Ubiquitin-dependent proteolysis can initiate at ribosomes for myriad reasons including misfolding of a nascent chain or stalling of the ribosome during translation of mRNA. Clearance of a stalled complex is required to recycle the ribosome for future use. Here we show that the ubiquitin (Ub) pathway segregase Cdc48/p97 and its adaptors Ufd1-Npl4 participate in ribosome-associated degradation (RAD) by mediating the clearance of ubiquitinated, tRNA-linked nascent peptides from ribosomes. Through characterization of both endogenously-generated and heterologous model substrates for the RAD pathway, we conclude that budding yeast Cdc48 functions downstream of the Ub ligases Ltn1 and Ubr1 to release nascent proteins from the ribosome so that they can be degraded by the proteasome. Defective RAD could contribute to the pathophysiology of human diseases caused by mutations in p97.https://doi.org/10.7554/eLife.00308.001
Ribosomes are complex molecular machines that translate the sequence of bases in a messenger RNA (mRNA) transcript into a polypeptide that subsequently folds to form a protein. Each ribosome is composed of two major subunits: the small subunit reads the mRNA transcript, and the large subunit joins amino acids together to form the polypeptide. This process stops when the ribosome encounters a stop codon and releases the completed polypeptide.
It is critical that cells perform some form of quality control on the polypeptides as they are translated to prevent a build up of incomplete, incorrect or toxic proteins in cells. Problems can occur if a ribosome stalls while translating the mRNA transcript, or if the mRNA transcript is defective. For example, most mRNA transcripts contain a stop codon, but some do not, and these non-stop mRNA transcripts result in a non-stop polypeptide that remains tethered to the ribosome. It is important that the cell identifies and removes these faulty polypeptides so as to leave the ribosome free to translate other (non-faulty) mRNA transcripts. A regulatory protein called ubiquitin is responsible for marking and sending proteins that are faulty, or are no longer needed by the cell, to a molecular machine called the proteasome, where they are degraded by a process called proteolysis. In 2010 researchers identified Ltn1 as the enzyme that attaches ubiquitin to non-stop proteins in yeast.
Now, building on this work, Verma et al. identify additional proteins involved in this process. In particular, an ATPase enzyme called Cdc48 (known as p97 or VCP in human cells) and two co-factors—Ufd1 and Npl4—promote release of the ubiquitinated non-stop polypeptides from the ribosomes, thus committing the marked polypeptide to destruction by the proteasome. Verma et al. also show that the Cdc48-Ufd1-Npl4 complex is involved in other aspects of quality control of newly synthesized proteins within cells. Collectively these processes are known as ribosome-associated degradation.
Mutations of the gene that codes for human p97 can cause a number of diseases, including Paget's disease of the bone and frontotemporal dementia, so an improved understanding of ribosome-associated degradation could provide new insights into these diseases.https://doi.org/10.7554/eLife.00308.002
Maintaining protein homeostasis is key for the healthy lifespan of the organism (Koga et al., 2011) and cells have evolved sophisticated mechanisms to control the quality of newly synthesized proteins (Bukau et al., 2006; Smith et al., 2011). Dysfunction of these quality control (QC) pathways can tip the balance towards the accumulation of toxic proteins and manifestation of disease, most notably neurodegeneration (Powers et al., 2009; Hartl et al., 2011; Dennissen et al., 2012).
There are multiple pools of QC substrates in cells. A relatively well-characterized substrate pool arises from misfolding of nascent chains that have been properly translated. Depending upon the relative rate at which malfolded sequences that comprise degrons form and bind their Ub ligase receptors vs the rate at which translation is completed, ubiquitination and degradation of misfolding proteins may initiate on the ribosome. It has been shown, for instance, that the acetylated N-terminus recognized by the Ub ligase Doa10 (Hwang et al., 2010) is generated co-translationally (Gautschi et al., 2003; Polevoda et al., 2008), and that the Ub ligase Ubr1 can initiate degradation of an N-end rule substrate prior to completion of its translation (Turner and Varshavsky, 2000).
A second pool of QC substrates arises from failure to complete translation successfully. This can occur because the mRNA is defective or the ribosome stalls due to either irresolvable structures in the mRNA or interactions between the nascent peptide and the ribosome (Lu and Deutsch, 2008; Kramer et al., 2009; Ingolia et al., 2011). Defective mRNAs are recognized by a cytosolic mRNA surveillance machinery that mediates their destruction. There are at least three pathways: no-go decay (NGD) targets mRNAs with strong stalls in translation elongation leading to endonucleolytic cleavage of the mRNA, nonsense-mediated decay (NMD) targets messages containing premature termination codons (PTC), and non-stop decay (NSD) targets mRNAs that lack a stop codon. Within this broad scheme, there are many variations by which aberrant mRNAs are generated (Parker, 2012). Interestingly, recent data suggest an intimate coupling between QC of defective mRNAs and the nascent peptides they produce (Shoemaker and Green, 2012). For example, Upf1 is a positive effector of NMD that is also needed for proteasome-mediated degradation of the prematurely terminated products (Takahashi et al., 2008; Kuroha et al., 2009).
Quality-control of mRNAs that lack a stop codon and the proteins produced from them has been the focus of considerable recent attention. Translation of these ‘non-stop’ mRNAs yields a ribosome-tethered polypeptide that is targeted for ubiquitination and degradation (Ito-Harashima et al., 2007; Dimitrova et al., 2009; Bengtson and Joazeiro, 2010). Notably, the mRNA may be processed by multiple pathways (e.g., NSD and NGD) because absence of a stop codon can cause translation to stall either because the end of the message is encountered or polylysine encoded by the poly(A) tail interacts with the negatively charged exit tunnel of the ribosome. Non-stop mRNAs can arise naturally through premature termination or polyadenylation within ORFs, which are estimated to occur for up to 10% of all transcriptional events (Frischmeyer et al., 2002). Proteins encoded by these messages could potentially impose a considerable burden on QC pathways. Thus, disposal of proteins produced from non-stop messages is likely to be of general significance to understanding human diseases that result from defects in protein homeostasis.
