|Home | About | Journals | Submit | Contact Us | Français|
Human DNA polymerase η (HsPolη) plays an important role in translesion synthesis (TLS), which allows for replication past DNA damage such as UV-induced cis-syn cyclobutane pyrimidine dimers (CPDs). Here, we characterized ApPolη from the thermophilic worm Alvinella pompejana, which inhabits deep-sea hydrothermal vent chimneys. ApPolη shares sequence homology with HsPolη and contains domains for binding ubiquitin and proliferating cell nuclear antigen. Sun-induced UV does not penetrate Alvinella's environment; however, this novel DNA polymerase catalyzed efficient and accurate TLS past CPD, as well as 7,8-dihydro-8-oxoguanine and isomers of thymine glycol induced by reactive oxygen species. In addition, we found that ApPolη is more thermostable than HsPolη, as expected from its habitat temperature. Moreover, the activity of this enzyme was retained in the presence of a higher concentration of organic solvents. Therefore, ApPolη provides a robust, human-like Polη that is more active after exposure to high temperatures and organic solvents.
Although genomic DNA contains genetic information that should be error-free for proper cellular function, it is continually subjected to ubiquitous DNA-damaging agents of both environmental and endogenous origins, such as UV and ionizing radiation and reactive oxygen species (ROS) [1–3]. To maintain genomic integrity, cells possess several repair pathways, including nucleotide excision repair (NER), base excision repair (BER), and recombination repair, to cope with the various resulting lesions. However, some lesions are not repaired and are encountered by the replication machinery. During DNA replication, these lesions block high-fidelity replicative DNA polymerases, and if not processed correctly, eventually lead to mutagenesis, carcinogenesis, or cell death. To avoid such catastrophic consequences, cells have a translesion DNA synthesis (TLS) mechanism that allows efficient and accurate DNA synthesis past lesions [4–6].
The importance of TLS in humans has been indicated by studies of an inherited human disease called xeroderma pigmentosum variant (XP-V), which is characterized by the hypersensitivity of skin to sunlight and the high incidence of sunlight-induced skin cancer [7, 8]. The XPV gene encodes human DNA polymerase η (HsPolη), a 713 amino acid protein that is a member of the Y-family DNA polymerases that includes human DNA polymerases ι, κ, and Rev1 [6, 9, 10]. Cells from XP-V patients are defective in the replication of damaged DNA and show hypermutability after exposure to UV radiation or DNA-damaging agents. These results indicate that HsPolη is at least involved in the accurate translesion pathway to avoid mutations by UV-induced lesions in vivo. Consistent with these observations, biochemical studies revealed that HsPolη, unlike the replicative Polδ and Polε, was able to catalyze efficient and accurate TLS past a UV-induced cis-syn cyclobutane pyrimidine dimer (CPD). In contrast, DNA containing other UV-induced lesions, such as the pyrimidine(6–4)pyrimidone photoproduct (6–4pp) and its Dewar valence isomer (Dewar), which are efficiently repaired by NER in vivo [11, 12], is not replicated by HsPolη [13, 42].
Furthermore, this enzyme was reportedly able to bypass not only UV-induced lesions but also various other lesions induced by both environmental and endogenous reactive oxygen species. For instance, HsPolη bypasses 7,8-dihydro-8-oxoguanine (8-oxoG), 5R-thymine glycol (5R-Tg), and 5S-thymine glycol (5S-Tg), but not an apurinic/apyrimidinic (AP) site [13–19], although these lesions, which have small alterations in their chemical structures, are mainly repaired by BER in vivo. Thus, these findings indicate that HsPolη also plays an important function in the replication of DNA containing ROS-induced lesions in vivo.
In addition to its role in TLS, HsPolη can extend DNA synthesis from D-loop recombination intermediates, and its activity is stimulated by Rad51 recombinase . Moreover, Polη-disrupted DT40 cells show significant decreases in the frequencies of both immunoglobulin-variable gene conversion and double-strand break-induced homologous recombination . Taken together, these reports indicate that Polη is involved in homologous recombination repair, and thus, Polη seems to be important for DNA damage tolerance in living cells.
