INTRODUCTION

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Adeno-associated virus type 2 (AAV) is a nonpathogenic human parvovirus that generally depends on coinfection with a helper virus (adenovirus or herpesvirus) for efficient replication (reviewed in reference 10). The linear, single-stranded DNA genome of AAV contains two open reading frames (rep and cap) flanked by 145-bp inverted terminal repeats (ITRs) (62). Replication of the AAV genome requires two viral components, the ITR that serves as the origin of replication (26, 55, 57, 63) and the rep gene products (27, 57, 65). The rep gene encodes four multifunctional proteins (27, 45, 65, 67) that are expressed from two promoters at map units 5 (p5) and 19 (p19). The larger Rep proteins transcribed from the p5 promoter (Rep78 and Rep68 [Rep78/68]), are essentially identical except for a unique carboxy terminus generated from unspliced (Rep78) and spliced (Rep68) transcripts (62). Two smaller Rep proteins (Rep52 and Rep40), transcribed from the p19 promoter, are amino-terminal truncations of Rep78 and Rep68, respectively.

Several biochemical activities of Rep78/68 have been characterized as being necessary for AAV replication. These include specific binding to the AAV ITR (4, 30, 59) and site-specific endonuclease cleavage at the terminal resolution site (trs) (31, 32, 58, 60). Rep78/68 also possess ATP-dependent DNA-DNA helicase (31, 32) and DNA-RNA helicase (73) as well as ATPase (73) activities. In addition to these activities, which are required for replication, Rep78/68 also regulate transcription from the viral promoters (8, 38, 39, 50, 66) and have been shown to mediate viral targeted integration (6, 40, 51, 74). How Rep78/68 mediate these diverse activities in vivo is still under investigation.

Mutant studies of the Rep proteins have indicated that the activities of Rep can be divided into partially distinct functional domains (Fig. 1A) that are spread throughout the protein (14, 21, 43, 48, 68-71, 77). These include regions required for binding to the ITR, a putative nucleoside triphosphate (NTP) binding/ATPase domain, a nuclear localization domain, and residues putatively required for nicking and helicase functions. Rep proteins with mutations within the NTP binding/ATPase domain that lacked trs endonuclease and viral replication were also defective for transactivation functions, suggesting a need for further mutant analysis (43). Since most mutants disrupt multiple Rep-mediated functions for the AAV life cycle, the detailed characterization of distinct functions has been difficult (21, 43, 48, 68-71, 77).

View larger version (25K): [in this window] [in a new window]   FIG. 1.   AAV Rep78. (A) Schematic diagram of previously described functional domains (see text) within Rep78/68. Regions described as required for binding (vertical stripes), nuclear localization (black box) (amino acids 483 to 519), oligomerization (gray box) (amino acids 466 to 476), and ATPase and helicase activities (black line) (amino acids 334 to 421) and the unique region between Rep78 and Rep68 (horizontal stripes) (amino acids 537 to 621) are indicated. Overlapping DD35E motifs are indicated as boxed residues corresponding to one motif at D368, D429, and E465 and as circled residues corresponding to a second motif at D412, D468, and E504. (B) Eucaryotic expression cassette (pHIV-78) for generating Rep78 proteins. Protein expression is under control of the HIV LTR promoter and the poly(A) signal from simian virus 40. The initiation codon (ATG) at p19 was changed to GGG to eliminate expression of Rep52 and Rep40, and the splice donor site was modified (spl) as described previously (74) to eliminate expression of Rep68. (C) Positions of point and clustered alanine mutations (open boxes) within the pHIV-78 expression plasmid. Amino acid changes are indicated by the nomenclature for each construct.

The use of temperature-sensitive (ts) mutations has proven to be an effective method for elucidating the essential functions of viral proteins (11, 17, 46, 53). One approach for generating ts mutants has been to utilize the charge-to-alanine mutagenesis strategy (7, 9, 18, 22, 49, 72). This approach has been utilized by others to characterized AAV Rep functions (21, 68); however, none of these mutants were assayed for temperature sensitivity. The rationale of this approach is that since most charged residues are found on the protein surface, they are expected to exert little effect on protein folding or stability (18, 19, 72), but could feasibly make a protein more thermosensitive by disrupting electrostatic and H-bonding interactions (22).

