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A nucleotide binding rectification Brownian ratchet model for translocation of Y-family DNA polymerases
- Ping Xie1Email author
https://doi.org/10.1186/1742-4682-8-22
© Xie; licensee BioMed Central Ltd. 2011
- Received: 22 March 2011
- Accepted: 24 June 2011
- Published: 24 June 2011
Abstract
Y-family DNA polymerases are characterized by low-fidelity synthesis on undamaged DNA and ability to catalyze translesion synthesis over the damaged DNA. Their translocation along the DNA template is an important event during processive DNA synthesis. In this work we present a Brownian ratchet model for this translocation, where the directed translocation is rectified by the nucleotide binding to the polymerase. Using the model, different features of the available structures for Dpo4, Dbh and polymerase ι in binary and ternary forms can be easily explained. Other dynamic properties of the Y-family polymerases such as the fast translocation event upon dNTP binding for Dpo4 and the considerable variations of the processivity among the polymerases can also be well explained by using the model. In addition, some predicted results of the DNA synthesis rate versus the external force acting on Dpo4 and Dbh polymerases are presented. Moreover, we compare the effect of the external force on the DNA synthesis rate of the Y-family polymerase with that of the replicative DNA polymerase.
Keywords
- Ternary Form
- Translesion Synthesis
- Unpaired Base
- Interaction Potential Versus
- Thumb Domain
Introduction
DNA polymerases (Pols) are enzymes to add free nucleotide to the 3' end of the newly-forming DNA strand. They play an essential role in the maintenance of genome integrity. On the basis of sequence similarity, DNA Pols can be broadly classified into A-, B-, C-, D-, X- and Y-families [1–3]. In general, most Pols in A-, B-, C-, and D-families are high-fidelity enzymes primarily involved in faithful DNA replication and in repair of replication mistake. The X-family Pols are involved in a number of DNA repair processes such as base excision repair (BER) and repair of double-strand breaks (DSBs) [4, 5]. The Y-family Pols represent a number of recently identified Pols characterized by low-fidelity synthesis on undamaged DNA and the ability to bypass DNA lesions which normally block replication by members of the A-, B-, C-, D-, or X-family Pols [6–12].
The Y-family Pols are ubiquitous and are distributed among the three kingdoms of life. They include E. coli Pol IV (also known as DinB) [13] and Pol V (also known as UmuC) [14, 15], yeast Pol η [16] and Rev1 [17], human Pols η [18], ι [19, 20], κ [21] and Rev1 [22], and archaeal Dbh [23] and Dpo4 [24], etc. Although there is no detectable sequence identity with other family Pols, available crystal structures of some Y-family Pols such as Dbh [25–27], Dpo4 [28], Pol η [29, 30], Pol ι [31, 32], Pol κ [33, 34] and Rev1 [35] reveal that they retain a catalytic core consisting of fingers, palm and thumb subdomains found in other family Pols. However, the fingers and thumb subdomains of the Y-family Pols are significantly smaller than the corresponding subdomains of the other DNA Pols. In addition to the conserved polymerase core, the Y-family Pols possess also a unique C-terminal domain termed the little finger (LF), wrist or polymerase-associated domain (PAD). In this paper we will use the acronym, LF, to denote this domain. The LF domain is the least conserved of the four domains in the Y-family Pols.
Besides the intensive structural studies of the Y-family Pols, which include the structures in apo, binary and ternary forms as well as the structures complexed with DNA substrates containing different lesions [11, 25–42], a variety of biochemical assays have provided insight into the catalytic mechanism, lesion-bypassing property, processivity and fidelity of the Pols [12, 43–55]. Both the biochemical and single-molecule assays for Dpo4 indicated that the binding of a nucleotide induces a fast DNA translocation event [55, 56], which is consistent with the structural studies showing that, in both of the binary complexes (pre- and post-insertion), the primer terminus occupies the site where the next incoming nucleotide will bind [28, 41, 42]. However, the structural studies for Dbh showed that, in the pre-insertion binary complex, the templating base and the primer terminus are already positioned so that space is available for the incoming nucleotide to bind and form the ternary complex, while in the post-insertion binary complex, the DNA is located in nearly the same position on the Pol [27]. Similar to Dbh, two pre-insertion binary complexes of Pol ι showed that space is available for the incoming nucleotide to bind [32].
Recently, a Brownian ratchet model has been proposed for the translocation of the high-fidelity replicative DNA Pols, where the translocation depends on the change of the interaction of the fingers subdomain with the single-stranded DNA (ssDNA) template upon a correct incorporation [57, 58]. In this work, based on the available structural, biochemical and single-molecule studies for the Y-family Pol, we modify the previous Brownian ratchet model for the replicative Pol to be applicable to the Y-family Pol, where the directed translocation is rectified by the nucleotide binding. Thus, the model can be called nucleotide binding rectification (NBR) Brownian ratchet model, which is abbreviated as the NBR model. Using the model, the observed different features of the structures for Dpo4, Dbh and Pol ι in binary and ternary forms [27, 28, 32, 41, 42] can be easily explained. Other dynamic properties for the Y-family Pols such as the considerable variations of the processivity among the Pols and the fast translocation event upon dNTP binding for Dpo4 can also be explained by using the model. In addition, some predicted results of the DNA synthesis rate versus the external force acting on Dpo4 and Dbh Pols are presented. Moreover, we compare the effect of the external force on the DNA synthesis rate of the Y-family Pol with that of the replicative Pol.
Methods
Brownian ratchet translocation model for replicative DNA Pols
Since the NBR model for the Y-family Pol is modified from the previous model for the replicative Pol [57–59], for convenience of reading, in this section we re-present the latter model. Briefly, the model was based on the Brownian ratchet mechanism (e.g., see [60, 61]) and the directed translocation of the Pol along the template resulted from the potential change induced by dNTP incorporation. The model was built up based on two arguments.
Schematic illustrations of the translocation model for replicative DNA Pols (see text for detailed description). The green circles in (a), (c) and (b') denote open fingers while the green ellipses in (b) and (a') denote closed fingers.
The second argument is on the rotation of the fingers subdomain from open (closed) to closed (open) conformation upon the binding (release) of dNTP (pyrophosphate, PPi), which is consistent with the structural studies on bacteriophage T7 DNA Pol [65], Taq DNA Pol [66] and HIV-1 reverse transcriptase [67]. The closed conformation of the fingers activates the phosphodiester bond formation (or nucleotide incorporation), while the open conformation of the fingers opens the polymerase active site for nucleotide binding. Moreover, the closed fingers could potentially enhance the interactions of binding sites S1 and S2 with the DNA substrate.
Based on the two arguments, the translocation model for the replicative DNA Pol is schematically shown in Figure 1[57–59]. We begin with the binding site S1 of the Pol binding strongly to the ssDNA at the replication fork, with the binding site S2 binding to the dsDNA and no nucleotide being in the polymerase active site (Figure 1a). In this nucleotide-free state, either a matched or a mismatched dNTP can bind to the active site, although the matched dNTP has a much larger probability to bind. Thus, we consider the two cases separately. (i) First, consider a correct incorporation. The binding of a matched dNTP induces the fingers to rotate from open to closed conformations (Figure 1b). The closed conformation activates nucleotide incorporation. After the incorporation, the release of PPi induces the fingers to return to the open conformation. At the same time, the binding site S1 would bind to new nearest unpaired base (i.e., the next unpaired base) of the ssDNA template, because the previous unpaired base where the binding site S1 has just bound has disappeared due to base pairing (Figure 1c). Then, the next nucleotide-incorporation cycle will proceed. (ii) Second, consider an incorrect incorporation. We still begin with Figure 1a. The binding of a mismatched dNTP also induces the fingers to rotate from open to closed conformations, activating nucleotide incorporation (Figure 1a'). After the incorporation, the release of PPi induces the fingers to return to the open conformation. Now, although the sugar-phosphate backbone of the mismatched dNTP has been connected to the backbone of the already formed dsDNA, the mismatched base is not paired with the sterically corresponding base on the ssDNA template. Thus, the binding site S1 is still binding strongly to the same unpaired base of the ssDNA template (Figure 1b'). Thus, the polymerization cannot proceed. In other words, the polymerization becomes stalled. In Figure 1b', after the mismatched base is excised, the polymerization will proceed again (Figure 1a).
