INTRODUCTION

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The adenovirus expression system (AES) is routinely used both for protein production and for gene transfer experiments (reviewed in references 2, 4, 5, 14, 31, and 34). Among the attractive features of the AES are the high gene transfer capacity of adenovirus vectors (AdV) in a wide range of cell types both in vitro and in vivo and very efficient transgene expression. We recently reported on an adenovirus major late promoter (MLP) expression cassette, pAdBM5, which allows for the production of heterologous proteins in the human 293 cell line at levels of 15 to 20% total cell protein (TCP) (23). Successful overexpression with pAdBM5 and with similar vectors during the course of adenovirus replication in permissive 293 cells is due both to the efficiency of the expression cassette and to gene amplification in combination with the selective expression of viral genes during the late phase of the adenovirus lytic cycle. Thus, the level of transgene expression with AdV having deletions of E1 following infection of nonpermissive cells even at a high multiplicity of infection (MOI) is much lower than that in 293 cells. For gene transfer experiments in nonpermissive cells, most AdV make use of the cytomegalovirus (CMV) immediate-early (IE) promoter-enhancer in the expression cassette, since this promoter is one of the strongest in a wide range of cell types (reviewed in references 22 and 36). Despite this fact, AdV with CMV-based expression cassettes rarely produce protein exceeding 1 to 2% TCP after infection of either nonpermissive cells or 293 cells (1, 18, 25, 37, 38, 40).

In addition, the utility of the AES is limited to the expression of proteins that either do not produce cytotoxic effects or interfere with AdV replication, since these situations make it impossible to generate recombinants (15). Among the genes that we were unable to rescue into AdV using the pAdBM5 transfer vector (5% of our attempts; unpublished data) are a series of deletion mutants of the herpes simplex virus type 2 (HSV-2) ribonucleotide reductase R1 subunit. To overcome this limitation, an ideal expression cassette should be regulated in such a way that the basal level of transgene expression is low enough to avoid any interference with adenovirus replication and yet is capable of becoming very high when fully induced. Although several inducible promoters are available, the tetracycline-controllable transactivator system is becoming the most widely used in mammalian cells in cultures (11-13, 20, 24, 27, 28) and in transgenic mice (29). This system makes use of a trans-acting factor (tTA) formed by the fusion of the activation domain of HSV protein VP16 to the Escherichia coli tetracycline repressor protein (12). The tTA transactivator can stimulate transcription from a promoter containing the tetracycline operator sequences (tetO) but is prevented from interacting with tetO by tetracycline concentrations that are not toxic for eukaryotic cells (reviewed in reference 11). A modified tTA (rtTA) which interacts with tetO only when certain tetracycline analogs are present has also been developed (13).

Here, we describe pAdTR5, an AdV containing a tetracycline-regulated expression cassette that inducibly overexpresses nontoxic proteins such as the HSV-2 R1 subunit at levels as high as 20 to 25% TCP in both 293 cells and nonpermissive cells. When compared with that of our newly optimized constitutive CMV-based expression cassette, pAdCMV5, the performance of pAdTR5 was found to be roughly equivalent. Moreover, we have constructed with this controllable vector a recombinant adenovirus expressing a putatively toxic R1 protein truncated at its amino-terminal end (R1). tTA-expressing cells infected with this recombinant produced, before their death, R1 at a level approaching 10% TCP. As the abrogation of R1 synthesis with anhydrotetracycline prevented cell death, we could conclude that recombinant protein expression was responsible for the death process.

	MATERIALS AND METHODS

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Cells and viruses. The conditions for culturing of human 293 cells, either the original anchorage-dependent 293A line (16) or 293S, an anchorage-independent clone, were as described previously (9, 23). HeLa S3 and A549 cells were obtained from the American Type Culture Collection and cultured with the same medium as that used for 293A cells. Ad5/E1E3 was used as the parent virus in our viral constructs (10). Viruses were purified from infected cells and titers were determined by standard protocols (23).

