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Conceived and designed the experiments: NA OOP GC MAC. Performed the experiments: NA OOP GC MAC. Analyzed the data: NA OOP GC MAC. Wrote the paper: NA OOP GC MAC. Created most of the strains used in this work: MAC. Performed all of the Tap-tag purifications and did the mass spectrometry analyses: NA. Performed part of the co-immunoprecipitation experiments: NA OOP. Performed the glycerol gradient analyses and northern blot analyses: GC.
Ccr4-Not is a highly conserved multi-protein complex consisting in yeast of 9 subunits, including Not5 and the major yeast deadenylase Ccr4. It has been connected functionally in the nucleus to transcription by RNA polymerase II and in the cytoplasm to mRNA degradation. However, there has been no evidence so far that this complex is important for RNA degradation in the nucleus.
In this work we point to a new role for the Ccr4-Not complex in nuclear RNA metabolism. We determine the importance of the Ccr4-Not complex for the levels of non-coding nuclear RNAs, such as mis-processed and polyadenylated snoRNAs, whose turnover depends upon the nuclear exosome and TRAMP. Consistently, mutation of both the Ccr4-Not complex and the nuclear exosome results in synthetic slow growth phenotypes. We demonstrate physical interactions between the Ccr4-Not complex and the exosome. First, Not5 co-purifies with the exosome. Second, several exosome subunits co-purify with the Ccr4-Not complex. Third, the Ccr4-Not complex is important for the integrity of large exosome-containing complexes. Finally, we reveal a connection between the Ccr4-Not complex and TRAMP through the association of the Mtr4 helicase with the Ccr4-Not complex and the importance of specific subunits of Ccr4-Not for the association of Mtr4 with the nuclear exosome subunit Rrp6.
We propose a model in which the Ccr4-Not complex may provide a platform contributing to dynamic interactions between the nuclear exosome and its co-factor TRAMP. Our findings connect for the first time the different players involved in nuclear and cytoplasmic RNA degradation.
In eukaryotic cells RNAs are synthesized by 3 different RNA polymerases and they are extensively processed to reach their mature forms. In many cases the processing is accompanied by degradation of processed RNA fragments and degradation of aberrantly processed RNAs occurs through surveillance pathways. The exosome is a conserved multi-subunit 3′ to 5′ exoribonuclease complex that plays a central role in a large number of the pathways related to RNA degradation. It also plays a major role in RNA processing pathways, both in the cytoplasm and in the nucleus (for review see ). The targets for the exosome are multiple since the exosome contributes to the turnover of cytosolic mRNAs, the normal processing of nuclear rRNAs and snoRNAs, and it participates in surveillance mechanisms leading to degradation of aberrant forms of different RNAs in the nucleus. The eukaryotic exosome is made up of 9 core subunits, with 6 subunits carrying the fold of bacterial RNase PH, a phosphorolytic RNase, namely Rrp41, Rrp42, Rrp43, Rrp45, Rrp46 and Mtr3, and 3 putative RNA-binding proteins, Csl4, Rrp4 and Rrp40 . It is constitutively associated with a processive hydrolytic exoribonuclease, Rrp44, which is the only active nuclease of the yeast core exosome . In the nucleus, the core exosome is associated with 2 additional proteins, Rrp6 , another hydrolytic RNase, which provides hydrolytic activity to the nuclear exosome but might also function independently of the core exosome , and Rrp47, which cooperates with Rrp6 , . In general, the activity of the exosome is regulated through association with co-factors such as Ski7 and the Ski2, 3, and 8 complex in the cytoplasm  or the TRAMP complex in the nucleus , , .
TRAMP is particularly important for surveillance pathways in the nucleus, where it is thought that it recognizes structural features of aberrant RNAs, leading to their selective polyadenylation, followed by recruitment and activation of the nuclear exosome (for review see ). TRAMP is composed of a poly(A) polymerase, either Trf4 or Trf5, a putative RNA binding protein, Air1 or Air2, and a 3′ to 5′ RNA helicase Mtr4 , , . TRAMP also functions with the nuclear exosome to degrade cryptic non-protein coding transcripts generated by RNA polymerase II, rendering the transcripts highly unstable (CUTs) . Recent evidence has demonstrated that such transcripts control transcription initiation of stable mRNAs by RNA polymerase II using different mechanisms , , , .
