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Journal of Virology, October 2001, p. 9991-9994, Vol. 75, No. 20
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.20.9991-9994.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Novel cis-Acting Replication Element in the Adeno-Associated Virus Type 2 Genome Is Involved in Amplification of Integrated rep-cap Sequences

Pascale Nony,^1, Jacques Tessier,¹ Gilliane Chadeuf,¹ Peter Ward,² Aurélie Giraud,¹ Marc Dugast,¹ R. Michael Linden,^2,3 Philippe Moullier,¹ and Anna Salvetti^1,*

Laboratoire de Thérapie Génique, CHU Hotel Dieu, 44035 Nantes Cedex 01, France,¹ and Institute for Gene Therapy and Molecular Medecine² and Department of Microbiology,³ Mt. Sinai School of Medicine, New York, New York 10029

Received 7 May 2001/Accepted 9 July 2001

	ABSTRACT

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This study identifies a region of the adeno-associated virus type 2 (AAV-2) rep gene (nucleotides 190 to 540 of wild-type AAV-2) as a cis-acting Rep-dependent element able to promote the replication of transiently transfected plasmids. This viral element is also shown to be involved in the amplification of integrated sequences in the presence of adenovirus and Rep proteins.

	TEXT

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It was previously reported that efficient recombinant adeno-associated virus (AAV) production using stable rep-cap cell lines correlated with a 100-fold amplification of the AAV-2 genes upon adenovirus infection (3, 9). This phenomenon, which occurred despite the absence of inverted terminal repeats (ITRs) generated extrachromosomal double-stranded DNA molecules harboring the rep-cap genes and required the activity of the adenovirus DNA binding protein, cellular polymerases, and Rep proteins (9). A question that remained unanswered was whether the rep-cap amplification was dependent on the activity of an as-yet-unidentified viral origin of replication present within the viral genome.

To answer this question, we investigated if a rep-cap-containing plasmid was able to replicate following transient transfection into adenovirus-infected cells. 293 cells were transfected with plasmid pRCtag containing the rep-cap genome with the ITRs deleted, ligated to a 3' tag sequence, and then mock or adenovirally infected. After DNA extraction, replication was assessed by digestion with DpnI or MboI followed by Southern blot analysis using a tag probe (Fig. 1). Cleavage by DpnI indicates that both strands are methylated in the absence of replication of the transfected DNA; cleavage by MboI occurs only if both strands are unmethylated as a result of two rounds of replication. In the absence of adenovirus, the pRCtag plasmid did not replicate (Fig. 1B, lanes 5 and 6). In contrast, upon adenoviral infection, a fraction of the plasmid DNA was susceptible to MboI digestion (Fig. 1B, lane 9), indicating that some input rep-cap molecules had replicated. After DpnI digestion, high-molecular-weight resistant bands were detected as weak signals, suggesting that pRCtag replication generated products which are heterogenous in size (Fig. 1B, lane 8).

View larger version (50K): [in this window] [in a new window]   FIG. 1.   In vivo replication analysis of pRCtag and pRCtag plasmids. (A) Circular map of the pRCtag and pRCtag plasmids: the tag located at the 3' end of the rep-cap genes (hatched area) corresponds to a 404-bp X174-derived sequence. Plasmid pRCtag differs from pRCtag by a 350-bp deletion in the 5' portion of the rep gene (nt 190 to 540 of wild-type AAV-2) that removes the entire p5 promoter and the 5' portion of the rep open reading frame. The positions of the two relevant DpnI-MboI sites are indicated. (B) 293 cells were transfected with the pRCtag or the pRCtag plasmid in the presence (+pRep) or absence (pRep) of the pRep plasmid, encoding for the Rep proteins under the control of the AAV-2 p5 and p19 promoters, and subsequently infected (+Ad) or not infected (Ad) with adenovirus. (C) pRCtag and pRCtag were similarly transfected into HeRC32 cells that harbor one integrated copy of the ITR-deleted AAV-2 genome (1). Total genomic DNA was extracted 48 h later, digested with DpnI (D) or MboI (M), and analyzed on a Southern blot by using a tag probe. As a control (lanes 1, 2, and 3), untransfected pRCtag plasmid DNA mixed with 10 µg of total DNA from 293 cells was digested with DpnI or MboI and similarly analyzed using the tag probe. The expected 1,430-bp DpnI-MboI fragment hybridizing to the tag probe is indicated.