Stalled ribosomes that trigger NGD/NSD are recognized by the Dom34–Hbs1 complex which is structurally related to the termination factors eRF1 and eRF3 but lacks the residues necessary for both stop codon recognition and hydrolysis of peptidyl-tRNA and instead binds to the empty A site in the stalled ribosome (Doma and Parker, 2006; Becker et al., 2011; Tsuboi et al., 2012). Dom34–Hbs1 works in concert with a member of the ABC family of ATPases, known as ABCE1 in mammalian cells (Pisareva et al., 2011) or Rli1 in budding yeast (Shoemaker et al., 2010; Shoemaker and Green, 2011), to disassemble stalled ribosomes for subsequent reuse. Additionally, the translational GTPase Ski7, which is closely related to Hbs1 (and thus to eRF3), has been proposed to recognize ribosomes stalled at the 3′ end of non-stop messages (van Hoof et al., 2002). However, no Dom34/eRF1-like molecule has been identified to date that can interact with Ski7 specifically so it remains unknown if it can promote recycling of ribosome subunits. Following dissociation of subunits, the mechanism by which the associated nascent peptide is extricated remains poorly understood. What has been shown so far is that the Ub ligase Ltn1 can bind the ribosome and ubiquitinate NSD substrates that contain a polylysine tract (Bengtson and Joazeiro, 2010). Ltn1 belongs to the RING domain family of E3 Ub ligases that ubiquitinate substrates targeted for degradation by the 26S proteasome (Deshaies and Joazeiro, 2009; Finley, 2009). However, the mechanism by which the nascent non-stop peptide is released from the ribosome and degraded remains unknown. Nevertheless, the underlying biochemistry is likely to be important for human health, because point mutations in mouse Ltn1 result in neurodegeneration and a null allele is lethal (Chu et al., 2009).
Budding yeast Cdc48 (the human protein is known as p97 or valosin-containing protein [VCP]) is a member of the AAA (ATPases associated with diverse cellular activities) family of proteins. Cdc48 has intrinsic Ub-binding affinity that is greatly enhanced by the binding of UBX domain proteins or the Ufd1–Npl4 heterodimer to its N-terminus and Ufd2 to its C-terminus (Ye, 2006; Meyer et al., 2012). Cdc48/p97 is widely believed to function as a ‘segregase’ that uses the free energy released upon ATP hydrolysis to remodel ubiquitinated substrate complexes, usually, but not always, as a prelude to their degradation by the 26S proteasome (Jentsch and Rumpf, 2007). In the work reported here, we show that Cdc48–Ufd1–Npl4 promotes the release of tRNA-linked ubiquitinated nascent chains as well as aberrant non-stop and prematurely terminated polypeptides from the ribosome. Our findings establish a new function for Cdc48/p97 in RAD.
In an effort to systematically elucidate cellular functions of Cdc48 and its adaptors, mutants were subjected to chemical profiling by determining growth in the presence of various drugs, including translation inhibitors. All mutants were insensitive to anisomycin, an inhibitor that blocks the peptidyl transferase reaction on ribosomes (not shown). However, low concentrations of hygromycin B and paromomycin inhibited growth of multiple cdc48 mutants and the adaptor mutants npl4-1, ufd1, ubx1Δ, and ubx2Δ (Figure 1—figure supplement 1A,B and data not shown). Hygromycin B and paromomycin belong to the aminoglycoside class of antibiotics that bind close to the decoding center and affect translational fidelity (Carter et al., 2000; Kim and Craig, 2005). Deletion of LTN1 leads to hygromycin-sensitivity and since Ltn1 is involved in QC of NSD pathway substrates (Bengtson and Joazeiro, 2010), we explored the possibility that Cdc48–Ufd1–Npl4 and one or more Ubx proteins also function in this pathway.
To determine if Cdc48 contributes to protein degradation at the ribosome in unperturbed, exponentially growing cells, we purified ribosomes using a rapid, one-step affinity method designed to isolate 60S subunits, 80S monosomes and polysomes (Oeffinger et al., 2007; Halbeisen and Gerber, 2009; Halbeisen et al., 2009). Coomassie blue staining of purified ribosomes confirmed that Cdc48 activity was not required for their assembly (Figure 1, Figure 1—figure supplement 2A, lane 3), a conclusion that was further validated by sucrose gradient fractionation of ribosomes from wildtype, cdc48-3, and ufd1-2 whole cell lysates (Figure 1—figure supplement 2B). However, the mutants do appear to have a slightly lower ratio of polysomes:80S monosomes. Immunoblotting for Ub revealed strong accumulation of Ub conjugates on ribosomes affinity-purified from cdc48-3 cells (Figure 1A). To ascertain if the epitope tag on the ribosome subunit was exacerbating the effect of the cdc48-3 mutation, we isolated ribosomes from untagged cells by pelleting through a sucrose cushion (Halbeisen and Gerber, 2009). Again, Ub conjugates were observed to accumulate on ribosomes in cdc48-3 and npl4-1 mutants (Figure 1B). Because the proteolytic defects of npl4-1 are manifested at the semi-permissive temperature of 30°C (Bays et al., 2001), we carried out the experiment in Figure 1B at 30°C. The data indicate that cdc48-3 does not have to be shifted to the fully non-permissive temperature to observe Ub conjugate accumulation at the ribosome. Additionally, conjugate accumulation on cdc48-3 and npl4-1 ribosomes exceeded that observed for ribosomes isolated from cells treated with the proteasome inhibitor MG132, a result that will be further discussed below.
To determine whether the ATPase activity of Cdc48 was required to prevent accumulation of ribosome-associated Ub conjugates, ribosomes were pelleted from cdc48-3 mutant cells expressing plasmid-borne wildtype CDC48, or a mutant (Q2) deficient in ATPase activity (Ye et al., 2003). Whereas CDC48 complemented the cdc48-3 phenotype, high levels of Ub conjugates were detected on ribosomes isolated from cells expressing the cdc48-Q2 mutant (Figure 1C). Consistent with the idea that Cdc48 ATPase functions at the ribosome to mediate release of ubiquitinated nascent peptides, both Cdc48 and Ufd1 were found to cofractionate with affinity-purified ribosomes isolated under stringent conditions (Figure 1D).
