A257T Linker Region Mutant of T7 Helicase-Primase Protein Is Defective in DNA Loading and Rescued by T7 DNA Polymerase*

The helicase and primase activities of the hexameric ring-shaped T7 gp4 protein reside in two separate domains connected by a linker region. This linker region is part of the subunit interface between monomers, and point mutations in this region have deleterious effects on the helicase functions. One such linker region mutant, A257T, is analogous to the A359T mutant of the homologous human mitochondrial DNA helicase Twinkle, which is linked to diseases such as progressive external opthalmoplegia. Electron microscopy studies show that A257T gp4 is normal in forming rings with dTTP, but the rings do not assemble efficiently on the DNA. Therefore, A257T, unlike the WT gp4, does not preassemble on the unwinding DNA substrate with dTTP without Mg(II), and its DNA unwinding activity in ensemble assays is slow and limited by the DNA loading rate. Single molecule assays measured a 45 times slower rate of A257T loading on DNA compared with WT gp4. Interestingly, once loaded, A257T has almost WT-like translocation and DNA unwinding activities. Strikingly, A257T preassembles stably on the DNA in the presence of T7 DNA polymerase, which restores the ensemble unwinding activity of A257T to ∼75% of WT, and the rescue does not require DNA synthesis. The DNA loading rate of A257T, however, remains slow even in the presence of the polymerase, which explains why A257T does not support T7 phage growth. Similar types of defects in the related human mitochondrial DNA helicase may be responsible for inefficient DNA replication leading to the disease states.

Helicases are molecular motors that are involved in almost all of the metabolic processes of the nucleic acids in the living cell. Helicases catalyzing genome replication and recombination assemble into six-membered ring-shaped proteins around DNA (1)(2)(3)(4)(5)(6)(7). Bacteriophage T7 encodes a ring-shaped helicase, the gp4 protein, which has served as a model system to understand the mechanisms of this class of helicases (3,4,7). The human mitochondrial DNA helicase Twinkle is homologous to T7 gp4, showing 46% overall sequence similarity (8).
T7 gp4 is a bifunctional helicase-primase protein with helicase conserved motifs in the C-terminal domain and the primase motifs in the N-terminal domain. The two domains of the T7 gp4 are structurally independent, but each enzyme depends on the other for optimal activity (9,10). Crystal structures of T7 gp4 have shown that the primase and helicase domains of T7 gp4 are connected via a linker region made of a helix-loop region (Fig. 1A) (11)(12)(13). The linker region is an important element that forms the subunit interface for assembling the helicase domains into a compact ring. A helix and loop in the linker region of one subunit interact with three helices of a neighboring subunit to connect the six subunits of the hexamer in a head-to-tail fashion (Fig. 1B).
Genetic screening has identified helicase-deficient but primase-proficient mutants that lie in the linker region (14,15). Many of the disease-causing mutations in the human mitochondrial helicase Twinkle are also found in the highly homologous linker region (8,16,17). These mutations are linked to autosomal dominant progressive external opthalmoplegia, a human disease characterized by multiple mitochondrial DNA deletions (8,18,19). Individuals carrying this mutation suffer from early or late onset progressive external eye muscle weakness, neuropathy, depression, ataxia, and deafness.
One of the linker region mutations of the T7 gp4 is A257T, which was originally isolated from a genetic screen for helicasedeficient and primase-proficient mutants of gp4 (14,15). An analogous mutation, A359T, is found in the human Twinkle protein (8). Twinkle contains a C-terminal helicase and N-terminal primase-like domain separated by a linker region that is highly homologous to the linker region of T7 gp4 (20). The similarity between T7 gp4 and human Twinkle indicates that the detailed characterization of the linker region mutant of T7 gp4 can provide important insights into the mechanisms that lead to mitochondrial deletions in humans. Biochemical studies of A257T or A257V have shown that the mutant protein is defective in DNA unwinding, and it was proposed that this might be due to its defect in translocating along single-stranded DNA (ssDNA) 2 (15,21). However, the precise mechanism by which A257T/A257V mutation causes this defect in translocation was not elucidated.
