AAA-ATPases fulfil essential roles in different cellular pathways and often act in form of hexameric complexes. Interaction with pathway-specific substrate and adaptor proteins recruits them to their targets and modulates their catalytic activity. This substrate dependent regulation of ATP hydrolysis in the AAA-domains is mediated by a non-catalytic N-terminal domain. The exact mechanisms that transmit the signal from the N-domain and coordinate the individual AAA-domains in the hexameric complex are still the topic of intensive research. Here, we present the characterization of a novel mutant variant of the eukaryotic AAA-ATPase Drg1 that shows dysregulation of ATPase activity and altered interaction with Rlp24, its substrate in ribosome biogenesis. This defective regulation is the consequence of amino acid exchanges at the interface between the regulatory N-domain and the adjacent D1 AAA-domain. The effects caused by these mutations strongly resemble those of pathological mutations of the AAA-ATPase p97 which cause the hereditary proteinopathy IBMPFD (inclusion body myopathy associated with Paget’s disease of the bone and frontotemporal dementia). Our results therefore suggest well conserved mechanisms of regulation between structurally, but not functionally related members of the AAA-family.
The protein family of AAA-ATPases (ATPases associated with a variety of cellular activities) achieves functional diversity by a shared core mechanism combined with pathway-specific adaptors1,2,3. Coordinated ATP hydrolysis in oligomeric complexes enables them to fulfil difficile cellular functions by unfolding of proteins and remodelling of protein complexes. Most AAA-ATPases form barrel-shaped hexameric rings, where each monomer consists of either one (type I) or two (type II) functional ATPase domains (named D1 and D2) accompanied by a regulatory N-terminal domain. The twelve ATPase domains present in a type II AAA-protein are arranged as two superimposed rings that can perform a rotary movement relative to each other4,5,6. To convert this motion into a vectored mechanical force required for substrate remodelling, it is crucial that the single domains act in a coordinated manner. The mechanisms that synchronize the individual sites are still under investigation and belong to the most discussed topics in the field7.
Well-studied models like the yeast ribosome biogenesis factor Drg1 or the multifunctional mammalian protein p97 have provided deep insights into the mechanisms of inter- and intramolecular synchronization of ATP binding and hydrolysis7,8,9. A central role in the regulation of activity can be assigned to the non-catalytic N-terminal domain that acts as connecting link between the enzymatic machinery and the target protein or protein-complex10,11. High resolution cryo-EM and crystal structures of p97 revealed that the position of the N-domain strongly depends on the nucleotide-binding states of the AAA-modules5,12,13,14,15; reviewed in7. In the ADP-bound state, the N-domain is found in the “down”-position co-planar to the D1 ring. In contrast, in the presence of the ATP-analogue ATPγS, the N-domain can adopt the “up”-conformation elevated above the D1 ring12,14,16. This conformational change was suggested to be a main regulatory switch for the ATPase activity of p97.
The N-domain of p97 mediates the direct physical interactions with the majority of co-factors and adaptor proteins that recruit the enzyme to the target pathways7,10,17. Adaptor-binding to the N-domain can either stimulate or inhibit the ATPase activity of p97 as exemplified by the adaptor proteins p37 and p47, respectively18. Beyond that, short linker segments between the individual domains serve as routes for the inter-domain signal transmission14,19. All these data indicate that the correct arrangement of the N-D1 segment (including the N-D1 linker) is crucial for regulation and intramolecular signal transmission in p97. This is further affirmed by the location of mutations in the p97 gene that cause the complex hereditary proteinopathy IBMPFD (inclusion body myopathy associated with Paget’s disease of the bone and frontotemporal dementia20,21,22) which is also being referred to as MSP1 (multisystem proteinopathy type 123). These mutations cause amino acid substitutions at the N-D1 interface of the protein and affect the nucleotide-dependent positioning of the N-domain and the interaction with specific adaptor proteins13,14. Most p97 IBMPFD variants also exhibit increased basal (unstimulated) ATPase activity and for three of them (A232E, L198W, R155H) it was already shown that they additionally fail to be stimulated by the adaptor protein p3711,13,18,24. Structural characterization of pathological p97-IBMPFD variants revealed that these single amino acid exchanges at the N-D1 interface can also cause rearrangements of the distal C-terminal D2 AAA-domain and increase its hydrolytic activity24,25. This further strengthens the model of a regulatory link between the N-domain and both AAA-domains. The exact molecular basis of the detrimental effects caused by p97-IBMPFD mutations, however, is still a matter of debate. Recent NMR experiments with the p97 N-D1 fragment suggest that the position of the N-domain is in a dynamic, nucleotide-dependent equilibrium between the up- (ATP-dependent) and down-position (ADP-dependent)26. In IBMPFD variants this equilibrium is shifted towards the up-position.