We next wished to ascertain if the Ub conjugates were derived from nascent polypeptides that were linked to tRNA. Magnetic beads containing bound ribosomes from wildtype or cdc48-3 cells were treated with TEV protease, which cleaves between Rpl18B and the TAP tag. The TEV cleavage was carried out in the presence or absence of puromycin. Puromycin causes premature termination of translation by binding in the A-site of the ribosome and reacting with peptidyl-tRNA in the P-site, yielding a peptide-puromycin conjugate (Nathans, 1964). Thus, we expected that puromycin would induce the release of peptidyl-tRNA from the ribosome as a peptide-puromycin conjugate. The supernatants were then bound to UBA Sepharose resin to enrich for Ub conjugates. The rationale behind this step was that ribosome-associated Ub conjugates that remained bound to the ribosome would bind poorly to UBA beads because ribosomes do not efficiently penetrate the pores of a Sepharose resin, whereas Ub conjugates released from the ribosome by puromycin would be able to bind more efficiently to UBA beads. Puromycin treatment of ribosomes from cdc48-3 but not wildtype cells released ubiquitinated proteins that were enriched on the UBA resin (Figure 2A, top panel). A similar result was obtained with ribosomes isolated from npl4-1 and ufd1-1 mutants (Figure 2—figure supplement 1A,B). The conjugates observed in Figure 2A were indeed linked to puromycin because they cross-reacted with an antibody specific for puromycin (Figure 2A, bottom panel). The same was true for Ub conjugates released from npl4-1 and ufd1-2 ribosomes (Figure 2—figure supplement 1C). The fact that no Ub immunoreactivity was recovered from mutant ribosomes in the absence of puromycin treatment validated our assumption that the UBA resin largely excluded mega-complexes. This experiment also suggests that at least some of the Ub conjugates that accumulated on cdc48 and npl4 ribosomes (Figure 1A,B) must be ubiquitinated nascent proteins linked to tRNA.
To further confirm that the Ub conjugates that accumulated on ribosomes in cdc48 cells were ubiquitinated nascent peptides linked to tRNA we did three additional experiments. First, ribosomes affinity-purified from cdc48-3 were treated with RNAse A or not before incubation with puromycin followed by binding to the UBA resin. Immunoblotting for Ub revealed that both the control and RNAse-treated ribosomes contained Ub conjugates that bound the UBA beads (Figure 2B, top panel, lanes 2 and 3). However, ribosomes pre-treated with RNAse no longer yielded puromycin-reactive conjugates (Figure 2B, bottom panel). By contrast, pre-treating lysate with RNAse before affinity purification of ribosomes eliminated recovery of both Ub-, and puromycin immunoreactivity (Figure 2B, lane 4, top and bottom panels).
The second experiment that we did to confirm tRNA linkage was to treat affinity-purified ribosomes with CTAB. CTAB is an ionic detergent that disrupts protein structure and precipitates peptidyl-tRNA molecules selectively (Hobden and Cundliffe, 1978; Mariappan et al., 2010). In parallel with results obtained previously using puromycin, Ub conjugates were precipitated from cdc48-3 ribosomes in an RNAse-sensitive manner (Figure 2C).
As a final test of the idea that the Ub conjugates that accumulated on cdc48-3 ribosomes were attached to nascent chains, wildtype and mutant cells were pulsed with radioactive methionine for 90 s and then chased with cold methionine. Ribosomes were affinity-purified from cells sampled at different times of chase and treated with puromycin to release tRNA-linked nascent chains. This material was then fractionated on UBA resin to enrich for discharged Ub conjugates. Strikingly, ribosomes from both cdc48-3 and ufd1-2 cells contained far higher levels of radiolabeled high MW Ub conjugates than wildtype ribosomes, and a substantial portion of this signal persisted on ribosomes for 10–20 min (Figure 2D), which is considerably longer than the time required to synthesize a protein. Importantly, the low signal on wildtype ribosomes was not due to inefficient incorporation, because the WT inputs for the UBA fractionation step actually contained slightly more total pulse-labeled species (Figure 2—figure supplement 1D). Taken together, the experiments described thus far indicate that Cdc48 and its cofactors Ufd1 and Npl4 prevent accumulation of ubiquitinated, tRNA-linked nascent chains on the ribosome. For simplicity, we hereafter refer to these species as tUNPs (tRNA-linked, ubiquitinated nascent polypeptides). Notably, other Cdc48 cofactors including Ubx2, Ubx4, Ubx6, and Ufd2 did not appear to contribute to clearance of tUNPs from the ribosome (Figure 2—figure supplement 1C). These cofactors were tested because they had scored positively in the hygromycin-sensitivity assay whereas ubx3Δ, ubx5Δ, and ubx7Δ were hygromycin-insensitive, and therefore not pursued further. Hygromycin-sensitive ubx1Δ/shp1Δ was also not pursued further, because this mutant is extremely sick.
The findings summarized above raised the question: what is the composition of the tUNPs? One possibility is a class of aberrant proteins arising from translation of mRNAs that lack stop codons (‘non-stop mRNA’). Translation through the poly(A) tail of these mRNAs can result in a ribosome that stalls either because it reaches the end of the message, or the polylysine encoded by the poly(A) tail interacts with the negatively charged exit tunnel of the ribosome (Dimitrova et al., 2009). Prior work has demonstrated that the Ub ligase Ltn1 targets proteins translated from mRNAs that lack a stop codon or that contain polylysine stretches (Bengtson and Joazeiro, 2010). We therefore employed the puromycin release/UBA bead capture protocol to test whether deletion of LTN1 diminished the accumulation of tUNPs on ribosomes in cdc48-3 cells. We also tested the impact of ubr1Δ, because of prior reports that Ubr1 promotes co-translational ubiquitination (Turner and Varshavsky, 2000), and because ubr1Δ mutants, like ltn1Δ, are hygromycin-sensitive (not shown, but see below). The data in Figure 3A demonstrate that additional loss of LTN1 or UBR1 resulted in a marked decrease in the level of tUNPs on cdc48-3 ribosomes. This result encouraged us to evaluate the steady state levels of the Gfp-FLAG-His3Non-Stop (GFHNS) fusion protein shown earlier to be an Ltn1 substrate at the ribosome that is degraded by the proteasome (Bengtson and Joazeiro, 2010). Amongst the Cdc48 pathway mutants examined, GFHNS accumulated maximally in ufd1 mutants (similar to levels observed for ltn1Δ), and also exhibited significant accumulation in npl4-1 and cdc48-3 (Figure 3B). Cycloheximide chase analysis in ufd1-2 cells indicated that accumulation resulted from stabilization of the non-stop reporter (Figure 3C). As observed in earlier studies (Bengtson and Joazeiro, 2010), the same reporter containing a stop codon was not degraded and accumulated at a much higher level than the NS reporter (Figure 3C; amounts loaded were adjusted to yield signals of equal intensity at 0 min).
If the Cdc48–Ufd1–Npl4 complex functions downstream of Ltn1 to mediate clearance of tUNPs from the ribosome, as suggested by the data in Figure 3A, we anticipated that ubiquitinated species of the non-stop reporter should accumulate upon inactivation of Cdc48 complex. To address this question, we prepared SDS lysates of wildtype and ufd1 mutant cells expressing GFHNS, diluted the lysates with Triton X-100 to sequester the SDS in micelles, and immunoprecipitated with anti-FLAG. Immunoblotting for Ub demonstrated that GFHNS accumulated in an ubiquitinated form in ufd1-1 and ufd1-2 but not in ltn1Δ mutants (Figure 3D).
