompassed by the present invention.
Substantially similar nucleic acid fragments of the instant invention may also be characterized by the percent identity of the amino acid sequences that they encode to the amino acid sequences disclosed herein, as determined by algorithms commonly employed by those skilled in this art.
Methods of alignment of sequences for comparison are well known in the art. Thus, the determination of percent identity between any two sequences can be accomplished using a mathematical algorithm. Non-limiting examples of such mathematical algorithms are the algorithm of Myers and Miller (1988. CABIOS 4:11-17), the local homology algorithm of Smith at al. (1981. Adv. Appl. Math. 2:482); the homology alignment algorithm of Needleman and Wunsch (1970. J. Mol. Biol. 48:443-453); the search-for-similarity-method of Pearson and Lipman (1988. Proc. Natl. Acad. Sci. 85:2444-2448; the algorithm of Karlin and Altschul (1990. Proc. Natl. Acad. Sci. USA 87:2264), modified as in Karlin and Altschul (1993. Proc. Natl. Acad. Sci. USA 90:5873-5877).
Computer implementations of these mathematical algorithms can be utilized for comparison of sequences to determine sequence identity. Such implementations include, but are not limited to: CLUSTAL in the PC/Gene program (available from Intelligenetics, Mountain View, Calif.); the ALIGN program (Version 2.0) and GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Version 8 (available from Genetics Computer Group (GCG), 575 Science Drive, Madison, Wis., USA). Alignments using these programs can be performed using the default parameters.
Unless otherwise indicated, sequence alignments and percent identity calculations were performed using the Megalign program of the LASERGENE bioinformatics computing suite (DNASTAR Inc., Madison, Wis.), or any equivalent program. Multiple alignment of the sequences was performed using the Clustal W method of alignment (Higgins and Sharp (1989. CABIOS 5:151-153) with the default parameters (GAP PENALTY=10, GAP LENGTH PENALTY=1.0), while default parameters for pairwise alignments using the Clustal W method were GAP PENALTY=10, GAP LENGTH PENALTY=1.0, Slow-Accurate unless otherwise indicated.
As used herein, “sequence identity” or “identity” in the context of two nucleic acid or polypeptide sequences makes reference to the residues in the two sequences that are the same when aligned for maximum correspondence over a specified comparison window. When percentage of sequence identity is used in reference to proteins, it is recognized that residue positions which are not identical often differ by conservative amino acid substitutions, where amino acid residues are substituted for other amino acid residues with similar chemical properties. (e.g., charge or hydrophobicity) and therefore do not change the functional properties of the molecule.
As used herein, “percentage of sequence identity” means the value determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid base or amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison, and multiplying the result by 100 to yield the percentage of sequence identity.
As used herein, “reference sequence” is a defined sequence used as a basis for sequence comparison. A reference sequence may be a subset or the entirety of a specified sequence; for example, as a segment of a full-length cDNA or gene sequence, or the complete cDNA or gene sequence.
The term “substantial identity” of polynucleotide sequences means that a polynucleotide comprises a sequence that has at least 80% sequence identity, preferably at least 85%, more preferably at least 90%, most preferably at least 95% sequence identity compared to a reference sequence using one of the alignment programs described using standard parameters. One of skill in the art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning, and the like. Substantial identity of amino acid sequences for these purposes normally means sequence identity of at least 80%, preferably at least 85%, more preferably at least 90%, and most preferably at least 95%. Preferably, optimal alignment is conducted using the homology alignment algorithm of Needleman et al. (1970. J. Mol. Biol. 48:443).
Another indication that nucleotide sequences are substantially identical is if two molecules hybridize to each other under stringent conditions. Generally, stringent conditions are selected to be about 5° C. lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH. However, stringent conditions encompass temperatures in the range of about 1° C. to about 20° C., depending upon the desired degree of stringency as otherwise qualified herein.
A “substantial portion” of an amino acid or nucleotide sequence comprises an amino acid or a nucleotide sequence that is sufficient to afford putative identification of the protein or gene that the amino acid or nucleotide sequence comprises. Amino acid and nucleotide sequences can be evaluated either manually by one skilled in the art, or by using computer-based sequence comparison and identification tools that employ algorithms such as BLAST. In general, a sequence of ten or more contiguous amino acids or thirty or more contiguous nucleotides, is necessary in order to putatively identify a polypeptide or nucleic acid sequence as homologous to a known protein or gene. Moreover, with respect to nucleotide sequences, gene-specific oligonucleotide probes comprising 30 or more contiguous nucleotides may be used in sequence-dependent methods of gene identification and isolation. In addition, short oligonucleotides of 12 or more nucleotides may be used as amplification primers in PCR in order to obtain a particular nucleic acid fragment comprising the primers. Accordingly, a “substantial portion” of a nucleotide sequence comprises a nucleotide sequence that will afford specific identification and/or isolation of a nucleic acid fragment comprising the sequence. The instant specification teaches amino acid and nucleotide sequences encoding polypeptides that comprise a particular plant protein. The skilled artisan, having the benefit of the sequences as reported herein, may now use all or a substantial portion of the disclosed sequences for purposes known to those skilled in this art. Thus, such a portion represents a “substantial portion” and can be used to establish “substantial identity”, i.e., sequence identity of at least 80%, compared to the reference sequence, AltMV. Accordingly, the instant invention comprises the complete sequences as reported in the accompanying Sequence Listing, as well as substantial portions at those sequences as defined above.