In an attempt to generate ts Rep mutants, we used alanine substitution to target a number of the functional domains critical for Rep-mediated activities. We describe the effects of these mutations on Rep78-mediated replication of an ITR-containing vector in adenovirus-infected human cells. We also assayed several biochemical activities in vitro (i.e., ITR binding, trs endonuclease, and helicase) by using Rep68 His-tagged fusion proteins expressed and purified from bacteria. From these analyses, we identified three classes of mutants (Table 1). Class I mutants were normal by in vivo replication and in vitro biochemical analyses. A class II mutant (D40,42,44A-78) was ts for expression and intracellular replication of AAV, resulting in a 3-log-unit difference in viral titer between the permissive and nonpermissive temperatures. In addition, a class III mutant demonstrated a defect for replication, but protein stability was wild type (wt) in nature. Further analysis of this mutant demonstrated Mg²⁺-dependent trs endonuclease activity, which was unrelated to either DNA helicase or DNA binding activity. This mutant Rep suggests that a specific interaction between residue D412 and Mg²⁺ is critical for endonuclease activity. These data represent the first description of a ts AAV Rep protein as well as the putative identification of an Mg²⁺ binding pocket required for Rep-specific DNA nicking activity. Further characterization of these mutants should prove useful in studying AAV replication and integration and should provide new strategies for AAV vector-packaging cell lines.

	MATERIALS AND METHODS

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Plasmids and site-directed mutagenesis. All recombinant DNA manipulations were performed by standard protocols (5). Unless otherwise noted, all enzymes were purchased from New England Biolabs and used according to supplier recommendations. The mutants used in this study were originally generated in the plasmid pHIV-78 (74). pHIV-78 (Fig. 1B) is a derivative of pHIV-Rep (2). pHIV-Rep contains a wt rep gene and expresses all four Rep proteins from the human immunodeficiency virus (HIV) long terminal repeat (LTR). To express Rep78 in the absence of the other rep gene products, the splice site was modified to prevent splicing and subsequent generation of the Rep68 and Rep40 proteins (74). In addition, the initiation codon following the p19 promoter was changed to GGG (13) to abrogate expression of Rep52. For simplicity, we have designated the Rep78 protein expressed from pHIV-78 the wt Rep78 control, with the recognition that the rep gene has been modified as described above.

Intracellular replication assays and viral replication time course. Subconfluent 293 cells were cotransfected with mutant or wt pHIV-78 helper constructs and the rAAV plasmid (pAB-11) at a 3:1 molar ratio, respectively, via Lipofectin (Gibco/BRL) essentially as described in the supplier protocol. After 14 h, the DNA-Lipofectin complexes were replaced with medium containing enough adenovirus type 5 (dl309 [33]) to infect cells at a multiplicity of infection (MOI) of 5. When transfections were performed to evaluate ts activity of the mutants, all reagents for transfection, including the cells and medium, were prewarmed and incubated at the appropriate temperatures (32, 37, or 39°C) following transfection. At 48 h postinfection, low-molecular-weight DNA was extracted (28), treated with RNase A, and digested extensively with DpnI to remove input plasmid DNA. Southern blots were performed on digested DNA (5) and probed with ³²P-labeled -galactosidase. Viral replication was determined by coinfecting subconfluent human embryonic kidney (HEK) 293 cells with rAAV-UF5 (MOI = 5) and adenovirus type 5 (MOI = 5) and simultaneously transfecting with the mutD40A,D42A,D44A or pIM45 plasmid. Hirt DNA was analyzed by Southern blotting with a vector GFP-specific probe.

Production of rAAV GFP virus by using ts Rep plasmids. In order to produce rAAV-UF5 virus, HEK 293 cells were cotransfected by the CaPO₄ method as previously described (61) with pTRUF5 (79), helper plasmid pXX6 to supply adenovirus functions (75), and either wt pIM45 or mutD40,42,44A to supply Rep functions. Following transfection, the cells were incubated for 48 h, harvested, and subjected to three successive freeze-thaw cycles to liberate the virus. Incubations were performed at 32, 37, and 39.5°C. The crude viral preparations containing rAAV-UF5 were then titrated by counting GFP single-cell fluorescence.

ECL-Western blotting. ECL-Western blots analyses were performed on transfected-cell lysates essentially as recommended by the supplier (Amersham), and blots were probed with a monoclonal antibody raised against all four of the AAV Rep proteins (29).