The above data indicate that the non-stop, but not the stop codon-containing reporter was targeted for degradation by the combined actions of Ltn1 and Cdc48–Ufd1–Npl4. The role of the Cdc48 complex in reporter degradation appeared to be direct, because both Cdc48 and Ufd1 were co-immunoprecipitated with GFHNS, but not GFHStop, even though GFHStop was more abundant (Figure 3E).
GFHNS accumulates on 80S ribosomes in ltn1Δ mutants (Bengtson and Joazeiro, 2010). To evaluate if any of these molecules are linked to tRNA, we sedimented ribosomes rapidly through sucrose cushions and treated the pellet with RNAse A (or not). Strikingly, immunoblotting revealed an RNAse-sensitive species on ribosomes from ltn1Δ, as well as those from cdc48-3 and ufd1-2 mutants, but not from wildtype cells (Figure 3—figure supplement 1). The fraction of GFHNS linked to tRNA was low. It is not clear whether this was due to hydrolysis of the tRNA linkage in vivo or in vitro.
For our subsequent experiments, we decided to focus on Protein A-NS (PrANS), a non-stop reporter utilized in earlier studies (Wilson et al., 2007; Bengtson and Joazeiro, 2010). Unlike GFHNS, the RNAse-sensitive, tRNA-linked form of PrANS accumulated more efficiently and could be detected even in total cell extracts. We first examined the steady-state levels of PrANS in several mutants. Interestingly, levels of tRNA-linked PrANS in cdc48-3 and ltn1Δ cell lysates were equivalent to those detected in dom34Δ and ski7Δ, bona fide components of the NSD pathway (Figure 4A; equivalent loading confirmed by staining with Ponceau S and immunoblotting for tubulin, Figure 4—figure supplement 1A).
To more precisely determine which subset of ribosomes contained tRNA-linked PrANS, we performed sucrose gradient fractionation. Shallow gradients (10–30%) were set up, enabling good resolution of the subunits, monosomes, and polysomes (Figure 4—figure supplement 1B). Immunoblotting for PrANS revealed that the RNAse-sensitive species peaked in the 80S fractions isolated from ltn1Δ mutants but was found in both the 60S and 80S-containing fractions from cdc48-3 cells (Figure 4B). Additionally, modified forms of slower mobility than the tRNA-linked species were detected in 60S ribosomes from cdc48-3 but not ltn1Δ, suggesting that these high MW species are Ltn1-dependent Ub conjugates. Only a small fraction of the PrANS detected on ribosomes migrated as Ub-conjugated species. This is consistent with what is typically observed for most Ub-dependent substrates upon inhibition of their degradation, and presumably reflects robust cytosolic deubiquitination activity. In addition, overproduction of PrANS from the GAL promoter may overwhelm Ltn1, which is inabundant (Bengtson and Joazeiro, 2010). Besides the modified forms of PrANS, unmodified protein was observed throughout the gradient and peaked in the ribosomal fractions. We do not know whether this latter form arose from hydrolysis of the peptidyl-tRNA linkage in cells or in vitro.
Our data thus far indicate that in cdc48, npl4, and ufd1 mutants, nascent proteins were targeted for degradation by Ltn1- and Ubr1-dependent ubiquitination but became stuck on 60S and 80S ribosomes as peptidyl-tRNAs, implying that Cdc48 activity promotes release of stalled, ubiquitinated peptides, which are then degraded by the proteasome. This hypothesis predicts that ribosomes isolated from cells in which proteasome activity is compromised should accumulate less tUNPs than cdc48 mutants. To test this prediction, we used the sucrose cushion method to isolate ribosomes from cdc48-3 and npl4-1 mutants, as well as pdr5Δ cells treated with or without the proteasome inhibitor MG132 (pdr5Δ enables cellular accumulation of this compound). The ribosome pellet was then treated with puromycin and incubated with UBA resin to enrich for tUNPs. Ribosomes isolated from cells with inhibited proteasomes contained far less tUNPs than ribosomes from cdc48-3 and npl4-1 cells (Figure 5A; the input lysates and ribosome pellets for this experiment are shown in Figure 1B). This result is in striking contrast to what we previously reported for proteasomes isolated from cdc48-3 and MG132-treated cells—both contained very high levels of accumulated Ub conjugates (Verma et al., 2011). A similar result was obtained using the cim3-1 mutant instead of MG132 treatment (Figure 5—figure supplement 1A; cim3-1 is a ts allele of the gene that encodes the proteasome subunit Rpt6).
We next sought to evaluate the effect of proteasome deficiency on accumulation of a specific peptidyl-tRNA on the ribosome. To evaluate the subcellular distribution of the PrANS species that accumulate upon inhibition of Cdc48 or proteasome function, we sedimented extracts through sucrose cushions to generate ribosome pellets and post-ribosomal supernatants from wildtype, cdc48-3 and cim3-1 cells (Figure 5B). Notably, whereas most of the PrANS fractionated in the ribosome pellet in cdc48-3 cells (a substantial portion of which remained linked to tRNA), the opposite was true in cim3-1 cells, where the bulk of the PrANS was recovered in the supernatant fraction (Figure 5B). Comparison of extracts made by lysing cells directly in SDS (Figure 5—figure supplement 1B) or under native conditions (Figure 5B) revealed that the proportion of PrANS that accumulated as full length or truncated species in vivo and its susceptibility to proteolytic clipping in native cell extract differed for cdc48-3 and cim3-1 mutants. We do not know the basis for these differences.