Drg1 (Diazaborine resistance gene 1) is an essential type II AAA-ATPase in the yeast Saccharomyces cerevisiae and is highly related to mammalian p97 and its yeast orthologue Cdc4827. In previous works we have characterized Drg1 as a key player of eukaryotic ribosome biogenesis that initiates the final maturation of the large ribosomal 60S-subunit in the cytoplasm8,28,29. Drg1 binds to the C-terminal extension of the ribosome biogenesis factor Rlp24 (Ribosomal-like protein 24) and releases this shuttling protein from pre-60S particles shortly after their export from the nucleus8. This release is an essential prerequisite for all downstream maturation steps and therefore a crucial event in the highly regulated ribosome biogenesis pathway. Consequently, inactivation of Drg1 results in a failure to release and recycle Rlp24 as well as other shuttling proteins and export factors, also causing a block in early ribosome biogenesis steps28. The C-terminal extension of Rlp24 is not only responsible for the recruitment of Drg1 but also stimulates ATP hydrolysis in both AAA-domains8. The D2 domain is thereby essential for the energy dependent release of Rlp24 from the pre-ribosomal particle whereas the D1 domain modulates hexamerization and the interaction with Rlp24.
The AAA-domains of Drg1 and p97 show an amino acid sequence identity of about 50%, while the N-domains exhibit a significantly smaller degree of sequence conservation (Fig. S1). Nevertheless, fold recognition and secondary structure prediction indicate that the general architecture of the N-domain including the N-D1 interface are well conserved. In this study, we present novel mutations in the N-domain of Drg1 that cause a disturbed regulation of ATPase activity and altered nucleotide-dependent interaction with the substrate protein Rlp24. Concerning positioning within the protein and effects on basal and co-factor stimulated ATPase activity, these substitutions strikingly resemble the IBMPFD variants of p97. These findings suggest that exchanges at the N-D1 domain interface affect general properties of AAA-ATPases and indicate that the regulatory interplay between the N-domain and the two catalytic domains is shared by functionally unrelated members of this protein family.
Mutations in the N-domain of DRG1 cause a dominant negative growth phenotype
Random mutagenesis of DRG1 and screening for mutations conferring temperature-sensitive growth phenotypes resulted in isolation of the novel drg1-21 allele. This allele contains two point mutations causing two amino acid exchanges in the N-domain of Drg1; an exchange of threonine 100 for isoleucine (T100I) and of leucine 108 for proline (L108P), which together cause a pronounced growth defect at 37 °C (Fig. 1a,b). Individual analyses of these two substitutions showed that the L108P exchange was mainly responsible for the failure to grow at elevated temperature (Fig. 1b). In addition the L108P mutant showed a slight dominant negative growth defect upon overexpression from the copper inducible CUP1 promoter in wildtype background (Fig. 1c). However, the full growth defect at 37 °C and a strong dominant negative effect were only observed when both exchanges were present, pointing at a synthetic enhancement of these two mutations. Interestingly, we found a similar dominant negative effect by overexpression of a Drg1 variant with inhibited ATP hydrolysis in the D2 AAA-domain (E617Q, designated Drg1-EQ2) but not for D1 (E346Q, designated Drg1-EQ1) as shown in Fig. 1d. In addition, the growth defect caused by the drg1-21 allele was enhanced in combination with the EQ2 exchange, but not when combined with the EQ1 mutation. This is obvious on the SD-ura plate lacking copper where the CUP1 promoter shows only low activity, but strong growth inhibition is observed for the allele containing the two drg1-21 exchanges (T100I/L108P) in combination with the EQ2 exchange (Fig. 1d). This enhancement shows that the combination of both defects is extremely toxic for the cell indicating an intricate connection between the N-domain and the D2 domain of Drg1.