Here, we report an in-depth characterization of the biochemical and structural properties of the T7 gp4 A257T mutant to understand its helicase defect. Our studies show that A257T is not defective in translocation on ssDNA and DNA unwinding, but has a defect in DNA loading. We find that T7 DNA polymerase stabilizes the binding of A257T to the DNA. However, the assembly rate of A257T gp4 on the DNA remains critically slow, even in the presence of T7 DNA polymerase, which explains why it does not support T7 phage growth.

EXPERIMENTAL PROCEDURES
Reagents and Buffers-Chemical reagents were purchased from Sigma and JT Baker. Radionucleotides were purchased from PerkinElmer Life Science or GE Healthcare. Oligodeoxynucleotides were purchased from Integrated DNA Technology (IDT, Coralville, IA). 5Ј,6Ј-Fluorescein carboxyamide succinamidyle ester was purchased from Molecular Probes. All reactions were carried out at 25°C in the T7 helicase buffer containing 50 mM Tris-Cl, pH 7.5, 40 mM NaCl, and 10% glycerol.
DNA Substrates-Oligodeoxynucleotides purchased from IDT were PAGE-purified and electroeluted (Schleicher & Schuell Elutrap). DNA concentrations were determined from absorption at 260 nm and calculated extinction coefficients after digestion with snake venom phosphodiesterase I (24). The DNA strand was radiolabeled using [␥-32 P]ATP and polynucleotide kinase. Labeled DNA was cleaned using Sephadex G-25 spin columns. Unwinding substrates were prepared by annealing together complementary DNA strands in the T7 helicase buffer. The 70-bp minicircle substrate was made using a DNA splint as reported (25,26).
Ensemble Fluorescence-based DNA Unwinding-Fluorescence-based DNA unwinding experiments were performed in a stopped-flow instrument (Kin Tek Instruments, Austin, TX) (27). An equal volume of fluorescein-labeled 30-bp unwinding fork (20 nM), WT or A257T gp4 (200 nM hexamer), dTTP (4 mM), EDTA (6 mM), BSA (2 M) in T7 helicase buffer from one syringe was rapidly mixed with MgCl 2 (14 mM, and final free concentration of 2 mM), BSA (2 M) with and without 3 M dT90-DNA trap from a second syringe. The reaction mix was excited at 480 nm through a slit width of 2 mm (ϳ8-nm spectral bandwidth), and the increase in fluorescence was detected by monitoring light filtered through a long pass filter with a cutoff of 515 nm. The unwinding rates were determined from fitting as described (27).
In the DNA unwinding experiments involving mixed WT and A257T hexamers, the proteins were mixed in different molar proportions (40/0, 40/20, 40/40, 40/80, 40/200) in T7 helicase buffer and incubated on ice for 30 min, followed by the addition of EDTA, dTTP, BSA, and DNA and incubated for 10 min. The reaction was then carried out as indicated above.
Single Molecule DNA Unwinding-The single molecule DNA unwinding experiments were carried out as described previously (28) at 8-piconewton force using 2 mM dTTP. The raw initiation time under single molecule conditions was measured as the time period between rapid unzipping of ϳ2000 bp of the double-stranded DNA (dsDNA) and when the helicase begins to unwind the dsDNA. This time periods were corrected for the time it takes to translocate on an average of 1000 nucleotides to determine the initiation time.
Electron Microscopy-WT or A257T gp4 (2.1 M) was incubated at 25°C for 20 min in 25 mM triethanolamine buffer, pH 7.2, with the nucleotides and DNA, applied to glow discharged grids, stained with 2% (w/v) uranyl acetate, and imaged under minimal dose conditions in a Tecnai T12 electron microscope, at a nominal magnification of ϫ30,000 and an accelerating voltage of 120 keV.