Alvinella pompejana is a polychaetous annelid that inhabits active deep-sea hydrothermal vent sites along the East Pacific Rise, where it colonizes the walls of actively venting high-temperature chimneys. The average temperature is about 68°C, with spikes up to 81°C, and thus exceeds the predicted 55°C limit for the survival of eukaryotes [22, 23]. The ability of this worm to survive in such an extreme environment suggests that A. pompejana may contain highly stable proteins that can be used for biology, biotechnology, and industry. Several proteins have been characterized from A. pompejana and the analyses have revealed the proteins have enhanced thermostability [24–26], which include A. pompejana superoxide dismutase (SOD) and U2AF65, which are more stable than their human homologs.
In this study, we cloned an A. pompejana gene with homology to the HsPolη gene. The encoded full-length recombinant protein was produced in Escherichia coli. Characterization of ApPolη revealed that it had the ability to bypass CPD, 8-oxoG, 5R-Tg, and 5S-Tg, but did not bypass either 6–4pp, Dewar, or an AP site analog. This substrate specificity is similar to that of the HsPolη, yet ApPolη is comparatively more thermostable than HsPolη and retains activity in the presence of organic solvents. Therefore, ApPolη is a robust human-like Polη that is useful to complement and expand ideas on TLS mechanisms by virtue of its eukaryotic origin and enhanced stability.
Recombinant HsPolη tagged with (His)6 at its C-terminal end was produced in Sf9 insect cells using the baculovirus expression system and was purified by sequential column chromatography on HiTrap Q, Ni-NTA agarose, and MonoS, as described previously . Klenow fragment 3′–5′ exonuclease minus (KF) and T7 DNA polymerase were purchased from New England Biolabs and USB, respectively. Oligonucleotides containing CPD , 6–4pp , Dewar , 5R-Tg , and 5S-Tg  were synthesized on an Applied Biosystems 3400 DNA synthesizer, as described, and those containing 8-oxoG and the AP site analog (dSpacer) were synthesized using phosphoramidite building blocks purchased from Glen Research.
Full-length ApPolη cDNA was isolated by RACE PCR, using cDNA prepared with the GeneRacer kit (Invitrogen) from total RNA isolated from frozen whole worm samples. A 2.5cm frozen section of the posterior end of A. pompejana collected with the DSV Alvin submersible  was ground using a mortar and pestle in liquid nitrogen. The ground tissue was aliquoted into eppendorf tubes, and after the addition of Trizol (Invitrogen) (1.4mL), the mixture was incubated at room temperature for 10 minutes. After centrifugation at 12,000×g for 10 minutes, the supernatant (1mL) was mixed with chloroform (250μl), and was incubated at room temperature for 2 minutes. The samples were then centrifuged at 12,000×g for 15 minutes to separate the total RNA into the aqueous layer. The RNA was then precipitated by adding isopropanol (500μl) to the aqueous solution (600μl), and was incubated at 4°C for 1.5 hours. After centrifugation at 12,000×g for 10 minutes at 4°C, the pellet was washed with 75% ethanol (1.4mL) and then stored in 75% ethanol (1mL) at −80°C. The stored RNA was pelleted by centrifugation and resuspended in diethylpyrocarbonate-treated water (20μl), and the concentration was determined by measuring the absorbance at 280nm. A 5μg portion of the total RNA was used to prepare cDNA using the GeneRacer kit (Invitrogen), according to the manufacturer's instructions. In brief, total RNA was dephosphorylated using calf intestinal alkaline phosphatase, extracted with phenol-chloroform, and precipitated with ethanol. The RNA was decapped using tobacco acid pyrophosphatase, extracted, and precipitated, and then the GeneRacer 5′ oligo was ligated to the 5′ ends. Finally, the RNA was subjected to the reverse transcription reaction using a poly-T primer containing the GeneRacer 3′ oligo sequence, to generate a single-stranded cDNA library with known 5′ and 3′ sequences.