Drg1-21 inhibits maturation of pre-60S particles
In order to assess the physiological implications of the exchanges leading to temperature sensitivity of the drg1-21 allele we investigated binding of Drg1-21 to pre-ribosomal particles. For this purpose, we performed Tandem Affinity Purifications (TAP) using the shuttling pre-60S maturation factor Arx1 as bait protein (Fig. 2a). As controls, strains expressing either wildtype Drg1 or the temperature-sensitive Drg1-18 variant were used. Analysis of the protein composition of the purified Arx1-TAP particles revealed that Drg1-21 fails to stably associate with the pre-60S particle, just as we showed previously for the Drg1-18 protein8. As a consequence, shuttling proteins (exemplified by Nog1 and Rlp24) and export factors (Mex67 and Mtr2) accumulated on the pre-60S particles, while late joining proteins (Sqt1 and Rpl10) showed reduced levels. These findings are in line with results obtained with the Drg1-18 protein and suggest loss of function of Drg1-21. However, in contrast to drg1-18, which is recessive, drg1-21 shows a dominant negative behaviour which is not easy to reconcile with a failure of the protein to bind to the pre-ribosome substrate. We therefore also purified pre-60S particles from a wildtype strain overexpressing the Drg1-21 protein. As shown in Fig. 2b, lower amounts of GST-Drg1-21 were recovered with the Arx1-TAP particles compared to overexpressed wildtype GST-Drg1 suggesting that it binds less efficiently or is lost more rapidly during purification. Nevertheless, more GST-Drg1-21 was present on the Arx1-TAP particles (lane 2) than wildtype Drg1 in the non-overexpressing strain (vector control). Moreover, the untagged wildtype copy of Drg1 was not detected in the purification of wildtype GST-Drg1 (lane 1) or GST-Drg1-21 (lane 2) overexpressing strains. This indicates that both, GST-Drg1 and GST-Drg1-21 are capable of competing with untagged wildtype Drg1 for binding. However, albeit the high levels of Drg1-21 on the Arx1-TAP particle compared to the vector control, shuttling proteins (as exemplified by Nog1) and export factors (as exemplified by Mex67) accumulated on the pre-60S particles of the Drg1-21 overexpressing strain. The accumulation of pre-60S factors suggests a defect in substrate release and shows that Drg1-21, even when it binds to the pre-60S particle, is unable to perform its function, which likely explains the dominant negative behaviour.
The Drg1-21 variant shows a dysregulated ATPase activity
Since the Drg1-21 protein, despite binding to the pre-60S particle, was unable to perform the release of shuttling proteins, we examined whether the two exchanges in the N-domain affect the ATPase activity of Drg1-21 (Fig. 3). In addition, we analysed the effects of the single exchanges. Our previous studies showed that the ATPase activity of both domains of Drg1 is stimulated by the C-terminal fragment of the substrate protein Rlp24 (Rlp24C)8. Therefore we also determined the stimulated ATPase activity in the presence of Rlp24C. Notably, the basal activity of the Drg1-21 variant was increased 5-fold compared to wildtype Drg1 (Fig. 3a). This elevated basal ATPase activity of Drg1-21, however, was not further stimulated by Rlp24C. Examination of the proteins containing the single exchanges demonstrated that both showed basal ATPase activity on wildtype level. While Drg1-T100I was stimulated by Rlp24C, Drg1-L108P showed no increase in ATP hydrolysis in the presence of the substrate. Interestingly, we found that the addition of ADP during the purification procedure significantly increased the yield of otherwise badly purifying Drg1-21 and Drg1-L108P, but decreased the yield of wildtype Drg1 and Drg1-T100I. This prompted us to analyse the ATPase activity of proteins purified in the presence of ADP (Fig. 3b). Under these conditions the Drg1-T100I variant exhibited increased basal activity like Drg1-21, whereas Drg1-L108P showed the same basal activity as the wildtype protein (Fig. 3b). This indicated that the T100I exchange is responsible for the elevated basal activity of Drg1-21 and that this effect is ADP dependent. Interestingly, the failure of Drg1-L108P to be stimulated by Rlp24C was not observed when the protein was purified in the presence of ADP. This is in sharp contrast to Drg1-21 that exhibited elevated basal activity and a failure to be stimulated under both purification conditions (Fig. 3a,b). Taken together these results suggest that the two exchanges in Drg1-21 exhibit a synergistic behaviour which is modulated by ADP.
Drg1-21 fails to dissociate from the substrate protein Rlp24
In order to examine whether the dysregulation of the ATPase activity of Drg1-21 is the result of an altered interaction with the substrate protein Rlp24, we performed in vitro binding experiments using Surface Plasmon Resonance (SPR). We immobilized GST-Rlp24C and injected purified Drg1 variants to analyse their interaction properties with the substrate. We demonstrated previously that Drg1 requires the presence of nucleotides to form hexamers and that only the hexameric form of the protein is able to interact with Rlp24C8. Consequently, during the dissociation phase in Surface Plasmon Resonance, Drg1 detached from Rlp24C rapidly in the absence of ATP, but dissociated more slowly when ATP was constantly present8. Interestingly, binding to Rlp24C was much stronger when Drg1 was pre-incubated with ATP than with ADP (Fig. 4a). Therefore, 1 mM ATP was added to the Drg1 preparations five minutes prior to injection as well as to the running buffer.