Minicircle Rolling Circle DNA Synthesis-The rolling circle DNA synthesis of WT and A257T was carried out on the 70-bp minicircle substrate at 22°C as reported (25).
Radiometric DNA Unwinding Assay-The rapid kinetics of dsDNA unwinding by WT and A257T was measured using the radiometric assay. WT or A257T (200 nM) was incubated for 30 min with 5 nM 40-bp replication fork (GC 20%), 5 mM EDTA, and 4 mM dTTP substrate in reaction buffer on ice in one syringe of the RQF-3 Quench-Flow apparatus (Kin Tek Instruments) and mixed with 13 mM MgCl 2 and 3 M dT90-DNA trap in the same buffer from a second syringe for 0.02 to 3 s and stopped by the addition 1.5 volume of 100 mM EDTA and 1% SDS. T7 DNA polymerase was preassembled by mixing gp5 and E. coli thioredoxin in 1:5 ratio at 22°C for 5 min in reaction buffer containing freshly made 5 mM DTT. When present, T7 DNA polymerase (200 nM) was added to WT or A257T and DNA mix and further incubated at room temperature for 30 min. The quenched unwinding reaction with and without T7 DNA polymerase was loaded on a native 12% polyacrylamide gel for resolving the duplex and unwound DNA substrates, and the fraction of DNA unwound was determined and quantitated using the PhosphorImager (Molecular Dynamics, Sunnyvale, CA) instrument and ImageQuant5 software. The data were analyzed as described previously (29).

RESULTS
DNA Unwinding Activity of the gp4 A257T-The DNA unwinding activity of gp4 WT and A257T was measured by the real-time fluorescence assay (27). T7 gp4 WT or A257T (100 nM hexamer) was preincubated with the fluorescein-labeled fork DNA (10 nM) in the presence of dTTP (without Mg 2ϩ ), and the reaction was initiated by rapid mixing with MgCl 2 ( Fig. 2A).
A time-dependent increase in fluorescence was observed in the WT gp4 reaction within 100 ms of reaction start (Fig. 2B). The fast kinetics indicates that WT gp4 is preassembled on the fork DNA and immediately initiates DNA unwinding upon addition of Mg(II) with rates of 67 bp/s at 25°C. In the same time span, no fluorescence increase was observed in the A257T reaction; however, when the reaction was monitored for longer periods, we did observe a slow increase in fluorescence that indicated ϳ1500-fold slower rate of unwinding by A257T compared with WT gp4 (Fig. 2C). As indicated previously, these experiments show that A257T has a defect in DNA unwinding (15,21). However, the exact reason for the defect was not determined.
One reason for the defect might be that the mutant does not translocate along ssDNA. We therefore used a single molecule assay to measure the translocation rate of T7 gp4 on ssDNA. In this assay, one strand of a 4.1-kb length dsDNA molecule is attached to an optically trapped microsphere and the other strand is attached to the surface of a glass coverslip (30,31) (Fig.  2D). By pulling on the ends of the two strands, ϳ400 bp of dsDNA is rapidly unzipped by mechanical movement of the coverslip relative to the trapped microsphere, creating ssDNA loading region for freely diffusing T7 gp4 hexamers to bind. Following binding of the gp4 to the ssDNA loading region, several hundred bp of dsDNA are quickly unzipped in front of the helicase, allowing the helicase to translocate on ϳ500 nucleotides of ssDNA without working against the DNA fork junction (28). The translocation rate is then determined by measuring the time for the helicase to travel across the unzipped ssDNA region. Using such experiments, we found that A257T can translocate on ssDNA, and the translocation rate of A257T is nearly the same as WT gp4 (Fig. 2E).