The amino acid sequence of HsPolη was used for a in-house TBLASTN search of a translated A. pompejana expressed sequence tag (EST) database comprised of sequences derived from collaborations with the Joint Genome Institute (Walnut Creek, CA) and Genome Therapeutics (Waltham, MA). A positive hit at the 5′ end of the gene was identified on EST CAGA3172. The 3′ sequence was determined from the prepared A. pompejana GeneRacer cDNA library by 3′ RACE PCR, using a gene specific primer (AlviXPVF1 5′GG GAC TGG TCT GTG CTG GCC GTG GAA AT 3′) and the GeneRacer 3′ oligo primer, together with the touchdown PCR strategy and KOD polymerase (Novagen). The PCR product was TOPO cloned into the pCR2.1 vector (Invitrogen) and was analyzed by restriction enzyme digestion and sequencing. The full-length ApPolη gene was amplified from the cDNA library, using two gene-specific primers, AlviXPVF1 (the above sequence) and AlviXPVR2 (5′ GGG ATG ATT CTA CAC TTT GCT GAA AAA TCT ATC CA 3′), and KOD polymerase under the standard PCR conditions. The 2.2kb product was gel-purified and TOPO cloned into the pCR4 vector (Invitrogen) and was analyzed by restriction enzyme digestion and sequencing. Restriction sites were added to the ends by a subsequent round of PCR and TOPO cloning. The full-length ApPolη cDNA was then subcloned into pET21a (Novagen), using the Nde I and Eco RI restriction nucleases and T4 DNA ligase, and was analyzed by restriction enzyme digestion and sequencing.
Recombinant ApPolη gene was expressed in E. coli Rosetta2 (DE3) (Novagen). The cells were grown at 37°C to an absorbance at 600nm of 0.6. The cultures were placed in an ice slurry for 20 minutes, and then isopropyl-β-D-thiogalactopyranoside was added to a final concentration of 0.5mM. After the cultures were incubated at 12°C for 40 hours, the cells were collected by centrifugation, rinsed with buffer A containing 10mM sodium phosphate (pH 7.4), 10% glycerol, and 300mM NaCl, and resuspended in buffer A containing p-amidinophenylmethanesulfonyl fluoride hydrochloride and a protease inhibitor cocktail (complete, EDTA free (Roche)). The lysate mixtures were mixed with powdered lysozyme at a final concentration of 2mg/mL for 10 minutes on ice, and then were subjected to ultrasonicationn. The lysates were centrifuged, and the supernatants were mixed with Talon resin (Clontech) (50% w/v, equilibrated with lysis buffer containing 10mM sodium phosphate (pH 7.4), 10% glycerol, 300mM NaCl, and 5mM imidazole). The resin was washed with the same buffer, and the bound proteins were eluted with eluate buffer (lysis buffer containing 300mM imidazole). The eluate was diluted and applied to a HiTrap Heparin HP column (GE Healthcare) equilibrated with buffer B (50mM sodium phosphate (pH 7.4), 1 mM EDTA, 1 mM β-mercaptoethanol, and 0.01% Triton X-100) containing 0.1M NaCl. Elution was performed by a stepwise gradient of 0.2M to 0.6M NaCl in buffer B. The peak fractions containing ApPolη eluted at 0.5M NaCl, and were stored at –80°C.
The 5′-32P-labeled primer-template was prepared by mixing a 16-mer primer labeled at its 5′ end with each of the 30-mer templates, at a molar ratio of 1:1. Standard reaction mixtures (10μl), containing 40mM Tris–HCl (pH 8.0), 1mM MgCl2, 100mM dNTPs, 10mM DTT, 0.24mg/mL BSA, 60mM KCl, 2.5% glycerol, 40nM 5′-32P-labeled primer-template, and purified ApPolη, were incubated at 37°C. The reaction times and the enzyme amounts are indicated in the figure legends. The reactions were terminated by the addition of stop solution (8μl), containing 95% formamide, 20mM EDTA, 0.025% bromophenol blue, and 0.025% xylene cyanol. The protein was denatured by boiling, and the products were separated by electrophoresis on a denaturing 16% polyacrylamide gel. Dried gels were analyzed on a FUJIFILM BAS 1800 bioimage analyzer.