Interestingly, the wildtype protein purified in the presence of ADP showed lower response units than the protein purified in the absence of nucleotide (compare Fig. 4b,c, note the different scales). Since the protein was pre-incubated with ATP in both cases, this finding suggests that ADP was stably bound to one of the two ATPase domains and could be less efficiently displaced by ATP. The importance of nucleotide binding for the interaction with Rlp24C prompted us to investigate the contribution of the two domains. To dissect the individual sites we tested Drg1 variants containing K292A (KA1) and K563A (KA2) exchanges in the Walker A motifs of each ATPase site. These exchanges are known to prevent nucleotide binding in the respective domains, allowing selective examination of the binding properties of the non-mutated domain. As shown in Fig. S2, the Drg1-KA1 protein did not interact with Rlp24C, while Drg1-KA2 was still able to bind to Rlp24C but dissociated more rapidly from the substrate compared to wildtype. This finding suggests that ATP binding into D1 is essential for substrate recognition and loading of D2 with ATP is required to provide stable association. Measurement of ATP binding to these KA mutants using differential scanning fluorimetry (DSF) suggests a Kd(ATP) of about 20 μM for the D1 domain and about 80 μM for the D2 domain (Fig. S3). These values are in good agreement with earlier estimates obtained by radioactive nucleotide binding studies with wildtype Drg127. With respect to ADP binding we measured a Kd(ADP) of about 120 μM for the D1 domain, while binding to D2 was below the detection limits of our experimental setup. Together with our previous finding that blockage of ATP hydrolysis in D1 results in more stable interaction with the substrate8, these results suggest that the D1 domain is the main determining factor for substrate interaction. Therefore we speculate that ADP is stably bound to D1 during purification and cannot easily be displaced by ATP added during the pre-incubation and the association phase of the SPR experiments. However, since nucleotide loading of D2 is required for stable interaction (Fig. S2), we cannot exclude that ADP binding into this domain also modulates substrate interaction.
The different behaviour of the Drg1-21, Drg1-T100I and Drg1-L108P variants in respect to stimulation of ATPase activity depending on purification in the presence or absence of ADP prompted us to investigate each protein for binding to Rlp24C under both conditions. The Drg1-L108P protein purified in the absence of nucleotide did not interact with Rlp24C, while it showed interaction when purified in the presence of ADP (compare Fig. 4b,c). The inability to interact with the substrate protein explains the failure of Drg1-L108P purified in the absence of ADP to be stimulated for ATP hydrolysis (Fig. 3a). The Rlp24C binding characteristics of Drg1-T100I were similar to those of the wildtype protein (Fig. S4). These results indicate that the L108P exchange is the major determinant for the altered interaction of Drg1-21 with Rlp24C.
Drg1-21 showed similar binding to Rlp24C under both conditions and this binding was comparable to the binding of the other Drg1 variants purified in the presence of ADP (Fig. 4b,c). However, in contrast to the other proteins, Drg1-21 failed to be released from Rlp24C during the dissociation phase. Together our findings demonstrate a synergistic effect of the T100I and L108P exchanges also with respect to substrate interaction.
An intragenic suppressor mutation partially restores the regulation of ATPase activity of Drg1-21
In order to understand the molecular mechanisms causing the failure in activation of the Drg1-21 protein by the substrate Rlp24C we screened for suppressor mutants restoring growth at 37 °C. After PCR mutagenesis of the drg1-21 allele, we isolated 28 mutants that permitted growth at the restrictive temperature. 12 of these mutants contained reversions of at least one of the two original mutations of the drg1-21 allele. 15 additional mutants contained codon changes leading to other amino acids instead of either I100 or P108. We identified four substitutions for lysine codons in position 100. In position 108 we found four exchanges for threonine, six for serine and one for alanine. Finally, we isolated one mutant that still contained the original exchanges (T100I and L108P) but was able to grow at 37 °C (Fig. 5a,b). This mutant carried an additional mutation leading to an N77K exchange in the N-domain and was designated drg1-21sup. To investigate whether the restoration of growth is due to a recovery of the stimulatability in this mutant we purified the Drg1-21sup protein and analysed its basal ATPase activity and its stimulation by Rlp24C (Fig. 5c). As a control we included the Drg1-N77K variant that carries the N77K exchange alone (without the T100I/L108P exchanges). Notably, when purified in the absence of ADP, Drg1-21sup could not be stimulated by Rlp24C and showed elevated basal activity, which closely reflects the situation with Drg1-21. However, both proteins, Drg1-21sup and the Drg1-N77K variant, showed similar basal activity as the wildtype protein and were stimulated by Rlp24C when purified in the presence of ADP. Although Drg1-21sup did not reach the full wildtype activity in the presence of Rlp24C, the regulation was partially restored.