Construction of the transfer vectors pAdCMV5 and pAdTR5 and of recombinant adenoviruses. All recombinant DNA molecules were constructed by standard cloning and site-directed mutagenesis procedures and propagated in E. coli DH5. The transfer vector pAdCMV5 was derived from pAdCMV/(rabbit -globin)-poly(A) (18) by several subcloning steps resulting in the insertion, downstream of the +1 start site for the transcription of the human CMV IE promoter-enhancer, of a PCR fragment containing the adenovirus tripartite leader with the adenovirus major late enhancer bracketed by splice donor and acceptor sites, as found in pAdBM5 (23). In the process, an additional unique 8-bp cutter cloning site (PmeI) was added before the BamHI site (Fig. 1). pAdTR5 (tetracycline regulatable) was derived from pUHD10-3 (12) and pAdCMV5 in two steps. The same PCR fragment containing the adenovirus tripartite leader and enhancer sequences from pAdBM5 was first subcloned in pUHD10-3 downstream of the minimal CMV TATA box (P_hCMV-1) of the tetracycline-regulated promoter. This modified tetracycline-regulated promoter was then subcloned as an AatII-BamHI fragment, blunted at the AatII site, into pAdCMV5, in place of the CMV IE promoter-enhancer, between the BglII (at map position 9.4) and BamHI sites. This was realized by blunting the BglII sites, after BglII partial digestion, followed by BamHI digestion and ligation of the insert to obtain pAdTR5 (Fig. 1).

View larger version (28K): [in this window] [in a new window]   FIG. 1.   Genetic maps of pAdTR5 and pAdCMV5 transfer vectors. (A) Most of the genetic elements present in these transfer vectors have been described in detail by Massie et al. (23), and the full sequences of the plasmids are available upon request. The inner numbers on the vectors refer to map units (m.u.) on the Ad5 genome. pML2 is the E. coli replicon; the segments with dots (0 to 1 and 9.4 to 15.5 m.u.) bracketing the expression cassettes (between 1 and 9.4 m.u.) are Ad5 subgenomic portions involved in homologous recombination used to generate adenovirus recombinants. (B) Schematic representation of the expression cassettes. The expression cassettes are identical from the TATA box to the poly(A) site (pA), the main difference being upstream of the TATA box, where the tetracycline operator binding sequences (tetO) replace the CAAT box and the enhancer of the CMV major IE promoter. The diagrams are not drawn to scale. SS, splicing signal; SD, splice donor; SA, splice acceptor; tpl, tripartite leader; enh, enhancer; tet, tetracycline; Ori, origin of replication; pro, promoter. The expression cassettes contain two SDs as a result of the insertion of the MLP enhancer sequence into a small intron located downstream of the tpl in pAdBM1 (19). The first SD is the one found after the third segment of the tpl, whereas the second SD is the one found after the first segment of the tpl and was added when the MLP enhancer mapping at +30 to +130 relative to the MLP transcription start site was cloned as a fragment of 108 nucleotides (23).

Selection of cells expressing the tetracycline-regulated transactivator. Three different selection schemes were used to facilitate the screening of stable cell lines expressing tTA. The 293-tTA cell line was obtained by cotransfection of calcium phosphate precipitates of the tTA expression and reporter plasmid ptTA-lux with the p3'SS plasmid (Stratagene), which allows for hygromycin resistance selection. The ptTA-lux plasmid contains the CMV promoter and tTA gene derived from pUHD15-1 (12) and the firefly luciferase gene under the control of the tTA-responsive promoter pCMV-1 derived from pUHC13-3 (12). Individual clones resistant to hygromycin (450 µg/ml) were subcultured into either tetracycline-free media or media containing 40 ng of anhydrotetracycline (Spectrum Chemical, Gardena, Calif.) per ml and screened for functional tTA expression 2 days later by assaying cell extracts for luciferase activity with the Promega luciferase assay system (Promega Corp., Madison, Wis.). An A549 cell line expressing tTA (A549-tTA) was generated by cotransfection of plasmid pUHD15-1 together with a plasmid that contains the SH-GAL gene under the control of the tTA-responsive promoter. This reporter plasmid, pTR/SH-GAL, was constructed by inserting the SH-GAL gene from plasmid pUT535 (Cayla, Toulouse, France) into the tTA-responsive expression vector pUHD10-3 (13). The SH-GAL protein is a hybrid containing functional domains of the -galactosidase and zeocin-phleomycin resistance proteins. A549 cells were transfected with calcium phosphate precipitates and selected for resistance to phleomycin at a dose of 30 µg/ml. Resistant clones were tested for functional tTA activity by comparing the levels of expression of -galactosidase in live cells that had been cultured in the presence of 5 µg of tetracycline per ml or in tetracycline-free medium by use of a flow cytometric -galactosidase assay (8). A HeLa S3 cell line expressing the reverse tTA protein was established by transfection with the rtTA expression vector pUHD172-1neo followed by selection in media containing G418 (13). The resulting clones were screened by transient transfection with a tTA-regulated reporter plasmid pTR/GFP encoding the green fluorescence protein (GFP) as detailed previously (24).