Illustrations of the translocation model for replicative DNA Pols by using interaction potentials of binding sites S 1 and S 2 with ssDNA and dsDNA segments, respectively, of a DNA substrate. (a) Top diagram shows the DNA substrate before the incorporation of the nucleotide paired with the (n+1)th base on the template. Potential V1(x) describes the interaction of the binding sites S1 with the ssDNA segment, while potential V2(x) describes the interaction of the binding sites S2 with the dsDNA segment. (b) The DNA substrate and potentials V1(x) and V2(x) after the incorporation of the nucleotide paired with the (n+1)th base on the template. (a') The DNA substrate and the potentials V1(x) and V2(x) before the incorporation of an incorrect nucleotide opposite to the (n+1)th base on the template, which is the same as (a). (b') The DNA substrate and potentials V1(x) and V2(x) after the incorporation of an incorrect nucleotide opposite to the (n+1)th base on the template.
However, after an incorrect incorporation of the nucleotide opposite to the (n+1)th base (see top of Figure 2b'), the forms of V1(x) and V2(x) are shown in Figure 2b', which are the same as those before the incorporation. This is because, after the incorrect incorporation, the (n+1)th base has not formed a base pair with the newly incorporated primer base and, thus, the Pol is still located at the position of the (n+1)th base, i.e., the position of the deepest well.
In this model, the translocation step occurs following the incorporation of a correct nucleotide. This is supported by the comparison of the binary (Pol-DNA) with ternary (Pol-DNA-dNTP) structures for the replicative Pol (see, e.g., [66]). Upon an incorrect incorporation, the Pol becomes stalled, which is also consistent with the experimental data [68]. For a lesion such as an abasic lesion having a weak effect on distortion of the DNA structure so that the damaged base still has a high affinity for the binding site S1, an incorporated base opposite to the lesion, which is equivalent to a mismatched base, also induces the stall of the polymerization. This is consistent with the structural observation [69]. During the stalled period, the mismatched base would be excised. Then another base opposite to the lesion site would be incorporated. Thus, the Pol cannot perform the translesion synthesis. For lesions that severely distort the DNA structure causing damaged DNA substrate not to be tolerated by the replicative Pol, e.g., with the template base being flipped out of the active site, this would preclude closing of the fingers subdomain upon nucleotide binding, as observed by Li et al. [70] for bacteriophage T7 DNA Pol complexed with a DNA template containing a cis-syn cyclobutane pyrimidine dimer. Without the activation by the closed conformation, the nucleotide incorporation cannot proceed and, thus, the Pol cannot also perform the translesion synthesis.
Nucleotide binding rectification Brownian ratchet model for Y-family DNA Pols
The NBR model for the Y-family DNA Pol is modified from the above model for the replicative Pol. The model is also constructed based on two arguments, which are presented in the following two sections.
Interaction of Pol with DNA substrate
Interaction potentials between a Y-family DNA Pol such as Dpo4, in which the active site is very close along the x direction to the nearest residue of the binding site S 2 located in the LF domain, and a DNA substrate shown in top of (b). (a) Schematic diagram of the Pol complexed with the DNA substrate. (b) V1(x) represents the potential of the binding site S1 interacting with the ssDNA segment, while V2(x) represents the potential of the binding site S2 interacting with the dsDNA segment. (c) Schematic diagrams of the position of the Pol along the DNA substrate, with blue dots representing the active site.
Interaction potentials between a Y-family DNA Pol such as Dbh, in which the active site is, along the x direction, distanced away from (or not close to) the nearest residue of the binding site S 2 located in the LF domain, and a DNA substrate shown in top of (b). (a) Schematic diagram of the Pol complexed with the DNA substrate. (b) V1(x) represents the potential of the binding site S1 interacting with the ssDNA segment, while V2(x) represents the potential of the binding site S2 interacting with the dsDNA segment. (c) Schematic diagrams of the position of the Pol along the DNA substrate, with blue dots representing the active site.
As in Figure 2, the potential V1(x) of the binding site S1 interacting with the ssDNA is shown in Figures 3b and 4b, with E1 denoting the binding affinity for N1 bases of the ssDNA template while E'1 the binding affinity for (N1-1) bases. However, E'1 and E1 have very small or nearly zero values.
Then, consider the potential V2(x) of the binding site S2 interacting with the dsDNA. Since the binding site S2 in the Y-family Pols is composed of residues located in the thumb domain and mainly in the LF domain, the form of potential V2(x) depends on the distance, L, from the active site to the nearest residue (red dots in Figures 3a and 4a) of the binding site S2 located in the LF domain along the x direction.
(i) For the case that the active site is very close along the x direction to the nearest residue of the binding site S 2 located in the LF domain (see Figure 3a), as seen from the structure of Dpo4 [28, 41, 42], the interaction potential V 2(x) can be simply shown in Figure 3b, where L = 0. If binding site S 2 is considered to cover N 2 base pairs of the dsDNA, E 2 is the binding affinity for the sugar-phosphate backbones connecting N 2 base pairs on the dsDNA while E' 2 is the binding affinity for the backbones connecting only (N 2-1) base pairs. Moreover, in the potential it is implicated that the primer 3' terminus, due to the structural restriction (see, e.g., [27, 28, 32, 41, 42]), is not allowed to move forwards relative to the Pol when its active site is located at the primer 3' terminus. In addition, from the Pol structures complexed with the DNA substrate, it is inferred that that the interaction between the binding site S 2 and the dsDNA is via the hydrogen-bonding, van der Waals and mainly electrostatic forces. On the other hand, the interaction distance of the electrostatic force that is approximately equal to the Debye length (~ 1 nm) in solution is larger than the distance p = 0.34 nm between two successive base pairs. Thus, the value at maxima of V 2(x) increases as the binding site S 2 deviates away from the dsDNA segment along the x direction.
(ii) For the case that the active site is, along the x direction, distanced away from (or not close to) the nearest residue of the binding site S 2 located in the LF domain (Figure 4a), as evidently seen from the structure of Dbh [27], the interaction potential V 2(x) can be simply shown in Figure 4b, where we take L = 1 bp. From available structures of the binary and ternary complex for Pol ι [31, 32], it is also noted that, if the active site is positioned opposite to the first unpaired base on the template, the first unpaired base is distanced by L = 1 bp away from the nearest residue of the binding site S 2 located in the LF domain. Thus, the interaction potential V 2(x) for Pol ι also has the form of Figure 4b rather than that of Figure 3b. Similarly, from the available structure of the ternary complex for Pol η [30], we infer that the interaction potential V 2(x) for Pol η also has the form of Figure 4b.