Fragments and variants of the disclosed nucleotide sequences and proteins encoded thereby are also encompassed by the present invention. By “fragment” a portion of the nucleotide sequence or a portion of the amino acid sequence and hence protein encoded thereby is intended. Fragments of a nucleotide sequence may encode protein fragments that retain the biological activity of the native protein and hence have AltMV protein-like activity. Alternatively, fragments of a nucleotide sequence that are useful as hybridization probes may not encode fragment proteins retaining biological activity.
By “variants” substantially similar sequences are intended. For nucleotide sequences, conservative variants include those sequences that, because of the degeneracy of the genetic code, encode the amino acid sequence of one of the AltMV viral polypeptides of the invention. Naturally occurring allelic variants such as these can be identified with the use of well-known molecular biology techniques, as, for example, with polymerase chain reaction (PCR), a technique used for the amplification of specific DNA segments. Generally, variants of a particular nucleotide sequence of the invention will have generally at least about 90%, preferably at least about 95% and more preferably at least about 98% sequence identity to that particular nucleotide sequence as determined by sequence alignment programs described elsewhere herein.
By “variant protein” a protein derived from the native protein by deletion (so-called truncation) or addition of one or more amino acids to the N-terminal and/or C-terminal end of the native protein; deletion or addition of one or more amino acids at one or more sites in the native protein; or substitution of one or more amino acids at one or more sites in the native protein is intended. Variant proteins encompassed by the present invention are biologically active, that is they continue to possess the desired biological activity of the native protein. Such variants may result from, for example, genetic polymorphism or from human manipulation. Biologically active variants of a native AltMV viral protein of the invention will have at least about 90%, preferably at least about 95%, and more preferably at least about 98% sequence identity to the amino acid sequence for the native protein as determined by sequence alignment programs described elsewhere herein. A biologically active variant of a protein of the invention may differ from that protein by as few as 1-15 amino acid residues, or even one amino acid residue.
The polypeptides of the invention may be altered in various ways including amino acid substitutions, deletions, truncations, and insertions. Novel proteins having properties of interest may be created by combining elements and fragments of proteins of the present invention, as well as with other proteins. Methods for such manipulations are generally known in the art. Thus, the genes and nucleotide sequences of the invention include both the naturally occurring sequences as well as mutant forms. Likewise, the proteins of the invention encompass naturally occurring proteins as well as variations and modified forms thereof. Such variants will continue to possess the desired AltMV viral activity. Obviously, the mutations that will be made in the DNA encoding the variant must not place the sequence out of reading frame and preferably will not create complementary regions that could produce secondary mRNA structure.
The deletions, insertions, and substitutions of the protein sequences encompassed herein are not expected to produce radical changes in the characteristics of the protein. However, when it is difficult to predict the exact effect of the substitution, deletion, or insertion in advance of doing so, one skilled in the art will appreciate that the effect will be evaluated by routine screening assays where the effects of AltMV viral protein can be observed.
“Codon degeneracy” refers to divergence in the genetic code permitting variation of the nucleotide sequence without affecting the amino acid sequence of an encoded polypeptide. Accordingly, the instant invention relates to any nucleic acid fragment comprising a nucleotide sequence that encodes all or a substantial portion of the amino acid sequences set forth herein.
It is to be understood that as used herein the term “transgenic” includes any cell, cell line, callus, tissue, plant part, or plant the genotype of which has been altered by the presence of a heterologous nucleic acid including those transgenics initially so altered as well as those created by sexual crosses or asexual propagation from the initial transgenic. The term “transgenic” as used herein does not encompass the alteration of the genome (chromosomal or extra-chromosomal) by conventional plant breeding methods or by naturally occurring events such as random cross-fertilization, non-recombinant viral infection, non-recombinant bacterial transformation, non-recombinant transposition, or spontaneous mutation.
As used herein, the term “plant” includes reference to whole plants, plant organs (e.g., leaves, stems, roots, etc.), seeds, plant cells, and progeny of same. Parts of transgenic plants are to be understood within the scope of the invention to comprise, for example, plant cells, protoplasts, tissues, callus, embryos as well as flowers, stems, fruits, leaves, roots originating in transgenic plants or their progeny previously transformed with a DNA molecule of the invention and therefore consisting at least in part of transgenic cells, are also an object of the present invention.
As used herein, the term “plant cell” includes, without limitation, seeds suspension cultures, embryos, meristematic regions, callus tissue, leaves, roots, shoots, gametophytes, sporophytes, pollen, and microspores. The class of plants that can be used in the methods of the invention is generally as broad as the class of higher plants amenable to transformation techniques, including both monocotyledonous and dicotyledonous plants.
Having now generally described this invention, the same will be better understood by reference to certain specific examples, which are included herein only to further illustrate the invention and are not intended to limit the scope of the invention as defined by the claims.