Purification of mutant and wt Rep68 His-tagged fusion proteins. His-tagged Rep68 fusion proteins (Rep68H6) were purified from SG13009 cells (Qiagen) by passage over nickel columns as previously described (78a) with minor modifications. Briefly, cleared cell extracts were incubated with Ni-nitrilotriacetic acid agarose (Qiagen) for 3 to 4 h at 4°C, followed by elution with a 0.1 to 0.5 M imidazole linear gradient. Eluted proteins were analyzed by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis and silver staining (see Fig. 4) according to the manufacturer's protocol (Bio-Rad Silver Stain Plus). Protein concentrations were determined with a bicinchoninic acid kit (Pierce) with bovine serum albumin (BSA) as a standard and by direct comparison to known amounts of BSA on a silver-stained SDS-polyacrylamide gel.

DNA substrates for in vitro biochemical assays. The AAV TR hairpin DNA used in the majority of the biochemical assays was prepared by EcoRI digestion of pDD (76), generating a 171-bp DNA fragment with D sequences flanking either side of the TR (D' A C' C B' B A' D). The substrate was boiled and snap cooled to form a hairpin with a double-stranded trs and then labeled with [-³²P]ATP by using T4 polynucleotide kinase to generate the substrate, ³²P-TR.

Electrophoretic mobility shift assays. Electrophoretic mobility shift assays were performed essentially as previously described (44). Briefly, 0.01 to 0.02 pmol of ³²P-TR was incubated with up to 9 ng (~0.15 pmol) of mutant or wt Rep68H6 protein in 20-µl binding reaction mixtures (40 mM KCl, 10 mM HEPES-KOH [pH 7.5], 0.2 mM dithiothreitol, 5% [vol/vol] glycerol, 0.5 µg of BSA, and 1 µg of poly[dI-dC]) at 25°C for 30 min. Protein-DNA complexes were resolved on 5% nondenaturing polyacrylamide gels and quantitated with a phosphorimager. Assays were performed in triplicate, and standard errors are indicated in the figures.

trs endonuclease assays. Site-specific endonuclease activity was screened by trs endonuclease assays as previously described (32), except where indicated otherwise. Briefly, 20-µl reaction mixtures (25 mM HEPES-KOH [pH 7.5], 5 mM MgCl₂, 1 mM dithiothreitol, 0.4 mM ATP, 10 µg of BSA per ml) containing 0.005 to 0.02 pmol of ³²P-TR (or ³²P-TRss) and up to 9 ng (~0.15 pmol) of mutant or wt Rep68H6 were incubated at 37°C for 60 min. Reaction products were treated with protease K for 60 min, extracted with phenol-chloroform, precipitated, and resolved on denaturing sequencing gels. The amount of product formed was determined with a phosphorimager. Assays were performed in triplicate, and standard errors are indicated in the figures.

Helicase assays. The helicase assays (31) were performed in the same reaction buffer as for the trs endonuclease assay except where indicated otherwise. Briefly, 20-µl reaction mixtures containing 0.01 to 0.02 pmol of M13/24 and up to 9 ng of mutant or wt Rep68H6 protein were incubated for 30 min at 37°C. Reactions were terminated by addition of 10 µl of stop solution (0.5% SDS, 50 mM EDTA [pH 7.5], 50% glycerol, 0.1% bromphenol blue, 0.1% xylene cyanole), resolved by electrophoresis on a 5% nondenaturing polyacrylamide gel, and quantitated with a phosphorimager. Assays were repeated a minimum of three times, and standard errors are indicated in the figures.

Structural modeling. Computational results were obtained by using software programs from Molecular Simulations Inc. Dynamics calculations were performed with the Discover Æ program, using the CFF91 forcefield; ab initio calculations were done with the DMol program; and graphical displays were printed out from the Cerius2 molecular modeling system.

	RESULTS

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Generation of mutant and "wt" Rep78 constructs. In an attempt to generate ts Rep mutants, we used a charge-to-alanine substitution strategy (7, 9, 18) to target a number of the putative functional domains critical for Rep-mediated activities (Fig. 1A). Site-directed mutations were generated in a eucaryotic expression construct, pHIV-78 (74), that expresses only the 78-kDa AAV Rep protein (Fig. 1B). In this construct, the rep gene has been altered to prevent p19 protein expression (ATG converted to GGG), as previously described (13). In addition, the 5' splice site was inactivated so that only the Rep78 protein initiated from the p5 promoter was expressed (as described in Materials and Methods) (74). For simplicity, we have designated the Rep78 protein expressed from pHIV-78 the wt Rep78 control. By using intracellular expression, AAV-mediated replication, and in vitro biochemical assays, the mutants described in Fig. 1C were grouped into three classes (class I, non-ts and normal; class II, ts for replication; and class III, non-ts and defective for replication) (Table 1).