Our observation that Ubr1 contributed to ubiquitination of tUNPs (Figure 3A) led us to wonder about the diversity of the QC mechanisms that underlie their formation. To determine if the role of Cdc48 is limited to the non-stop pathway or whether it plays a more global role in degradation of proteins encoded by aberrant messages, we also assessed the stability of endogenous phosphogluconate dehydrogenase truncated by a premature termination codon (Gnd1PTC) in the middle of a folded domain at residue 368. Over-produced Gnd1PTC was shown to be a substrate of the Ubr1 cytosolic quality control pathway in a prior study (Heck et al., 2010). The data in Figure 6A confirmed stabilization of Gnd1PTC in ubr1Δ. Notably, cdc48-3 and ufd1-2 mutations also stabilized Gnd1PTC, but ltn1Δ was without effect (equivalent loading confirmed in Figure 6—figure supplement 1). Gnd1PTC was also stabilized in upf1Δ. Upf1 is a RING domain Ub ligase (Takahashi et al., 2008) that plays a crucial role in NMD and stimulates the degradation of aberrant PTC translation products (Kuroha et al., 2009). The dependence of Gnd1PTC degradation on Cdc48 and Upf1 suggested that tRNA-linked Gnd1PTC might become stuck on ribosomes, as observed for the non-stop reporters. To test this possibility we used the sucrose cushion method to isolate ribosomes from various mutants, and evaluated the ribosomal pellets for their content of Gnd1PTC. Analysis of total cell lysates revealed strong accumulation of Gnd1PTC in cdc48-3, ubr1Δ, and upf1Δ cells (Figure 6B). Fractionation of lysates prepared in an identical manner revealed an RNAse-sensitive species on ribosomes but not in post-ribosomal supernatants isolated from cdc48-3 mutants (Figure 6C) as well as ufd1-2, ubr1Δ and upf1Δ mutants (data not shown). In contrast, little tRNA-linked substrate was found in dom34Δ mutants (Figure 6C). Strikingly, the tRNA-linked species was not detected on ribosomes from ltn1Δ (data not shown).
Whereas QC of defective mRNAs and recycling of ribosomes stalled on these templates has received considerable attention in prior studies, much less is known about what happens to the nascent polypeptides, some of which accumulate as peptidyl-tRNA. Some proteins encoded by non-stop mRNAs, including the reporter proteins used here (GFHNS and PrANS), are degraded by the ubiquitin-proteasome system (UPS) (Wilson et al., 2007; Bengtson and Joazeiro, 2010). The Ub ligase Ltn1 binds 60S ribosomes and promotes ubiquitination of stalled GFHNS (Bengtson and Joazeiro, 2010). Our data suggest that Cdc48–Ufd1–Npl4 acts downstream of Ltn1 to promote release of the non-stop peptide from the ribosome, so that it can be degraded by the proteasome. How Ltn1 and the Cdc48 complex does this remains unknown. Indeed, this remains unknown for any NSD or NGD pathway substrate; the Dom34-Hbs1 complex lacks the residues necessary for hydrolysis of the peptidyl-tRNA bond, and the two budding yeast peptidyl-tRNA hydrolases, Pth1 and Pth2, are non-essential mitochondrial proteins whose transmembrane configurations are currently unknown (Rosas-Sandoval et al., 2002). An interesting question for the future will be to determine whether Ltn1 and Cdc48–Ufd1–Npl4 act together with, or in a redundant pathway parallel to Ski7 or Dom34–Hbs1-Rli1.
We observed direct physical association of Cdc48 and Ufd1 with both affinity-purified ribosomes and the NSD pathway substrate GFHNS. This interaction was highly specific, because Cdc48 and Ufd1 did not bind the same substrate when it was translated from a message that includes a stop codon. While this manuscript was in revision, it was reported that Cdc48, Ufd1, and Npl4 are components of the newly identified Ribosome Quality Control (RQC) complex, which also contains Ltn1, Rqc1 and Tae2 and associates with the 60S ribosomal subunit. The latter two proteins, like Ltn1 and Cdc48–Ufd1–Npl4, are highly conserved and have mammalian homologs (Brandman et al., 2012). Both Ltn1 and Rqc1 help link Cdc48–Ufd1–Npl4 to RQC. Rqc1 associates with and is required for the degradation of an Ltn1 substrate that contains an internal polyarginine sequence, but a functional role for Cdc48–Ufd1–Npl4 in RQC was not established by Brandman et al. (2012).
A key question that emerges from this work is, what is the signal that differentiates ribosomes engaged with NSD or other aberrant substrates from normally translating ribosomes? Ltn1 (Bengtson and Joazeiro, 2010) and RQC (Brandman et al., 2012) are reported to be predominantly bound to 60S ribosomal subunits, suggesting that they may act downstream of the initial recognition and splitting of a stalled ribosome. However, in ltn1Δ cells, GFHNS accumulates on 80S monosomes (Bengtson and Joazeiro, 2010). Likewise, we report here that tRNA-linked PrANS appeared to be concentrated in monosomes in ltn1Δ. By contrast, tRNA-linked PrANS was spread more broadly across 60S and 80S fractions in extracts from cdc48-3 cells. The different fractionation behavior of tRNA-linked PrANS in ltn1Δ and cdc48 mutants may reflect leakiness of the cdc48 mutation (the experiment was done at the semi-permissive temperature of 30°C) or Cdc48-independent ribosome splitting. Detailed resolution of the exact sequence of events will require reconstitution of the overall process with defined components.
In addition to observing accumulation of engineered NSD pathway reporter proteins in Cdc48 pathway mutants, we also observed extensive accumulation of endogenous, tRNA-linked ubiquitinated nascent polypeptides (tUNPs) on ribosomes in these cells. These tUNPs could potentially arise from multiple sources including misfolded domains (Turner and Varshavsky, 2000), mRNAs whose transcription was prematurely terminated, mRNAs or nascent peptides containing sequences that cause ribosome pausing (Ingolia et al., 2011) or mRNAs that encode premature termination codons (e.g., Figure 6C). Thus it is perhaps not surprising that at least two Ub ligases (Ltn1 and Ubr1) contributed to their accumulation. In any event, we believe it is unlikely that there is a single pathway or mechanism for disposing of tUNPs. Even in the seemingly simple case of a ribosome that translates into the poly(A) tail of an mRNA that is prematurely polyadenylated within the coding sequence, the 3′-most ribosome may be stalled because it reached the end of the message, or because polylysine encoded by the poly(A) tail bound the exit channel of the ribosome (Ito-Harashima et al., 2007). Because stalls in translation elongation lead to endonucleolytic cleavage of the mRNA upstream of the 3′-most ribosome (Tsuboi et al., 2012), each trailing ribosome will present a unique substrate to the UPS, and may be processed by a different mechanism.
The intimacy with which protein biosynthesis is coupled to protein degradation is highlighted by the identification of the translasome, a supercomplex defined by mass spectrometric analysis of the translation initiation factor eIF3 and found to contain both ribosome and proteasome subunits as well as chaperones involved in protein QC (Sha et al., 2009). A tight coupling of these processes may be particularly important for neurons, which are post-mitotic and need to remain robust for the life of the organism (Segref and Hoppe, 2009). Indeed, homozygous lister mice deficient in Listerin (Ltn1) function exhibit severe neurological dysfunction (Chu et al., 2009), whereas mutations in human Ubr1 result in the Johanson–Blizzard syndrome characterized by, amongst other phenotypes, frequent mental retardation (Hwang et al., 2011). Mutations in p97 contribute to 1–2% of familial ALS (Johnson et al., 2010) and are the root cause of a syndrome, IBMPFD, that includes frontotemporal dementia (Watts et al., 2004). Defects in metabolism of protein aggregates (Manno et al., 2010), endosomal trafficking (Ritz et al., 2011) and autophagy (Ju et al., 2009; Tresse et al., 2010) have been previously suggested to contribute to the pathophysiology that results from mutation of p97. As the molecular mechanisms underlying these diseases are unraveled, it will be interesting to see if ribosome-associated degradation contributes to their etiology.