Protein extraction and analysis. For analysis of recombinant protein synthesis or accumulation, petri dishes of subconfluent cells at a density of 5.0 × 10⁵ cells/dish were infected with viral inocula corresponding to MOIs of 10 to 20 PFU/cell for 293 cells and 50 to 800 PFU/cell for A549 or HeLa S3 cells. At different times postinfection (p.i.), total protein extracts were prepared by lysing phosphate-buffered saline-washed cells with 2% sodium dodecyl sulfate (SDS) in 80 mM Tris-HCl (pH 6.8)-10% glycerol. Before protein analysis by SDS-polyacrylamide gel electrophoresis and Western blotting, performed as described previously (19), the extracts were sonicated to shear the DNA. Quantification of the percentages of recombinant R1 and R1 in total protein extracts was done by densitometric scanning of the lanes of Coomassie blue-stained gels with a Jandel Scientific video analysis system as detailed previously (23). Protein radiolabeling with [³⁵S]methionine was done as detailed previously (19).

Flow cytometry analysis of GFP expression. Exponentially growing cells (10⁶) seeded in duplicate 60-mm plates were either infected with pAd5TR5GFP at increasing MOIs (A549-tTA cells) or coinfected with pAd5CMVtTA at 500 PFU/cell (HeLa S3 and A549 cells). After 40 h at 37°C with or without doxycycline (1 µg/ml), the cells were fixed with 2% paraformaldehyde for 30 min at 4°C. GFP emission was analyzed with an EPICS XL-MCL flow cytofluorometer (Coulter, Miami, Fla.) equipped with a 15-mW argon ion laser and the following filters: 488-nm laser blocking, 488-nm long-pass dichroic, 550-nm long-pass dichroic, and 525-nm band-pass.

Ribonucleotide reductase assay. Ribonucleotide reductase activity of proteins R1 and R1 was measured in crude protein extracts obtained by 2 min of sonication followed by centrifugation at 12,000 × g for 10 min at 4°C as previously detailed (23).

	RESULTS

Top Abstract Introduction Materials & Methods Results Discussion References

Construction of the transfer vectors pAdTR5 and pAdCMV5. We have been using the AES to produce sufficient amounts of HSV-2 R1 and R2 proteins for structural studies. Although the AES was very successful for the R2 protein, the R1 protein could not be obtained with a similar yield, partly due to poor solubility (23). HSV-2 R1 is a more complex protein than cellular R1: it contains, in addition to a reductase domain, an amino-terminal domain of unknown function with an associated kinase activity (26). Since the cellular R1 overexpressed with the AES was more soluble, we attempted to produce only the reductase domain of HSV-2 R1 by deleting the first 357 amino acids. Surprisingly, we were unable to generate an adenovirus recombinant expressing this R1 protein with vector pAdBM5, even after 10 carefully controlled transfections.

Expression of HSV-2 R1 in pAdTR5- and pAdCMV5-derived recombinants. The performance of our new vectors was first assessed with the HSV-2 R1 gene by producing the adenovirus recombinants Ad5TR5R1 and Ad5CMV5R1. Our best previously produced adenovirus recombinant for the R1 gene, Ad5BM5R1, yielded in permissive 293 cells R1 levels exceeding 20% TCP (more than 60 µg/10⁶ cells) (23). To complement the tetracycline-regulated expression cassette, stable clones expressing tTA or rtTA were derived from 293S (24), A549, and HeLa S3 cells as described in Materials and Methods. With a tetracycline-regulated reporter gene, the cell lines used in this study were further selected for their ability to retain, in the absence of selective pressure, both high and inducible levels of expression.