To identify the cis element(s) involved in pRCtag replication, we focused on the 5' portion of the rep gene which includes a Rep binding site (RBS). (nucleotides [nt] 260 to 284 of wild-type AAV-2) and a trs-like motif (nt 287 of wild-type AAV-2) (4, 12). The presence of both elements in the ITRs is known to be essential for wild-type AAV-2 replication (6, 8). A rep-cap plasmid containing a deletion in the 5' portion of the rep gene (nt 190 to 540 of wild-type AAV-2) was generated (pRCtag) and evaluated as described above. Because pRCtag no longer produced the large Rep proteins (data not shown), its replicative activity was tested with or without a cotransfected pRep plasmid to provide Rep proteins in trans. In adenovirus-infected 293 cells, replication of the pRCtag plasmid was undetectable and only partially restored in the presence of Rep proteins (Fig. 1B, lanes 15 and 18). To exclude the possibility that the low level of pRCtag replication was due to the inefficient transfection of plasmid pRep, the same experiment was reproduced using HeRC32 cells, a stable cell line which expresses the four Rep proteins upon adenovirus infection (1). Again, plasmid pRCtag replicated much less efficiently than plasmid pRCtag (Fig. 1C, lanes 21 and 24). Overall, these data suggested that this 350-nt region of the rep gene behaved as a cis-acting replication element (CARE). The residual level of pRCtag replication observed with 293 and HeRC32 cells could be due either to a recombination event between the plasmid and the cotransfected or endogenous rep sequences or to the presence of additional replication element(s) in the deleted rep-cap genome.

To confirm the role of this viral region in replication, the CARE element was cloned upstream of the lacZ gene in the same or opposite orientation and tested as previously described (Fig. 2). Both pCARE.LZ¹ and pCARE.LZ² plasmids replicated in the presence of Rep proteins and adenovirus (Fig. 2B, lanes 15 and 18), whereas no replication products were detected with a pLZ control plasmid (lanes 1 to 3). The ability of CARE to promote replication in a Rep-dependent manner was further evidenced by two additional experiments. First, a cell-free DNA replication assay was performed, in which EcoRI-digested pLZ, pCARE.LZ¹ or pCARE.LZ² plasmids were incubated with cell extracts from uninfected HeLa cells with or without purified Rep68 protein (7, 13). Despite a significant level of DNA repair which occurred with each DNA template, addition of purified Rep68 resulted in a 13- and 8.5-fold increase in the incorporation of labeled nucleotides only in the upper band containing the CARE sequence, for both plasmids CS pCARE.LZ¹ and pCARE.LZ², respectively (Fig. 3, lanes 4 and 6). Second, the RBS and the trs-like elements contained in the p5 region were individually mutated in the pCARE.LZ¹ plasmid (Fig. 4A). When tested in a replication assay, mutation of either the RBS or the trs element impaired replication of the pCARE.LZ¹ plasmid despite the presence of Rep proteins and adenovirus (Fig. 4B, lanes 9 and 12). The same result was obtained upon transfection in HeRC32 cells (data not shown).

View larger version (68K): [in this window] [in a new window]   FIG. 2.   In vivo replication assay of pCARE.LZ plasmids. (A) Circular map of pCARE.LZ plasmids. The CARE sequence (190 to 540 bp of wild-type AAV-2), indicated by the hatched area, was introduced upstream of the CMVLacZ cassette either in the same (pCARE.LZ1) or opposite (pCARE.LZ2) orientation. The positions of the relevant DpnI-MboI sites are indicated. (B) 293 cells were transfected with the indicated plasmid in the presence or absence of the pRep plasmid and adenovirus infection. DNA was analyzed as described in the legend of Fig. 1 by using a lacZ probe. The expected 552-, 426-, and <100-bp DpnI-MboI fragments hybridizing to the lacZ probe are indicated.

View larger version (43K): [in this window] [in a new window]   FIG. 3.   In vitro replication assay of pCARE.LZ plasmids. (A) Circular map of the pLZ and pCARE.LZ1/2 plasmids. Two major linear species are generated upon EcoRI digestion: one of 3,077 bp that is common to both plasmids and corresponds to the lacZ gene and one of 3,261 and 3,690 bp for pLZ and pCARE.LZ1/2, respectively, that corresponds to the CARE sequence associated with the rest of the plasmid. (B) The EcoRI-digested plasmid DNA was used directly in the in vitro replication assay, so each reaction mixture contained equimolar amounts of the two larger DNA fragments. Replication assays were performed as previously described using a cellular extract from uninfected HeLa cells, supplemented or not with purified Rep68 protein (13).