All strains used in this study are listed in Supplementary file 1. They were derived from the W303 or S288C backgrounds. Deletion strains were acquired from Open Biosystems (Waltham, MA). All crosses were confirmed by auxotrophic marker selection and genomic PCR. Temperature-sensitive strains were confirmed by incubating the plate at the restrictive temperature for 4–5 days. Cultures were grown in YPD, or if cells contained plasmids, in synthetic selection medium. For expression of PrANS from the GAL1,10 promoter, induction was typically for 2 hr. Temperature-sensitive mutants and their congenic wildtypes were grown at 25°C and temperature shifts were for 90 min at 37°C, or two cell division cycles at 30°C. Any exceptions to these regimens are noted in the respective figure legends.
Cells were grown as described in the respective figure legends to a final O.D.600 (optical density at a wavelength of 600 nm) between 1.0 and 2.0, harvested by centrifugation, and drop-frozen in liquid nitrogen. Frozen cell pellets were thawed and washed with ice-cold buffer containing 50 mM Tris, pH 7.5, 10 mM sodium azide, 10 mM EDTA, 10 mM EGTA, 1× protease inhibitor tablet (Roche, Basel, Switzerland), 10 mM NEM, 50 mM NaF, 60 mM β-glycerophosphate, 10 mM sodium pyrophoshate. An equal volume of glass beads (Sigma, St Louis, MO; 425–600 μm, acid washed) was added and the cell pellets were immersed in boiling water for 3 min. They were then suspended in 1× SDS buffer (37.5 µl/O.D. unit) and cells were lysed by vortexing in Fast Prep-24 (MP) for 45 s at a setting of 6.5, and boiled again for 4 min. Boiled lysates were centrifuged at 16,000×g for 1 min. Aliquots were resolved by SDS-PAGE. In some instances, particularly when tRNA-linked substrate was being detected, washed cell pellets were brought up in 1× SDS buffer containing 1× Secure (Ambion, Carlsbad, CA), heated at 65°C for 5 min, lysed by glass beads as described above, and loaded on NuPAGE gels (Invitrogen, Carlsbad, CA). For immunoblot detection, gels were transferred to nitrocellulose and filters were stained with Ponceau S to determine equivalent loading of protein extracts. If loading was not equivalent, the experiment was repeated. The nitrocellulose filters were immunoblotted with desired antibody and developed by ECL or Super Signal (Pierce, Rockford, IL). Anti-Gfp was from Clontech (Mountain View, CA), Peroxidase Anti-Peroxidase Soluble Complex (for all Protein A detections, PAP), anti-Tubulin and anti-Flag were from Sigma, anti-TAP was from Thermo (Waltham, MA), anti-HA (12CA5) was from Roche, and anti-Ub antibodies were from Chemicon (Millipore, Billerica, MA), Stressgen (Enzo Life Sciences, Farmingdale, NY), and Abcam (Cambridge, MA). Puromycin antibody was a gift from Peter Walter, and anti-Rpl32 a gift from Jonathan Warner.
Ribosomes were affinity-purified using TAP-tagged RPL18B by following a protocol established in prior studies with some modifications as follows (Halbeisen and Gerber, 2009; Halbeisen et al., 2009). Exponential cultures were grown at either 30°C or 37°C for 1.5 hr before being harvested by filtration using 0.2 µm Nalgene filters. In some experiments 0.1 mg/ml cycloheximide was added during filtration, and was omitted when no difference was observed in the experimental outcome. Cells were washed with a buffer containing 50 mM Tris, pH 7.5, 10 mM NEM, 10 mM sodium pyrophosphate, 0.1 mg/ml cycloheximide and frozen in liquid nitrogen. Pellets were ground in liquid nitrogen. Cell powder was weighed and resuspended in twice the volume of lysis buffer (buffer A) containing 20 mM Tris–HCl (pH 8.0), 140 mM KCl, 5 mM MgCl2, 1% Triton-100, 10% glycerol, 0.2 mg/ml heparin, 0.1 mg/ml cycloheximide, 5 mM NEM, 0.5 mM AEBSF, protease inhibitor cocktail (EDTA-free; Roche), 20 U/ml DNAse I, 0.05 U/µl of RNaseOut (Invitrogen), 0.05 U/µl of SUPERase-In (Ambion), 0.5 mM DTT. Lysate was centrifuged at 5000 rpm for 5 min and the supernatant reclarified at 14,000 rpm for 10 min in a refrigerated microfuge (Eppendorf, Hamburg, Germany; 5417R). Lysate was bound to rabbit IgG conjugated to superparamagnetic Dynabeads (Invitrogen) as described by (Oeffinger et al., 2007). Using beads of this diameter enables the isolation of large complexes such as polysomes. Magnetic beads were washed twice with wash buffer (buffer B) containing 20 mM Tris–HCl, pH 8.0, 140 mM KCl, 5 mM MgCl2, 10% glycerol, 0.025 U/µl RNaseOut, 0.025 U/µl of SUPERase-In, 1 mM DTT, 0.1% NP40, supplemented with 0.1 mg/ml cycloheximide and 5 mM NEM, and then twice with buffer B lacking supplements. Elution was in buffer B containing 0.3 U/µl of Tobacco Etch Virus (TEV) protease at 16°C for 2 hr with intermittent shaking in the presence (or absence) of 2 mM puromycin, following which samples were adjusted to 0.6 M KCl and 3 mM puromycin and incubated at 37°C for 7 min. Eluates were removed after immobilization of beads with a magnet and characterized by Coomassie blue staining, immunoblotting, and RNA analysis using RNeasy mini columns (Qiagen, Valencia, CA).
A total of 25 A260 units of cultures lysed in buffer A were loaded on top of a 10–50% sucrose gradient prepared in buffer A lacking Triton X-100, glycerol and NEM. The samples were centrifuged in an SW-41 rotor for 180 min at 35,000 rpm at 4°C and fractionated while continuously recording the absorbance at 254 nm with a flow cell UV detector (ISCO, Lincoln, NE). Fractions of 0.5 or 0.75 ml were collected and analyzed by Coomassie blue staining and immunoblotting with various antibodies, including Rpl32, to identify 40S, 60S, 80S and polysomal fractions. An aliquot (100 µl) of each fraction was also analyzed for RNA using RNeasy mini columns (Qiagen). Figure 1—figure supplement 2B is representative of this protocol.