The defects of Drg1-21 are caused by exchanges at the N-D1 interface
Structural investigations of p97 showed that the protein can adopt different conformations depending on the nucleotide-binding state of the ATPase domains7. In the presence of ADP the N-domain is positioned coplanar with the D1 ring (down-position), while in the presence of ATPγS it is found elevated above the D1 ring (up-position)12. These positions are supposed to be in a dynamic, nucleotide-dependent equilibrium26. Structural investigations of the pathogenic IBMPFD mutants showed that they preferentially adopt the up-position even in the ADP-bound state and shift the equilibrium to the elevated position13,26. To investigate the structural impact of the Drg1-21 mutations, we analysed our previously built homology model of Drg129 as well as five newly built models based on the recently released high resolution cryo-EM structures of human p9712. While the alignment in the D1 and D2 domains is highly confident with about 50% sequence identity (Fig. S1), the N-domains of Drg1 and p97 have diverged considerably, making homology-based conclusions more difficult. Nevertheless, we found a 23-residue stretch in the N-domain (Drg1 residues I95 to K117) where the alignment is securely anchored based on several conserved residues including the triplet ‘LGD’ and a perfect match of predicted and actual secondary structure in p97 (Fig. S1). To further validate our predictions we compared several N-domain models based on different template structures (including high resolution cryo-EM structures of p97 and more distantly related templates). Comparison of these models suggests that the general architecture of the N-domains of these proteins is well conserved (Fig. S5). Compared to p97, the N-domain of Drg1 contains an N-terminal extension of 28 residues and an insertion from residue 136 to 156 for Drg1 (Fig. S1). Nevertheless, all models based on p97 structures with the N-domain in the down-position predicted positioning of T100I and L108P at the N-D1 domain interface (Fig. S5; Fig. 6a,b).
Remarkably, the location of these residues resembles the positions of exchanges in p97 leading to the hereditary disease IBMPFD/MSP1, which also cluster at the contact area between these two domains (Fig. 6c,d). Our models predict that threonine 100 of Drg1, which is changed to isoleucine in the drg1-21 mutant, faces towards the N-D1 linker. This linker is thought to play an important role in signal transduction from the N- to the D1 domain14,19. Moreover, in a superposition of the Drg1 model and the p97 structure, shown in Fig. 6e, T100 matches with arginine 86 of p97, which is known to cause IBMPFD-like features when mutated to alanine14. The exchange of leucine 108 for proline seems to be the major determinant for the temperature sensitivity and growth phenotype of drg1-21. In the superposition it is located between two p97 residues, arginines 93 and 95, for which IBMPFD/MSP1 exchanges were reported30. This further strengthens the hypothesis that the drg1-21 mutations resemble those pathological exchanges in p97.
According to our Drg1 structural model, the N77K exchange, which suppresses the temperature sensitive growth phenotype of the drg1-21 allele, is located at the surface-exposed side of the N-domain in the down-position. As a consequence of the structural change of the N-domain from the down- to up-position, however, N77 is relocated towards the D1 domain (Fig. S6). The insertion of the larger lysine residue in this position instead of the smaller asparagine might lead to structural changes at the N-D1 interface which are likely connected to the suppression mechanism.
Drg1 and p97 (or its yeast orthologue Cdc48) act in physiologically unrelated pathways. While Drg1 is specific for one distinct pre-ribosomal maturation step, p97 acts in a variety of cellular pathways by means of different adaptor proteins7,31,32. Nevertheless, our data suggest that both proteins use conserved mechanisms for the regulation of ATPase activity.
This idea became obvious by comparing both, structural and functional features of the IBMPFD variants of p97 on the one hand and the Drg1-21 variant on the other hand. These include positioning of the exchanges at the N-D1 interface30, elevated basal ATPase activity13,18,25, changes in adaptor protein/substrate binding13,33 and a dominant negative phenotype upon overexpression34. In addition, a failure to stimulate ATPase activity through binding of adaptor (p37 for p9718) or substrate proteins (Rlp24 for Drg1) was also found for mutated forms of both AAA-ATPases. In contrast to p97, where single exchanges cause these phenotypes, we have found a combination of two mutations to be responsible in Drg1-21. None of the single exchanges manifests the full severity of the phenotypes observed for the Drg1-21 variant but they exhibit a synergistic behaviour with respect to ATPase activity, substrate interaction and dominant negative growth phenotype. Interestingly, the behaviour of the proteins containing the single exchanges was modulated by the presence of ADP. This indicates an important role of this nucleotide for causing the deleterious effect of Drg1-21.