From Figure 3b it is seen that, when the active site is positioned at the n th base pair (top of Figure 3c), the affinity of the Pol for the DNA substrate is E n = E'1 + E2; while when the active site is positioned at the (n+1)th base (bottom of Figure 3c), the affinity is En+1= E1 + E'2. Since E'1 and E1 are much smaller than E'2 and E2 and E2 > E'2, it is expected that E n > En+1. Similarly, from Figure 4b it is seen that, when the active site is positioned at the n th base pair (top of Figure 4c), the affinity of the Pol for the DNA substrate is E n = E'1 + E2; while when the active site is positioned at the (n+1)th base (bottom of Figure 4c), the affinity is En+1= E1 + E2. Since E'1 and E1 are much smaller than E2, it is expected that En+1is slightly larger than (or nearly equal to) E n . Moreover, from both Figure 3 and 4 it is noted that, when the active site is positioned at the (n+1)th base, the jumping of the Pol from the (n+1)th site to the (n+2)th site is required to overcome a larger energy barrier than the backward jumping to the n th site. For approximation, we do not consider the jumping to the (n+2)th site in this work.
The binding of dNTP induces a slight conformational change, enhancing the interaction of the Pol with DNA substrate
As evidenced from the FRET experimental data [56], it is argued that the dNTP binding involves (at least) two substeps, E · DNA + dNTP → E · DNA · dNTP → E* · DNA · dNTP, where E represents the DNA Pol. The transition from the unactivated E · DNA · dNTP ternary complex to activated E* · DNA · dNTP ternary complex induces a slight conformational change of the Pol, enhancing its interactions with both the DNA substrate and dNTP. Similarly, the PPi releasing also involves (at least) two substeps, E* · DNA · PPi → E · DNA · PPi → E · DNA + PPi, where the transition from the activated E* · DNA · PPi ternary complex to unactivated E · DNA · PPi ternary complex results in a reverse slight conformational change of the Pol, reducing its interactions with both the DNA substrate and PPi.
Since in the activated E* · DNA · dNTP (or E* · DNA · PPi) complex the Pol has a stronger interaction with DNA substrate and nucleotide than in the unactivated E · DNA · dNTP (E · DNA · PPi) complex, for simplicity of analysis, it is considered that in the activated state the Pol is unable to move relative to the DNA substrate and the dNTP or PPi bound to the active site has a negligible probability to release.
Model for Pol translocation
Schematic illustrations of the nucleotide binding rectification Brownian ratchet model for the Y-family DNA Pol translocating along DNA substrate (see text for detailed description).
We begin with the Pol positioned at the n th site (Figure 5a), just after the incorporation of a nucleotide. In Figure 5a, the active site is occupied by the primer 3'-terminus, which sterically prevents a dNTP from binding to the active site. Due to the thermal noise, the Pol in this nucleotide-free state can jump from the n th site to the (n+1)th site (from Figure 5a to 5b) and vice verse (from Figure 5b to 5a). For the case that the active site is very close along the x direction to the nearest residue of the binding site S2 located in the LF domain (Figure 3a), E n > En+1(see above). Thus, the Pol in the binary E · DNA state stays most of the time at the n th site (Figure 5a), as will be shown in the Results, which is consistent with the availably resolved binary E · DNA structure for Dpo4 [28, 41, 42]. For the case that the active site is, along the x direction, distanced away from (or not close to) the nearest residue of the binding site S2 located in the LF domain (Figure 4a), En+1is slightly larger than (or nearly equal to) E n (see above). Thus, the Pol in the binary E · DNA state shows slightly larger (or nearly equal) probability to stay at the (n+1)th site (Figure 5b) than (or to) that at the n th site (Figure 5a), implying that the binary E · DNA structure for this case would be observed to be either at the (n+1)th site or at the n th site. This is consistent with the observations that the pre-insertion binary E · DNA structures for Dbh [27] and Pol ι [32] showed that their active sites are at the (n+1)th site, while the post-insertion binary E · DNA structure for Dbh [27] showed that the active site is at the n th site.
When the Pol jumps to the (n+1)th site, since the active site is nucleotide free, a dNTP becomes able to bind to it, as shown in Figure 5b that is equivalent to the state shown at bottom of Figure 3c or Figure 4c. Consider that the dNTP binds to the active site during the period when the Pol stays at the (n+1)th site (Figure 5c). Due to the structural restriction (see, e.g., [27, 28, 32, 41, 42]), the occupation of the active site by the dNTP sterically prevents the Pol from moving backwards to the n th site unless the dNTP is dissociated, which is consistent with the available structures showing that the active site of the Pols such as Dbh, Dpo4, Pol ι, Pol η, Pol κ and Rev1 in ternary forms is at the (n+1)th site [11, 27, 28, 30, 32, 34, 35, 41, 42]. Then, the transition from the unactivated ternary complex E · DNA dNTP to the activated E* · DNA dNTP complex enhances the interactions of the Pol with the DNA substrate and with the dNTP, thus preventing both the DNA substrate and the dNTP from dissociating from the Pol.
After the phosphodiester bond formation and then the release of PPi, except that the dsDNA segment is elongated by one base pair and the Pol has moved forwards by one base pair, the Pol-DNA complex returns to the state shown in Figure 5a. Correspondingly, the potentials V1(x) and V2(x) in Figure 3b and in Figure 4b are shifted by one base pair along the x direction. Then, the next round of the nucleotide incorporation would proceed continuously.
Equations for Pol motion
Here the potential U(x,r) can be written as U(x,r) = V(x)[2exp (-r/r d ) - exp (-2r/r d )], with V(x) = V1(x) + V2(x) + V0, where V1(x) and V2(x) have the forms shown in Figures 3b and 4b, and V0 ≡-E0 < 0 results from the fact that the electrostatic interaction distance of the Pol with the DNA in solution is larger than the distance between two successive base pairs. The magnitude of V(x) is defined as follows: its minimum value at the n th site is - (E n + E0), while at the (n+1)th site the value is - (En+1+ E0). The term [2 exp (-r/r d ) - exp (-2r/r d )], which has the Morse form, denotes the potential change along the r direction, with 2r d = 1 nm (the Debye length) characterizing the interaction distance. The parameter Γ is the frictional drag coefficient on the Pol and ξ i (t) (i = x, r) is the fluctuating Langevin force with 〈ξ i (t)〉 = 0 and 〈ξ i (t)ξ j (t')〉 = 2k B T Γδ ij δ(t - t'). The drag coefficient is calculated by Γ = 6πηR, where η is the viscosity of the aqueous medium and the Pol is approximated as a sphere with radius R = 5 nm. As the previous experiment showed that the viscosity of the aqueous cytoplasm does not differ from water [71], we take the viscosity of aqueous to be the same as that of water in the calculation, i.e., η = 0.01 g cm-1 s-1, which gives Γ = 9.4 × 10-11 kg s-1. Moreover, the effect of the viscosity variation on the results will be discussed.
Results
Processivity of the Y-family Pol
To study the processivity of the Y-family Pol, we determine the dissociation probability of the Pol from the DNA substrate during one cycle of nucleotide incorporation. To this end, we calculate the mean dissociation time, T d , of the Pol from the DNA substrate.
where it is seen that T d is proportional to the viscosity η.
It is noted from Eqs. (3) and (4) that P d is inversely proportional to the viscosity η.
Based on the model, only during the time period, T
p1
, after transition to the unactivated E · DNA PPi ternary complex but before the dNTP binding and during the time period, Tp 2, after the dNTP binding but before transition to the activated E* · DNA dNTP ternary complex, can the Pol be dissociated from the DNA substrate. During the time period Tp 1, the Pol can jump between the well at the n th site and the well at the (n+1)th site along the x direction. As our results show (see additional file 1), the dissociation probability P
d1
during this time period Tp 1is approximately only dependent on the value of
(m = n or n + 1), with
, where C = 1 ~ 2 and
represents P
d
given by Eqs. (3) and (4) but with
(m = n if E
n
> En+1, m = n + 1 if E
n
< En+1). During the time period Tp 2, the Pol is positioned at the (n+1)th site and the dissociation probability P
d2
is calculated by
, where
represents P
d
given by Eqs. (3) and (4) but with
.