To determine whether A257T can unwind dsDNA, we used the same single molecule assay described above. T7 gp4 was allowed to reach the unwinding fork junction, and the unwinding reaction was monitored by measuring the increase in the length of ssDNA region. To our surprise, we found that the A257T is capable of unwinding a kilobase pair length of dsDNA with rates that are only a little slower than WT gp4 (Fig. 2F). The only defect we observed was that we needed higher A257T concentrations to detect enough unwinding molecules. WT gp4 at 0.3 nM hexamer concentration initiated DNA unwinding with an average initiation time of ϳ60 s. To get a comparable initiation time (ϳ60 s) with A257T, the concentration of A257T had to be increased to 30 nM. These results indicate that contrary to what was concluded from previous ensemble reactions (15,21), A257T is not defective in ssDNA translocation and DNA unwinding. The requirement of higher A257T protein indicates a defect in initiation; hence, we designed single molecule experiments to measure the initiation times to unwinding.
To measure the initiation time, about 2000 bp of the dsDNA was mechanically unzipped rapidly to create ssDNA region for the helicase to bind. Then, the time between mechanical unzipping of DNA and the beginning of the dsDNA unwinding reaction was measured. After correcting for the time it takes to translocate on the ssDNA (using the ssDNA translocation rates determined from Fig. 2E), we determined that at 5 nM hexamer, 2 mM dTTP, and 5 mM MgCl 2 , it takes on an average 3.7 s for the gp4 WT to initiate unwinding, and it takes A257T about 165 s to initiate unwinding at the same 5 nM concentration (Fig. 2G). These results indicate that A257T is 45 times slower at initiation compared with WT gp4. However, once it is bound to DNA, A257T unwinds with almost a WT rate. At 5 nM, we do not expect to have multiple A257T hexamers unwinding DNA because the initiation time of 165 s on an average is much longer than its unwinding time of Ͻ30 s.
A defect in assembling around DNA can explain the slow rate of unwinding by A257T detected in the ensemble assays (Fig.  2C). However, in the ensemble assays preincubation of A257T should have bypassed any slow assembly steps. WT gp4 preassembles on the fork DNA with dTTP without Mg(II), and in this manner we can bypass the assembly steps and synchronize the unwinding reaction, which allows us to measure the intrinsic unwinding rate. But this was not observed with A257T. This indicates that A257T does not preassemble on the fork DNA in the presence of dTTP without Mg(II). This is consistent with the filter binding assays that showed very little or no binding of A257T on ssDNA in the presence of dTTP without Mg(II) (supplemental Fig. 1). However, once Mg(II) is added, A257T must load on the DNA, as we observe DNA unwinding, but the loading rate must be slow, as measured by the single molecule assays above. Thus, the observed rate of DNA unwinding by A257T is slow under ensemble conditions because it is limited by the slow rate of DNA loading. The inefficient loading of A257T on the DNA also explains the lower DNA-stimulated V max of dTTPase (supplemental Fig. 2). The WT-like dTTP K m indicates that A257T is not defective in binding dTTP.
A257T Forms Rings-To determine whether the reason for not binding DNA in the presence of dTTP without Mg(II) is due to a defect in ring formation, we imaged WT and A257T gp4 proteins by electron microscopy (32,33). Both WT and A257T gp4 assemble into ring-shaped structures in the presence of dTTP or dTMPPCP (Fig. 3A, supplemental Fig. 3), and the rings with dTMPPCP and MgCl 2 bind to M13 ssDNA like beads on a string (Fig. 3B), consistent with the NC-DEAE binding assay with dTMPPCP (supplemental Fig. 1). In the presence of MgdTTP, WT gp4 binds to DNA like beads on a string, but A257T forms bullet-like structures, which is either an aggregate or a structure bound to DNA (Fig. 3C). With dTTP without Mg(II), the rings of A257T do not bind DNA (Fig. 3D). We conclude that A257T gp4 is normal in forming rings with dTTP; however, the rings do not bind DNA in the presence of dTTP without Mg(II).