The relative thermostabilities of ApPolη and HsPolη were compared by heating each enzyme to temperatures ranging between 37°C and 58°C for 5 minutes. An aliquot of each enzyme was then used for the standard 20 minutes TLS reaction at 37°C to measure the incorporation of a single nucleotide, dCMP, opposite the template G residue (see the TLS reactions described above). The enzyme concentrations used in the reactions were initially determined by making serial dilutions of each enzyme and identifying the concentration necessary to give the same extension level of the labeled primer. These amounts were 1.8 and 5.9fmol for HsPolη and ApPolη, respectively. The ability of each enzyme to extend the primer was quantified with MultiGauge software (FUJIFILM), and the specific activity, compared to the activity of each enzyme heated to 37°C, was calculated. The specific activity was plotted as a function of the temperature to which the enzyme was exposed.
A cDNA sequence with homology to that of HsPolη was cloned from an A. pompejana cDNA library by RACE PCR. The open reading frame encoded a predicted product of 745 amino acid residues, with a calculated molecular mass of 83kDa. Alignment of the amino acid sequence against HsPolη revealed 38.1% identity and 57.6% similarity overall (identities = 283/708 (39%), positives = 414/708 (58%), gaps = 68/708 (9%)). The alignment (Figure 1(a)) also indicated the high conservation within the N-terminal region and the presence of the four structural domains (finger, palm, thumb, and little finger) that are the hallmarks of the Y-family translesion DNA polymerases [32, 33]. Ubiquitin (Ub)-binding domains [34–36] and a proliferating cell nuclear antigen (PCNA)-binding domain [37, 38], located in the C-terminal region of Polη, were identified in the ApPolη amino acid sequence, suggesting that Ub and/or PCNA regulate this protein.
The Y-family DNA polymerases ι (Polι) and κ (Polκ) and the B-family DNA polymerase ζ (Polζ) are known to share sequence homology with the Y-family HsPolη. To analyze the relationship between this A. pompejana protein and other translesion DNA polymerases, a phylogenetic tree was produced on the basis of the amino acid sequences of these DNA polymerases, by the unweighted pair group method with arithmetic mean (UPGMA). The tree revealed that this protein was not related to Polκ , Polι, or Polζ, but was more closely related to Polη (Figure 1(b)). Therefore, we concluded that this protein is a member of the DNA polymerase η group, and thus referred to the protein as A. pompejana DNA polymerase η.
To examine the biological activities of the protein encoded by the ApPolη cDNA, we prepared the recombinant ApPolη protein with a C-terminal (His)6 tag in E. coli. The extract was first fractionated on Talon beads, and then purified on a Heparin column. The recombinant protein was eluted by a step gradient of NaCl (Figure 2(a)). As expected from the calculated relative molecular mass, the purified recombinant ApPolη bearing the (His)6 tag migrated as a single band of approximately 85kDa in the SDS-PAGE analysis (Figure 2(b)), and exhibited DNA polymerase activity (Figure 3(a)). The recombinant human Y-family polymerases, for example, Polη, Polι, and Polκ, are usually prepared from baculovirus-infected insect cells, as reported previously [13, 17, 39, 40]. In the present study, the incubation of the cultures at a low temperature after induction enabled the production of full-length ApPolη in E. coli, as was also reported by Hoffman et al.  for Polη from other species. The yield of the purified protein was 15.5μg per liter of the culture.