From Eqs. (5) and (6), it is seen that, whether E n > En+1or E n ≤ En+1, the polymerization processivity is mainly determined by the binding affinity, En+1, of the Pol at the (n+1)th site along the DNA substrate. Moreover, it is noted that N p is proportional to the viscosity η.

Results for processivity of the Y-family Pol. (a) Mean dissociation time T d of the Pol from the DNA substrate versus the binding affinity E r between them. (b) Mean number of processive incorporation cycles N p versus E r .
In addition, from Figure 6b it is interesting to see that, if E r is decreased from 20.8k B T to a value below 16k B T, N p is decreased from about 100 to a value smaller than 1. This implies that only an about 5k B T decrease in the binding affinity can induce the processive polymerization of a hundred nucleotides to a distributive polymerization. From this result, it is also concluded that the considerable variations of the processivity among Y-family Pols result mainly from slight changes in their binding affinities for the DNA substrate. Moreover, since the LF domain is the least conserved of the four domains in the Y-family Pols, the slight differences in the binding affinity of different Pols are mainly due to different interaction strengths of the LF domain with the DNA. For example, comparison of the LF structure of Dpo4 with that of Dbh showed that the DNA-contacting surface in LF domain of Dpo4 is slightly more positively charged than Dbh, and, correspondingly, Dpo4 is much more processive than Dbh [48]. Since the LF domain has a large binding affinity for the DNA, it is expected from Figure 6a that the deletion of the LF domain will significantly reduce the association time of the Pol with the DNA, thus resulting in much less active than the full-length Pol. This is also consistent with the experimental data [28].
Moving time of the Y-family Pol

The mean moving time, T(n+1)→ n, from the (n+1)th site to the n th site also has the form of Eq. (7) but with E n and En+1being exchanged with each other. From Eq. (7) and D = K B T/Γ, it is noted that the mean moving time is proportional to the viscosity η.
Results of the mean time T n→(n+1) ( T (n+1)→n ) for the Y-family Pol to move from the n th (( n +1)th) site to the ( n +1)th ( n th) site versus E n ( E n+1 ) for different values of E n+1 ( E n ) (indicated in the figure) before dNTP binding to the active site. Note that the four curves of Tn→(n+1)(T(n+1)→n) versus E n (En+1) for different values of En+1(E n ) are nearly coincident.
Effect of external force on DNA-synthesis rate of the Y-family Pol
For Dpo4, since E n > En+1, it is thus noted from Eq. (8) that the active site has a much larger probability to stay at the n th site than to stay at the (n+1)th site. For the value of E n -En+1= 3k B T ~ 5k B T, T n /Tn+1≈ 20 ~ 100. For Dbh, Pol ι and Pol η, En+1is slightly larger than (or nearly equal to) E n . From Eq. (8) it is noted that the Pols show slightly larger (or nearly equal) probability to stay at the (n+1)th site than (or to) that at the n th site.

where k
c
is the dNTP-incorporation rate at saturating dNTP concentration and
. It is noted from Eqs. (8) - (11) that the DNA-synthesis rate k is independent of the viscosity η.


Predicted results of DNA-synthesis rate k ( F ) under the effect of the external force F for Dbh. (a) DNA-synthesis rate k(F) versus F for different values of [dNTP]. (b) DNA-synthesis rate k(F) versus [dNTP] for different values of F, with curves from upper to lower corresponding to F = 1 pN, 10 pN, 20 pN and 30 pN, respectively.
Predicted results of DNA-synthesis rate k ( F ) under the effect of the external force F for Dpo4. (a) DNA-synthesis rate k(F) versus F for different values of [dNTP]. (b) DNA-synthesis rate k(F) versus [dNTP] for different values of F, with curves from upper to lower corresponding to F = 1 pN, 10 pN, 20 pN and 30 pN, respectively.
Comparison of the effect of external force on dNTP-binding rate of the Y-family Pol with that of the replicative Pol
Based on the model for the replicative Pol (Figure 2) and the modified model for the Y-family Pol (Figures 3, 4, and 5), the dNTP-binding rate k b (F) versus the external force F satisfies Eq. (10), where E n -En+1= E'1-E1 < 0 for the replicative Pol (see Figure 2) while E n -En+1≥ 0 for the Y-family Pol. For the replicative Pol, E'1-E1 represents the binding affinity of binding site S1 for one base of the ssDNA template (or the binding affinity of the binding site S1 residue that is closest to the palm subdomain for ssDNA), and it is estimated that E'1-E1 = -5k B T ~ -3k B T. As mentioned before, for Dbh, Pol ι and Pol η, E n -En+1≈ 0, while for Dpo4, E n -En+1= 3k B T ~5k B T.

Predicted results of ratio, , versus the external backward force F acting on the Pol for different values of E n - E n+1 , where k b ( F ) is the dNTP-binding rate under effect of the external force F and is the dNTP-binding rate under no external force. Curves from upper to lower are for E n -En+1= -5k B T, -4k B T, -3k B T, 0, 3k B T and 5k B T, where E n -En+1= -5k B T, -4k B T, -3k B T correspond to replicative Pols, E n -En+1= 0 corresponds to Dbh, Pol ι and Pol η and E n -En+1= 3k B T and 5k B T correspond to Dpo4.
The biological implication of these different characteristics between the Y-family and replicative Pols might be imagined as follows. At the replication fork, the replicative Pol generally feels a backward force by the front DNA helicase [73]. Thus, the slight effect of the backward force on the DNA synthesis rate by the replicative Pols is purposed to have little impact on the DNA replication. However, when the replicative Pol becomes stall at the lesion site, since the front helicase is still unwinding the dsDNA, the Pol would not feel a backward force now. Thus, when the relicative Pol is replaced by the Y-family Pol, the latter would also not feel a backward force at the lesion site. After bypass the lesion site, the Y-family Pol would continue to make processive DNA synthesis and, if the Y-family Pol catches up with the helicase, the backward force induced by the front helicase would greatly reduce the DNA synthesis rate, thus enhancing the probability of the Y-family Pol to dissociate from the DNA substrate or the probability of the Y-family Pol to be replaced by the replicative Pol.
The Y-family Pol can easily bypass a mismatched base pair or a lesion site
In this section, we will show how the Pol that uses the NBR mechanism for translocation can easily bypass a mismatched base pair or a lesion site. As an example, we will use Dpo4 to illustrate this bypass ability, in which the active site is very close along the x direction to the nearest residue of the binding site S2 located in the LF domain.
Interaction potentials between a Y-family DNA Pol and a DNA substrate with a mismatched base pair at the n th site shown in top of (a). For clarity, the mismatched base is drawn in pink. (a) V1(x) represents the potential of the binding site S1 interacting with the DNA substrate, while V2(x) represents the potential of the binding site S2 interacting with the DNA substrate. (b) Schematic diagrams of the position of the Pol along the DNA substrate, with blue dots representing the active site.
Now we compare the case of a matched incorporation at the n th site (Figure 3) with the case of a mismatched incorporation (Figure 11). Since E'1 and E1 are much smaller than E'2 and E2, we have
, where
and
represent E
n
for cases of matched incorporation and mismatched incorporation, respectively. Thus, from the results shown in Figure 7, it is seen that the mean moving time Tn→(n+1)for the case of mismatched incorporation is shorter than the case of matched incorporation. Moreover, it is noted that the value of
is close to that of
, since both value of E'2-E''2 and that of E2-E'2 correspond to the affinity of the binding site S2 for the backbones connecting one base pair on the dsDNA. Thus, from Eq. (8), the ratio (T
n
/Tn+1)(mismatch)is close to (T
n
/Tn+1)(match). As a result, we conclude that the Pol that uses the NBR mechanism for translocation has nearly the same rate to bypass a mismatched base pair as that to bypass a matched base pair. Similarly, for the case of an abasic lesion located at the n th site, the interaction potential V2(x) is the same as shown Figure 11a. Thus, as in the case of a mismatched base, the Pol that uses the NBR mechanism for translocation can also easily bypass the lesion site.