Seed of N. benthamiana were sown in 10 cm pots and grown either in a greenhouse, or in plant growth chambers at 22° C. with a 16 h/8 h light/dark regime. Three- to four-week old N. benthamiana plants were used for virus infection and agroinfiltration. Alternanthera dentate ‘Purple Knight’ was raised from seed and propagated by cuttings. For temperature treatments, inoculated plants were grown in greenhouses maintained at 15° C. and 25° C. under a 14 h light regime.
AltMV-SP was isolated from Phlox stolonifera cv. Sherwood Purple by mechanical transmission to N. benthamiana, and serially passaged in this host over several years; AltMV-Po was isolated from Portulaca grandiflora and maintained in N. benthamiana (Hammond et al. 2006a,b, supra). Tissue of N. benthamiana infected with AltMV-SP and stored frozen at −70° C. from various timepoints (serial passages) was used to re-initiate the culture; total RNA was isolated from leaves of N. benthamiana using the RNeasy Mini Kit (Qiagen, Valencia, Calif.). Two micrograms of total RNA were used to generate cDNA using SuperScript III RNase H-Reverse Transcriptase (Invitrogen, Carlsbad, Calif.) separately with an oligo (dT)20 primer and an internal reverse primer (MluI-R) containing an Mlu I site that is unique in the sequence of AltMV-PA (Hammond et al. 2006a, supra) at nt3125. Two cDNAs were amplified by a) a 5′ non coding region primer including a T7 promoter sequence upstream of AltMV nt1 (PstI-F; CTGCAGTAATACGACTCACTATAGAAAAGTAAAGCAAAGCA; SEQ ID NO:6) paired with MluI-R (AGAGCAGAATTTGCACGCGTGGGGCTG; SEQ ID NO:7), and b) MluI-F (CAGCCCCACGCGTGCAAATTCTGCTCTCA; SEQ ID NO:8) and XbaI-R1 (GAGAGTCTAGATTTTTTTTTTTTTTTTTTTT; SEQ ID NO:9) respectively; the two PCR products were separately cloned to the TOPO vector (Invitrogen, Carlsbad, Calif.), yielding four clones containing the 5′ portion of the genome (nt 1-3143), and seven clones containing the 3′ region (nt3117 to the poly(A) tail); each clone contains an MluI site at nt3125. The seven 3′ region clones were each digested individually with MluI and XbaI, and each insert individually ligated into each of the 5′ region clones similarly cleaved with MluI and XbaI to create 28 distinct full-length AltMV clones. Each of the full-length clones was linearized with XbaI for in vitro T7 RNA transcript production (see below); transcripts were inoculated to young plants of N. benthamiana (3 plants per transcribed clone). Inoculated plants were tested for infection by RT-PCR using AltMV-specific primers PP12 (AATCCTTGCCCTGCTGTC; SEQ ID NO:10) and PP15 (TCAGAAGCACTATGTGACAT; SEQ ID NO:11).
3′ region TOPO clones 1 and 7 were used for preparation of chimeric vectors. The Pol domain of mild symptom 3′ region clone 1 was digested with Mlu I (at nt3125) and Bam HI (at nt4484) and the Pol domain exchanged with the Mlu I/Bam HI Pol fragment of severe symptom clone 7. To replace both the Pol and TGB1 domains, clone 1 was digested with Mlu I (nt3125) and Xma I (nt5480) and this fragment replaced with the clone 7 Mlu I/Xma I Pol+TGB1 fragment. The Clone 1 TGB1 fragment was substituted by the clone 7 TGB1 fragment using the Bam HI/Xma I fragment of clone 7, and the TGB1 fragment of clone 7 similarly substituted by the Bam HI/Xma I fragment of clone 1. Because the Bam HI/Xma I fragment also included the P(1535)S difference between clones 1 and 7, P(1535) was altered to S(1535) so that the differences due to TGB1 residue 88 could be evaluated independently. Overlap PCR (Wurch et al. 1998. Biotech. Techniques 12: 653-657) was used to substitute S(1535) into clone 1 using primers Pol-F (GGAGTTCTGTGGATACAGGATTACGCCCA [SEQ ID NO:12])/(P to S)-R (TTCATCTTTGGAAGAAAAGTTTT [SEQ ID NO:13]) and (P to S)-F (CCCAAAGAT GAATCACTTTACT [SEQ ID NO:14])/Pol-R (TAGGGACCTCCAAAGGGCAGTTGATG AATATT [SEQ ID NO:15]). The structures of all chimeric clones were confirmed by sequence analysis. The chimeric 3′ subclones were then digested with Mlu I and Xba I and combined with appropriate Mlu I/Xba I cleaved 5′ region TOPO clones to create chimeric full-length clones 4-1PRK (4-1 with Pol from clone 7); 4-1L (4-1 with TGB1 from clone 7); 4-1PRKL (4-1 with Pol+TGB1 from clone 7); and 3-7Pol 4-1 (3-7 with Pol from clone 1).