For some p97-IBMPFD variants it was demonstrated that they co-precipitate increased levels of ubiquitinated proteins34 (their native substrates) suggesting a substrate release defect. In addition, altered nucleotide-dependent binding and a strongly reduced dissociation from the adaptor proteins p37 and p47 was shown for the p97-IBMPFD variants R155H and A232E33. Analogously, Drg1-21 fails to be released from its substrate Rlp24. Despite all these similarities, p97 and Drg1 differ with respect to the nucleotide states of the isolated proteins, as purified p97 usually retains ADP bound to at least some of its ATPase domains7. For Drg1, nucleotide binding to D1 is crucial to allow initial substrate recognition, but subsequent loading of ATP into D2 stabilizes the interaction. Due to this complex relationship, we cannot determine yet, how exactly ADP interferes with substrate binding and stimulation of ATP hydrolysis. However, the differential effects of ADP on Drg1-T100I and Drg1-L108P suggest the existence of an ADP containing intermediate state which is crucial for substrate handling. Based on the higher affinity of D1 we speculate that the ADP-dependent effects are linked to ADP binding into D1. To unravel the role of ADP in Drg1 regulation, high resolution structures of Drg1 bound to different nucleotides will be required.
The dysregulation of Drg1-21 suggests that binding of the substrate cannot be transmitted to the ATPase domains and the N-domain cannot fulfil its regulatory function. According to our structural models, T100 corresponds to R86 of p97. A mutation to alanine at this position is linked to “IBMPFD-like” structural alterations in p9714. Disturbed interactions of the N-domain with residues of the N-D1 linker were suggested to be the molecular basis for the conformational changes of the p97-R86A variant. In all calculated structural models of Drg1, T100 is predicted in close proximity to the N-D1 linker and mutating this residue is sufficient to increase the basal ATPase activity of Drg1. This further corroborates that interactions at the N-D1 interface are crucial for the regulation of ATP hydrolysis. Importantly, the Drg1-T100I exchange alone does neither cause temperature sensitivity nor exhibit a dominant negative effect on growth. Therefore, the enhanced ATP hydrolysis of Drg1-21 is not directly linked to the dominant negative behaviour but might rather be a consequence of disturbed interactions between N-domain and D1. Only the additional L108P substitution, which itself only causes a mild temperature sensitive phenotype and a mild dominant negative growth defect, results in full appearance of the deleterious effects of Drg1-21. We conclude that the two exchanges present in the Drg1-21 variant uncouple the combination of phenotypes caused by single amino acid exchanges in p97-IBMPFD variants and could therefore help to dissect the mechanism underlying the disease. Our results raise the speculation that the elevated basal ATP hydrolysis may not be causally linked to the pathogenesis, but might merely be a consequence of the failure of the N-domain to correctly interact with substrate and adaptor proteins and transmit a regulatory signal via the N-D1 linker.
Our screen for suppressor mutants showed that incorporation of a polar sidechain at position 100 of Drg1-21 is sufficient to restore activity of the protein. Polar and hydrophobic interactions at the N-D1 interface seem to be critical determinants for the positioning of the N-domain relative to the D1 domain. In p97, R86 forms multiple polar contacts with residues of the N-D1 linker (D204 and D205) and similar interactions were also predicted for the IBMPFD residues R93 and R9514. These interactions are lost when the N-domain changes its position. In other mutants, identified by the suppressor screen, the rigid proline in position 108 was exchanged for more flexible residues. Proline108 (L108P) might further dislocate residues responsible for inter-domain contacts (including threonine 100) and thereby explain the synergistic effect of both mutations. Interestingly, the only suppressor that retained the two original exchanges had an additional N77K substitution. This change obviously compensates for alterations introduced by T100I and L108P and therefore allows a positioning of the N-domain relative to the D1 domain that restores its function as regulator of ATPase activity. The fact that Rlp24C is able to stimulate ATP-hydrolysis by the Drg1-21sup protein explains the suppression of the temperature sensitive phenotype of Drg1-21. In cryo-EM structure of p97 obtained in the presence of ATPγS, where the N-domain adopts an elevated position reminiscent of the IBMPFD variants, residue R65 (which corresponds to N77 in Drg1), is rotated towards the N-D1 linker which undergoes a loop to helix transition upon ADP to ATPγS loading into D114. Recently, NMR experiments showed that the N-D1 linker is an important component in transmitting perturbations of the N-domain “up/down” equilibrium in the IMBPFD mutant R95G to the nucleotide binding pocket of D1 (pathway I26). It is therefore tempting to speculate that the N77K exchange in Drg1 reverses the defects of Drg1-21 by interfering with the N-D1 linker. This could shift the up/down equilibrium of the N-domain towards the down-position and thus rescue the phenotype of the double mutation in Drg1-21. However, in the absence of an experimentally determined structure for Drg1, and given the fact that the region containing the N77 residue is less confidently represented in our Drg1 models, these explanations are largely speculative. Therefore the exact mechanism behind the suppressor exchange N77K has to remain elusive and awaits further investigations.