However, since
, it is noted from Figure 6a that the dissociation probability near the lesion site is larger than that in the absence of the lesion or mismatched base, which is in agreement with the experimental data for Dpo4 [52]. On the hand, it is seen from Figure 6b that, when there is no lesion or no mismatched base, for N
p
= 10 that corresponds to the case of Dbh [48]E
r
= 18.5k
B
T, while for N
p
= 100 that corresponds to the case of Dpo4 [48]E
r
= 20.8k
B
T. From the value of E1-E'1 = 3k
B
T ~ 5k
B
T (see above), we infer that E'1-E''1 ≈ 3k
B
T ~ 5k
B
T. Thus, at the lesion site, for the case of Dbh with E
r
= 13.5k
B
T ~ 15.5k
B
T, we have N
p
≈ 0.08 ~ 0.6 from Figure 6b; for the case of Dpo4 with E
r
= 15.8k
B
T ~ 17.8k
B
T, we have N
p
≈ 0.8 ~ 5.2 from Figure 6b. This implies that, at the lesion site, Dbh is prone to dissociate from the DNA substrate while Dpo4 is not easily to dissociate. In other words, Dpo4 can bypass the lesion site, yet Dbh does so with a much lower efficiency. These are consistent with the experimental data [24, 48, 50, 52]. Moreover, as the different lesion-bypassing abilities of the two Pols, Dpo4 and Dbh, are due to the different binding affinities, which in turn result mainly from the different interaction strengths of the LF domain with the DNA, it is inferred that, by interchanging the LF domains, the lesion-bypassing abilities of the two Pols will be exchanged. This is also consistent with the experimental data of Boudsocq et al. [48].
Similarly, we can easily show that the Pols such as Dbh and Pol ι, in which the active site is, along the x direction, not close to the nearest residue of the binding site S2 located in the LF domain, can also easily bypass the lesion site. Thus, we conclude that, although different values of distance L give different translocation features, all the Y-family Pols that use the NBR mechanism for translocation can easily bypass the lesion site, thus performing the translesion synthesis. By contrast, the replicative Pols that use other Brownian ratchet mechanism for translocation cannot bypass the lesion site and is thus unable to perform the translesion synthesis (see Figures 1 and 2).
Discussion
The explanation of the lesion-bypassing ability by a Y-family Pol in this work is focused only on the translocation activity of the active site from the position opposite to the lesion site to the next position. In fact, the lesion-bypassing ability is dictated by two activities. One is the translocation activity while the other one is the catalytic activity of the phosphodiester bond formation. The latter activity determines that rates of nucleotide incorporation opposite to the lesion site and one position downstream from the lesion site are slower than those at other sites [46]. Moreover, since the latter activity is determined by the structure of the catalytic core, single amino acid substitutions within the active site, palm or fingers subdomains can also have a profound effect on the ability of the enzyme to perform translesion synthesis [74, 75].
Distinct translocation features among the Y-family Pols in the NBR model depend on the distance L from the active site to the nearest residue of the binding site S2 located in the LF domain. It is important to note that this distance L in the model corresponds to the structure of the Pol only after binding to its DNA substrate. Although available structures showed a significant conformational change in the LF domain of the apo-Dpo4 upon binding to the DNA substrate [42], only a little change has been observed between the Pol complexed with the DNA substrate alone and that with both the DNA substrate and the dNTP nucleotide. Thus, the large conformational change in the LF domain of the Pol upon binding to the DNA substrate has no effect on the conclusion of the current work which is involved only with the structures of the Pol either complexed with the DNA substrate alone or complexed with both the DNA substrate and the dNTP nucleotide.
Further comments on the NBR translocation model
In the NBR model (Figure 5), it has been implicitly considered that the Pol has a rigid structure, i.e., different domains have been considered to be linked rigidly. In fact, the residues linking different domains may behave elastically. For example, for Dpo4, considering an elastic link between the palm and thumb domains. Upon nucleotide binding, after the active site, together with the fingers, palm and LF domains, move from the n th site to the (n+1)th site, the thumb domain may not move simultaneously due to the elastic link between the palm and thumb domains, i.e., the thumb contacts with the DNA may fluctuate by the thermal noise between pre- and post-translocation positions with nearly equal probability. This gives an explanation to the available structural data for Dpo4 showing that, upon nucleotide binding, the LF contacts with the DNA shift by one base pair but the thumb contacts do not shift simultaneously [41].
Potential implication of binding site S1 in the induced-fit mechanism
The strong interaction of the binding site S1 with the unpaired base on the template induces the conformational change in the residues of the binding site S1, which in turn results in the conformational change in the active site that is adjacent to the residues of the binding site S1. This unpaired-base-related conformational change thus results in the active site having a much higher affinity for the structurally compatible nucleotide than structurally incompatible nucleotides. This argument is consistent with the experimental data for high-fidelity DNA Pols showing that the shape of the nascent base pair is important regardless of whether the Watson-Crick hydrogen bonds can be formed [76]. It is also consistent with the recent FRET-based assay on Klenow fragment showing that base discrimination takes place within the open complex rather than occurs during the transition from open to closed fingers conformations [77]. Conversely, the interaction of the structurally incompatible nucleotide may have a negative effect on the conformational change in the active site, which in turn results in the inverse conformational change in the binding site S1, potentially reducing its binding affinity for the unpaired base on the template. This could account for the increased dissociation caused by the binding of a mismatched nucleotide, as observed by Joyce et al. [77].
Crystal structures of the Y-family DNA Pol complexed with DNA substrate showed weak or no interaction of the Pol with the ssDNA template [27, 28, 32, 41, 42]. The weak binding affinity would result in a minor or no conformational change in the active site that is related to the structure of the unpaired base on the template, giving a smaller difference in binding affinity between correct and incorrect nucleotides. This thus results in that the Y-family Pol has a low-fidelity synthesis, which is consistent with the available experimental data [43, 45]. Since minor or no conformational change in the active site occurs which is related to the shape of the template base, it is expected that the base discrimination in Y-family Pols should rely mainly on the Watson-Crick hydrogen bonding interaction, in sharp contrast to the high-fidelity replicative DNA Pols where the effect of the Watson-Crick hydrogen bonding interaction can be negligible compared to the dominant effect of the base shape. Indeed, steady state kinetic studies with incoming dNTP and DNA substrates containing difluorotoluene, which has the same shape as thymine but lacks the ability to form Watson-Crick hydrogen bonds, are poor substrates for Y-family pol η [78].
Conclusion
In conclusion, a NBR model is proposed for the translocation of the Y-family DNA Pol along the DNA substrate, which is modified from the translocation model proposed previously for the replicative DNA Pol. The observed different features of the structures for Dpo4, Dbh and pol ι in binary and ternary forms are consistent with the NBR model. Moreover, since the interaction potential V2(x) for Pol η has the form of Figure 4b rather than that of Figure 3b, it is predicted that Pol η would show the translocation feature similar to Dbh and Pol ι rather than Dpo4. The obtained theoretical results on dynamic properties of the Y-family Pols by using the NBR model are consistent with the available experimental data. To further verify the model, it is hoped to test the predicted results given in Figures 8, 9, 10.
Declarations
Acknowledgements
This work was supported by the National Natural Science Foundation of China (Grant No. 10974248).