Intracellular expression of mutant and wt Rep78 proteins. All of the mutant plasmids were sequenced and characterized for the ability to express full-length Rep protein by transfection in 293 cells. ts expression was determined by transfecting mutant and wt pHIV-78 constructs into 293 cells at 32, 37, and 39°C, followed by Western blot analysis. A representative blot of protein expression is shown in Fig. 2. Based on protein expression at different temperatures, we designated two classes of Rep mutants. The class I mutant proteins were expressed at normal levels from the HIV LTR promoter, whereas the class II mutant D40,42,44A-78 was present at levels below the detection sensitivity of the ECL-Western blot analysis at 37 and 39°C (Fig. 2, lanes 8 and 9). Expression of this class II mutant was confirmed at 37°C by overexposing Western blots (data not shown) and by comparing lysates prepared from cells transfected at 32°C (Fig. 2, lane 7). Detection of the class II mutant protein at 32°C but not at 37°C suggested a ts Rep phenotype (22).

View larger version (23K): [in this window] [in a new window]   FIG. 2.   Immunoblot analysis of the various Rep78 proteins expressed from the HIV LTR in transiently transfected 293 cells. Mutant and wt pHIV-78 constructs were transfected into 293 cells at 32, 37, and 39°C as described in Materials and Methods. A representative blot of protein expression is shown. With the exception of D40,42,44A, all lysates were prepared from cells transfected at 37°C. Blots were hybridized with a monoclonal antibody that recognizes all four Rep proteins. All lanes were loaded with 15 µl of cellular extract. *, proteins were detected after long-term exposure of blots.

Replication activities of mutant Rep78 proteins. The intracellular functional activities of the Rep mutants (Fig. 3A) and wt Rep78, wt Rep68, and a construct (wt Rep) expressing all four Rep proteins (Fig. 3A, compare lanes 1, 14, and 15) were determined by assaying the ability to mediate replication of an rAAV plasmid (pAB-11) in the presence of adenovirus. The replication activities of control plasmids expressing either wt Rep78 or Rep68 appeared to be equivalent (Fig. 3A, compare lanes 1 and 14). As expected, the construct expressing all four Rep proteins (wt Rep) generated slightly more replicated DNA in this assay (Fig. 3A, compare lanes 1 and 14 to 15). Mutants that had less than 50% of wt Rep78 activity at 37°C were considered to be defective for replication. Intracellular replication assays were also performed at 32 and 39°C to determine if the Rep mutants were ts in activity.

View larger version (82K): [in this window] [in a new window]   FIG. 3.   Southern blot analysis of intracellular replication mediated by various Rep78 proteins. (A) Representative Southern blot of rAAV-LacZ (pAB-11) replication mediated by mutant and wt Rep78 proteins expressed from the HIV LTR in adenovirus type 5-infected 293 cells. The replication assays shown were performed at 37°C, except as indicated for D40,42,44A (lanes 6 to 8). The pHIV-78 and pAB-11 constructs were transfected at a 3:1 molar ratio as described in Materials and Methods. Following transfection, the cells were incubated for 48 h with adenovirus type 5 (MOI of 5). At 48 h postinfection, Hirt DNA was extracted, digested with DpnI, and analyzed by Southern blotting with a 32P-labeled probe specific for -galactosidase sequences. Replicative monomer (M) and dimer (D) DNA forms are indicated. *, replicated forms of pAB-11 were detected only after long-term exposure of blots. Rep68 was expressed from pHIV-68, a derivative of the pHIV-78 construct that has the rep gene intron removed as described previously (74). wt Rep is expressed from the pHIV-Rep construct, which expresses all four rep gene products, as described in Materials and Methods. (B) Southern blot analysis of replication of an rAAV-UF5 virus (GFP) mediated by transfected wt pIM45 or mutD40A,D42A,D44A pIM45 Rep expression plasmids. The pIM45 constructs express all four rep gene products (see Materials and Methods). Transfection infections were performed at permissive (32°C) and nonpermissive (39.5°C) temperatures in adenovirus type 5-infected HEK 293 cells. Rep-containing plasmids (wt pIM45 or mutD40,D42,D44A pIM45) were transfected into subconfluent HEK 293 cells and simultaneously coinfected with adenovirus type 5 (MOI of 5) and rAAV-UF5 (MOI of 5). At various time points, Hirt DNA was extracted and analyzed by Southern blotting as described above with a 32P-labeled probe specific for GFP sequences. No-plasmid lanes, cells were infected with adenovirus type 5 only; pIM45 (wt) lanes, cells were coinfected with adenovirus type 5 and rAAV-UF5 and transfected with wt pIM45; mutD40,42,44A lanes, cells were coinfected with adenovirus type 5 and rAAV-UF5 and transfected with mutD40,D42,D44A,pIM45.

