Helicases are molecular engines which translocate along nucleic acids (NA) to unwind double-strands or remodel NA–protein complexes. While they have an essential role in genome structure and expression, the rules dictating their processivity remain elusive. Here, we developed single-molecule methods to investigate helicase binding lifetime on DNA. We found that UPF1, a highly processive helicase central to nonsense-mediated mRNA decay (NMD), tightly holds onto NA, allowing long lasting action. Conversely, the structurally similar IGHMBP2 helicase has a short residence time. UPF1 mutants with variable grip on DNA show that grip tightness dictates helicase residence time and processivity. In addition, we discovered via functional studies that a decrease in UPF1 grip impairs NMD efficiency in vivo. Finally, we propose a three-state model with bound, sliding and unbound molecular clips, that can accurately predict the modulation of helicase processivity.
Helicases are ubiquitous molecular motors found in all living organisms. These enzymes are organized around a core domain that simultaneously binds nucleotide triphosphates (NTPs) and nucleic acids (NA) in a sequence-independent manner, and converts the chemical energy of NTP hydrolysis into mechanical activities on NA. Hence, helicases can lock onto NA, translocate on single-strands (ss) or double-strands (ds), and apply a mechanical force either to unwind dsNA or to remodel NA–protein complexes1,2,3. This versatile ability to act on NAs justifies the ubiquitous involvement of helicases in every NA-related process including DNA replication, repair, recombination, transcription, and every event of post-transcriptional gene regulation2,4,5. Despite seemingly comparable cores, helicases intervene in precise processes and sometimes act on specific NA substrates. The specificity of their actions is conferred by accessory domains either flanking or inserted in the helicase core. These additional domains can carry complementary catalytic activities, affinity for specific NA sequences, or ensure interactions with protein partners, as most helicases are part of protein complexes6,7,8.
Helicase coding genes have been classified into six superfamilies (SF1-SF6) and subsequent subfamilies. SF1 and SF2 are the largest groups of RNA and DNA helicases generally acting as monomers or dimers while SF3–SF6 encompass multimeric ring-shaped helicases7,9. The helicase domain of SF1 and SF2 enzymes is composed of conserved and characteristic motifs2,7,10,11. However, the presence of signature motifs or the affiliation of a helicase to a specific family cannot foretell its intrinsic biophysical properties and physiological functions. The UPF1-like family is a good example of functional diversity occurring between sister helicases. This family is formed of a group of 11 enzymes belonging to the SF1-B 5′–3′ helicases10. Among them one finds IGHMBP2 (immunoglobulin helicase mu-binding protein 2), a helicase related to mRNA translation and responsible for distal spinal muscular atrophy with respiratory distress type 112,13, SetX/Sen1 (Senataxin), which is involved in transcription termination, R-loop resolving and is linked to amyotrophic lateral sclerosis14, and MOV10 (Moloney leukemia virus 10), which is involved in miRNA-dependent regulation15,16.
Members of UPF1-like helicases present a common helicase domain organization with two RecA-like domains (1A and 2A) containing conserved helicase motifs and two domains (1B and 1C) protruding from the first RecA domain 1A10,17,18,19,20. The prototype, UPF1 (Up-frameshift 1) is a multifunctional RNA and DNA helicase. It is implicated in telomere maintenance and telomerase activity regulation21 and various mRNA decay pathways22,23,24. UPF1 is best-known for its essential role in nonsense-mediated mRNA decay (NMD), an eukaryotic surveillance pathway that eliminates aberrant messenger RNAs (mRNAs) carrying premature termination codons (PTC) and modulates the expression level of normal mRNAs-presenting NMD substrate features25,26.
We recently assessed some of the biophysical properties of UPF1 by using magnetic tweezers to manipulate DNA and RNA hairpins at the single-molecule scale27. We monitored the activity of the helicase domain of human UPF1 (hUPF1) and discovered some unexpected properties. As a monomer, hUPF1 was able to unwind long dsNA and translocate onto ssNA with a processivity exceeding 10 kilobases (kb). Though the processivity of other UPF1-like helicases has not been determined, the processivity of hUPF1 exceeds that of the DNA helicases UvrD or Rep in their monomeric state when measured by single-molecule approaches28,29. The processivity of UPF1 is particularly surprising given that it translocates onto NA as a monomeric unit at a rate at least one order of magnitude slower than UvrD, Rep, or the SF2 RNA helicase NS327,29,30,31,32. Therefore, to cover similar distances, hUPF1 must stay a much longer time on its substrate. In addition, the progression of UPF1 onto RNA or DNA is not affected by NA-bound proteins27. These observations raise the question of whether these peculiar attributes are specific to hUPF1 or whether they are shared with the related UPF1-like helicases.