DNA Unwinding Activity of Mixed WT and A257T gp4-To determine whether mixed hexamers of WT gp4 and A257T are active in DNA loading, we measured the unwinding amplitude, which is a measure of the fraction of productive helicase bound to the forked substrate. WT gp4 at 20 nM was mixed with increasing amounts of A257T (10 -100 nM) (Fig. 4A), and the unwinding kinetics was measured using the fluorescence-based assay (Fig. 4B). The data were analyzed to determine the unwinding rates and amplitudes. The unwinding rate of the mixed hexamers was 70% of the WT level and remained at that level even at a high A257T:WT ratio of 5:1 (Fig. 4C). The unwinding amplitude, on the other hand, decreased linearly with increasing fraction of A257T over the entire sampled region and predicted a close to zero amplitude for A257T alone. This indicates that the mixed A257T-WT hexamers are active in DNA unwinding; however, as the number A257T subunits increase in the mixed hexamers, the rings become increasingly defective in productive assembly on the DNA.
A257T gp4 Supports DNA Replication-Previous studies had indicated that A257T supports DNA synthesis, but the mechanism of this rescue was not determined (15). We examined this reaction in more detail here with the minicircle replication assay (25,34). A257T or WT gp4 was preincubated with T7 DNA polymerase on the minicircle fork DNA in the presence of dNTPs without MgCl 2 (Fig. 5A). Reactions were initiated by adding MgCl 2 . Both WT and A257T supported the synthesis of kilobase pair size DNA products from rolling circle DNA synthesis (Fig. 5B). The only difference was the lower yield of DNA products in the A257T reactions, consistent with the lower efficiency of A257T assembly on the DNA.
T7 DNA Polymerase Rescues the Helicase Defect of A257T-There are two ways by which T7 DNA polymerase can rescue the activity of A257T gp4: (a) it helps load or stabilize the mutant helicase on the DNA, and/or (b) it "pushes" the helicase or prevents helicase slippage via its DNA synthesis activity. We did not observe any helicase slippage in the single molecule unwinding assays. However, we cannot eliminate the possibility that the rescue is because DNA polymerase pushes the helicase via DNA synthesis. To distinguish between possibilities (a) and (b), the 40-bp fork DNA with 5Ј-ssDNA overhang for helicase loading and 3Ј-primer-template region for polymerase binding was incubated with the helicase and dTTP without Mg(II) in the absence and in the presence of T7 DNA polymerase for at least 30 min, and then reactions were initiated with MgCl 2 (Fig. 6A). The 5Ј-strand was radiolabeled to monitor its conversion to ssDNA by the gel assay (27,29,35). We did not add the other three dNTPs required for DNA synthesis. Without the remaining dNTPs, the DNA polymerase incorporates one dTTP but cannot elongate the primer any further by DNA synthesis.
A257T gp4 without the polymerase does not unwind the fork DNA (Fig. 6B), consistent with the fluorescence-based unwinding assay. However, when A257T was preincubated with T7 DNA polymerase, it showed almost WT-like DNA unwinding activity (Fig. 6, B and C). WT gp4 unwinds the forked substrate in the absence of T7 DNA polymerase at ϳ82 bp/s and in the presence of T7 DNA polymerase at ϳ65 bp/s. The DNA polymerase in this case does not accelerate the DNA unwinding activity of WT as observed previously (36) because there is no DNA synthesis. In fact, it appears that a nonsynthesizing DNA polymerase slows the helicase. The unwinding rate of A257T gp4 in the presence of T7 DNA polymerase is ϳ50 bp/s (Fig.  6C), which is ϳ75% of WT. These results indicate that A257T can preassemble on the fork DNA in the presence of T7 DNA polymerase. The preassembled A257T on the DNA has almost WT-like unwinding activity, as observed in the single molecule unwinding assays (Fig. 2C).
How does T7 DNA polymerase help A257T preassemble on the fork DNA? It has been proposed that T7 DNA polymerase interacts with T7 gp4 via a basic loop that becomes exposed when T7 gp5 (DNA polymerase subunit of T7 DNA polymerase) interacts with thioredoxin (processivity factor). We therefore measured DNA unwinding by A257T without thioredoxin in the presence of T7 gp5 alone. We find that T7 gp5 alone was not able to rescue the helicase function of A257T (supplemental Fig. 4). These results indicate a specific mechanism involving the thioredoxin binding domain on gp5 in rescuing the helicase function of A257T.