In vitro expression and purification of mutant Rep proteins. In an effort to further characterize the non-ts Rep mutants initially evaluated in the intracellular replication study, several mutant constructs (Y311F, D412A, E465A, D468A, and E504A) were subcloned into the bacterial expression vector pStump68 (78a) for purification and characterized of Rep-specific biochemical activities. The pStump68 construct allowed for high-level expression and purification of Rep68 proteins from E. coli via a His₆-tag fusion. Overexpression and purification from this vector enabled us to compare the activities of the mutant Rep proteins to well-established biochemical activities previously assigned for wt Rep68 (30-32). Silver stained SDS-polyacrylamide gels (Fig. 4) and Western blot analysis (data not shown) demonstrated that the His₆-tagged proteins were purified to greater than 95% homogeneity. With the exception of mutant E504A-68, the Rep mutants expressed similar amounts of stable Rep68 protein (Fig. 4). Mutant E504A-68 required 50 times more total protein when assayed under these conditions and appeared to have a pronounced profile of breakdown products that were similar to those of Rep68 purified from baculovirus (Fig. 4, lanes 6 and 7). This was in contrast to its expression in 293 cells, which appeared to be normal (Fig. 2, lane 14). These two contradicting data suggest that this mutant may be unstable in the context of the His-tagged fusion protein. While this result exemplifies the concern of modifying Rep for E. coli expression, all other constructs generated identical protein profiles both in vivo and in vitro, supporting further analysis of their biochemical activities.

View larger version (64K): [in this window] [in a new window]   FIG. 4.   SDS-polyacrylamide gel electrophoresis-silver stain analysis of purified mutant and wt Rep68H6 proteins overexpressed in E. coli. Proteins were expressed from the inducible expression cassette pStump68 and purified via a His6 tag by passage over nickel-agarose columns (Qiagen) as described in Materials and Methods. The position of full-length Rep68H6 is indicated. The same amount of protein was loaded in each lane, except for E504A-68, which required 50-fold more protein to achieve the same level of full-length protein. The lower-molecular-weight products visible in the gel (especially in lanes 6 and 7) were mostly degradation products as indicated by Western blot analysis (data not shown). Rep68* was expressed in a baculovirus system and purified as described previously (30).

Interaction of Rep68H6 proteins with the AAV TR. Standard mobility shift assays were used to compare the specific binding of mutant and wt Rep68H6 proteins to the hairpin TR substrate (³²P-TR). Binding titration profiles performed with each class of mutant protein were similar to that for wt Rep68H6 (data not shown). A representative binding assay with a protein-to-DNA molar ratio of ~10:1 demonstrated that all of the His-tagged E. coli-produced proteins bound specifically to ³²P-TR (Fig. 5A). Specific binding to the TR suggested that neither the point mutations nor the addition of the His₆-tag significantly altered the DNA binding activities of these Rep68 proteins. However, as observed in the silver stain analysis, approximately 50-fold more total protein was used in the binding assays for E504A-68 relative to wt Rep68H6.

View larger version (290K): [in this window] [in a new window]   FIG. 5.   In vitro biochemical analyses of His-tagged Rep68 proteins. (A) Gel mobility shift assay of mutant and wt Rep68H6 proteins expressed in E. coli. Standard binding reaction mixtures contained 0.5 nM 32P-labeled AAV TR hairpin DNA (32P-TR) and 6 nM purified Rep68 protein containing the indicated mutation. Reactions were carried out in standard binding reaction buffer (see Materials and Methods) at 25°C for 30 min, and products were resolved on nondenaturing 5% polyacrylamide gels. Mutant and Rep68H6 (B) proteins were purified by one passage over nickel columns (batch) while Rep68H6 (M) was further purified by passage over a Mono Q column. (B) Terminal resolution by His-tagged Rep68 proteins. Standard trs endonuclease assays contained 0.5 nM 32P-TR substrate and 5 nM His-tagged protein. Nicking reactions were performed in standard nicking buffer (see Materials and Methods) for 60 min at 37°C, followed by protease K digestion and phenol-chloroform extraction, and products were resolved on denaturing polyacrylamide sequencing gels. Substrate (S) and cleavage products (P) are indicated. (C) Standard helicase reactions were performed at 37°C for 60 min in nicking buffer containing 0.5 nM substrate (M13/24) and 6 nM protein, and products were resolved on 5% nondenaturing polyacrylamide gels. Substrate (S) and released product (P) are indicated. Boiled, positive control. In all of the assays described for Fig. 5, E504A-68 required 50-fold more protein to achieve the level of activity shown.