In the present study, we show that the high processivity of hUPF1 is shared with its homolog from the yeast Saccharomyces cerevisiae (yUPF1) but not with the very similar human helicase IGHMBP2. Structural comparison between core helicase domains of both proteins led to the design of a series of mutants differentially affecting UPF1 processivity. Using a single-molecule binding assay, we measured the strength of UPF1 grip on NA and established a correlation between helicase grip, binding lifetime, and the duration of translocation. In addition, the study of a mutant affecting UPF1 grip in yeast demonstrates its relevance for UPF1 function in NMD.
Processivity is variable amid UPF1-like helicases
We first determined whether the helicase core of yeast UPF1 (yUPF1) is as processive as the helicase core of human UPF1 (hUPF1). Indeed, both proteins are key NMD factors, and both core domains present high sequence and structural similarities (Supplementary Figure 1 33). Using a magnetic tweezers setup, we manipulated single 1.2 kb DNA hairpins tethering super-paramagnetic beads to a glass surface. Using video-microscopy, we tracked the beads’ positions to monitor changes in the extension of the hairpins over time (Fig. 1a 27,34), all the while applying a controlled force on the hairpin fork using magnets to pull on the tethered beads. yUPF1 (in an appropriate buffer with ATP) was injected in this setup at the lowest possible concentration to observe monomeric single-molecule events. Under a constant tension of 7 pN and at saturating ATP concentration (2 mM), yUPF1 molecules generated characteristic saw-tooth tracks (Fig. 1b) similar to hUPF1 (Supplementary Figure 2A). The rising and falling edges correspond, respectively, to complete hairpin unwinding (Fig. 1a, steps 2–3) and rezipping in the wake of the enzyme following translocation on single strand (ss) (Fig. 1a, step 4). yUPF1 unwinding and ss translocation rates were significantly higher (10.2 and 13.4 bp s−1, respectively) than those of hUPF1 (0.32 and 1.92 bp s−1) consistent with their different ATP consumption rates (Supplementary Figure 2B). To assess yUPF1 processivity, we first calculated the probability of fully unwinding the 1.2 kb DNA hairpin using 58 events that initiated on fully closed hairpins. Using this probability, we estimated the unwinding processivity to be superior to 10 kb (n = 58) (Supplementary Figure 2C). We thus concluded that a high processivity is a conserved UPF1 feature shared between yeast and human homologs33.
As UPF1 is the prototype of the UPF1-like helicase family, we broadened our scope and examined whether high processivity is also a feature of other UPF1-like helicases. To this end, we selected the human IGHMPB2 protein, a helicase linked to DSMA1 respiratory disease12,13. Guenther et al.35 previously described the ATP-dependent 5′–3′ helicase activity of a recombinant full-length IGHMPB2 on small RNA and DNA duplexes. However, no unwinding assays on the human IGHMBP2 helicase domain alone have been done so far. Using our single-molecule conditions, we assayed the isolated helicase core of IGHMBP2, which did not display any observable unwinding activity (Fig. 1c) despite a detectable (albeit sevenfold lower) ATPase activity in vitro (Supplementary Figure 2B). However, when flanked by its C-terminal domain (Supplementary Figure 2D) which increases its binding affinity19, IGHMBP2 presented short unwinding events with a small processivity estimated to be 19 bp only (Supplementary Figure 2D, E; unwinding speed 5 bp s−1). Taken together, our experiments reveal that high processivity is not shared uniformly among the UPF1-like helicase family, in spite of similar core domains.
Binding lifetime varies between sister helicases
How to explain such a diverse behavior between closely related helicases? To travel over a long distance at slow speed, a helicase must remain bound to its NA substrate despite conformational changes occurring with every ATP hydrolysis cycle (Supplementary Figure 3A). In other words, a helicase with a short binding lifetime and a slow speed will only travel a few base pairs before falling off its substrate. Hence, to understand the differences between yUPF1 (UPF1 for simplicity hereafter) and IGHMBP2, we first compared their binding lifetime on a substrate. In bulk assays, both proteins bind NA in absence of ATP35,36, so we developed an ATP-free single-molecule binding assay (SMBA) to measure their residence time (τR) in a stationary state (Fig. 2a, b). In contrast to bulk assays, SMBA detects dissociation events and therefore measures the binding off rate. In each experiment, we injected the helicase in a buffer lacking ATP, then performed a series of cycles with 3-phases. During the first phase DNA hairpins are fully unzipped for 4 s at a force >15 pN, allowing random helicase binding to ssDNA (Fig. 2a, step 1). In the second phase, the force is reduced to 7 pN, and hairpins start refolding to their natural closed state, unless a helicase acts as a roadblock (Fig. 2a, step 2). While the force is held at 7 pN for 20–30 s, the closing hairpin fork constantly pushes on the bound helicase and challenges its binding. Thus, the helicase either remains on its substrate (Fig. 2a, step 3a) or is ejected (Fig. 2a, step 3b). A third phase is performed where force is reduced to 3 pN to verify complete hairpin closure. This force cycle is repeated multiple times over hundreds of seconds. During this test, single-UPF1 molecules attached and remained at their initial binding positions until recording was stopped, despite all opposing forces (n = 11) (Fig. 2c). UPF1 residence time was estimated to be larger than 5500 s (Supplementary Table 1). Under similar conditions, whether with or without its C-terminal domain, IGHMBP2 poorly resisted to the closing fork and was ejected after one or two cycles (Fig. 2d, Supplementary Figure 3B). IGHMBP2 residence times followed exponential distributions with a mean of 20 sec (no C-ter, n = 48) (Supplementary Figure 3C) or 60 s (with C-ter, n = 27). These results strongly suggested a tight link between residence time and unwinding processivity, which relies on the ability to remain bound to the NA substrate over multiple ATP hydrolysis cycles (Supplementary Figure 3A).