View larger version (88K): [in this window] [in a new window]   FIG. 2.   Constitutive or regulated overexpression of HSV-2 R1 in the absence of viral protein synthesis in A549 and HeLa S3 cells infected with AdV (A and B). Coomassie blue-stained gel of total proteins produced in either A549-tTA (A) or HeLa-rtTA (B) cells infected with Ad5CMV5R1 (lanes 2 to 6) or Ad5TR5R1 (lanes 7 to 11) and extracted at 48 h p.i. Both cell lines were mock infected (lane 1) or infected at MOIs of 50 (lanes 2 and 7), 100 (lanes 3 and 8), 200 (lanes 4 and 9), 400 (lanes 5 and 10), and 800 (lanes 6 and 11). Anhydrotetracycline (1 µg/ml) was added for the induction of R1 expression in HeLa-rtTA cells. (C and D) Expression of R1 compared in A549 (C) or HeLa (D) cells expressing tTA following pAdCMVtTA infection (MOI, 500) versus stable integration of the tTA or rtTA expression vectors. A549, A549-tTA, HeLa S3, or HeLa-rtTA cell lines were mock infected (lanes 1, C and D) or infected with pAdCMVtTA alone (lanes 2 and 8, C and D) or with Ad5TR5R1 at MOIs of 50 (lanes 5, C and D), 100 (lanes 6, C and D; lanes 10 in C and 9 in D), and 400 (lanes 7, C and D). Lanes 3 and 4 in C and D are control infections with Ad5TR5R1 alone at MOIs of 50 and 400, respectively, whereas lane 9 in C is an infection of A549-tTA with Ad5TR5R1 alone at an MOI of 100. For comparison, extracts of A549-tTA (lane 11 in C) or HeLa-rtTA (lane 10 in D) cells infected with Ad5CMV5R1 (MOI, 400) were loaded. Each lane was loaded with 10 µg of protein from total cell extracts. The position of R1 is indicated on the right. Molecular weight markers are shown on the left in thousands.

Regulation of gene expression by an AdV recombinant expressing the tTA protein. To increase the range of cell lines that could be efficiently transduced by our pAdTR5 cassette, we also constructed an AdV recombinant that could express the tTA protein under the control of the CMV promoter. In addition, as the high level of protein expression obtained in Ad5TR5R1-infected tTA cells was found to be dependent on the tTA clones used (data not shown), we hoped that higher levels of tTA could be expressed by AdV transduction than by our best stable clones and that this expression would further increase the production of R1 in Ad5TR5R1-infected cells. To determine the conditions for optimal gene expression with the tetracycline-regulatable expression system, we used AdTR5GFP, an adenovirus recombinant expressing the jellyfish GFP which is easily quantifiable by cytofluorometry (24). When A549 and HeLa S3 cells were coinfected with AdTR5GFP at an MOI of 50 and AdCMVtTA at increasing MOIs, we observed an increase in GFP expression that was approximately proportional to the MOI up to 500, where it plateaued (data not shown). With AdCMVtTA at this optimal MOI of 500, A549, A549-tTA, HeLa S3, and HeLa-rtTA cells were coinfected with Ad5TR5R1 at MOIs of 50, 100, and 400, and R1 accumulation was examined by SDS-polyacrylamide gel electrophoresis at 48 h p.i. As shown in Fig. 2C and D, the coinfection yielded, in A549 cells, slightly higher levels of R1 than the infection of A549-tTA cells with Ad5TR5R1 alone (compare lane 6 with lane 9 in Fig. 2C) and equivalent levels in HeLa-rtTA cells (compare lane 6 with lane 9 in Fig. 2D). In another experiment, at least a twofold-higher level of recombinant protein expression was measured following coinfection of A549 cells with Ad5CMVtTA and Ad5TR5GFP than following single infection of A549-tTA cells with Ad5TR5GFP (data not shown). Interestingly, infection with Ad5TR5R1 or Ad5CMVtTA alone did not produce the appearance of any new protein band detectable by Coomassie blue staining (Fig. 2C and D, lanes 3 and 4 and data not shown). This result indicated that, although being driven from a CMV-based promoter cassette, tTA was expressed at a much lower level than R1 and that R1 expression with the tetracycline-regulated promoter was very low in the absence of tTA. Altogether, these results showed not only that the tTA protein can be transduced by an adenovirus recombinant but also that in this way the transactivator appears to be produced in higher effective amounts than by the best stable cell lines.