Effect of mutations on Rep68H6 trs endonuclease activity. Site-specific and strand-specific endonuclease cleavage of the AAV TR by Rep78/68 is an essential part of AAV replication (47). All of the mutants examined specifically nicked the TR at the trs, generating the proper-sized product (Fig. 5B). In the nicking assay shown (Fig. 5B), a protein-to-DNA molar ratio of ~10:1 was used for all of the mutants except E504A-68, which required ~50-fold more total protein to obtain the same level of cleaved product.

Effect of mutations on Rep68H6 helicase activity. Under the reaction conditions used in these assays (~10:1 protein-to-DNA molar ratio), all of the Rep68H6 mutants examined exhibited helicase activity (Fig. 5C).

Affinity of D412A-68 versus Rep68H6 for the hairpin TR. In the assays described above, a difference in binding between D412A-68 and wt Rep68H6 was not detected. This suggested that the replication defect observed with D412A-78 in the intracellular assays was not due simply to an inability to interact efficiently with the viral TR. While we used 500-fold less Rep protein than used in other studies (69), we still had excess protein relative to the TR concentration, potentially masking any subtle differences in binding efficiency. In order to determine the concentrations of D412A-68 and wt Rep68H6 required to bind 50% of the substrate (K_D), binding assays were performed as a function of protein concentration. The apparent K_D values were determined from plots of the percentage of TR bound versus protein concentration (Fig. 6A). The apparent K_D values for wt Rep68H6 and D412A-68 for the TR were essentially the same, at about ~3 nM (Fig. 6A). These values, which were derived from assays performed in triplicate, were also within the nanomolar range previously described for baculovirus-purified Rep68 binding to a hairpin TR substrate (44).

View larger version (43K): [in this window] [in a new window]   FIG. 6.   Binding, trs endonuclease, and helicase activities of D412A-68 and Rep68H6 as a function of protein concentration. (A) Standard binding reactions were performed as described for Fig. 5A and carried out in triplicate with 1 nM substrate (32P-TR) and the indicated concentration of each protein. (B) Standard nicking reactions were performed as described for Fig. 5B and carried out in triplicate with 1 nM 32P-TR substrate and the indicated concentration of each protein. (C) Standard helicase reactions were performed as described for Fig. 5C and carried out four times in nicking buffer containing 1 nM substrate (M13/24) and the indicated concentration of protein.

Titration of trs endonuclease and helicase activities. In an effort to identify gross biological differences between the mutant and wt Rep (Fig. 5B and C), protein levels were in excess relative to the respective DNA substrates. In the following assays, the efficiency of D412A-68 compared to that of wt Rep68H6 in the trs endonuclease and helicase activities was determined as a function of protein concentration (Fig. 6B and C, respectively). In the nicking assay comparisons, nearly threefold more D412A-68 protein was required to nick 50% of the substrate, and about 25% less substrate was cleaved overall relative to that with wt Rep68H6 (Fig. 6B). In contrast, no significant differences were observed between the efficiencies of D412A and wt Rep68H6 in the helicase assay (Fig. 6C).

Effect of magnesium concentration on Rep68 functions. Previous studies have shown that the endonuclease activity of Rep68 requires magnesium (Mg²⁺) (31). In the nicking reactions described above, the Mg²⁺ concentration [Mg²⁺] was held constant at 5 mM, which is approximately 10-fold greater than would be present in the intracellular environment (1). Under such conditions, if an interaction between Mg²⁺ and Rep68 was necessary to form an active transition state for nicking, a difference in binding affinity for Mg²⁺ might go unnoticed. Excess Mg²⁺ in the nicking reactions should shift the equilibrium in favor of binding, therefore potentially masking a mutant protein phenotype. For this reason, nicking reactions were performed under conditions of low [Mg²⁺] (Fig. 7A). Neither of the proteins was very efficient at nicking the TR when the [Mg²⁺] was <500 µM. However, wt Rep68H6 activity increased linearly with [Mg²⁺] and cleaved about 14-fold more substrate at 250 µM Mg²⁺. In contrast, we could not detect any cleaved substrate with D412A-68 at <200 µM Mg²⁺. The sensitivity to [Mg²⁺] with D412A-68 suggested that this mutant had a diminished ability to bind Mg²⁺ and that an interaction between Mg²⁺ and D412 was necessary for efficient trs endonuclease activity in vitro.