The Ccr4-Not complex is another conserved eukaryotic multisubunit complex whose activity has been associated both with RNA degradation and transcriptional regulation (for reviews see , ). Indeed, one of its subunits, Ccr4, is the major yeast deadenylase , which catalyzes the first step leading to the subsequent degradation of cytoplasmic mRNAs. This activity is supported by another Ccr4-Not subunit, Caf1. Besides Ccr4 and Caf1, the yeast Ccr4-Not complex has 7 other subunits, Caf40, Caf130 and 5 Not subunits, Not1-Not5. The only subunit that is essential for yeast viability is Not1, the scaffold of the complex . Not4 is an E3 ligase whose only known substrate is the EGD/NAC complex , a chaperone associated with ribosomes that is in contact with nascent peptides , , . Ubiquitination of this chaperone by Not4 was recently shown to be important for its association with the ribosome and with the proteasome . The role of the other subunits has not been clearly defined. Several studies have demonstrated the importance of the Ccr4-Not complex for appropriate transcription initiation, in particular for the appropriate promoter distribution of the general transcription factor TFIID , and both genetic and physical interactions between the Ccr4-Not complex and TFIID have been described , . Transcription functions of the Ccr4-Not complex are also consistent with the observation that a mutation in NOT1 is suppressed by the deletion of SPT3 , encoding a subunit of the SAGA co-activator complex ,  and a protein that interacts with TBP. Though many studies have suggested roles of the Ccr4-Not complex in other cellular functions, such as resistance to ionizing radiation and DNA damage or replication stress , , mechanistic understanding of the connection between the Ccr4-Not complex and these other pathways is lacking. However, consistent with transcription and cytoplasmic RNA degradation functions, the Ccr4-Not complex, like the exosome, has been reported to have both cytoplasmic and nuclear localizations , . Indeed, while association of certain subunits with promoters has been described , , the presence of others was revealed in cytoplasmic P bodies .
A recent investigation of the role of the 8 non-essential Ccr4-Not subunits in the expression of the yeast genome revealed that each subunit had a very specific function in the expression of the genome . Surprisingly, an excessive presence of polyadenylated snRNAs and snoRNAs was highly and significantly identified in certain mutants. Such a phenotype is characteristic of nuclear exosome mutants that fail to degrade aberrant nuclear RNAs . In this study we demonstrate genetic and biochemical interactions between the Ccr4-Not complex and the nuclear RNA degradation machinery provided by TRAMP and the nuclear exosome. Our findings shed a new light on the functional organization of the Ccr4-Not complex and connect the different players involved in cellular RNA degradation.
Micro-array experiments designed to measure polyadenylated RNAs  revealed that U4 and U6 snRNAs, as well as many snoRNAs of all different types and origin (H/ACA or C/D boxes, intronic, mono-cistronic or polycistronic), were over-expressed in certain mutants of the Ccr4-Not complex, especially ccr4Δ, not2Δ, not4Δ and not5Δ (Fig. 1 and Table S1). These nuclear non-coding RNAs should in principle not be polyadenylated. However, transcripts for a wide variety of snoRNAs have been shown to accumulate as 3′-extended polyadenylated species in mutants of the nuclear exosome . In this context it is interesting to note that we isolated Rrp6, an exonuclease specific of the nuclear exosome, as a two-hybrid partner of Not1 in a genome-wide screen performed several years ago (described in ). These observations from former studies led us to investigate a possible link between the Ccr4-Not complex and the nuclear exosome in this work.
We created strains lacking Rrp6 and individual subunits of the Ccr4-Not complex. The double mutant strains displayed synthetic slow growth phenotypes when compared to the single mutants (Fig. S1). The most extreme phenotype was observed in the case of not5Δ, since the double mutant grew so poorly (Fig. 2) that it was very difficult to obtain a growth curve in liquid medium. To determine whether the synthetic growth phenotypes might correlate with synthetic defects in expression of nuclear snoRNAs, we studied the expression of one snoRNA identified in our micro-arrays, namely U14, in single or double mutant cells. Indeed, this snoRNA is processed from a polycistronic RNA  and is inappropriately processed and accumulates in larger polyadenylated forms in nuclear exosome mutants .