Structural features grant UPF1 a strong grip on substrates
The differences in residence time and processivity between UPF1 and IGHMPB2 helicases were intriguing, especially considering the structural similarities between their core domains. Lim et al.19 previously reported a superposition of IGHMPB2 and UPF1 structures, showing that both helicases share overall similar core motor domains (Supplementary Figure 4A, B). Hence, we looked for specific structural features likely impacting residence time and contributing to binding. Both UPF1 and IGHMBP2 are formed of two RecA-like domains designated as Rec1A and Rec2A. They also share distinctive protruding sub-domains 1B and 1C embedded within Rec1A, in contrast to SF1-A helicases such as Rep, UvrD, and PcrA, which have one protruding domain on each RecA contributing to processivity30. Both domains 1B and 1C could impact UPF1 and IGHMBP2 binding differently. Indeed, domain 1B shows different folding and movement upon RNA and/or nucleotide binding in each helicase, and deletion of domain 1C abolishes NA binding in UPF117,19,33. To evaluate their importance, we simultaneously swapped domains 1B and 1C between UPF1 and IGHMBP2 (UPF1/BC and IGHMPB2/BC) and investigated the resulting chimeric helicases. Remarkably, IGHMBP2/BC mimicked UPF1 behavior as its processivity markedly increased (>10 kb), along with its residence time (9540 s) during SMBA (Fig. 3a). In contrast, the swap negatively affected UPF1/BC residence time on DNA (930 s) and reduced its processivity (464 bp) (Fig. 3b), confirming the impact of these auxiliary domains on the residence time and unwinding processivity.
Interestingly, UPF1/BC also displays a singular binding property. As the force cycles proceeded during SMBA, UPF1/BC progressively slid along the hairpin from its initial binding position to a lower position (Fig. 3b). This sliding reflects a lower resistance to fork pressure and indicates a looser grip on DNA, which might account for the reduction in residence time. We further swapped the 1B or 1C domains, one at a time. IGHMBP2/B and IGHMBP2/C chimeras were insoluble or ATPase inactive, while UPF1 chimeras were active with reduced residence times and unwinding processivities (Supplementary Figure 4C–F; Supplementary Table 1). Taken together, these findings conclusively unravel a crucial role for protrusions 1B and 1C in regulating the binding and unwinding abilities of UPF1-like helicases.
As protrusions 1B and 1C are both attached to Rec1A and interact with the 3′-end of the NA substrates, we further looked in this area for key elements impacting helicase grip and inter-domain connection. We identified a small loop at the junction between domains 1A and 1C that undergoes conformational changes upon NA binding17,33 (Supplementary Figure 5A) and displays sequence variability between UPF1-like helicases (Supplementary Figure 5B). Additionally, in the UPF1 crystal structure, four amino acids (yUPF1 AKSR 484–487) contact NA at the loop level, whereas in the corresponding IGHMBP2 sequence (IGHMBP2, HPAR 267–270) only the arginine contacts NA19,33. To study the impact of this loop on UPF1 performance, we generated the following mutants: UPF1A484→H, UPF1K485→P, UPF1K485→A, UPF1S486→A, UPF1R487→S, and a triple mutant UPF1AKS→HPA. Only mutant UPF1S486→A behaved like wild-type UPF1. All other mutants suffered from a reduction in processivity and residence time in SMBA, and displayed a sliding rate that reflects a weaker grip on the substrate (Fig. 3c, d; Supplementary Figure 6A–F). Remarkably, all three parameters vary significantly among the different mutants, showing that small targeted mutations can result in profound behavioral diversity. However, the variation of these parameters was correlated: the mutants with the lower processivities also displayed faster sliding rates and shorter residence times. Altogether, these observations highlight the impact of UPF1 grip on its total residence time whether unwinding or just bound to its substrate.