Overexpression of the cytotoxic R1 protein. As mentioned above, the cytotoxic nature of R1 was initially suspected from our inability to generate a recombinant adenovirus expressing the deletion protein in several transfection experiments regardless of whether the pAdBM5 or pAdCMV5 vector was used. However, when the pAdTR5 vector was used, Ad5TR5R1, a recombinant adenovirus expressing R1(2-357), was readily obtained in the first attempt. An initial analysis of R1 expression in permissive 293-tTA cells infected with Ad5TR5R1 for 48 h indicated that the level of R1 accumulation was lower (10% TCP) than that of the full-length R1 in cells infected with either Ad5CMV5R1 or Ad5TR5R1 (20 to 25% TCP) (Fig. 3, compare lane 6 with lanes 2 and 4). Moreover, whereas in cells infected with Ad5TR5R1 the accumulation of several viral polypeptides, including the hexon and 100K protein, was severely reduced (Fig. 3, compare lanes 5 and 6), their accumulation was not compromised by the presence of a higher amount of full-length R1 in cells infected with Ad5TR5R1 (Fig. 3, compare lanes 2, 3, and 4). The reduction in the synthesis of viral polypeptides might explain why we were unable to generate a recombinant virus for R1 with a constitutive expression cassette. Consistent with this idea, the titer of Ad5TR5R1 grown on 293-tTA cells under induced conditions (in the absence of anhydrotetracycline) was 20-fold lower than when the expression of R1 was repressed (data not shown). The experiment presented in Fig. 3 also shows that the expression of R1 or R1 could be repressed about 25-fold by the addition of 40 ng of anhydrotetracycline per ml (compare lanes 3 and 5 with lanes 4 and 6). Repression was not complete, likely due to low-level transactivation of the minimal TATA box by adenovirus E1 proteins (17, 39) in combination with the high copy number of the viral vector following replication in permissive 293 cells. The extent of repression that could be achieved by this system was quantified more precisely with Ad5TR5GFP and nonpermissive A549-tTA cells. As can be seen in Table 1, it was greater than 50-fold at MOIs of 50 to 250 PFU/cell. Interestingly, at the highest MOI, the extinction factor was decreased to a value of 28, which corresponds to the repression observed in permissive 293 cells. The nearly linear relationship between the MOI of AdTR5GFP and the basal expression level indicates that the copy number of the tetracycline-regulated expression cassette is the most important factor which determines the basal expression level (Table 1).

View larger version (47K): [in this window] [in a new window]   FIG. 3.   Constitutive or regulated overexpression of HSV-2 R1 and HSV-2 R1 in 293-tTA cells infected with AdV. (A) Coomassie blue-stained gel of total proteins (10 µg) extracted from 293-tTA cells uninfected (lane 1) or at 48 h p.i. with Ad5CMV5R1 (lane 2), Ad5TR5R1 (lanes 3 and 4), and Ad5TR5R1 (lanes 5 and 6). The positions of the R1, hexon, and R1 proteins are indicated on the right. Molecular weight markers are shown on the left in thousands. + and , with or without anhydrotetracycline (40 ng/ml), respectively. (B) Immunoblot of the same total protein extracts probed with a rabbit polyclonal antiserum raised against a 19-mer peptide corresponding to amino acids 886 to 904 of HSV-2 R1 and visualized with an ECL detection kit (Amersham). The protein band comigrating with the 66-kDa marker is bovine serum albumin, which contaminated the cell extracts. Bovine serum albumin reacted strongly with this rabbit antiserum since it (bovine serum albumin) was coupled to the R1 peptide for the immunization.