As expected from previous studies , , northern blot analysis with a probe specific to the sequence downstream of the 3′ end of mature U14 revealed several 3′-extended heterogeneously polyadenylated forms of this snoRNA in cells lacking Rrp6 (Fig. 3, lane 2). In particular three stabilized U14 3′-extended-species were seen: the slowest migrating one indicated by D on the left of Fig. 3 may correspond to the dicistronic precursor thought to be stabilized in the absence of Rrp6 . The second one indicated by an arrow is likely to be the 3′-extended U14 precursor that does not get processed in the absence of Rrp6 , . Finally, the third one indicated by a star has not been clearly identified, but its accumulation has been reported to be specific to deletions of Rrp6 or Rrp47 . In the single mutants of the Ccr4-Not complex (Fig. 3, lanes 3 and 5), there appeared to be an accumulation of heterogenous U14 that was faint in this experiment, but more visible in others (Fig. S2, panel A). Strikingly, when NOT4 or NOT5 were deleted in the rrp6Δ mutant (Fig. 3, lanes 4 and 6), the largest precursor D accumulated less than in the single rrp6Δ mutant, whereas the faster migrating 3′-extended U14 precursor (indicated by a star) accumulated to a greater extent. It was difficult to assess the levels of precursor D in the not4Δ and not5Δ single mutants, though it seemed to accumulate somewhat (Fig. 3, lanes 3 and 5).
Hence, the profile of inappropriately processed and polyadenylated U14 forms that accumulate in rrp6Δ cells is affected by concomitant mutations of the Ccr4-Not complex. We extended this analysis to several other snoRNAs, namely U18, snR71 and U3 and observed that similarly to the situation described for U14, the profile of extended snoRNAs that accumulate in rrp6Δ cells is affected by concomitant deletion of either Not4 or Not5 (Fig. S2 panel B).
This effect of the Ccr4-Not complex on accumulation of aberrant U14 in the absence of Rrp6 led us to determine whether the Ccr4-Not complex might have an impact on the exosome. For this, we created wild-type and ccr4-not mutant strains expressing Tap-tagged Rrp41, a core exosome subunit. The expression of the tagged protein was similar in wild-type and mutant strains (Fig. 4A, upper panel) and the tagged protein could be affinity-purified from all strains (Fig. 4A, lower panel). Interestingly, a specific subunit of the Ccr4-Not complex, namely Not5, was recovered when Rrp41 was affinity purified from cells lacking Not4 or Caf40, but not from wild-type cells or from the other mutants (Fig. 4A, middle panel).
These observations led us to analyze the affinity-purified Rrp41 from wild-type, not4Δ or caf40Δ cells by separation on SDS-PAGE followed by mass spectrometry. We identified most of the exosome subunits, and the nuclear exosome subunit Rrp6, in all 3 purifications (Fig. 4B and Table S2), but the recovery of exosome seemed greater in the case of not4Δ and caf40Δ This was not due to increased expression of exosome subunits in mutants as verified by analyzing wild-type, not4Δ and caf40Δ strains expressing each of the exosome subunits as a Tap-tagged fusion protein (data not shown). The presence of Not5 in the purifications from the two mutants was confirmed by mass spectrometry (Table S2), and Not5 was not identified in the purification from the wild-type, supporting the analysis by western blot (Fig. 4A). Control affinity purifications performed with wild-type and ccr4-not mutant strains not expressing any Tap-tagged protein revealed the presence of a low level of proteins isolated non-specifically (Fig. S3), but none of them could be determined as exosome or Ccr4-Not subunits (data not shown).