Full-length AltMV cDNA clones were linearized with Xba I and transcript RNA was generated using T7 RNA polymerase as described by Petty et al. (1989). The transcribed RNAs were precipitated and resuspended in 20 μl of GKP buffer (50 mM glycine, 30 mM KHPO4, pH9.2, 1% bentonite, 1% celite) per 50 μl transcription reaction and 10 μl used per leaf to inoculate Nicotiana benthamiana (Petty et al. 1989. Virology 171:342-349).
Total RNA was isolated from leaves of N. benthamiana using the RNeasy Mini Kit (Qiagen, Valencia, Calif.) and the extracted RNA was treated with DNase I according to manufacturer's recommendation. Two micrograms of total RNA were used to generate cDNA in a 20 μl reaction using SuperScript III RNase H-Reverse Transcriptase (Invitrogen, Carlsbad, Calif.) with 0.5 μg of an oligo (dT)20 primer: Q-RTPCR was performed with the selected primer sets (Coat: Coat-F=ATCATCTGGAACCTCAG AACAGAC [SEQ ID NO:16], Coat-R=TGAAAGAGGTTTACCTGCTTGTTAG [SEQ ID NO:17]; RdRp: RdRp-F=AAGAGGTCCAAACTTCAATACTTCC [SEQ ID NO:18], RdRp-R=GAAGGAAGTGTAGTGTGTCTCCAAT [SEQ ID NO:19]; Actin: Actin-F=GTTGGCTTACATTGCTCTTGACTAT [SEQ ID NO:20], Actin-R=GTTTCCGTACAG ATCCTTTCTGAT [SEQ ID NO:21]) using an Mx3005P® QPCR System and Brilliant® SYBR® Green QPCR Master Mix (Stratagene, La Jolla, Calif.) as described by Bae et al. (2006. Plant Physiol. 141:1056-1057). Each 25 μl Q-RTPCR reaction contained 12.5 μL of 2× Brilliant SYBR® Green QPCR Master Mix, 5 μl of ten-fold diluted cDNA, 2.5 pM of each gene-specific primer and diluted reference dye (final concentration=300 nM). The conditions used for Q-RTPCR reactions were: 95° C. for 10 min, followed by 40 cycles of 95° C. for 30 sec, 60° C. for 1 min, and 72° C. for 30 sec. A putative EST sequence encoding a chlorophyll a-b binding protein 50 (LHCII type I CAB-50, LHCP) was obtained from the “The DFCI Nicotiana benthamiana Gene Index (NbGI)” (http://compbio.dfci.harvard.edu/tgi/cgi-bin/tgi/gireport.pl?gudb=N. benthamiana) and used as an internal control. Relative transcript levels of each target (AltMV CP or RdRp, LHCP) were normalized with respect to N. benthamiana ACTIN (accession no. AY179605) transcript levels (% of ACTIN), which is a constitutively expressed gene. Four biological replications were used to calculate mean values.
RNA was extracted and cDNA produced as described above, from an infection established from the oldest available tissue stored at −70° C. (frozen approximately 3 years prior to the passage from which the infectious clones were produced). A PCR product spanning the nt3125 MluI site junction of the 5′ and 3′ region clones was amplified with primers PP3 (CCCCCACGAAGCCCACAGTCATC [SEQ ID NO:22])/PP20 (CATTTGCACAAAGGTATCCTC [SEQ ID NO:23]). The PCR products were cloned into the TOPO vector, and 15 clones were sequenced using sequencing primers M13F and M13F (Invitrogen).
A multiple cloning site (MCS) including Nco I, Bam HI, Mlu I, Bgl II and Nhe I restriction sites was inserted immediately upstream of the CP gene in a 3′-terminal subclone of full-length clone 3-1 by overlap PCR (Wurch et al., supra). The TGB21TGB3 region was amplified using a forward primer (TGB2/3-F; GAGAAGCTTTCCCTCGCCC GGGGACAATATT; SEQ ID NO:24) introducing a Hind III site (to aid subcloning) upstream of the Xma I site at nt5480, and reverse primer MCS-R (CATAGATCTACG CGTGGATCCCATGGGATGACTTCAACTAGGA; SEQ ID NO:25) that added Bgl II, M/u I, Bam HI, and Nco I sites at the end of the TGB3/CP intergenic region; the CP-3′UTR fragment was amplified with forward primer MCS-F (GGGATCCACGCGTAGATCTAT GCTAGCATGTCTACACCATTTCCT; SEQ ID NO:26) adding Bam HI, Mlu I, Bgl II, and Nhe I sites immediately upstream of the CP gene, and reverse primer XbaI-R1 (see Example 2 above). These two fragments were then combined by amplification using the flanking. (TGB2./3-F and XbaI-R1[see just above]) primers, and the product cloned into the Hind III and Xba I sites of pUC18 to form pAltMV:MCS.
The CP subgenomic (sg) promoter was duplicated by amplification (from AltMV 3-1) of a fragment containing the sg promoter, CP, and 3′ UTR using Nhe I-modified forward primer NheI-F (GCTAGCCACCAGAGACCATCAGGG; SEQ ID NO:27) and reverse primer XbaI-R2 (TCTAGATTTTTTTTTTTTTTTTT; SEQ ID NO:28). The PCR product was digested with Nhe I and Xba I, and substituted for the Nhe I/Xba I CP-3′ UTR fragment of pAltMV:MCS to yield pAltMV:MCS:sg.