UV irradiation induces the formation of pyrimidine dimers, namely, CPD and 6–4pp. The latter is isomerized to Dewar by exposure to UVA/B. HsPolη catalyzed efficient and accurate TLS past CPD , but not 6–4pp  and Dewar (unpublished results). To examine whether ApPolη possessed TLS activity for UV-induced lesions, 30-mer oligonucleotide templates containing a single lesion were hybridized to a 5′-32P-labeled 16-mer oligonucleotide primer, and these duplexes were employed for the TLS reactions (Figure 3). Klenow fragment (KF) inserted one nucleotide opposite CPD, but did not elongate the primer (Figure 3(b), lane 1), whereas ApPolη could efficiently elongate the primer up to the end of the 30-mer, in an enzyme concentration-dependent manner (Figure 3(b), lanes 3–7). Similar experiments were performed with other UV-induced lesions, 6–4pp and Dewar. ApPolη could insert one nucleotide opposite these lesions, but elongation of the primers was not observed (Figures 3(c) and 3(d)), in a manner similar to HsPolη [13, 42].
To examine the preference for nucleotide incorporation opposite the lesion by ApPolη, the polymerization reactions were performed in the presence of only a single deoxyribonucleoside triphosphate (Figure 4). Although HsPolη replicates undamaged DNA with low fidelity [43, 44], it can accurately incorporate dATP opposite the TT sequence of CPD . On the undamaged template, ApPolη preferred to incorporate dATP correctly, and dGTP was incorporated less frequently (Figure 4(a)), indicating that ApPolη, like HsPolη, replicates undamaged DNA with low fidelity. When the template contained CPD, ApPolη incorporated dATP exclusively (Figure 4(b), lane 4), indicating that ApPolη, like HsPolη, can accurately perform TLS past CPD. For both 6–4pp and Dewar, primers that were elongated with dAMP and dGMP by ApPolη were detected, although the elongation efficiency was very low (Figures 4(c) and 4(d)). While we are able to test these activities biochemically, establishing the biological roles of ApPolη would require additional assays such as genetic complementation, however these results were also similar to those obtained for HsPolη.
Since A. pompejana inhabits deep sea thermal vent regions that are in excess of 1.5km under the ocean surface where UV-rays from the sun do not penetrate [45, 46], we thought that CPD containing DNA may not be a major template for ApPolη. Other candidates were assumed to be oxidative lesions, because the high temperature and the solutes at the hydrothermal vent sites might induce oxidative stress. Tg is one of the major DNA lesions produced by ROS, and two isomeric forms, 5R-Tg and 5S-Tg, are produced in DNA. Tg often blocks DNA replication by replicative DNA polymerases , but rarely induces mutation . However, HsPolη can catalyze efficient and accurate TLS past each Tg isomer .
Using the 30-mer oligonucleotides containing a single lesion at the 17th nucleotide from its 3′ end as templates, we examined the ability of ApPolη to replicate DNA past 5R-Tg and 5S-Tg. At both lesions, the replicative T7 DNA polymerase was blocked completely (Figures 5(a) and 5(b), lane 1), but ApPolη efficiently catalyzed the replication reaction (Figures 5(a) and 5(b), lanes 3–7). To examine the preference of nucleotide incorporation opposite each Tg isomer, the polymerization reactions were tested in the presence of only a single deoxyribonucleoside triphosphate (Figures 6(a) and 6(b)). ApPolη preferred to incorporate dATP (Figures 6(a) and 6(b), lane 4). Although dGTP was incorporated in the absence of the other nucleotides (lane 6), this product, which exhibited slightly slower migration in the PAGE analysis, was not detected when the four nucleotides were added (lane 3). These results indicated that ApPolη had the ability to catalyze TLS accurately past both 5R-Tg and 5S-Tg.
Another major oxidative DNA lesion induced by ROS is 8-oxoG, which is an important promutagen in vivo and in vitro . Similar experiments were performed with a template containing 8-oxoG, instead of Tg. No insertion of any nucleotide opposite the lesion by T7 DNA polymerase was observed (Figure 5(d), lane 1), whereas ApPolη could bypass 8-oxoG efficiently (Figure 5(d), lanes 3–7). For the nucleotide preference, ApPolη preferred to incorporate the correct dCTP opposite the undamaged template G (Figure 6(c)), whereas it mainly incorporated the incorrect dATP opposite 8-oxoG (Figure 6(d)). Thus, this enzyme replicates DNA containing 8-oxoG efficiently but incorrectly, leading to frequent G·C to T·A transversions. In addition, we investigated whether ApPolη has TLS activity on a template containing the AP site analog. However, like the other Y-family DNA polymerases, this enzyme was unable to catalyze TLS past this lesion (data not shown).