Authors’ Affiliations
References
- Braithwaite DK, Ito J: Compilation, alignment, and phylogenetic relationships of DNA polymerases. Nucleic Acids Res. 1993, 21: 787-802. 10.1093/nar/21.4.787.PubMed CentralView ArticlePubMedGoogle Scholar
- Cann IK, Ishino Y: Archaeal DNA replication: identifying the pieces to solve a puzzle. Genetics. 1999, 152: 1249-1267.PubMed CentralPubMedGoogle Scholar
- Ohmori H, Friedberg EC, Fuchs RP, Goodman MF, Hanaoka F, Hinkle D, Kunkel TA, Lawrence CW, Livneh Z, Nohmi T, Prakash L, Prakash S, Todo T, Walker GC, Wang Z, Woodgate R: The Y-Family of DNA Polymerases. Mol Cell. 2001, 8: 7-8. 10.1016/S1097-2765(01)00278-7.View ArticlePubMedGoogle Scholar
- Moon AF, Garcia-Diaz M, Batra VK, Beard WA, Bebenek K, Kunkel TA, Wilson SH, Pedersen LC: The X family portrait: structural insights into biological functions of X family polymerases. DNA Repair (Amst). 2007, 6: 1709-1725. 10.1016/j.dnarep.2007.05.009.PubMed CentralView ArticleGoogle Scholar
- Yamtich J, Sweasy JB: DNA polymerase family X: function, structure, and cellular roles. Biochim Biophys Acta. 2010, 1804: 1136-1150.PubMed CentralView ArticlePubMedGoogle Scholar
- Woodgate R: A plethora of lesion-replicating DNA polymerases. Genes Dev. 1999, 13: 2191-2195. 10.1101/gad.13.17.2191.View ArticlePubMedGoogle Scholar
- Goodman MF: Error-prone repair DNA polymerases in prokaryotes and eukaryotes. Annu Rev Biochem. 2002, 71: 17-50. 10.1146/annurev.biochem.71.083101.124707.View ArticlePubMedGoogle Scholar
- Friedberg EC, Wagner R, Radman M: Specialized DNA polymerases, cellular survival, and the genesis of mutations. Science. 2002, 296: 1627-1630. 10.1126/science.1070236.View ArticlePubMedGoogle Scholar
- Yang W, Woodgate R: What a difference a decade makes: Insights into translesion DNA synthesis. Proc Natl Acad Sci USA. 2007, 104: 15591-15598. 10.1073/pnas.0704219104.PubMed CentralView ArticlePubMedGoogle Scholar
- Lehmann AR, Niimi A, Ogi T, Brown S, Sabbioneda S, Wing JF, Kannouche PL, Green CM: Translesion synthesis: Y-family polymerases and the polymerase switch. DNA Repair (Amst). 2007, 6: 891-899. 10.1016/j.dnarep.2007.02.003.View ArticleGoogle Scholar
- Pata JD: Structural diversity of the Y-family DNA polymerases. Biochim Biophys Acta. 2010, 1804: 1124-1135.PubMed CentralView ArticlePubMedGoogle Scholar
- Washington MT, Carlson KD, Freudenthal BD, Pryor JM: Variations on a theme: Eukaryotic Y-family DNA polymerases. Biochim Biophys Acta. 2010, 1804: 1113-1123.PubMed CentralView ArticlePubMedGoogle Scholar
- Wagner J, Gruz P, Kim S-R, Yamada M, Matsui K, Fuchs RPP, Nohmi T: The dinB gene encodes a novel E. coli DNA polymerase, DNA pol IV, involved in mutagenesis. Mol Cell. 1999, 4: 281-286. 10.1016/S1097-2765(00)80376-7.View ArticlePubMedGoogle Scholar
- Reuven NB, Arad G, Maor-Shoshani A, Livneh Z: The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication. J Biol Chem. 1999, 274: 31763-31766. 10.1074/jbc.274.45.31763.View ArticlePubMedGoogle Scholar
- Tang M, Shen X, Frank EG, O'Donnell M, Woodgate R, Goodman MF: UmuD'2C is an error-prone DNA polymerase, Escherichia coli pol V. Proc Natl Acad Sci USA. 1999, 96: 8919-8924. 10.1073/pnas.96.16.8919.PubMed CentralView ArticlePubMedGoogle Scholar
- Johnson RE, Prakash S, Prakash L: Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, pol η. Science. 1999, 283: 1001-1004. 10.1126/science.283.5404.1001.View ArticlePubMedGoogle Scholar
- Nelson JR, Lawrence CW, Hinkle DC: Deoxycytidyl transferase activity of yeast REV1 protein. Nature. 1996, 382: 729-731. 10.1038/382729a0.View ArticlePubMedGoogle Scholar
- Masutani C, Kusumoto R, Yamada A, Dohmae N, Yokoi M, Yuasa M, Araki M, Iwai S, Takio K, Hanaoka F: The XPV (xeroderma pigmentosum variant) gene encodes human DNA polymerase η. Nature. 1999, 399: 700-704. 10.1038/21447.View ArticlePubMedGoogle Scholar
- Johnson RE, Washington MT, Haracska L, Prakash S, Prakash L: Eukaryotic polymerasesι and ζ act sequentially to bypass DNA lesions. Nature. 2000, 406: 1015-1019. 10.1038/35023030.View ArticlePubMedGoogle Scholar
- Tissier A, McDonald JP, Frank EG, Woodgate R: pol ι, a remarkably error-prone human DNA polymerase. Genes Dev. 2000, 14: 1642-1650.PubMed CentralPubMedGoogle Scholar
- Ohashi E, Ogi T, Kusumoto R, Iwai S, Masutani C, Hanaoka F, Ohmori H: Error-prone bypass of certain DNA lesions by the human DNA polymerase κ. Genes Dev. 2000, 14: 1589-1594.PubMed CentralPubMedGoogle Scholar
- Gibbs PEM, Wang X-D, Li Z, McManus TP, McGregor WG, Lawrence CW, Maher VM: The function of the human homolog of Saccharomyces cerevisiae REV1 is required for mutagenesis induced by UV light. Proc Natl Acad Sci USA. 2000, 97: 4186-4191. 10.1073/pnas.97.8.4186.PubMed CentralView ArticlePubMedGoogle Scholar
- Kulaeva OI, Koonin EV, McDonald JP, Randall SK, Rabinovich N, Connaughton JF, Levine AS, Woodgate R: Identification of a DinB/UmuC homolog in the archeon Sulfolobus solfataricus. Mutat Res. 1996, 357: 245-253.View ArticlePubMedGoogle Scholar
- Boudsocq F, Iwai S, Hanaoka F, Woodgate R: Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4): an archaeal DNA polymerase with lesion-bypass properties akin to eukaryotic pol η. Nucleic Acids Res. 2001, 29: 4607-4616. 10.1093/nar/29.22.4607.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhou BL, Pata JD, Steitz TA: Crystal structure of a DinB lesion bypass DNA polymerase catalytic fragment reveals a classic polymerase catalytic domain. Mol Cell. 2001, 8: 427-437. 10.1016/S1097-2765(01)00310-0.View ArticlePubMedGoogle Scholar
- Silvian LF, Toth EA, Pham P, Goodman MF, Ellenberger T: Crystal structure of a DinB family error-prone DNA polymerase from Sulfolobus solfataricus. Nat Struct Biol. 2001, 8: 984-989. 10.1038/nsb1101-984.View ArticlePubMedGoogle Scholar
- Wilson RC, Pata JD: Structural insights into the generation of single-base deletions by the Y family DNA polymerase Dbh. Mol Cell. 2008, 29: 767-779. 10.1016/j.molcel.2008.01.014.View ArticlePubMedGoogle Scholar