The eGFP and DsRed genes were amplified from pGDG and pGDR (Goodin et al. 2002. Plant J. 31: 375-383) respectively, using primers to introduce 5′ Nco 1 and 3′ Nu I or Nhe I sites (eGFP NcoI-F(GAGAACCATGGGTAAAGGAGAAGAACTTTT; SEQ ID NO:29)/eGFP MluI-R (AAAAAGATTAGTCTTCACCATGGACGCGT; SEQ ID NO:30); and DsRed NcoI-F(GAGAACCATGGCCTCCTCCGAGAACGTCAT [SEQ ID NO:31])/DsRed NheI-R (GACTAGCTAGCTTATCTCAGGAACAGGT [SEQ ID NO:32]), respectively, and separately inserted into the MCS of pAltMV:MCS:sg. The eGFP-containing 3′ region of the AltMV genome was then substituted into full-length mild clones 3-1 and 4-1 as an Xma I/Xba I fragment to form 3-1:eGFP and 4-1:eGFP, and the Xma I/Xba I fragment containing DsRed similarly substituted to the severe clones 3-7 and 4-7 to form 3-7:DsRed and 4-7:DsRed.
First we generated an AltMV RdRp construct with homologous AltMV 5′ and 3′ non-coding region. The AltMV 3′ non-coding region from nt 6482-6607 and poly(A) tail was amplified from pGD:AltMV using Spe I forward (AAAAACTAGTACTAGCATAAC CCCTTGGGG; SEQ ID NO:33) and Xba I reverse (XbaI-R1, see above) primers, and inserted into pGD-T7ttr digested with the same enzymes. The T7 promoter, AltMV 5′ non-coding region and complete RdRp coding sequence were amplified from pGD:AltMV using PstI forward (GAGCTGCAGTAATACGACTCACTATAGAAAAGTAA AGCAAAGCA; SEQ ID NO:34) and Spe I reverse (GAGACTAGTTAAGTAAAGTGAT TCATCTTTG; SEQ ID NO:35) primers, and inserted into the Pst I/Spe I digested pGD-T7ttr derivative already containing the 3′ non-coding region, creating pGD:5RdRp3. A construct containing the Triple Gene Block and CP gene between the 5′ and 3′ non-coding regions (pGD-5TGB123-CP3C) was prepared by digesting pGD:AltMV with Bam HI and religation lacking a Bam HI fragment (nt 224-4484); the resulting pGD-5TGB123-CP3C has an in-frame translational fusion of N- and C-terminal domains of RdRp, which overlaps TGB1. Each of constructs pGD:5RdRp3 and pGD-5TGB123-CP3C has both CaMV 35S and T7 promoters upstream of the AltMV sequence. Co-agroinfiltration of a susceptible host in the presence of pCAM:T7RNAP and pGD:p19 results in in vivo transcription and recombination to yield a full-length AltMV genome. Derivatives of pGD-5TGB123-CP3C with a multiple cloning site are suitable for expression of additional sequences for protein expression (with TGB1L88) or VIGS (with TGB1P88).
Substitution of a naturally occurring variant of AltMV TGB1, with residue Pro88 (TGB1P88) instead of Leu88 (TGB1L88) into pGD:AltMV3-7 (creating pGD:AltMV3-7P) resulted in a significant decrease in the efficacy of RNA silencing, milder symptoms, and a lower level of viral replication. Reduced silencing suppression efficacy of TGB1L88 was demonstrated in an in vivo silencing suppression assay.
Substitution by site-directed mutagenesis by overlap PCR (Wurch et al., supra) of PVX TGB1 residue Leu86 (PVX TGB1L86) with Pro86 (PVX TGB1P86) (PVX TGB1 L>P top=AGTATACTCCGGACAACACCACAAGG [SEQ ID NO:36], PVX TGB1 L>P bottom=TGTTGTCCGGAGTATACTCATCGAGGAT [SEQ ID NO:37], PVXTGB1 L(86)P forward=TAATGCACAGATTTTCCTAGGCACGTTATC [SEQ ID NO:38], PVXTGB1 L(86)P reverse=ACTAGTTTTTTTTTTTTTATTTATATTATTCAT[SEQ ID NO:39]), and of PIAMV-NMV TGB1 residues Leu(86,89) (NMV TGB1L86,89) with Pro(86,89) (NMV TGB1 LL>PP top=GCGCCCCAACCGCTCAAGGGCTCTT [SEQ ID NO:40], NMV TGB1 LL>PP bottom=CTTGGGCGGTTGGGGCGCTGCGTAT [SEQ ID NO:41], NMV TGB1-F=GAGACTCGAGAAATGGACGCAATTATTTCAACACTGA [SEQ ID NO:42], NMV TGB1-R=GAGAGGATCCTCAGTAGGTGGGGGTGAGGTG GTG [SEQ ID NO:43]) (NMV TGB1P86,89) had similar effect on efficacy of RNA silencing suppression activity in the in vivo silencing suppression assay, and the substitution of PVX TGB1P86 into an infectious clone of PVX demonstrated to have similar effects as for AltMV on symptom expression and viral replication. For each of the AltMV, PVX, and PIAMV-NMV TGB1 mutants, GFP:TGB1 fusions of TGB1 mutants with lower efficiency of RNA silencing suppression (Pro substitutions) were demonstrated to accumulate primarily at the periphery of the nucleus, whereas the efficient suppressors with wild-type Leu at the critical residue(s) accumulated to a significant extent within the nucleus, and particularly at the nucleolus.