Our findings suggest that the primary defect in the Drg1-21 mutant is the altered interaction between N- and D1-domain which might be counteracted by conformational rearrangements at the N-D1 interface. Taken together, the characterization of the Drg1-21 variant gave new insights into the regulation of ATPase activity of Drg1 as one of the crucial trans-acting enzymes during eukaryotic ribosome biogenesis. Our findings revealed a striking correlation with the pathological IBMPFD variants of p97. This indicates that despite low sequence conservation of the N-domain, the basic mechanisms of regulation of the ATPase activity are conserved among AAA-ATPases. In this context our work also contributes to the understanding of the molecular basis of the deleterious effects caused by dysregulated AAA-ATPases, including IBMPFD variants of p97.
Yeast Strains and Growth Conditions
All yeast and bacterial strains used in this study are listed in Supplementary Table S1, all plasmids are listed in Supplementary Table S2. Chromosomal deletions or gene fusions were generated by homologous recombination with PCR generated fragments as previously described35. Strains were grown either in YPD complex medium or for plasmid maintenance in synthetic dextrose complete medium supplemented with an appropriate amino acid mix to maintain selection. SD + all amino acids supplemented with 1 g/l 5-fluoroorotic acid (5-FOA, Thermo scientific) were used for plasmid shuffle experiments. Strains carrying temperature sensitive alleles were either incubated at permissive (25 °C) or restrictive (37 °C) temperatures.
Screening for temperature sensitive DRG1 mutants
Temperature sensitive alleles were generated by error prone PCR mutagenesis in the presence of 0.05 mM Mn2+. The mutagenized PCR fragments were cloned into a centromeric vector (pRS315) and transformed into the heterozygous diploid W303 DRG1/drg1-1::URA3 strain. After sporulation, random spore analysis was used to select for cells carrying the disrupted chromosomal copy of DRG1 as well as the mutagenized allele on the plasmid. Temperature sensitive alleles were identified by replica plating and incubation at permissive (25 °C) and restrictive (37 °C) temperatures. Localization of the mutations was identified by sequencing.
Construction of DRG1 shuffle plasmids
The centromeric plasmids containing the drg1-21 allele and the alleles with the single mutations were generated by overlap-PCR using primer pairs carrying point mutations followed by intragenic fragment swapping to exchange fragments from pRS315-DRG1 for mutagenized PCR fragments36. Mutagenic primers are listed in Supplementary Table S3.
Expression and purification of Drg1 variants
The pCUP1 expression plasmids in this study were derived from the pAZ7 (GST-DRG1) plasmid described in ref. 27. These constructs contain a uracil auxotrophy marker, the copper-inducible CUP1-promoter and an N-terminal GST-tag, which is separated from the DRG1-alleles by a PreScissionTM protease (GE Healthcare) site to allow removal of the GST-tag. The mutant drg1 alleles were introduced by intragenic fragment-swapping. The expression protocol of the Drg1 variants in this study is a modified version of the protocol for wildtype Drg1 which is described in detail elsewhere8,29. For expression of the Drg1-21 variant and the single mutant variants (L108P and T100I) two to twelve litres of SD-ura media were inoculated to an OD600 of 0.01 in baffled flasks and incubated at 25 °C under constant shaking at 110 rpm. At an OD600 of 0.2, protein expression from the CUP1 promoter was induced by adding 0.1 mM CuSO4. After another 18 hours at 25 °C the cells were harvested by centrifugation, washed with aqua bidest. and stored at −80 °C. Purification of the GST-fusion proteins was performed essentially as described in ref. 8 except that the pH of the crude extracts was adjusted to 7.4 with Tris base. When indicated 1 mM ADP was present in all purification buffers, since ADP proved to have a positive effect on the yield of the otherwise poorly purifying mutant fusion proteins. The concentration of the eluted proteins was determined using the Bradford assay (Biorad).