View larger version (56K): [in this window] [in a new window]   FIG. 4.   Cytoxicicity of HSV-2 R1. A549-tTA cells (105 in six-well plates) were infected 24 h after seeding with 100 PFU of Ad5TR5R1 (), Ad5TR5R1 (), or Ad5TR5R1 plus 30 ng of anhydrotetracycline per ml () per cell or were mock infected (). (A) Morphological appearance of Ad5TR5R1 (top)- and Ad5TR5R1 (bottom)-infected cells at 12 h (left) and 40 h (right) p.i. (B) Numbers of attached cells counted with a hemacytometer at various times p.i. (symbols are given above).

View larger version (105K): [in this window] [in a new window]   FIG. 5.   Time course of HSV-2 R1 and HSV-2 R1 synthesis in A549-tTA cells infected with tetracycline-regulatable AdV. A549-tTA cells were either uninfected (lane 1) or infected with Ad5TR5R1 (lanes 2 to 5) or Ad5TR5R1 (lanes 6 to 9) at an MOI of 100, and total proteins were extracted following 2 h of radiolabeling with [35S]methionine at 2 h (lanes 2 and 6), 6 h (lanes 3 and 7), or 24 h (lanes 4, 5, 8, and 9) p.i. Autoradiography was performed on a gel loaded with 10 µg of protein per lane. The positions of the R1 and R1 proteins are indicated on the right. + and , with or without anhydrotetracycline (40 ng/ml).

	DISCUSSION

Top Abstract Introduction Materials & Methods Results Discussion References

The pAdTR5 and pAdCMV5 transfer vectors significantly improved the utility of AdV for high-level transgene expression in mammalian cells. First, each of these vectors allowed for very high levels of recombinant protein production in nonpermissive cell lines. This fact greatly simplified the production and purification effort, since the recombinant protein could be produced at levels approaching 15 to 25% TCP in the absence of the synthesis of other viral proteins. Second, by incorporation of the tetracycline-regulated promoter into the expression vector, it was possible to use the AES to produce toxic proteins that interfered with adenovirus replication at levels approaching those which can be achieved by use of a constitutive expression cassette.

In comparison with the pAdTR5 and pAdCMV5 transfer vectors, adenovirus MLP-based expression cassettes such as pAdBM5-derived AdV, which yielded the best protein production levels in permissive 293 cells (23), typically yielded, at equivalent MOIs, three- to fivefold-lower expression levels in nonpermissive cells, depending on the transgene tested (unpublished results). This observation is consistent with previous reports showing that adenovirus MLP-based expression cassettes, even when modified with additional enhancer sequences, are less efficient than CMV promoter-based expression cassettes in most nonpermissive cell lines (38, 40). Although the relative contributions of the various elements cloned downstream of the CMV TATA box to the improvement in transgene expression in AdV were not systematically assessed, we suspect that in nonpermissive cells the most significant cis-acting elements are the adenovirus tripartite leader and splice sites. In fact, the adenovirus major late enhancer is not likely to be active in the absence of viral protein IVa2, which is normally expressed after DNA replication begins (21); even at a high MOI in A549 or HeLa cells, we did not find evidence that the adenovirus late proteins were expressed at significant levels, suggesting that levels of IVa2 were minimal. Nevertheless, the adenovirus major late enhancer was included in the expression cassette both to take advantage of its activity in permissive 293 cells and also to obtain a direct comparison with pAdBM5, our best-characterized transfer vector (23).

The high level of expression attained in nonpermissive cell lines with our new vectors is substantially greater than the previously reported expression levels of about 2% TCP obtained with nonoptimized CMV promoter-based expression cassettes (1, 18, 25, 37, 38, 40; unpublished results). The exception is a study by Wilkinson and Akrigg in which an expression level in the range of 20% TPC was obtained in MRC5 cells infected with an AdV expressing the E. coli lacZ gene (37). However, this high level of expression of -galactosidase required the addition of forskolin, which stimulated the CMV promoter more than 10-fold. Furthermore, overexpression of -galactosidase was obtained only after 144 h p.i.; at 48 h p.i., a time corresponding to the peak of expression with our optimized expression cassettes, the expression of -galactosidase was fivefold lower.