Ribosomes were also analyzed on 10–30% gradients prepared in 50 mM Hepes, pH 7.4, 2.5 mM MgCl2 and 100 mM KOAc using the SW55Ti rotor at 50,000 rpm for 100 min with slow acceleration /deceleration. 0.2 ml fractions were collected from the top. Aliquots were resolved by SDS-PAGE and immunoblotted with anti-Rpl32 and the Ab for the specific NS substrate. To aid in tRNA detection, samples were also precipitated with 10% TCA following the addition of 0.02% deoxycholate. Pellets were washed with ice-cold acetone, resuspended in 2× Laemmli buffer containing RNA secure and analyzed by NuPAGE. Representative data are shown in Figure 4B.
For analysis of tRNA-linked substrates in Figures 5B and 6B and Figure 3—figure supplement 1, we employed the method described by (Tsuboi et al., 2012). Ribosomes were sedimented at 49,000 rpm for 45 min (RP100AT4 rotor in Sorvall RC M120EX ultracentrifuge) through 0.5 M sucrose cushions in buffer C containing 20 mM Hepes, pH 7.4, 5 mM MgOAc, 100 mM KOAc, 0.5 mM DTT, 100 µg/ml cycloheximide, 200 µg/ml heparin, and the protease and RNAse inhibitor cocktails described above. Ribosome pellets were resuspended in the same buffer in the presence (or absence) of 0.5 M KCl, 3 mM puromycin, 2 µM Ub aldehyde and incubated for 15 min on ice and 30 min at 25°C. RNAse inhibitors were omitted when ribosomes were treated with 10 or 100 µg/ml RNAse A at 30°C for 10 min.
Two types of UBA resins were used to bind multiubiquitinated substrates: purified and dialyzed recombinant Gst-Dsk2 immobilized on glutathione-sepharose beads (Figures 2, 5A and Figure 2—figure supplement 1C), TUBE2-UBA (Boston Biochem, Cambridge, MA; Figure 2—figure supplement 1B, and Figure 3A). Purified ribosomes in high salt and puromycin were diluted with buffer containing 20 mM Tris–HCl, pH 7.5, 5 mM NEM, 0.1% NP40 and bound to UBA resin at 4°C for 1.5 hr. Beads were washed three times with 25 mM Tris, pH 7.5, 150 mM NaCl, 0.2% NP40 and a final wash was performed with the same buffer minus detergent. Beads were re-suspended in 2× SDS-PAGE buffer and loaded on 4–12% Tris-Glycine gels (Invitrogen). Following transfer, they were typically immunoblotted with anti-Ub antibody.
Samples to be precipitated were adjusted to 2% CTAB (Hexadecyltrimethyl-ammonium bromide; Sigma) and mixed with an equal volume of 0.5 M sodium acetate containing 0.2 mg/ml bacterial tRNA (Hobden and Cundliffe, 1978; Mariappan et al., 2010). Samples were incubated at 30°C for 10 min and then centrifuged for 10 min at room temperature. Precipitates were washed with 1% CTAB, 0.25 M sodium acetate at room temperature and resuspended in SDS-PAGE buffer.
Wildtype and mutant cells growing in synthetic medium were temperature shifted to 36°C for 1 hr and starved for methionine for 30 min. Cells were then harvested by centrifugation, resuspended in one-tenth the original volume, and pulse-labeled with 150 µCi/ml 35S-methionine (>600 Ci/mmol, cell-labeling grade; Perkin Elmer, Waltham, MA) for 90 s. Aliquots were immediately withdrawn into collection tubes containing 2× stop solution (0.2 mg/ml cycloheximide and 500 mM sodium azide), and the remainder of the cultures chased for the indicated times with 0.2 mg/ml cycloheximide and 10 mM unlabeled methionine. Ribosomes were affinity-purified from cell pellets drop-frozen in liquid nitrogen by resuspending in buffer A and lysing cells with glass beads using a Fast-Prep. Elution with TEV protease was done in the presence of 2 mM puromycin, following which eluates were bound to recombinant Gst-Dsk2 UBA resin. Washed beads were eluted in 2× SDS-PAGE buffer, and aliquots were resolved by SDS-PAGE. Gels were dried and exposed to film (Kodak, Rochester, NY).
Cell pellets were resuspended in lysis buffer A described above except that the buffering reagent was 20 mM Hepes, pH 7.4, and glycerol was omitted. Lysate was incubated on ice for ten minutes and then spun at 20,000×g for 10 min. Ribosomes were sedimented at 80,000 rpm for 65 min (RP100AT4 rotor in Sorvall RC M120EX ultracentrifuge) through 1.0 M sucrose cushions. Ribosome pellets were resuspended in SDS sample buffer and evaluated by Coomassie blue staining, or immunoboltting with anti-Ub antibodies.
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Ivan DikicReviewing Editor; Goethe University, Germany
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.
Thank you for choosing to send your work entitled “Cdc48/p97 promotes degradation of aberrant nascent polypeptides bound to the ribosome” for consideration at eLife. Your submission has been evaluated by three reviewers, two of whom are members of our Board of Reviewing Editors, and the decision has been discussed further with one of eLife's Senior Editors. The following reviewer wants to reveal his identity: Roy Parker.
General assessment and substantive concerns: This manuscript addresses the role of Cdc48 in targeting nascent aberrant polypeptides for degradation. The main conclusion is that the Cdc48 complex plays a role in disassembling tRNA-peptide-ubiquitin conjugates from the ribosome. Cdc48 has been previously characterized as a “seggregase” to remodel certain ubiquitinated substrate complexes prior to their proteasomal degradation, but these findings are relevant because they describe a new role for Cdc48 in ribosome-associated protein quality control pathways. All of the reviewers have credited the quality of the work but they also indicated that mechanistic understanding of this new pathway is missing. For example, no evidence is presented that the Cdc48 role in this process is direct and it remains possible that Cdc48 affects other aspects of the cell that indirectly lead to this phenotype. Further detailed analyses of the pathway and a better mechanistic understanding of the process are needed for publication in eLife.https://doi.org/10.7554/eLife.00308.017
The main changes from the original submission are as follows:
1. The main criticism of the original submission was that there was not sufficient mechanistic insight into how Cdc48–Ufd1–Npl4 promotes degradation of tUNCs and non-stop decay (NSD) pathway substrates that are translated from messages that lack a stop codon. In particular, we provided no evidence to indicate that the role of Cdc48–Ufd1–Npl4 in this process is direct. In a series of email and telephone discussions with the editors, we were advised that providing evidence to support a direct role for Cdc48–Ufd1–Npl4 in RAD might suffice to address the concern that the reviewers raised about mechanism. We have addressed this criticism by showing in the revised manuscript that Cdc48 and Ufd1 were associated specifically with stringently-washed, affinity-purified ribosomes (Figure 1D). We also show that Cdc48 and Ufd1 bound the NSD substrate GFHNS, but not the control GFHStop (Figure 3E), despite the latter being present at much higher levels than the NS reporter.