Tandem affinity purification of pre-60S particles
Tandem affinity purifications of pre-60S particles were performed as described in ref. 8 adapted from the standard protocols37,38. Cells were grown in YPD to an OD600 of 2.0, harvested by centrifugation and stored at −80 °C. For overexpression of the DRG1 alleles from pCUP1-plasmids, the cells were grown in SD-ura to an OD600 of 1.0 (early log-phase) and overexpression of the GST-Drg1 variants was induced by addition of 0.5 mM CuSO4 for 3 hours. Afterwards, cells were harvested by centrifugation and stored at −80 °C. Cell lysis and pre-60S particle purification was performed as described in ref. 8. After elution from calmodulin beads, proteins were concentrated by TCA precipitation.
SDS-PAGE and Western Blotting
Protein samples were separated using NuPAGE™ Novex™ 4–12% Bis-Tris gradient Protein Gels (Thermo scientific). Western blot detection of specific proteins after transfer to PVDF membranes (Millipore) was described in ref. 8 including sources of the used antisera.
Affinity purification of Rlp24C
Purification of the Hexahistidine-tagged (HIS6) and GST-tagged Rlp24C fragments was performed as described in detail in ref. 8.
ATPase activity assay (Malachite green phosphate assay)
ATPase activity was measured using the Malachite green phosphate assay (Bioassay systems) and was carried out as described previously8,29 with the exception that 5 μg (98 nM hexamer) of Drg1 or its variants were used. The absorbance of the samples at 600 nm was measured using a TECANTM plate reader (GeniusPro). For the measurement of the stimulated activity, saturating concentrations of purified HIS6-Rlp24C (1.68 μM) were added. All values were calculated as specific activity (μmol ATP h−1 mg−1 Drg1. Error bars represent standard deviations of means calculated from at least two biological replicates each measured in triplicate. P-values were calculated by an unpaired t-test (two-tailed, 95% confidence intervals); for pairs with unequal variances (confirmed by F-test) p-values were calculated by an unpaired t-test with Welsh’s correction. All calculations were performed using the GraphPadTM Prism software (version 3.03).
Surface plasmon resonance
SPR binding experiments with immobilized GST-Rlp24C were performed on a BiacoreXTM system as described previously8. Purified Drg1 variants were injected at concentrations of 10-100 nM at a constant flow rate of 40 μl/min (120 seconds contact time) at a constant temperature of 22 °C. As in-line control the signal measured in the control flow cell (immobilized GST-tag) was subtracted for each sensorgram. After each cycle, the binding surface was regenerated using running buffer containing 1 M sodium chloride to remove bound analyte. Sensorgrams were analysed using the BIAevaluation software (version 3.2). Kinetic parameters were calculated using the BIAevaluation software (version 3.2) and fitting to a two state (conformational change) model. Data were collected from at least two biological replicates over at least two CM5 sensor chips
Generation of random mutations of the drg1-21 allele was performed by mutagenic PCR in the presence of 0.05 mM Mn2+. The mutagenized PCR fragments were cloned into centromeric pRS315-plasmids and used for transformation of the drg1-21 shuffle strain [pRS316-drg1-21]. To identify mutations that suppressed the temperature sensitivity caused by the drg1-21 allele, the transformants were plated on SD-leu agar plates and incubated at 37 °C. Plasmid shuffling was performed on SD-agar plates containing 1 g/L 5-FOA (5-Fluorootic acid). Plasmids of transformants with restored growth at 37 °C were isolated and the location of the mutation was identified by sequencing.
Generation of a Drg1 homology model based on p97 crystal structures
For structural analysis of the mutants, we re-used the model built previously with YASARA29,39 based on murine p97 crystal structures 3CF3 and 1R7R as templates, and with the same protocol built five more models using the recently released cryo-EM structures of human p9712 (PDB codes 5FTJ, 5FTK, 5FTL, 5FTM and 5FTN). Modelling was also performed using the Phyre2 web service for fold recognition40. The Images were generated with PyMOL (The PyMOL Molecular Graphics System, Version 184.108.40.206 Schrödinger, LLC) which was also used for structure alignment. PDB files of all models are available from the authors upon request.
How to cite this article: Prattes, M. et al. A conserved inter-domain communication mechanism regulates the ATPase activity of the AAA-protein Drg1. Sci. Rep. 7, 44751; doi: 10.1038/srep44751 (2017).
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This work was supported by grants from the Austrian Science Fund FWF (Grants P 26136 and 29451 to HB).
The authors declare no competing financial interests.
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Prattes, M., Loibl, M., Zisser, G. et al. A conserved inter-domain communication mechanism regulates the ATPase activity of the AAA-protein Drg1. Sci Rep 7, 44751 (2017). https://doi.org/10.1038/srep44751
Nature Communications (2021)