View larger version (51K): [in this window] [in a new window]   FIG. 7.   trs endonuclease and helicase activities of D412A-68 and Rep68H6 as a function of magnesium concentration. (A) Endonuclease reactions were performed as described for Fig. 5B and carried out in triplicate. Nicking buffer contained 1 nM substrate (32P-TR) with a double-stranded (ds) nicking site (trs), 3 nM protein, and the indicated [Mg2+]. (B) Helicase assays were performed as described for Fig. 5C and carried out in triplicate in nicking buffer that contained 1 nM helicase substrate (M13/24), 3 nM protein, and the indicated [Mg2+]. (C) Nicking reactions were performed as described for Fig. 5B and carried out in triplicate. Nicking buffer contained 1 nM substrate (32P-TRss) with a single-stranded (ss) nicking site (trs), 3 nM protein, and the indicated [Mg2+].

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

In the absence of a crystal structure, assignment of structure-function activities to the AAV Rep proteins has relied on mutational analysis studies. Mutational analysis of the AAV Rep proteins has indicated that Rep-mediated activities can be attributed to somewhat distinct functional domains (Fig. 1A) (14, 21, 43, 48, 68-71, 77). However, in these mutational studies, multiple effects were observed due to the disruption of more than one Rep biological activity. In this study we used a charge-to-alanine mutagenesis strategy (7, 9, 18) to target a number of Rep78/68 functional domains in an attempt to generate a collection of ts mutants (22, 49, 72). We describe the effects of these mutations on Rep78-mediated replication of an rAAV vector in adenovirus-infected 293 cells and on in vitro biochemical assays with purified Rep68 His-tagged fusion proteins expressed in bacteria. Using this alanine substitution strategy, we generated mutants that were grouped into three classes based on their functional activities (Table 1). These included class I mutants (E245A,D246A, Y311F, I330C, E465A, D468A, K474A,D475A, and E504A), which retained normal activity; a class II mutant (D40,42,44A), which was ts for replication; and a class III mutant (D412A), which was not ts but was defective for replication and more [Mg²⁺] dependent for in vitro endonuclease activity.

The expression and replication activity of the mutant Rep proteins relative to those of a wt Rep78 protein in 293 cells at permissive and nonpermissive temperatures were characterized. Similar to results of previous alanine mutagenesis studies (9), the majority of the mutants (class I and III) were stably expressed at levels similar to those of wt protein (wt Rep78) (Fig. 2). The class I mutants also exhibited wt activities in the intracellular replication assays (Fig. 3A) and in the biochemical assays in vitro (Fig. 5). Interestingly, we determined that three of the mutants (Y311F, E465A, and K474,D475A) grouped within this class were active, whereas similar mutants have previously been shown to lack endonuclease activity in the context of the MBP-Rep68 fusion protein (21, 69). The discrepancy between these observations suggests a need for concern when evaluating only in vitro Rep activity by using fusion proteins. For this reason, we first assayed all of the mutants in intracellular replication assays in the context of the Rep78 protein (Fig. 3A) and supported these analyses by in vitro studies. Of the mutant Rep proteins that we analyzed in vitro, only mutant E504A displayed protein stability characteristics contrary to those seen in in vivo analysis (compare Fig. 2, lane 14, to Fig. 4, lane 6). Since completion of our study, Davis et al. (21) generated an MBP Rep fusion protein with mutations identical to that of the ts mutant we describe here. In these in vitro studies, D40,42,44-MBP-68 does not bind or nick the TR, contrary to our in vitro and in vivo results.

While steady-state protein levels for the class II ts mutant (D40,42,44A) at 37°C were generally below the sensitivity limits of the ECL-Western blot analyses (Fig. 2), expression was shown to be at wt levels at 32°C. This class II mutant was also notably defective for replication under physiological conditions (Fig. 3A). D40,42,44A-78 mediated replication much more efficiently at 32°C (~3-fold) than at 37°C and was essentially inactive at 39°C. The instability of the class II mutant Rep protein (D40,42,44A) corroborated ts replication data (Fig. 3), allowing us to assign a ts replication phenotype. When this mutant was assayed in the context of all four Rep proteins (pIM45 plasmid), its activity was similar to that seen with the HIV construct (Fig. 3B), although the stability of the pIM45 mutant Rep was not characterized. In addition, a 3-log-unit difference in titer was observed when permissive and nonpermissive temperatures were compared (Table 2). All of these analyses support Rep mutant D40,42,44A-78 having a ts phenotype. The 3-log-unit difference in Rep function demonstrates that this is a tight mutant and should be useful in further analysis of Rep function.