Substitution of PVX TGB1P86 into an infectious clone of PVX reduced RNA silencing suppression activity, creating a vector more suitable for VIGS usage. The PVX TGB1P86 was substituted into pGD-PVX, and WT (TGB1L86) and mutant (TGB1P86) clones were agroinoculated separately to N. benthamiana. Symptoms of the WT (TGB1L86) were typical mosaic, whereas the TGB1P86 mutant induced significantly milder mottle symptoms, and western blotting of equivalent leaf extracts with PVX-specific antibodies revealed a significantly lower amount of coat protein, consistent with lower levels of replication, and the differences in RNA silencing suppression observed in the agroinfiltration assay.
When pGD:AltMV was co-agroinfiltrated with pGD:p19 alone, only 10 of 15 N. benthamiana plants were infected, with visible symptoms appearing at about 15 days post inoculation (dpi). When construct pCAM:T7RNAP was included in addition to pGD:AltMV and pGD:p19, 15 of 15 agroinfiltrated plants were infected, with visible symptoms appearing at 7 dpi.
Nicotiana benthamiana was co-infiltrated with pGD-5RdRp3 paired with pGD-5TGB123-CP3C, in the presence or absence of pCAM-T7TRNAP. Symptoms of infection were observed within 8-10 dpi when pCAM-T7RNAP was included; no symptoms were detected in the absence of pCAM-T7RNAP. To determine whether the bipartite nature of the virus was maintained in infected plants, total RNA was purified from symptomatic leaves of systemically infected plants, and amplified using primers specific for the 5′ (CTGCAGTAATACGACTCACTATAG; SEQ ID NO:44) and 3′ (GAGAGTCTAGATTTTTTTTTTTTTTTTTTTT; SEQ ID NO:45) UTRs. A single large PCR product equivalent to that from plants infected with pGD-AltMV was detected, without significant products representing the RdRp and TGB123-CP genome fragments, indicated that the two RNAs had recombined in planta. Sequence analysis of progeny virus across the RdRp:TGB1 junction revealed an identical sequence to the parental full-length clone in all six PCR clones examined, indicating that precise recombination had occurred in the region of overlap between the RdRp and TGB123-CP constructs.
The CP gene and 3′ UTR of portulaca isolate AltMV-Po (Hammond et al., 2006a,b) was amplified using primer Po-CP-F (GAGCCATGGCCATGTCCACTC CATTTCCTCAAGTC; SEQ ID NO:46) adding an Nco I site immediately upstream of the CP gene, paired with vector primer XbaI-R1 (see [0148] above), and substituted into pAltMV:MCS; the Xma I/Xba I fragment of pAltMV:MCS:Po-CP was then substituted into full-length clone 3-7 to form AltMV 3-7Po-CP.
Overlap PCR (Wurch et al., supra) was utilized to mutate selected residues of the AltMV 3-7 CP to the residues present in AltMV-Po. Thus mutants MN(13,14)ID, T(66)A, LA(76,77)IS, T(154)A, and MN(13,14)ID+LA(76,77)IS were produced using the primers indicated (for CP MN(13,14)ID: TGB2start F=ATGTCCGGGCTCCCCCACT CCCTGA [SEQ ID NO:47], (MN to ID)-R=GTctATCTGTTCCTGGGTGACTTG [SEQ ID NO:48], (MN to ID)-F=GAACAGATagACGCCTTCACCCC [SEQ ID NO:49], and XbaI-R1 [see 0148]; for CP (T66 to A):TGB2start F (see just above), (T66 to A)-R=GGcACT GGAGCCATTGTCATAAC [SEQ ID NO:50], (T66 to A)-F=GGCTCCAGTgCCTACAC AGCGGT [SEQ ID NO:51], XbaI-R1 [see 0148]; for CP(LA76,77 to IS): TGB2start F (see just above), (LA to IS)-R=GagAtTGAAGAAGGGCCCACCACC [SEQ ID NO:52], (LA to IS)-F=CCCTTCTTCAaTctCAGAGGTCT [SEQ ID NO:53], XbaI-R1 (see [0148]; for CP(T154 to A): TGB2start F (see just above), (T154 to A)-R=GAGcCCTAACCAA CCCTCCTGGTGG [SEQ ID NO:54], (T154 to A)-F=TTGGTTAGGgCTCCCAGCCAAG CAG [SEQ ID NO:55], XbaI-R1 (see [0148]).