A mechanistic model links helicase grip and processivity
Our study encompasses a large set of functional helicases presenting variable grips on their substrate as well as different binding lifetimes in the absence of ATP and during unwinding. This variety offers the opportunity to rationalize the link between helicase grips and the time they spend on NA. We thus propose a mechanistic model (detailed in the Supplementary Note) in which the helicase behaves as a molecular clip with three different states. In the ground state, the clip is strongly bound to its substrate, in the sliding state the clip is partially opened, and in the unbinding state, the clip is fully opened and falls off (Fig. 4a). To build our model, we measured several parameters gathered in Supplementary Table 1. Using SMBA, we measured for each helicase the average sliding time per nucleotide τS as a marker of grip tightness, and the total residence time τR in absence of ATP. τS and τR, respectively, represent the time necessary to shift from the ground state to the sliding state and to the unbinding state. Our data revealed a covariation of τS and τR (Supplementary Figure 7A). These times are set by an Arrhenius law37, and define how long it takes for thermal fluctuations to reach an energy level sufficient to either slide or fall-off. By fitting our molecular clip model, we calculated the binding energy difference each mutant requires to slide or fall in reference to the enzyme having the smallest energetic needs (UPF1AKS→HPA). We further plotted the values of the binding energy differences versus the corresponding τR and τS (Fig. 4b). Remarkably, τR and τS almost perfectly follow the model predictions (Fig. 4b) demonstrating that a small alteration in binding energy directly impacts helicase grip and residence time. Furthermore, while τR and τS widely vary among mutants, the ratio τR/τS is constant, indicating that the transition state to sliding or detaching is the same for all mutants. Similarly, we measured the unwinding time τU in presence of ATP. τU is the time each helicase spent unwinding before falling from its substrate. This time also showed a covariation with τR (Supplementary Figure 7B). Our model reveals that τU correlates with the binding energy (Fig. 4b), showing that the binding lifetime in presence of ATP also depends on the binding energy. Furthermore, τU is always smaller than τR (τR/τU is constant), indicating that helicases are more likely to fall-off during ATP hydrolysis. To test this hypothesis, we chose the moderately affected mutant UPF1R487→S and tested by SMBA the impact of ADPNP, a non-hydrolysable analog of ATP. Interestingly, the addition of ADPNP reduced the binding lifetime of this mutant and steepened its sliding slope (Supplementary Table 1). This result strongly suggests that during a power stroke, the binding energy is reduced due to conformational changes, and a smaller fluctuation is required to reach the opening threshold of detachment. Despite this fragile state, UPF1 manages to keep a tight grip on NA and avoids a detrimental fall while moving thanks to its large binding energy. In contrast, UPF1 mutants suffer from a looser grip and have a higher probability of falling, leading to their reduced processivity. Thus, our model demonstrates that aside from NA composition and fork pressure31,38, binding energy is a major parameter that determines helicase processivity.
Loss of UPF1 processivity reduces NMD efficiency
We wondered if the mechanistic conclusions described above were relevant for UPF1 function in vivo. As UPF1 is an essential NMD factor among all eukaryotes, we evaluated the necessity of its grip and processivity during this quality control pathway. Overexpression of yeast UPF1 C-terminal fragment (UPF1-C-ter) encompassing the helicase core was previously reported to partially restore NMD after deletion of the UPF1 gene39. We took advantage of our functional UPF1AKS→HPA mutant and designed wild-type and mutant UPF1 expression vectors under doxycycline repressible tetO7 promoter, which we used to transform S. cerevisiae upf1∆ strains. We first assessed UPF1 protein levels in wild-type and mutant strains to verify that the mutation does not alter the protein expression (Fig. 5a). We then assessed NMD efficiency in both contexts. To do so, we performed qPCRs on RNA extracts and quantified the expression level of DAL7, a natural transcript targeted by yeast NMD40. Overexpression of a wild-type UPF1-C-ter allowed recovery of a 30% efficient NMD in a yeast upf1Δ strain. This partial complementation effect was abolished when we used a mutant UPF1AKS→HPA version (Fig. 5b), suggesting that under limiting conditions, UPF1 tight binding and/or translocation processivity are required for NMD.
The human genome codes for more than 100 helicases implicated in multiple steps of both DNA and RNA metabolisms3,41. Each of them is involved in a specific pathway, and many are related to variable diseases, from cancers to developmental defects and neurodegenerative disorders42,43,44. Even though similarities in their helicase cores point towards a common ancestor, it has become evident that every helicase is unique and possesses structural elements leading to several layers of complexity.