Slow Assembly of A257T gp4 on the DNA-If A257T can unwind DNA to almost WT level in the presence of T7 DNA polymerase, then why does it not support phage growth? One reason could be that the loading of A257T on the DNA although rescued by T7 DNA polymerase is too slow to support  T7 DNA synthesis. To measure the DNA loading rate in the presence of T7 DNA polymerase, we designed the following experiment (Fig. 7A): WT or A257T gp4 was incubated with T7 DNA polymerase and the replication fork substrate in the presence of dTTP without MgCl 2 , and this incubation time was controlled from 5 s to 30 min. Following controlled incubation, the unwinding activity was assayed within 5 s, which is enough time for the helicase to unwind the 40 bp duplex fully (see Fig.  6B). The unwinding activity here is a readout of the assembly process around DNA. The results showed that WT gp4 assembles on the fork at a rate of 0.03 s Ϫ1 and A257T assembles with a rate of 0.001 s Ϫ1 (Fig. 7, B and C), which is similar to the ensemble unwinding rate of A257T shown in Fig. 2F that we propose is limited by the DNA loading rate. Thus, T7 DNA

DISCUSSION
The studies in this paper show that the defect in the helicase function of the linker region mutant, A257T gp4, is caused by a defect in DNA loading rather than a defect in DNA unwinding, as previously thought. Both single molecule and ensemble assays indicate that A257T loads 30 -45 times slower on DNA compared with WT gp4, but once it is assembled on the DNA into a stable complex, A257T has almost WT-like ssDNA translocation and unwinding activities.
The linker region between the N-terminal primase and the C-terminal helicase domain of T7 gp4 is an important element that forms the subunit interface for assembling the helicase domain into a compact ring (11)(12)(13). The helix and the loop of the linker region interact with three helices of the neighboring subunit to form a clasp of subunit interface (Fig. 1A). The primase domains are independent structural units emerging out of each subunit of the helicase ring, with their primase active sites pointing toward the neighboring subunit primase domain.
The residue Ala 257 is located at the beginning in the loop of the linker region, close to the N-end, (Fig. 1B). Mutation of Ala 257 to Val, Leu, Pro, Glu, Asp, Asn, Thr, His, or Tyr is lethal, and the mutant protein does not support T7 phage growth (21). These results suggest that the small size of Ala 257 is important for its function. Because Ala 257 lies closer to the primase domain than the helicase, it is unlikely that A257T mutation affects the folding of the helicase domain. This is consistent with the observation that A257T mutation does not affect ring formation, which occurs primarily through interactions between the helicase domains. Our modeling experiments using the crystal structure of the gp4 heptamer suggest that the position of Ala 257 is such that any change to a bulky amino acid will produce a clash with the nearby amino acids (Fig. 1, C and  D). The A257T change results in a clash with Gln 253 and Val 230 , which both reside in the helix next to the linker region and in the primase domain. To accommodate the A257T change, therefore, the protein must undergo local structural changes. It appears that these local changes near the linker region affect the DNA loading mechanism of T7 gp4.
Previous studies have suggested a role of the primase domain in DNA loading by the ring-opening mechanism (37,38). Based on the DNA binding kinetics, it was proposed that ssDNA initially interacts with the primase domain, which chaperones the ssDNA into the central channel. It was proposed that the binding of the DNA to the primase domain causes the linker region clasp to weaken and to open the subunit interface like a lock washer, allowing the DNA to bind in the central channel. It has been shown that the A257T gp4 has primase activity; hence, the primase domain must be proficient in DNA binding (15,21). However, local changes caused by the A257T mutation may restrict loading of the DNA into the central channel. The single molecule assays show that indeed A257T DNA loading rate is ϳ45 times slower than WT gp4. The single molecule assay is sensitive to detect the small number of A257T molecules that load on the ssDNA, and hence it is able to observe the almost WT like unwinding and ssDNA translocation activities of A257T.