- Ling H, Boudsocq F, Woodgate R, Yang W: Crystal structure of a Y-family DNA polymerase in action: a mechanism for error-prone and lesion-bypass replication. Cell. 2001, 107: 91-102. 10.1016/S0092-8674(01)00515-3.View ArticlePubMedGoogle Scholar
- Trincao J, Johnson RE, Escalante CR, Prakash S, Prakash L, Aggarwal AK: Structure of the catalytic core of S. cerevisiae DNA polymerase η: implications for translesion DNA synthesis. Mol Cell. 2001, 8: 417-426. 10.1016/S1097-2765(01)00306-9.View ArticlePubMedGoogle Scholar
- Alt A, Lammens K, Chiocchini C, Lammens A, Pieck JC, Kuch D, Hopfner KP, Carell T: Bypass of DNA lesions generated during anticancer treatment with cisplatin by DNA polymerase eta. Science. 2007, 318: 967-970. 10.1126/science.1148242.View ArticlePubMedGoogle Scholar
- Nair DT, Johnson RE, Prakash S, Prakash L, Aggarwal AK: Replication by human DNA polymerase-iota occurs by Hoogsteen base-pairing. Nature. 2004, 430: 377-380. 10.1038/nature02692.View ArticlePubMedGoogle Scholar
- Jain R, Nair DT, Johnson RE, Prakash L, Prakash S, Aggarwal AK: Replication across template T/U by human DNA polymerase-iota. Structure. 2009, 17: 974-980. 10.1016/j.str.2009.04.011.PubMed CentralView ArticlePubMedGoogle Scholar
- Uljon SN, Johnson RE, Edwards TA, Prakash S, Prakash L, Aggarwal AK: Crystal structure of the catalytic core of human DNA polymerase kappa. Structure. 2004, 12: 1395-1404. 10.1016/j.str.2004.05.011.View ArticlePubMedGoogle Scholar
- Vasquez-Del Carpio R, Silverstein TD, Lone S, Swan MK, Choudhury JR, Johnson R, Prakash S, Prakash L, Aggarwal A: Structure of human DNA polymerase kappa inserting dATP opposite an 8-OxoG DNA lesion. PLoS ONE. 2009, 4: e5766-10.1371/journal.pone.0005766.View ArticlePubMedGoogle Scholar
- Nair D, Johnson R, Prakash L, Prakash S, Aggarwal A: Rev1 employs a novel mechanism of DNA synthesis using a protein template. Science. 2005, 309: 2219-2222. 10.1126/science.1116336.View ArticlePubMedGoogle Scholar
- Ling H, Boudsocq F, Plosky BS, Woodgate R, Yang W: Replication of a cis-syn thymine dimer at atomic resolution. Nature. 2003, 424: 1083-1087. 10.1038/nature01919.View ArticlePubMedGoogle Scholar
- Ling H, Boudsocq F, Woodgate R, Yang W: Snapshots of replication through an abasic lesion; structural basis for base substitutions and frameshifts. Mol Cell. 2004, 13: 751-762. 10.1016/S1097-2765(04)00101-7.View ArticlePubMedGoogle Scholar
- Ling H, Sayer JM, Plosky BS, Yagi H, Boudsocq F, Woodgate R, Jerina DM, Yang W: Crystal structure of a benzo[a]pyrene diol epoxide adduct in a ternary complex with a DNA polymerase. Proc Natl Acad Sci USA. 2004, 101: 2265-2269. 10.1073/pnas.0308332100.PubMed CentralView ArticlePubMedGoogle Scholar
- Trincao J, Johnson RE, Wolfle WT, Escalante CR, Prakash S, Prakash L, Aggarwal AK: Dpo4 is hindered in extending a GT mismatch by a reverse wobble. Nat Struct Mol Biol. 2004, 11: 457-462. 10.1038/nsmb755.View ArticlePubMedGoogle Scholar
- Vaisman A, Ling H, Woodgate R, Yang W: Fidelity of Dpo4: effect of metal ions, nucleotide selection and pyrophosphorolysis. EMBO J. 2005, 24: 2957-2967. 10.1038/sj.emboj.7600786.PubMed CentralView ArticlePubMedGoogle Scholar
- Rechkoblit O, Malinina L, Cheng Y, Kuryavyi V, Broyde S, Geacintov NE, Patel DJ: Stepwise translocation of Dpo4 polymerase during error-free bypass of an oxoG lesion. PLoS Biol. 2006, 4: e11-10.1371/journal.pbio.0040011.PubMed CentralView ArticlePubMedGoogle Scholar
- Wong JH, Fiala KA, Suo Z, Ling H: Snapshots of a Y-family DNA polymerase in replication: substrate-induced conformational transitions and implications for fidelity of Dpo4. J Mol Biol. 2008, 379: 317-330. 10.1016/j.jmb.2008.03.038.View ArticlePubMedGoogle Scholar
- Kokoska RJ, Bebenek K, Boudsocq F, Woodgate R, Kunkel TA: Low fidelity DNA synthesis by a Y family DNA polymerase due to misalignment in the active site. J Biol Chem. 2002, 277: 19633-19638. 10.1074/jbc.M202021200.View ArticlePubMedGoogle Scholar
- Fiala KA, Suo Z: Mechanism of DNA polymerization catalyzed by Sulfolobus solfataricus P2 DNA polymerase IV. Biochemistry. 2004, 43: 2116-2125. 10.1021/bi035746z.View ArticlePubMedGoogle Scholar
- Fiala KA, Suo Z: Pre-steady-state kinetic studies of the fidelity of Sulfolobus solfataricus P2 DNA polymerase IV. Biochemistry. 2004, 43: 2106-2115. 10.1021/bi0357457.View ArticlePubMedGoogle Scholar
- Fiala KA, Hypes CD, Suo Z: Mechanism of abasic lesion bypass catalyzed by a Y-family DNA polymerase. J Biol Chem. 2007, 282: 8188-8198. 10.1074/jbc.M610718200.View ArticlePubMedGoogle Scholar
- Washington MT, Prakash L, Prakash S: Yeast DNA polymerase η utilizes an induced-fit mechanism of nucleotide incorporation. Cell. 2001, 107: 917-927. 10.1016/S0092-8674(01)00613-4.View ArticlePubMedGoogle Scholar
- Boudsocq F, Kokoska RJ, Plosky BS, Vaisman A, Ling H, Kunkel TA, Yang W, Woodgate R: Investigating the role of the little finger domain of Y-family DNA polymerases in low fidelity synthesis and translesion replication. J Biol Chem. 2004, 279: 32932-32940. 10.1074/jbc.M405249200.View ArticlePubMedGoogle Scholar
- Gruz P, Pisani FM, Shimizu M, Yamada M, Hayashi I, Morikawa K, Nohmi T: Synthetic activity of Sso DNA polymerase Y1, an archaeal DinB-like DNA polymerase, is stimulated by processivity factors proliferating cell nuclear antigen and replication factor C. J Biol Chem. 2001, 276: 47394-47401. 10.1074/jbc.M107213200.View ArticlePubMedGoogle Scholar
- Potapova O, Grindley ND, Joyce CM: The mutational specificity of the Dbh lesion bypass polymerase and its implications. J Biol Chem. 2002, 277: 28157-28166. 10.1074/jbc.M202607200.View ArticlePubMedGoogle Scholar
- McCulloch SD, Kokoska RJ, Masutani C, Iwai S, Hanaoka F, Kunkel TA: Preferential cis-syn thymine dimer bypass by DNA polymerase η occurs with biased fidelity. Nature. 2004, 428: 97-100. 10.1038/nature02352.View ArticlePubMedGoogle Scholar
- Kokoska RJ, McCulloch SD, Kunkel TA: The efficiency and specificity of apurinic/apyrimidinic site bypass by human DNA polymerase η and Sulfolobus solfataricus Dpo4. J Biol Chem. 2003, 278: 50537-50545. 10.1074/jbc.M308515200.View ArticlePubMedGoogle Scholar