UPF1-like helicases show a large functional diversity, with members involved in a variety of RNA regulation pathways. Their helicase core domains share a similar structural organization formed of two RecA-like domains and two extra domains protruding from the RecA domain 1A17,18,19,20,33,45 that are flanked by different and specific N-terminal and C-terminal accessory domains. One could imagine that helicase cores from the same subfamily have conserved comparable intrinsic properties. Unexpectedly, our study shows that UPF1 and IGHMBP2 cores present contrasting helicase activities. IGHMBP2 is not capable of unwinding on its own and requires assistance of its C-terminal domains to unwind dsDNA with a very low processivity estimated to 19 bp, in clear contrast with the processivity of UPF1 estimated to more than 10 kb. We questioned the role of protrusions 1B and 1C in this disparity as the deletion of domains 1C or 1B leads respectively to a loss of UPF1 NA binding, or to uncoupling between NA binding and ATP hydrolysis in vitro, both abolishing NMD in vivo17. By simultaneously swapping 1B and 1C domains between UPF1 and IGHMBP2, we reveal that these protruding domains most likely co-evolved to dictate the processivity of the helicase core to which they are attached. In the case of UPF1, domain 1B moves away from the RecA surface and towards 1C, possibly to form a circular channel for NA17,33. In the case of IGHMPB2, domain 1B is rather distorted and collapsed on bound NA19 potentially disturbing the unwinding mechanism. Structural data of both parental and chimera helicases bound to NA would be needed to precisely understand how domains 1B and 1C contribute to the formation of the clip around the NA substrate.
The impact of protruding domains on the helicase processivity has been previously observed for SF1-A helicases for which the interaction between the domains 1B and 2B that protrude from each RecA domain directly alters the movement of the helicase core1,30. Recent structures of several UPF1-like helicases put forward the variability of protruding domains between these related enzymes. The nuclease/helicase DNA2 presents a C-terminal domain highly resembling to IGHMBP2 helicase20. Sen1 presents a shorter protrusion 1C, called the prong, and a supplementary brace that restricts the movement of protrusion 1B18. In the splicing factor Aquarius/IBP160, a domain called the pointer replaces the protrusion 1C at the exact same position and is probably responsible for the reversed 3′–5′ polarity of this helicase45. Using comparable methods, it will be particularly interesting to explore the mechanical variety of these motors and the role of protruding domains.
Mechanistic insights into the remarkable processivity of UPF1 came from the study of a large series of mutants that gradually affect its grip tightness. In addition to protruding domains swapping, we targeted a flexible loop at the hinge between 1C and the RecA domain 1A. This loop drew our attention due to its position outside any conserved helicase motif, its contribution to NA binding, its divergence among UPF1-like helicases, and its conformational changes upon NA binding17,33. We assessed our mutants with a combination of two single-molecule assays: (i) an unwinding assay in the presence of ATP, to measure helicase processivity in distance and in time; and (ii) a binding assay in absence of ATP, to measure the residence time of the enzyme once bound to NA as well as its sliding speed against the opposing force of hairpin closure. The sliding phenomenon shows that the tested helicases are comparable to molecular binders with C-shaped spring clips that exist in three different states: a ground closed binding state with an initial binding energy, a partially opened sliding state and a fully opened unbinding state. For each enzyme, the transition from the ground state to the sliding or to the unbinding state follows an Arrhenius law since it depends on the energy fluctuation needed to alter the binding energy and open the clip: The stronger the initial grip, the higher is the energy fluctuation required to slide or fall, the more time is needed for the event to occur. In fact, the total residence time we measured for each of our enzymes is none-other than the time it takes for the clip to open sufficiently and fall, while the sliding time per base corresponds to smaller events where the clip opens just enough to slide by one base. For instance, wild-type UPF1 has a very tight grip on NA, and a very high binding energy in the ground state. Thus, a large energy fluctuation is required to lead to sliding or unbinding, and such events happen with an extremely low frequency.
Furthermore, in this clip model, two parameters govern binding to NA: the NA binding pocket constituted by a specific set of amino acids, and the inner stiffness of the clip, arising from the overall helicase structure. We suggest that the total binding energy (EBi) governing the clip state is the sum of the interaction energy (EInt) inside the cavity of the clip, and the mechanical energy (EM) stored in the spring of the clip when it is stretched. The differences in unbinding rates we recorded between the tested enzymes led us to calculate EBi differences between the mutants. Using these values, we tested two possible models to see which of the two energies EInt and EM is altered by the mutations. Our data well fit a model in which mutations negatively alter EInt and not EM (see Supplementary Note) suggesting that all UPF1 variants tested in this study have roughly the same spring stiffness conferred by the protein scaffold, but diverge in their binding interactions with NA inside the clip.
Our clip model also explains the impact of the grip on helicase processivity. During ATP hydrolysis, power strokes drive consecutive conformational changes to move forward, but weaken helicase binding. Less energy is therefore required to open the clip, making it easier to fall during translocation, especially for enzymes with a weaker grip.