To understand why Not5 co-purified with Rrp41 specifically in certain mutants of the Ccr4-Not complex, we determined the size distribution of Rrp41-containing complexes in wild-type and mutant cell extracts. This was investigated by glycerol gradient fractionation of total cell extracts followed by western blot analysis of the fractions with antibodies against the calmodulin binding peptide entity of the Tap-tag (CBP). In wild-type cells Rrp41 eluted with a very broad profile suggesting that it was present in complexes of very different sizes (Fig. 4C), including very large complexes (fractions 17–21 at the bottom of the gradient, in which both 25S and 18S rRNAs could be found (Fig. S4)). Not5 also eluted with a broad profile, consistent with previous studies using superose 6 gel filtration analyses of total protein extracts . In particular, it was also present in fractions 17–21 (Fig. 4C). The deletion of Not4 and Caf40 lead to a loss of Not5 in the fractions corresponding to these largest complexes (see fractions 17–21 in Fig. 4C). This was not surprising for Not5 in not4Δ, since previous studies have already demonstrated a partial disruption of Ccr4-Not complexes in this deletion strain , , but it was new for Not5 in caf40Δ, since the importance of Caf40 for Ccr4-Not complex integrity has not yet been studied. Surprisingly however, these mutations of the Ccr4-Not complex also had a great impact on the elution profile of Rrp41, since the largest Rrp41-containing complexes were disrupted in caf40Δ and not4Δ (Fig. 4C, see fractions 13–21). Thus the more efficient purification of Rrp41 in caf40Δ and not4Δ in one hand and the co-purification of Not5 with Rrp41 in other hand are correlated with the release of Rrp41 from large soluble structures.
These results are compatible with the idea that the Not5-associated Rrp41 that was affinity purified in the mutants might have been released from the larger Rrp41 complexes in not4Δ and caf40Δ. However, it could also be that co-purification of Not5 with Rrp41 was detectable in the mutants simply because Rrp41 itself was more efficiently purified. Finally, the association of Not5 with Rrp41 could be an aberrant mutant phenotype resulting from the disruption of the Ccr4-Not complex.
To first exclude this latter possibility, and to additionally determine whether Not5 interacted with the entire exosome or only with Rrp41, we determined whether Not5 co-purified with any other exosome subunit in wild-type and mutant cells. Indeed, detectable levels of Not5 co-immunoprecipitated with Tap-tagged Csl4 from wild-type cell extracts and from extracts of cells lacking Caf40 (Fig. 5A). The purification of Tap-tagged Csl4 from total extracts of wild-type cells was generally more efficient than that of Rrp41 (data not shown) suggesting that the tag on Csl4 might be more accessible in the different exosome-containing complexes. In any event, these results indicate that Not5 is likely to interact with the exosome, and that this interaction occurs in wild-type cells. Indeed, Not5 could also be co-immunoprecipitated with several other Tap-tagged exosome subunits from wild-type cells (Fig. S5).
We next wanted to determine the nature of the large Rrp41-containing structures whose integrity was dependent upon the Ccr4-Not complex. In particular we wanted to determine whether they might contain RNA, since both the Ccr4-Not complex and the exosome are RNA-degrading machines. For this purpose, we prepared total protein extracts from wild-type cells expressing Tap-tagged Rrp41 that we treated or not with RNAse A prior to tandem affinity purification of Rrp41. In both cases the exosome was purified, as determined by western blot analysis with antibodies against CBP (to detect Rrp41), and against Rrp4 or Rrp43 (Fig. 5B). Not5 co-purified with Rrp41 from wild-type cell extracts treated with RNAse A but not from untreated wild-type cell extracts (Fig. 5B). Thus, in wild-type cell extracts RNA limits the accessibility of Not5-associated Rrp41. In good correlation with this finding, digestion of RNA in total cellular extracts prior to their separation by glycerol gradient centrifugation showed that the integrity of the largest Rrp41-containing complexes was indeed RNA-dependent (Fig. S6).