Plants of N. benthamiana inoculated with pGD:AltMV3-7, pGD:AltMV4-7, developed severe mosaic, and if grown at 15° C., developed systemic necrosis and typically died within 30 days. Inoculated plants of Alternanthera ‘Purple Knight’ developed premature anthocyanin coloration at 25° C., and stunting. In contrast, when the AltMV-Po CP was substituted for the AltMV-SP CP of severe clones 3-7 or 4-7 (AltMV 3-7CP-Po, AltMV 4-7CP-Po), plants of N. benthamiana developed mild mosaic, even if grown at 15° C., and no necrosis developed; plants of Alternanthera ‘Purple Knight’ did not develop premature anthocyanin coloration, and were not stunted. Thus substitution of AltMV-Po CP reduces symptom severity in N. benthamiana and Alternanthera ‘Purple Knight’.
Soybean plants inoculated with pGD:AltMV3-7, pGD:AltMV4-7, or pGD:AltMV4-1, plants either died as a result of apical necrosis, or the inoculated leaves became necrotic and abscised without systemic infection occurring. Soybean plants inoculated with AltMV 3-7CP-Po or AltMV 4-7CP-Po became systemically infected, with mild mosaic symptoms. Thus substitution of AltMV-Po CP allows AltMV to be used as a vector in soybean, as well as reducing symptom severity in N. benthamiana and Alternanthera ‘Purple Knight’.
The infectious clone pGD:AltMV contains the AltMV sequence immediately downstream of the bacteriophage T7 polymerase, with the CaMV 35S promoter an additional 54 nucleotides upstream. Agroinfiltration of N. benthamiana with pGD:AltMV in the presence of pGD:p19 resulted in infection of 10 of 15 plants, with visible infection by 15 dpi. When pGD:AltMV was agroinfiltrated in the presence of both pGD:p19 and pCAM:T7RNAP, 15/15 plants were infected, with visible symptoms at 7 dpi. In vitro RNA transcripts from pGD:AltMV inoculated to N. benthamiana resulted in infection of 15/15 plants with visible symptoms at 7 dpi.
A new infectious clone of PVX, under the control of the T7 promoter, was produced in the TOPO vector (TOPO-PVX), and in vitro transcripts were shown to be infectious on N. benthamiana. The PVX genome, including the T7 promoter, was then transferred to pGD-T7ttr. The resulting clone, pGD-PVX, was infectious by both in vivo transcription following agroinfiltration in the presence of pCAM-T7RNAP, or from in vitro transcripts (data not shown), as previously demonstrated with pGD-AltMV variants.
This contrast with reports for other viruses, where separate constructs have proven necessary for 35S (in vivo) transcription and 17, T3 or SP6 in vitro transcription (e.g. Baulcombe, 1995, supra), or where non-viral nucleotides between the promoter and the 5′ end of the viral sequence have significant compromised or abolished transcript infectivity (e.g. Boyer and Haenni, 1994, Virology 198: 415-426).
All binary vectors used in these studies were derived from pGD or pGDG as previously described (Goodin et al., supra). The TGB1 gene of AltMV 3-1 and 3-7 (TGB1 XhoI-F=GAGACTCGAGAAATGAATCACTTTACTAACCTCA[SEQ ID NO:56], TGB1 BamHI-R=GAGAGGATCCTTTATTACTAAAGCTAAACTAACT [SEQ ID NO:57]), and TGB2 (TGB2 XhoI-F=GAGACTCGAGAAATGTCCGGGCTCCCCCA [SEQ ID NO:58], TGB2 BamHI-R=GGATCCCTAAGAGCAGCAAGGA [SEQ ID NO:59]) and TGB3 (TGB3 XhoI-F=CTCGAGAAATGCCCTATCTTGTAGAG [SEQ ID NO:60], TGB3 BamHI-R=GGATCCCTAAAACCTAAGCCAAAGCAGAG [SEQ ID NO:61]) of 3-7 were separately amplified and inserted to the Xho I and Bam HI sites of pGD. Constructs pGD:smGFP (soluble modified GFP), and pGD:p19 (Tomato bushy stunt virus p19) were a gift of Andy Jackson (Bragg and Jackson. 2004. Molecular Plant Path. 5: 465-481). pGD:HC-Pro (Soybean mosaic virus [SMV] HC-Pro) was created by amplification of HC-Pro using HC-Pro XhoI-F (GATCTCGAGAAATGTTTTTCCGT GGTTGGAAAAAGGTGT [SEQ ID NO:62])/HC-Pro XmaI-R (GAGCCCGGGTAG AATTTCATCTCACTCTG [SEQ ID NO:63]) from pG5-Hc-Pro (Lim et al. 2005. Plant Physiol. Biochem. 43: 1014-1021). AltMV-SP CP and AltMV-Po CP were separately amplified (Coat XhoI-F=GAGACTCGAGATATGTCTACACCATTTCCT [SEQ ID NO:64], Coat BamHI-R=GAGA GGATCCTCA CTCAGGTCCTGGGAG [SEQ ID NO:65]), and each inserted into both pGD (as free CP) and pGDG (as a GFP:CP fusion) vectors at the Xho I and Bam HI sites.