Finally, previous modeling of helicase processivity has considered the impact of NA sequence31 and the destabilizing effect of the NA fork pushing the helicase38, but no attempt has been made so far to look at helicase binding lifetime and its impact on processivity. Our model demonstrates that a helicase grip dictates its binding lifetime, which in turn limits its processivity. Remarkably, both our data and our model reveal that a single-residue mutation outside the conserved helicase motifs, that slightly reduces the binding energy of the helicase, is sufficient to drastically reduce its processivity. Lastly, we previously showed that UPF1 is an efficient NA–protein interaction remodeler that can notably melt biotin–streptavidin interaction27. We expect that the strong grip of UPF1 is probably necessary to displace stable NA-binding proteins.
The notion of helicase processivity is intuitively associated to the distance traveled by the enzyme. Progression over long distances is clearly essential for processes like genome replication for which important portions of dsDNA must be unwound to allow duplication. Such events also involve fast helicases as replication is under time constraint to be achieved before cell division. In contrast, in multiple cases, DNA and RNA helicases only need to translocate over short distances to unwind short dsNA regions, to move over a short distance or to remodel proximal NA–protein interactions. Does this imply that most helicases are not processive? Here, the thorough study of UPF1 helicase core attributes revealed that its processivity coincides with the enzyme ability to remain bound to its substrate for long periods of time without detaching. We assume that the residence time of a helicase onto NA is an important parameter for its function, notably to offer a time window long enough to guarantee process completion. The process of NMD requires several successive steps including translation-dependent recognition of a premature termination codon, ribosome dissociation, mRNP remodeling, and recruitment of RNA decay factors25. In addition to the observation that ATP-dependent activities of UPF1 are essential for NMD, several evidences showed that UPF1 is involved in every successive step of NMD25,46,47. So, it has been proposed that ATP-dependent activities of UPF1 orchestrate the conformational and compositional transitions between PTC recognition and mRNA decay25,48,49. Here, the observation that UPF1 altered grip reduces NMD efficiency in yeast also argues for the notion that the residence time of UPF1 onto its substrate is an important parameter for NMD completion. The importance of UPF1 processivity is further supported by the observation that during HTLV infection in human cells, the viral protein Tax directly targets UPF1 translocation and reduces its processivity to decrease NMD efficiency50. Some helicases, like the SF2 RNA helicase eIF4A3, are deposited onto NA to form a stable and sequence-independent clamp without necessity to use ATPase activities51,52. In the case of UPF1, we suggest that it combines its tight grip and its ability to translocate both to serve as a binding platform for NMD factors and to remodel RNA–proteins complexes. Future investigations will be necessary to determine the precise site of action of UPF1 during NMD and whether NMD partners modulate its residence time and its processivity. Exploration of the biophysical attributes of closely related UPF1-like helicases will be necessary to better understand their action in vivo and the consequences of their mutations linked to several human disorders13,14,53.
cDNA cloning and protein purification
We produced helicase domains of Homo sapiens UPF1 (295-914), Saccharomyces cerevisiae UPF1 (221–851) and Homo Sapiens IGHMPB2 (1–652), as well as the full-length form of IGHMPB2 (1–993, IGHMPB2-FL) (Uniprot accession codes Q92900-2, P30771, and P38935, respectively). Boundaries were defined according to previous structural studies17,19,33. IGHMPB2, IGHMPB2-FL, and yeast UPF1 coding sequences were PCR amplified using oligos HLH 2696/2697, HLH 2696/2698, and HLH 2705/2706, respectively. Purified PCR fragments were inserted in a home-made variant of pET28a plasmid pHL5 (Novagen) between NdeI/NotI (IGHMPB2) and NheI/XhoI (yUPF1) restriction sites. To generate UPF1 mutants, we modified the wild-type coding sequence of plasmid pHL 1281 (yeast UPF1 helicase domain) through PCRs followed by ligation reactions using amplification oligos carrying the corresponding mutations at the targeted sites. Chimeric forms of UPF1 and IGHMPB2 were engineered using Gibson cloning strategy. Required fragments were amplified from yUPF1 (pHL 1281) and IGHMPB2 (pHL 1278). Domain frontiers selected for the swaps are indicated in Supplementary Figure 8A. After amplification and purification, the fragments were ligated through Gibson reactions. All recombinant proteins were fused to a CBP-tag at their N terminus and a hexa-histidine tag at their C terminus, and expressed using Escherichia coli BL21 competent strains (DE3) grown in LB medium and induced overnight at 16°C. Cells were harvested and lysed in buffer A [1.5× PBS pH 7.5, 225 mM NaCl, 1 mM magnesium acetate, 0.1% (w/v) NP-40, 20 mM imidazole, 10% (w/v) glycerol] Supplemented with 100 mg ml−1 of egg white lysozyme (Sigma-Aldrich) and 1× protease inhibitor cocktail EDTA-Free (Sigma-Aldrich). Proteins were first purified on Nickel columns (Ni-NTA, Qiagen) and further purified on a calmodulin affinity column. Collected proteins were dialyzed against 1.5× PBS, 10% (w/v) glycerol, 1 mM magnesium diacetate and 2 mM DTT, then stored at −80 °C.