We used the tetracycline-regulatable adenovirus cassette to produce, at high levels, a protein that was suspected to be cytotoxic, and we confirmed the cytotoxic nature of the R1 protein by showing that infection of A549-tTA cells with the Ad5TR5R1 vector brought about an eventual demise of the infected cells. The cytotoxicity of the R1 protein was totally unexpected. Although we do not have any clues to explain it at this point, it is evident that overexpression per se was not the cause, since the R1 protein was expressed at even higher levels. Furthermore, preliminary experiments indicated that cytotoxicity could be observed at levels lower than 0.01% TCP (19a). This cytotoxic effect and the synthesis of the R1 protein could be nearly completely abrogated by inhibition of the activity of the tTA protein with anhydrotetracycline in Ad5TR5R1-infected cells.

We have also generated a number of other recombinant adenovirus using the pAdTR5 vector. The vector has made it possible to overexpress, at more than 10% TCP, the human enzyme methenyltetrahydrofolate synthetase, the heat-inducible chaperone protein hsp70, the adenovirus E1B-19K protein, and the viral protein encoded by ORF5 of the porcine reproductive and respiratory syndrome virus (unpublished data). This last protein was recently shown to induce apoptosis when expressed in BSC40 cells with the T7 vaccinia virus system (32). We have also shown that the expression of R1 by infection with Ad5TR5R1 induces the death of A549 and HeLa S3 cells by an apoptotic process (19a). The characterization of the apoptotic behavior of R1 or any other proteins with similar behavior will be facilitated by the use of an expression system allowing for the tight regulation of gene expression in the absence of any other toxic effects resulting from the infection of permissive cells, such as is the case with vaccinia virus vectors. Curiously, the adenovirus E1B-19K protein, which exhibited potent antiapoptotic activity in both adenovirus-infected cells and stable cell lines (35; reviewed in reference 33), could be overexpressed only with the pAdTR5 vector. We found that at high MOIs in nonpermissive cells, the overexpression of E1B-19K (>2% TPC) was very toxic, killing the cells by necrosis (unpublished results).

Another elegant molecular switch, based on the Cre-loxP recombination system, has been described for the regulation of gene expression in AdV (3). With this system, the transgene is placed under the control of a strong constitutive promoter, such as the CMV promoter, and its expression is silenced by the inclusion of a spacer fragment of 1.3 kbp between the promoter and the open reading frame. This spacer fragment is flanked by two lox sites, upon which the Cre recombinase acts to precisely excise it, thereby restoring efficient expression of the transgene. Although this vector system has the potential of expressing toxic gene products in AdV, overexpression of toxic proteins has not been reported thus far with it. Furthermore, the Cre-loxP system is less flexible than the tetracycline-regulated gene switch described here in two respects. First, the need for a spacer fragment larger than 1 kbp limits the available space for the cloning of transgenes into AdV, thereby reducing the option for cloning large cDNAs or constructing AdV with double expression cassettes (6). Second, since it is not possible to regulate the Cre recombination switch with chemical inducers, one is restricted to the scenario of coinfection with two viruses instead of being able to combine the transactivator with the inducible expression cassette in one virus, as we are currently doing with the tetracycline-regulated gene switch. This latter approach was reported to be more efficient for the generation of transgenic animals with regulated transgene expression (29) and should prove to be equally efficient for gene transfer experiments with AdV.

Finally, in addition to the application of the AES to protein production in animal cell cultures, the pAdCMV5 and pAd5TR5 vectors will be useful for functional studies and gene therapy applications. Adenoviruses are already well established as effective vectors for human gene therapy applications. The higher level of expression that can be achieved with these AdV in nonpermissive cells will make it possible to express transgenes at significant levels in vivo at lower MOIs, thereby allowing minimization of the toxic side effects associated with the load of adenovirus particles. For example, Connelly et al. recently reported that a threefold improvement in the level of expression of blood coagulation factor VIII following AdV transduction allowed for the injection of significantly lower vector doses while still providing factor VIII at therapeutic levels (7). Furthermore, the tTA system has been shown to be highly effective for the regulated expression of recombinant proteins in transgenic animals (29). The tetracycline-regulated AES that we have described here will make it possible to express in vivo by coinfection with an AdV expressing tTA a therapeutic protein at levels that can be precisely regulated by the in vivo concentration of the effector molecule tetracycline. We are currently assessing the usefulness of such an inducible vector for in vivo gene transfer experiments.