The co-purification of Not5 with the exosome isolated via Rrp41 or Csl4 raised the question of whether the entire Ccr4-Not complex interacts with the exosome, or whether Not5 interacts with the exosome independently of the Ccr4-Not complex. Indeed to date it is still unclear whether Ccr4-Not subunits function outside the context of a complex or not. The improved recovery of the exosome by affinity purification of tagged Rrp41 when the Ccr4-Not complex was compromised supported the idea that the entire Ccr4-Not complex was involved, but its role could have been indirect. To address this issue, we first purified Tap-tagged Not5 itself and identified Not1, Not2, Not3, and Caf40, as well as Rrp41, as co-purifying proteins (Fig. 6A and Table S3). These results confirmed an interaction between Not5 and Rrp41, but did not clearly determine whether the Ccr4-Not subunits co-purifying with Not5 were within the same complex as Rrp41. We next tandem-affinity purified the Ccr4-Not complex through different subunits from wild-type cells or from the caf40Δ mutant in which accessibility of the Not5-exosome complexes was improved (see above). Depending upon which subunit of the Ccr4-Not complex was tagged, the success in purifying intact Ccr4-Not complexes from wild-type cells was variable. For instance, purification of Tap-tagged Not4 led to isolation of complexes lacking Not2 and Caf130, purification of Tap-tagged Not2 led to isolation of complexes lacking Caf130, whereas purification of Tap-tagged Caf130 was inefficient, and only led to co-purification of Not1 (Fig. 6B). The deletion of Caf40 had a major impact in all cases. For Not2 or Not4, the co-purification of several subunits of the Ccr4-Not complex, namely Not3, Ccr4 and Caf1, was less efficient, suggesting that the core Ccr4-Not complex might be less stable in the absence of Caf40. In contrast, for Caf130 the co-purification of Not2 and Not5 was greater, suggesting that the tag on Caf130 within Ccr4-Not complexes might have become more accessible because of the Caf40 deletion. Most importantly, for the caf40Δ strains, Rrp41 and Rrp42 co-purified with the Tap-tagged Ccr4-Not subunits (Fig. 6B and Table S3). Thus, the isolation of exosome subunits by purifying different Ccr4-Not subunits besides Not5 suggests that these exosome subunits most likely interact with the integral Ccr4-Not complex.
The purification of Not2 and Not4 from caf40Δ cell extracts also led to the co-purification of Mtr4, an RNA helicase of the TRAMP complex, which serves as a co-factor for the nuclear exosome (Fig. 6B and Table S3). Mtr4 also co-purified with Tap-tagged Caf40 from wild-type cell extracts (data not shown). To confirm this interaction between Mtr4 and the Ccr4-Not complex, Mtr4 was immunoprecipitated from extracts prepared from not4Δ cells expressing myc-tagged Not4 from an episome or from caf40Δ cells expressing HA-tagged Caf40 from an episome. Both Caf40 and Not4 co-immunoprecipitated with Mtr4, and these interactions were RNA-independent (Fig. 7A and Fig. S7). We also observed the co-immunoprecipitation of other subunits of the Ccr4-Not complex (Ccr4, Not3, Not5 and Caf1) with Mtr4, using Tap-tagged Mtr4, and polyclonal antibodies against the Ccr4-Not complex subunits (data not shown). RNA degradation had no effect on the co-precipitation of Caf40 with Mtr4, whilst the co-precipitation of Not4 with Mtr4 was improved. Since Mtr4 was the bait protein each time, these results suggested that complexes containing Mtr4 and Caf40 might not entirely overlap those containing Mtr4 and Not4. We hence tested the association of Mtr4 with Not4 in caf40Δ, and the association of Mtr4 with Caf40 in not4Δ. The deletion of Not4 led to a reduced co-precipitation of Mtr4 with Caf40. In contrast, the co-precipitation of Mtr4 with Not4 was improved in the absence of Caf40 (Fig. 7B) and the same was observed for the co-precipitation of Mtr4 with the other subunits of the Ccr4-Not complex mentioned above (not shown). Hence Not4 contributes to the interaction between Caf40 and Mtr4, but Caf40 seems to be in competition with the interaction between Mtr4 and other subunits of the Ccr4-Not complex. Interestingly, Caf40 co-immunoprecipitated with another subunit of the TRAMP complex, the Trf4 polymerase, and this co-immunoprecipitation was also decreased in cells lacking Not4 (Fig. 7C). In addition, Not5 co-immunoprecipitated not only with Tap-tagged Mtr4 (as mentioned above) and with Tap-tagged Air1 (data not shown) but also with Tap-tagged Air2 (Fig. S5). These results suggest that the Ccr4-Not complex interacts with TRAMP and that probably in this context Not4 contributes to the association of Caf40 with TRAMP.