We did notice in the electron microscopy studies that A257T has a greater tendency to form aggregates in the presence of Mg 2ϩ . These aggregates appear as short filament type structures, which could be formed by altered interactions between subunits. It is possible that the local changes in the linker region alter interactions between the subunits, causing hydrophobic residues to be exposed that lead to protein aggregation. Perhaps these higher order oligomers or aggregates of A257T are refractory to DNA loading.
We find it curious that although both dTMPPCP and dTTP nucleotides promote ring formation, A257T binds DNA only in the presence of dTMPPCP, but not with dTTP. The decreased aggregation and increased rings around DNA with MgdTMP-PCP as opposed to MgdTTP could be because dTMPPCP does not get hydrolyzed and interacts more tightly with the subunits than dTTP.
When A257T was preincubated with T7 DNA polymerase and fork DNA, the helicase could be stably assembled on the DNA such that it now displayed almost WT-like unwinding activity. This recovery was observed even in the absence of DNA synthesis. Hence, T7 DNA polymerase is able to restore the function of A257T gp4 by stabilizing the binding of the helicase on the replication fork.
T7 DNA polymerase interacts with T7 gp4 via the basic loops of the thioredoxin binding domain (39). The processivity factor thioredoxin binds to the thioredoxin binding domain of gp5 and causes exposure of the basic loops, which stimulate interaction between the helicase and polymerase. It appears that this interaction between the helicase and polymerase stabilizes A257T on the DNA. This is supported by our finding that T7 gp5 by itself (or thioredoxin by itself) does not stimulate the helicase activity of A257T. Although T7 DNA polymerase rescues the helicase function of A257T gp4, it does not accelerate the DNA loading rate. Measurement of the kinetics of protein assembly on the fork DNA showed that the loading time of A257T is about 30 times slower than of the WT gp4. Thus, it appears that T7 DNA polymerase rescues A257T by stabilizing the helicase complex on the DNA.
The slow assembly of A257T gp4 on the DNA explains why it is not a viable mutation and why it does not support phage growth. Helicase loading is a key step during the initiation of DNA replication, in addition to being required for processive DNA replication. Thus, any defect in helicase loading will lead to a defect in DNA replication. Although T7 DNA polymerase is able to rescue the DNA loading defect of A257T, the loading process is still inefficient to support the propagation of T7 phage, whose entire infection cycle lasts for 25-30 min at 30°C (40).
The importance of studying the A257T mutation of T7 gp4 lies in the fact that an analogous mutation of A359T is naturally found in the human mitochondrial DNA helicase Twinkle (8). The Twinkle helicase contains a C-terminal helicase and N-terminal primase-like domain separated by a linker region that is highly homologous to the linker region of T7 gp4. Modeling studies suggest that the linker region of Twinkle plays a role similar to that of gp4 in connecting the helicase domains to form a hexameric ring (20). Many of the disease-causing Twinkle mutations are found within or near the linker region, including A359T.
The detailed studies of the T7 gp4 A257T mutant reported here potentially elucidate the defects of other helicases with similar conserved linker region. A biochemical study of A359T Twinkle has shown that the protein is not defective in oligomerization, but has reduced helicase and replication properties (20). If A359T Twinkle mutant cannot assemble efficiently on the DNA, it will hinder normal replication fork initiation and progression (41). A mutant defective in loading on DNA will also have problems with reinitiation of DNA replication following stalling or collapse of the replication fork. Mixed hexamers of T7 gp4 A257T and WT gp4 are more active in DNA loading even when 85% of the population was made of A257T. This is consistent with what has been observed with the A359T mutation in Twinkle. In the heterozygous form the symptoms are mild, but in the homozygous form of A359T, early onset autosomal dominant progressive external opthalmoplegia is observed.