Agrobacterium tumefaciens infiltrations of N. benthamiana leaves were performed essentially as described by Johansen and Carrington (2001. Plant Physiol. 126:930-938). Agrobacterium EHA105 was separately transformed with each of the pGD-derived constructs; colonies were scraped from fresh plates and diluted to approximately A600=0.4 in infiltration buffer (10 mM MES pH 5.6, 10 mM MgCl2) containing 150 μM 3′,5′-dimethoxy-4′-hydroxyacetophenone (Aldrich, Milwaukee, Wis.). When more than one culture was used for co-agroinfiltration, each culture was diluted to OD600=0.4 before adding to the mixture. The bacteria were then incubated at room temperature for 2 to 3 h before pressure infiltration with a 1-cc syringe at the underside of the leaf.
To test silencing suppressor activity, we used an smGFP suppression assay as described (Bragg and Jackson, supra). Because 35S promoter-controlled GFP induces silencing of GFP expression (Silhavy and Burgyán. 2004. Trends Plant Sci. 9:76-83; Shiboleth et al. 2007. J. Virol. 81: 13135-13148), we used only pGD:smGFP co-infiltrated with the silencing suppressor. Construct pGD:smGFP was co-infiltrated with pGD:AltMV TGB1(3-7[88(L)]; and 3-1 [88(P)]), pGD:TGB2, pGD:TGB3, pGD:CP (AltMV-SP, 3-7) and pGD:p19, respectively.
AltMV infections were confirmed as necessary using western blotting as previously reported (Hammond et al. 2006b, supra) using a 1:2000 dilution of AltMV-specific antibody (a gift of Andrew Geering; Geering and Thomas, supra). PVX infections were detected using a 1:400 dilution of PVX-specific antibody (Agdia). GFP fusion proteins were detected using anti-GFP Living Colors monoclonal antibody diluted as recommended by the manufacturer (Clontech). T7 RNA polymerase was detected using anti-T7 RNA polymerase monoclonal antibody diluted as recommended by the manufacturer (Novagen).
Expression of smGFP in leaves of whole plants was detected using a Fujifilm LAS-1000 imaging system (Fujifilm USA, Stamford, Conn.). Fluorescence in epidermal cells of N. benthamiana leaves was visualized by laser scanning confocal microscopy (LSCM) using a Zeiss LSM 410 or a Zeiss LSM 710 microscope (Carl Zeiss MicroImaging, Inc., Thornwood, N.Y.). For the Zeiss LSM 410, an Argon laser was used to excite GFP at 488 nm and an emission band pass was detected between 500 to 520 nm. DsRed was excited at 543 nm, and the emission was passed to the PMT detector through the same filter as used for GFP, as well as through a LP570 nm emission filter.
For the Zeiss LSM 710, an Argon laser was used to excite eGFP at 488 nm and emission was monitored between 500 to 520 nm. The images were observed using an AxioObserver inverted microscope with a 40×1.2 NA water immersion Plan Apochromatic objective. A photomultiplier tube captured the light emitted from a 488 nm argon laser with a pin hole of 3.7 μm passing through a MBS 488 filter with limits set between 492-543 nm. The Zeiss Zen software package was used to obtain the images. Cell wall staining experiments utilized 70 μg/ml of Calcofluor Blue (Sigma-Aldrich) that was added to 0.7 M sucrose and infiltrated for 30 min before observing with the microscope. Nuclear localization was confirmed as necessary by staining nuclei with DAPI (Deng et al., 2007).
Yeast two-hybrid vectors (James et al. 1996. Genetics 144: 1425-1436), were designed to produce fusions of either the Gal4 activation domain (AD) or the Gal4 binding domain (BD) to the N-terminus of the proteins to be tested for interactions. To construct fusions to the AD (pGAD:Coat, pGAD:Coat-Po) and the BD (pGBDU:Coat, pGBDUCoat-Po), CP sequences were amplified using primers Y2H EcoRI-F (ATCGAATTCATGTCTACACCATTTCCTCAA; SEQ ID NO:66) and Y2H BamHI-R (GAGAGGATCCTCACTCAGGTCCTGGGAG; SEQ ID NO: 67) and introduced into the EcoRI and BamHI sites of pGDBU, and of pGAD. The yeast strain PJ69-4A was transformed with LEU2 selected activation domain (AD) and URA3 selected binding domain (BD) constructs as previously described (Becker et al. 1991. Proc. Natl. Acad. Sci. USA 88: 1968-1972). To select for transformants containing both the AD and BD plasmids, transformed yeast were plated on SD-glucose medium containing 20 mg/L Ade, Met, Trp, and His, and 30 mg/L Lys and were grown for 3 days at 28° C. Yeast colonies were tested for interactions through expression of the reporter genes ADE2 and HIS by streaking on SD-glucose medium containing 20 mg/L Met and Trp, and 30 mg/L Lys and growing for three to five days at 28° C. or at room temperature.
All publications and patents mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication or patent was specifically and individually indicated to be incorporated by reference.
The foregoing description and certain representative embodiments and details of the invention have been presented for purposes of illustration and description of the invention. It is not intended to be exhaustive or to limit the invention to the precise forms disclosed. It will be apparent to practitioners skilled in this art that modifications and variations may be made therein without departing from the scope of the invention.
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| Number | Date | Country | |
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| 20110154538 A1 | Jun 2011 | US |