View larger version (28K): [in this window] [in a new window]   FIG. 4.   Mutational analysis of CARE element. (A) Sequence of the wild-type (wt) and mutated CARE element between nt 227 and 294 of wild-type AAV-2. The mRBS mutation was previously described by Pereira et al. (5). The mtrs mutation was introduced by changing 6 bp surrounding the trs site described by Wang et al. (12). The presence of each mutation was verified by sequencing. (B) 293 cells were transfected with the indicated construct with or without the pRep plasmid and adenovirus infection. DNA was analyzed as described in the legend of Fig. 1 by using a lacZ probe.

Altogether, these findings established the presence of a Rep-dependent replication element between nt 190 and 540 of wild-type AAV-2. These results support and extend the observation made by Tullis and Shenk (10), who demonstrated the presence of a positive cis-acting element between nt 194 and 1882 of AAV-2. Furthermore, CARE features resembled those already described for the chromosome 19 AAVS1 region that also contains an RBS and a trs element (2, 11, 14).

Finally, we wanted to determine if CARE could also induce the amplification of an integrated sequence. A stable cell line (HeCARE.LZ) was obtained by cotransfection of pCARE.LZ¹ and the PGK-Neo plasmids into HeLa cells. Control cells (He.LZ) that integrated a lacZ sequence without CARE were obtained similarly. The cells were then tested for the amplification of integrated lacZ sequences. As seen by Southern blot analysis using a lacZ probe, an increase in the lacZ copy number was observed in HeCARE.LZ cells upon adenovirus infection and transfection of plasmid pRep, but not in control He.LZ cells (Fig. 5, lanes 8 and 4). The level of lacZ gene amplification measured in HeCARE.LZ cells was likely underestimated due to the low transfection efficiency of HeLa cells (less than 10%). Importantly, neither adenovirus infection alone nor expression of the rep gene under the control of either the p5 (plasmid pRep) or the cytomegalovirus (CMV) promoter (plasmid pCMVRep) was sufficient to induce lacZ gene amplification in HeCARE.LZ cells (Fig. 5, lanes 6, 7, and 13). These results indicated that integration of CARE can lead to the amplification of an heterologous adjacent sequence and that Rep proteins are necessary together with adenovirus for this phenomenon to occur. This finding suggests that the amplification of an integrated rep-cap genome, which shares this dual requirement (9), is also CARE dependent. As such, the identification of CARE has important implications for the design of stable AAV-2-packaging cells.

View larger version (28K): [in this window] [in a new window]   FIG. 5.   Analysis of lacZ amplification in stable CARE-lacZ HeLa cells. He.LZ or HeCARE.LZ cells, containing an integrated lacZ or a CARE-lacZ sequence, respectively, were either transfected with a Rep-expressing plasmid (+pRep or +pCMVRep), infected with wild-type adenovirus (+Ad), or both. Total genomic DNA extracted 48 h later was digested with HincII and analyzed on a Southern blot by using a lacZ probe. The position of the expected 1.8-kb lacZ band is indicated. The standard samples with 0.1, 1, and 10 lacZ, copies per cell were obtained by adding 4, 40, and 400 pg of pCARE.LZ plasmid, respectively, to 10 µg of total genomic DNA from noninfected HeLa cells.

	ACKNOWLEDGMENTS

Pascale Nony and Jacques Tessier contributed equally to this work.

This work was supported by the Association Française contre les Myopathies (AFM), Vaincre les Maladies Lysosomales (VML), Association Nantaise de Thérapie Génique (ANTG), and the Fondation pour la Thérapie Génique en Pays de la Loire. It was also supported, in part, by NIH grants DK55609 and DK57746 to R.M.L.

	FOOTNOTES

^* Corresponding author. Mailing address: Laboratoire de Thérapie Génique, CHU Hotel Dieu, Bâtiment Jean Monnet, 30 avenue Jean Monnet, 44035 Nantes cedex 01, France. Phone: (33) 240087490. Fax: (33) 240087491. E-mail: salvetti{at}sante.univ-nantes.fr.

Present address: CNRS-UMR5641, Domaine Rockefeller, 69373 Lyon Cedex O9, France.

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Journal of Virology, October 2001, p. 9991-9994, Vol. 75, No. 20
0022-538X/01/$04.00+0   DOI: 10.1128/JVI.75.20.9991-9994.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

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