ATP hydrolysis assays
ATP hydrolysis was performed in steady-state conditions. Proteins (10 pmol) were incubated at 30 °C in a 20 µl reaction mixture containing 1× ATPase buffer [20 mM MES pH 6.0, 100 mM potassium acetate, 1 mM DTT, 0.1 mM EDTA, 1 mM magnesium acetate, 1 mM zinc sulfate, and 5% (v/v) glycerol], 2 µCi of [γ32P]-ATP (3000 Ci/mmol, Perkin Elmer), 25 µM ATP and 50 µM polyC (concentration of binding sites). Reaction aliquots (2 µl) were withdrawn at various times and quenched with a buffer (5 µl) containing 10 mM EDTA and 0.5% (v/v) SDS. Samples were separated using thin layer chromatography on polyethyleneimine cellulose plates (Merck) with a 0.35 M potassium phosphate (pH 7.5) solvent, then analyzed using a Typhoon Phosphorimaging system. Quantification was performed using Fiji/ImageJ analysis package.
Mutant UPF1 yeast expression vectors
UPF1 wild-type and the mutant UPF1AKS→HPA variant expressions in yeast were done with plasmids based on pCM189-NTAP a single copy vector derived from pCM189 with a doxycycline repressible tetO7 promoter and an N-terminal TAP tag, an intermediate in the construction of pTG189. We amplified the 208–971 region of UPF1 coding sequence with oligonucleotides CS1362 (TTAAGAAAATCTCATCCTCCGGGGCACTTGATGCGAATAAAGACGCTACAATTAATGATATTGACG) and CS1364 (ATAACTAATTACATGATGCGGCCCTCCTGCAGGGCTTATATTCCCAAATTGCTGAAGTC), having 35 nucleotides extremities identical with regions in the destination vector. NotI digested pCM189-TAP was used in a hot-fusion in vitro version of Gibson assembly followed by direct transformation in E. coli. To generate the AKS484–486HPA mutant, three partially overlapping PCR fragments were obtained on the UPF1 plasmid template and on pHL1376. All the constructs were verified by Sanger sequencing. The plasmids were transformed in yeast wild-type and LMA1667 (upf1∆) for RNA quantitation and immunoblotting.
Yeast RNA quantitation
Total RNA was extracted from cells grown to mid-exponential phase in rich medium (YPD, yeast extract, peptone, glucose) using the hot acid phenol protocol. DNAse-treated samples of equal total RNA amounts were reverse transcribed using specific oligonucleotides (CS888—CTCAGTTTGCGATGGAAGAG, CS1430—TCCCAACGACCACAGTTCAAACC and CS1077—AACCGTCGTCTCTCTCGAAG). Q-PCR estimation of initial RNA amounts were done on eightfold dilutions of the RT reaction using oligonucleotides CS1429 (TGAAACTTTGCCAGCGGCCTTC)/CS1430 (DAL7) and CS1076 (GTTAGAAAAGGCGCTTTGGTATATG)/CS1077 (RIM1). We used the amount of RIM1 mRNA for normalization and used differences in Ct to estimate RNA fold change in comparison with the wild-type strain, as reference. Each experiment was performed at least three times.
Protein extracts were obtained by boiling equal numbers of mid-exponential growth cells in denaturing electrophoresis sample buffer. Two-fold dilutions of protein extracts were separated on 4–12% polyacrylamide gels (Novex NuPAGE MOPS running buffer, Life Technologies). The proteins were transferred by electroblotting on nitrocellulose membranes and probed with PAP (peroxidase-anti-peroxidase antibodies, Sigma P1291, 1:2000), followed by a control test with polyclonal anti-Zwf1 (glucose-6-phosphate dehydrogenase) antibodies (Sigma A9521, 1:20,000). Peroxidase activity was monitored with the Clarity Western ECL chemiluminescence kit (Bio-Rad) and pictured on a Bio-Rad GelDoc imaging system. Image processing was performed with FIJI/ImageJ and consisted in contrast adjustment. Uncropped blots are presented in Supplementary Figure 8B.
Single-molecule data acquisition
Camera images were used to collect the raw data of DNA extension. Raw data represented the real-time evolution of the DNA extension in nm, which was converted into the number of base pairs unzipped by helicases using a calibration factor determined from the elastic properties of ssDNA (Supplementary Figure 8C). Instantaneous unwinding and translocation rates were obtained from a linear fit to the traces filtered with a least square method over a time window define by the user mouse. The histograms of the instantaneous rates were fit to Gaussian functions when applicable. The error bars shown in the histograms are proportional to the inverse of the square root of the number of points for each individual bin.