2. In addition to the new figure panels described above (Figures 1D and 3E), we have added the following additional data panels to address the other criticisms made by the reviewers: (i) input controls for Figure 1B, (ii) evidence that accumulation of tUNCs in cdc48-3 cells is reversed by expression of wild type Cdc48 but not the ATPase-deficient Q2 mutant (Figure 1C), (iii) an expanded Figure 2B to include a control in which RNAse was added to cell lysate prior to isolation of ribosomes, (iv) a new version of Figure 3A showing the effect of ubr1Δ and ltn1Δ on accumulation of tUNCs in cdc48-3 mutants, (v) a new version of Figure 3B showing the effect of Cdc48 pathway mutations on accumulation of the NSD substrate GFHNS, including an anti-tubulin loading control, (vi) degradation assays for GFHNS in wild type, ltn1Δ, and ufd1-2 cells and GFHStop in wild type cells (Figure 3C), (vii) high-resolution sucrose gradient fractionation of lysates of ltn1Δ and cdc48-3 cells expressing PrANS (Figure 4B; these data replace the sucrose gradient fractionations of GFHNS that were previously shown in Figure 3D), (viii) levels of Gnd1PTC in total cell extracts of various mutants (Figure 6B), and (ix) post-ribosomal supernatants from the sucrose cushion fractionation of cells expressing Gnd1PTC (Figure 6C bottom panel).
3. Because we do not have direct mechanistic data on exactly what Cdc48 is doing to promote degradation of proteins encoded by mRNAs that lack a stop codon, we have attenuated our Discussion regarding the potential role(s) of Cdc48 in this process.
One week prior to the submission of this revised manuscript, a paper was published by Jonathan Weissman's group (Brandman et. al. 2012 Cell 151, 1042-54; http://www.ncbi.nlm.nih.gov/pubmed/23178123; doi:10.1016/j.cell.2012.10.044) that partially overlaps with our own work in a complementary manner. Weissman's group was studying the heat shock response in yeast, which is mediated by the transcription factor HSF1. This led them to discover the Ribosome Quality Control (RQC) protein complex, which contains Rqc1, Tea2, Ltn1, Cdc48, Ufd1, and Npl4, as well as subunits of the 60S ribosomal subunit. Brandman et al show that Rqc1 and Ltn1 are required for association of Cdc48 with RQC, and hence they propose that Rqc1 and Ltn1 help recruit Cdc48 to the ribosome. Mutant rqc1Δ cells accumulate a model substrate (GFP–Arg12–RFP) with an internal polybasic tract that is designed to mimic an NSD pathway substrate, and Rqc1 and Cdc48 are shown to co-immunoprecipitate with this substrate. Although Weissman and colleagues propose that Cdc48 is involved in degradation of RQC substrates, no evidence is provided that Cdc48, Ufd1, or Npl4 are required for RQC function. This leaves open several possible interpretations. As but one example, their data are also consistent with the possibility that Cdc48–Ufd1–Npl4 serves as a negative regulator of RQC that blocks RQC from targeting inappropriate substrates, thereby determining the specificity of RQC action. In that sense, the two papers provide a nice complement to each other – Brandman et al describe a mechanism for how Cdc48 is recruited to NSD pathway substrates, whereas our work establishes that Cdc48, Ufd1, and Npl4 are required to release these substrates from the ribosome so that they can be degraded by the proteasome. We have modified our Discussion to incorporate the findings of Brandman et al and how they relate to our own.https://doi.org/10.7554/eLife.00308.018
- Raymond J Deshaies
The funder had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Drs. Tsui-Fen Chou, Andre Gerber, Dale Haines, Ambro van Hoof, Claudio Joazeiro, Ernst Jarosch, Roy Parker, Matthew Sachs, Thomas Sommer, Peter Walter and Jonathan Warner for reagents. David Akopian's help in using the sucrose gradient fractionator in the Shu-Ou-Shan laboratory is gratefully acknowledged. We thank current and ex-members of the Deshaies Lab for fruitful discussions, particularly Drs. Gary Kleiger and Willem den Besten. Finally, we thank Jonathan Weissman and Ramanujan Hegde for sharing data prior to publication.
- Ivan Dikic, Goethe University, Germany
- Received: October 6, 2012
- Accepted: December 21, 2012
- Version of Record published: January 22, 2013 (version 1)
© 2013, Verma et al.
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The nucleus of higher eukaryotes is a highly compartmentalized and dynamic organelle consisting of several biomolecular condensates that regulate gene expression at multiple levels (Banani et al., 2017; Shin and Brangwynne, 2017). First reported more than 100 years ago by Ramón y Cajal, nuclear speckles (NS) are among the most prominent of such condensates (Spector and Lamond, 2011). Despite their prevalence, research on the function of NS is virtually restricted to colocalization analyses, since an organizing core, without which NS cannot form, remains unidentified (Chen and Belmont, 2019; Galganski et al., 2017). The monoclonal antibody SC35, which was raised against a spliceosomal extract, is a frequently used reagent to mark NS since its debut in 1990 (Fu and Maniatis, 1990). Unexpectedly, we found that this antibody has been misidentified and the main target of SC35 mAb is SRRM2, a large (~300 kDa), spliceosome-associated (Jia and Sun, 2018) protein with prominent intrinsically disordered regions (IDRs) that sharply localizes to NS (Blencowe et al., 1994). Here we show that, the core of NS is likely formed by SON and SRRM2, since depletion of SON leads only to a partial disassembly of NS as reported previously (Ahn et al., 2011; Fei et al., 2017; Sharma et al., 2010), in contrast, combined depletion of SON together with SRRM2, but not other NS associated factors, or depletion of SON in a cell line where IDRs of SRRM2 are genetically deleted, leads to a near-complete dissolution of NS. This work, therefore, paves the way to study the role of NS under diverse physiological and stress conditions.
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