- Zang H, Goodenough AK, Choi JY, Irimia A, Loukachevitch LV, Kozekov ID, Angel KC, Rizzo CJ, Egli M, Guengerich FP: DNA adduct bypass polymerization by Sulfolobus solfataricus DNA polymerase Dpo4. J Biol Chem. 2005, 280: 29750-29764. 10.1074/jbc.M504756200.View ArticlePubMedGoogle Scholar
- DeLucia AM, Grindley ND, Joyce CM: An error-prone family Y DNA polymerase (DinB homolog from Sulfolobus solfataricus) uses a 'steric gate' residue for discrimination against ribonucleotides. Nucleic Acids Res. 2003, 31: 4129-4137. 10.1093/nar/gkg417.PubMed CentralView ArticlePubMedGoogle Scholar
- DeLucia AM, Grindley ND, Joyce CM: Conformational changes during normal and error-prone incorporation of nucleotides by a Y-family DNA polymerase detected by 2-aminopurine fluorescence. Biochemistry. 2007, 46: 10790-10803. 10.1021/bi7006756.View ArticlePubMedGoogle Scholar
- Xu C, Maxwell BA, Brown JA, Zhang L, Suo Z: Global conformational dynamics of a Y-family DNA polymerase during catalysis. PLoS Biol. 2009, 7: e1000225-10.1371/journal.pbio.1000225.PubMed CentralView ArticlePubMedGoogle Scholar
- Xie P: Model for forward polymerization and switching transition between polymerase and exonuclease sites by DNA polymerase molecular motors. Arch Biochem Biophys. 2007, 457: 73-84. 10.1016/j.abb.2006.09.019.View ArticlePubMedGoogle Scholar
- Xie P: A possible mechanism for the dynamics of transition between polymerase and exonuclease sites in a high-fidelity DNA polymerase. J Theor Biol. 2009, 259: 434-439. 10.1016/j.jtbi.2009.04.009.View ArticlePubMedGoogle Scholar
- Xie P: A polymerase-site-jumping model for strand transfer during DNA synthesis by reverse transcriptase. Virus Res. 2009, 144: 65-73. 10.1016/j.virusres.2009.03.022.View ArticlePubMedGoogle Scholar
- Magnasco MO, Stolovitzky G: Feynman's ratchet and pawl. J Stat Phys. 1998, 93: 615-632.View ArticleGoogle Scholar
- Kay ER, Leigh DA, Zerbetto F: Synthetic molecular motors and mechanical machines. Agnew Chem Int Ed. 2007, 46: 72-191. 10.1002/anie.200504313.View ArticleGoogle Scholar
- Delagoutte E, von Hippel PH: Function and assembly of the Bacteriophage T4 DNA replication complex. J Biol Chem. 2003, 278: 25435-25447. 10.1074/jbc.M303370200.View ArticlePubMedGoogle Scholar
- Turner RM, Grindley NDF, Joyce CM: Interaction of DNA polymerase I (Klenow fragment) with the single-stranded template beyond the site of synthesis. Biochemistry. 2003, 42: 2373-2385. 10.1021/bi026566c.View ArticlePubMedGoogle Scholar
- Datta K, Wowor AJ, Richard AJ, LiCata VJ: Temperature dependence and thermodynamics of Klenow polymerase binding to primed-template DNA. Biophys J. 2006, 90: 1739-1751. 10.1529/biophysj.105.071837.PubMed CentralView ArticlePubMedGoogle Scholar
- Doublie S, Sawaya MR, Ellenberger T: An open and closed case for all polymerases. Structure. 1999, 7: R31-R35. 10.1016/S0969-2126(99)80017-3.View ArticlePubMedGoogle Scholar
- Li Y, Korolev S, Waksman G: Crystal structures of open and closed forms of binary and ternary complexes of the large fragment of thermus aquaticus DNA polymerase I: structural basis for nucleotide incorporation. EMBO J. 1998, 17: 7514-7525. 10.1093/emboj/17.24.7514.PubMed CentralView ArticlePubMedGoogle Scholar
- Huang H, Chopra R, Verdine GL, Harrison SC: Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance. Science. 1998, 282: 1669-1675.View ArticlePubMedGoogle Scholar
- Donlin MJ, Patel SS, Johnson KA: Kinetic partitioning between the exonuclease and polymerase sites in DNA error correction. Biochemistry. 1991, 30: 538-546. 10.1021/bi00216a031.View ArticlePubMedGoogle Scholar
- Hogg M, Wallace SS, Doublie S: Crystallographic snapshots of a replicative DNA polymerase encountering an abasic site. EMBO J. 2004, 23: 1483-1493. 10.1038/sj.emboj.7600150.PubMed CentralView ArticlePubMedGoogle Scholar
- Li Y, Dutta S, Doublie S, Bdour HM, Taylor JS, Ellenberger T: Nucleotide insertion opposite a cis-syn thymine dimer by a replicative DNA polymerase from bacteriophage T7. Nat Struct Mol Biol. 2004, 11: 784-790. 10.1038/nsmb792.View ArticlePubMedGoogle Scholar
- Luby-Phelps K, Mujumdar S, Mujumdar RB, Ernst LA, Galbraith W, Waggoner AS: A novel fluorescence ratiometric method confirms the low solvent viscosity of the cytoplasm. Biophys J. 1993, 65: 236-242. 10.1016/S0006-3495(93)81075-0.PubMed CentralView ArticlePubMedGoogle Scholar
- Gardiner CW: Handbook of stochastic methods for physics, chemistry and the natural sciences. Springer-Verlag, Berlin. 1983Google Scholar
- Stano NM, Jeong Y-J, Donmez I, Tummalapalli P, Levin MK, Patel SS: DNA synthesis provides the driving force to accelerate DNA unwinding by a helicase. Nature. 2005, 435: 370-373. 10.1038/nature03615.PubMed CentralView ArticlePubMedGoogle Scholar
- Boudsocq F, Ling H, Yang W, Woodgate R: Structure-based interpretation of missense mutations in Y-family DNA polymerases and their implications for polymerase function and lesion bypass. DNA Repair (Amst). 2002, 1: 343-358. 10.1016/S1568-7864(02)00019-8.View ArticleGoogle Scholar
- Glick E, Vigna KL, Loeb LA: Mutations in human DNA polymerase η motif II alter bypass of DNA lesions. EMBO J. 2001, 20: 7303-7312. 10.1093/emboj/20.24.7303.PubMed CentralView ArticlePubMedGoogle Scholar
- Moran S, Ren RXF, Kool ET: A thymidine triphosphate shape analog lacking Watson-Crick pairing ability is replicated with high sequence selectivity. Proc Natl Acad Sci USA. 1997, 94: 10506-10511. 10.1073/pnas.94.20.10506.PubMed CentralView ArticlePubMedGoogle Scholar
- Joyce CM, Potapova O, DeLucia AM, Huang X, Basu VP, Grindley NDF: Fingers-closing and other rapid conformational changes in DNA polymerase I (Klenow fragment) and their role in nucleotide selectivity. Biochemistry. 2008, 47: 6103-6116. 10.1021/bi7021848.View ArticlePubMedGoogle Scholar
- Washington MT, Helquist SA, Kool ET, Prakash L, Prakash S: Requirement of Watson-Crick hydrogen bonding for DNA synthesis by yeast DNA polymerase eta. Mol Cell Biol. 2003, 23: 5107-5112. 10.1128/MCB.23.14.5107-5112.2003.PubMed CentralView ArticlePubMedGoogle Scholar
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