Mg²⁺ binding mutant. The mutant D412A was categorized in a separate class (class III), since it was expressed at wt levels (class I) but did not exhibit a temperature-dependent phenotype (class II). However, this mutant was markedly reduced in its ability to mediate replication in the intracellular assays (Fig. 3A). When the biochemical activities of D412A were analyzed in the context of the Rep68 His-tagged fusion protein, this mutant bound efficiently to the TR (Fig. 6A) but had a reduced level of endonuclease activity relative to wt Rep68H6 (Fig. 6B). The reduced nicking activity of D412A-68 was shown with both single-stranded and double-stranded substrates and appeared to be more Mg²⁺ dependent for activity (Fig. 7A and C). While Mg²⁺ is also required for Rep ATP-dependent helicase activity, we did not see an [Mg²⁺]-dependent phenotype for the D412A mutation in helicase assays (Fig. 7B). The biochemical assays that we have described support that the Rep mutant D412A has diminished ability to interact with Mg²⁺ and that an interaction between D412 and Mg²⁺ is necessary for efficient trs endonuclease activity. These results were reproducible with multiple Rep protein extracts, further supporting that the active DNA cleavage site of Rep78/68 consists, at least in part, of D412 and Mg²⁺.

DD35E motif. The D412 mutation maps to a region of Rep78/68 that contains a cluster of acidic amino acid residues that have the potential to form overlapping DD35E motifs (Fig. 1). The acidic amino acids of the DD35E motif have been shown to form an Mg²⁺ binding pocket that is critical for the nicking and strand transfer reactions of bacterial transposases and retroviral integrases (16, 36, 52). One might speculate that the decreased affinity for Mg²⁺ with D412A was consistent with the partial disruption of a similar putative Mg²⁺ binding domain. Based on this assumption, mutations at any of the conserved DD35E motif residues should result in the loss of some in vitro function as previously described (35, 36). Rep78/68 mutants generated within this putative DD35E motif (D468A and E504A) were identified as class I mutants with wt phenotypes, suggesting that these residues are not critical for catalytic function. However, this does not rule out the possibility that the second putative DD35E motif within Rep78/68 was involved in the coordination of the active-site Mg²⁺ ion(s). We also introduced a mutation at E465A within this second putative DD35E motif (at residues D368, D429, and E465) (71) to test the relevance of this DD35E cluster. The activity of this mutant was also similar to that of wt Rep78/68.

Mg²⁺ binding pocket. One of the reasons that we were originally intrigued by the DD35E motif was that Rep mediates targeted integration by an as-yet-unknown mechanism. Also, the DD35E motif is highly conserved among enzymes that mediate transposition and integration (16). A number of crystal structures have been solved for various Mg²⁺-dependent nucleases, such as HIV integrase (23, 41) and Mu transposase (54), which utilize the DD35E motif, as well as E. coli RNase H (34), HIV RNase H (20), and the E. coli resolvase RuvC (3). Genetic and crystallography studies have demonstrated that the catalytic cores of these enzymes consist of a cluster of acidic residues that interact directly with Mg. While the primary sequences of these proteins are quite diverse, the overall secondary and tertiary structures of these enzymes are strikingly similar (25, 78). As shown with HIV integrase (Fig. 8A), The active domains of these structures consist of five central beta strands flanked by a various number of alpha helices (23, 41).

View larger version (69K): [in this window] [in a new window]   FIG. 8.   Structural analysis of the magnesium binding pocket and catalytic active site for nuclease activity. (A) Crystal structure of the active site for the HIV integrase, INT (23). Residues critical for magnesium binding and nuclease activity are indicated; beta strands are colored blue, and helices are colored red. (B) Theoretical structural model of the Rep78/68 active site for nicking. Residues 391 to 534 were used to generate a theoretical model of the magnesium binding domain of Rep by using secondary structural predictions (64, 79a) and the computer software programs from Molecular Simulations Inc. (see Materials and Methods). Residues potentially critical for magnesium binding and Rep nuclease activity based on this model are shown.