Experiment with magnetic tweezers
The substrate used in single-molecule assays is a 1239 bp long DNA hairpin that has a 76-nt 5′-biotinylated ssDNA tail and a 146 bp 3′-digoxigenin-labeled dsDNA tail27,34. The biotinylated end of the hairpin is attached to a streptavidin coated paramagnetic bead while the digoxigenin end is attached to the surface of a flow cell via anti-digoxigenin. We used a picotwist magnetic tweezers to manipulate the DNA substrate. A tunable force can be applied to the substrate by applying a magnetic field on the paramagnetic bead via a pair of permanent magnets. Force applied on the hairpin can be precisely controlled by changing the position of the magnet over the substrate. DNA extension was measured in nanometers in real time via a 31 Hz video-camera (CM-140 GE Jai) and then converted to base pairs by exploiting the elastic properties of ssDNA. All the measurements were conducted at 30 °C, unless mentioned otherwise. The working buffer had a composition of 20 mM Tris-HCl, 75 mM potassium acetate, 3 mM magnesium chloride, 1% BSA, 1 mM DTT, and 2 mM ATP. The concentration of helicase used was the lowest possible to observe single-molecule events and varied between 1 and 20 nM.
Single-molecule binding assays (SMBA)
Binding of proteins to DNA in single-molecule configuration was measured in the working buffer in absence of ATP, using cycles of hairpin openings and closings. Briefly, after helicase injection in a helicase buffer free of ATP, a cyclic variation of force is executed. Starting from low force where the hairpin is closed, the force is first increased for 1 s to the test force = 7 pN, to check that the hairpin is in the closed state then the force is increased to >15 pN for 3 to 4 s (Fig. 2, step 1) then reduced to 7 pN and held for 20 to 30 s (Fig. 2, step 2). The force is finally reduced below 3 pN (Fig. 2, step 3). The whole process is repeated several times to form a cyclic assay. The 3 pN regime closes the hairpin in most cases, this offers the possibility to check that the hairpin does open and close at each cycle. Multiple openings and closings of the hairpins provide various instances for proteins to bind with most of the available substrates. Helicase concentration used is the lowest possible to observe single-binding events and varied between 1 and 20 nM.
Single-molecule data analysis
For unwinding processivity, large processivity was determined by taking into account only those traces where helicase starts unwinding the hairpin in fully closed state until it falls off. This leads to a histogram with a few points corresponding to excursion shorter than the hairpin length and a last bin of this precise length with many events (Supplementary Figure 2C). This truncated histogram was fitted to a truncated exponential providing a processivisity value usually larger than the hairpin length. For moderately processive helicase, the histogram of the length of unwound events was calculated. These histograms were exponential in nature, which gave the mean processivity of the helicase on fitting them. The errors in histograms are given by the square root of the number of events in each bin. For residence time measurement in ATP-free SMBA, binding time was obtained by measuring the inverse of the falling rate. That is by summing the time over which the fork remained blocked by the helicase and dividing it over the number of real unbinding events that we have recorded. As the binding time is often long, the experiment’s recording was often stopped before the binding event finished. Such event contributes to the total binding time but not to the number of unbinding events. The relative error on the binding time is computed as the NU−1/2.
The data that support the findings of this study are available from the corresponding authors upon reasonable request. Single-molecule data supporting the findings of this study are available at http://pimprenelle.lps.ens.fr/Magnetic_tweezers_graphs_Kanaan.zip (2.2 Go). Data analysis software (PlayItAgainSam) can be downloaded at (http://www.picotwist.com/download/Pias_setup.exe). Figures 1b, c, 2c, d and 3a–d in the main text have associated raw data. Supplementary Figures 2a, d, 3a, 4a–f, 6a–f, 7a, b and 8c have associated raw data.
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We thank E. Conti and B. Séraphin for plasmids, I. Barbosa and M.H. Pontier for experimental help, F. Fiorini for scientific advice, O. Bensaude, A. Jacquier, N. Leulliot and D. Bensimon for reading the manuscript, and members of our labs for discussion. This study was supported by the ANR CLEANMD grant (ANR-14-CE10-0014) from the French Agence Nationale de la Recherche to C.S., V.C., and H.L.H., by the program « Investissements d’Avenir » launched by the French Government and implemented by ANR (ANR–10–LABX-54 MEMOLIFE and ANR–10–IDEX–0001–02 PSL* Research University) to J.K. and H.L.H., by the European Research Council grant Magreps [267 862] to V.C. and S.R., by the Fondation ARC pour la recherche sur le cancer PhD fellowship to J.K., and by continuous financial support from the Centre National de Recherche Scientifique, the Ecole Normale Supérieure and the Institut National de la Santé et de la Recherche Médicale, France.
V.C. is the cofounder of PicoTwist. All the remaining authors declare no competing interests.
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Kanaan, J., Raj, S., Decourty, L. et al. UPF1-like helicase grip on nucleic acids dictates processivity. Nat Commun 9, 3752 (2018). https://doi.org/10.1038/s41467-018-06313-y
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