As A. pompejana colonizes the walls of actively venting high-temperature chimneys [23, 45, 46], we hypothesized that its enzymes may be more thermostable than those found in mesophilic organisms, as shown for other TLS polymerases derived from single cellular hyperthermophilic organisms such as Sulfolobus solfataricus DNA polymerase 4 (Dpo4) [47, 48]. To test this possibility, we compared the activity of ApPolη along with that of HsPolηafter heating both enzymes to various temperatures for 5 minutes. After this treatment, we tested the ability of both enzymes to incorporate a single dCMP opposite a template G. As shown in Figure 7, ApPolη retained the activity even after it was heated to 49°C. In contrast, the activity of HsPolη diminished rapidly after heating to temperatures higher than 43°C. Therefore, ApPolη is relatively more thermostable than HsPolη.
As a further test of ApPolη stability, we tested the ability of ApPolη to incorporate dCMP opposite a template G in the presence of various organic solvents. In these assays, dimethyl sulfoxide (DMSO), ethanol, and isopropanol (IPA) were used at concentrations of 20% (v/v). Similar experiments were performed in a study on TLS past a benzo[a]pyrene adduct by another thermostable Y-family DNA polymerase, archaeal Dpo4, although the organic solvents were added to stabilize the benzo[a]pyrene moiety in the major groove, rather than to test the protein stability . As shown in Figure 8(a), ApPolη exhibited higher activity than HsPolη in the presence of all of the solvents used in this study, although IPA greatly reduced the enzyme activity. In the presence of DMSO, ApPolη retained the full activity, even when the reaction mixture contained this solvent at a concentration of 20% (Figure 8(b)). These results support our conclusion that the full-length ApPolη protein is more stable than its human homolog.
In this study, we cloned the cDNA encoding the novel thermostable DNA polymerase η from A. pompejana, which colonizes deep-sea hydrothermal vents. This enzyme was produced in E. coli, and was purified as a full-length recombinant protein (85kDa) bearing a (His)6 tag. The purified ApPolη protein displayed DNA polymerase activity. This enzyme catalyzed TLS past CPD, 5R-Tg, 5S-Tg, and 8-oxoG, but not past 6–4pp, Dewar, or the AP site analog, in a similar manner to HsPolη (Table 1). We also demonstrated that ApPolη was more stable than HsPolη.
Despite the fact that A. pompejana inhabits the deep sea, where UV-rays do not penetrate, the UV-induced CPD was found to be an excellent template for ApPolη. Considering that a genetic defect in the HsPolη gene results in the XP-V syndrome, and that XP-V patients are sensitive to sunlight and highly prone to cancer development, the critical role of HsPolη is thought to be error-free TLS across CPD in human cells. As A. pompejana's environment is significantly less subject to UV radiation produced by the sun, we speculate that the inclusion of the TLS polymerase system within the organism may arise from specific environmental adaptations. Evidence for photosynthetic events at hydrothermal vent sites has been noted , where energy for the reactions may arise from vent activity. Moreover, the vent area is sporadically subject to periods of intense volcanic and geothermal activity that may cause production of bulky DNA lesions within these organisms. The presence of ApPolη may also play a role in protecting developing embryos, as embryos pass through a period of developmental arrest when passing from one colony site to another before renewed growth . In these cases, they may experience periods of geothermal light during passage and during their development at their new colonization site. Thus, these Polη proteins may protect the embryo until it becomes more self-motile and can build its housing tube.
Here, we also showed that this polymerase catalyzes efficient and accurate TLS past both 5R-Tg and 5S-Tg, which are generated by ROS. Since Tg can block DNA replication by replicative DNA polymerases and also induces cell death, the critical role of ApPolη might be error-free TLS across Tg in A. pompejana cells.
Since A. pompejana inhabits hydrothermal vent sites at temperatures that often measure within the representative classifications for thermophilic (40–60°C) and hyperthermophilic organisms (60°C and higher), we expected that ApPolη would be thermostable. In agreement with these expectations, we found that ApPolη was more thermostable than HsPolη (Figure 7), but less stable than an archaeal DinB-like polymerase from the hyperthermophile S. solfataricus P2 [47, 51] which lives at higher temperatures (>75°C) than A. pompejana. Posttranslational modification of proteins is sometimes important for their structure and function. Since the ApPolη used in this study was produced in E. coli, the measured thermostability was that without eukaryotic post-translational modifications. We expected that this enzyme may be modified in insect cells, which are more closely related to A. pompejana cells than to E. coli cells, and thus might gain higher thermostability. Therefore, we prepared ApPolη in Sf9 insect cells using the baculovirus expression system. The ApPolη protein produced in Sf9 cells could catalyze DNA synthesis at 37°C, but lacked translesion activity after it was heated to 55°C (data not shown).
There might be several reasons why ApPolη is not even more thermostable. (1) It has been reported that Polη functions in a replication complex during TLS [37, 38, 52]. Thus, it is possible that ApPolη becomes more heat resistant with the help of other thermostable replication proteins in A. pompejana cells. In fact, ApPolη has a PCNA binding motif (Figure 1(a)), indicating that ApPolη may exist in a replication complex with PCNA. (2) Y-family DNA polymerases replicate undamaged DNA in an error-prone manner [34–36, 38]. Hence, to maintain genetic integrity, it might not be favorable for cells to have an extremely stable mutator polymerase. The present study is the starting point for the elucidation of the temperature preference of each A. pompejana enzyme and its biological significance, which will further our understanding of the ecology of this unique living organism.
ApPolη could be useful for in vitro studies as a new paradigm system to understand TLS mechanisms and also could be a starting material for the development of a more stable eukaryotic-like TLS polymerase by directed evolution. Such an enzyme will enable us to amplify heavily damaged DNA, such as ancient DNA, by PCR-like methods.
In this study, we cloned an A. pompejana gene with homology to the HsPolη gene. The primary structure of the protein indicated the conservation of the PCNA binding domain and the ubiquitin-binding zinc finger motif. The encoded full-length recombinant protein, ApPolη, was readily produced in Escherichia coli and purified. We demonstrated that ApPolη could bypass CPD, 8-oxoG, 5R-Tg, and 5S-Tg, but not 6–4pp, Dewar, or any AP site analog revealing a similar spectrum of activities to those of the human homolog. ApPolη's properties of higher stability with human-like activities offer advantages over other known eukaryotic TLS polymerases for future basic and practical applications.
The authors thank S. C. Cary and B. R. Chapados for technical support. They thank the R/V Atlantis and DSV Alvin crews in aiding A. pompejana sample collection and the Department of Energy (DOE) Joint Genome Institute for partial EST sequencing for this work. This work was supported by Human Frontier Science Program (J. A. Tainer, F. Hanaoka, S. Iwai), by the 3rd Annual Incyte Discovery Award (D. S. Shin, J. A. Tainer), by the US National Institutes of Health Grants GM46312 (JAT), and by DOE program Integrated Diffraction Analysis Technologies (J. A. Tainer) and DOE Community Sequence Program award (D. S. Shin, J. A. Tainer). D. S. Shin and K. Hitomi were supported in part by Skaggs Institute for Chemical Biology, and D. S. Shin was further supported in part by a Ruth L. Kirschstein NSRA Fellowship. Bulky lesion repair in the Tainer lab is support by NIH grant R01 CA112093. J. O. Fuss and Q. J. Cheng were supported in part by the US National Cancer Institute Grant CA112093 and the US Department of Energy Molecular Assemblies: Genes and Genomes Integrated Efficiently Project (DE-FG0207ER64326), plus the NRSA Fellowship 1F32CA108393 to J. O. Fuss.