The results presented so far show that the Ccr4-Not complex can interact with the nuclear exosome on one hand and with Mtr4 on the other hand. This led us to question whether it might play a role in the interaction of the nuclear exosome with its co-factor. To address this question, we created wild-type and ccr4-not mutant strains expressing Tap-tagged Rrp6 and immunopurified Rrp6 using a single affinity step. Equal levels of Rrp6 were purified from all strains (Fig. 8A, upper panel), and Mtr4 generally co-purified with Rrp6, but to reduced levels from not4Δ compared to wild-type cells and not at all from caf40Δ (Fig. 8A, lower panel). However, expression of Mtr4 was similar in wild-type and ccr4-not mutant strains (Fig. 8B), and the co-purification of Rrp6 with the exosome was similar in wild-type and mutant strains (shown for not4Δ in Fig. 8C). Thus, it seems that the association of Mtr4 with Rrp6 might be compromised in caf40Δ. To confirm this finding we created wild-type and caf40Δ strains expressing myc-tagged Rrp6, and immunoprecipitated Mtr4 to determine the presence of Rrp6 in the immunoprecipitate. Though equal levels of Mtr4 were immunoprecipitated from both strains, no co-precipitation of Rrp6 with Mtr4 was detected in caf40Δ (Fig. 8D). Thus, the interaction between Mtr4 and Rrp6 is indeed compromised in caf40Δ.
In this work, we have made the exciting finding that the Ccr4-Not complex, whose role in cytoplasmic RNA degradation has been clearly demonstrated , is also connected to the nuclear RNA degradation machinery. Starting from our finding in a previous study of a very significant accumulation of polyadenylated snoRNAs in several mutants of the Ccr4-Not complex  we observed synthetic growth phenotypes when mutants of the Ccr4-Not complex were combined with the deletion of the nuclear exonuclease Rrp6, whose role in processing and degradation of aberrantly processed snoRNAs has been clearly established. These genetic interactions are consistent with our identification of a remarkable alteration in the profile of aberrantly processed and polyadenylated U14 snoRNA in rrp6Δwhen the Ccr4-Not complex was mutated. We could determine that these genetic and functional interactions correlate with physical interactions between the Ccr4-Not complex and the nuclear RNA degradation machinery provided by TRAMP and the nuclear exosome. Indeed, we demonstrated that Not5 co-purified with the exosome through Rrp41 or Csl4, that the purification of Ccr4-Not complexes through different subunits led to the co-purification of the Rrp41 and Rrp42 subunits of the exosome, and that the association of the exosome subunit Rrp41 in very large soluble structures was dependent upon subunits of the Ccr4-Not complex. We also provided evidence that the Ccr4-Not and exosome complexes are likely to be associated in RNA-containing structures. Finally, we showed that the Ccr4-Not complex was physically associated with the Mtr4 RNA helicase, a subunit of the TRAMP complex and co-factor of the nuclear exosome.
Though we did not demonstrate that Mtr4 and Rrp41 were a part of the same Ccr4-Not containing complex, it is interesting to note that Mtr4 and exosome subunits were purified together with the Ccr4-Not complex in the same affinity purifications. At present we cannot be sure that these interactions occur within a single soluble structure, but these results are nevertheless compatible with a model in which the Ccr4-Not complex physically connects the nuclear exosome and its co-factor Mtr4 of TRAMP. Because the exosome and Ccr4-Not interactions occur in RNA-containing structures, it is very tempting to speculate that the Ccr4-Not complex may contribute to the dynamic assembly of the nuclear RNA degradation machinery with its target RNAs.
It may seem surprising that such interactions have not been described so far, despite extensive work and purification of both TRAMP and exosome complexes in many different studies, including , , , , , , , , . However, we identified these interactions first in situations where the integrity of the Ccr4-Not complex was perturbed, situations in which the exosome and TRAMP have not been purified previously.
As mentioned above, our study revealed a series of physical interactions between Ccr4-Not, exosome or TRAMP subunits. However curiously, when purifying the Ccr4-Not complex in different ways, we only co-purified at most a couple of the exosome subunits and only Mtr4 of TRAMP, and similarly when purifying the exosome, we only co-purified Not5 of the Ccr4-Not complex. This raises the question of whether the partial entities that we isolated exist as such in vivo. However, we believe that this is highly unlikely and rather imagine that in vivo the Ccr4-Not complex interacts with the integral exosome and maybe also the integral TRAMP complex. Nevertheless, we cannot exclude that the Ccr4-Not complex might serve as some form of a chaperone for TRAMP and/or the exosome in vivo, and that this explains why it can be isolated interacting only with certain subunits of these complexes. Alternatively, it could be that the interactions between these entities are highly dynamic and only stabilized in the largest structures where however the accessibility to purification of the different components is reduced. Hence, partial disruption of these structures required to access the different components may also disrupt or destabilize certain entities such that only the directly interacting partners are captured during purification. If this is the case, according to the different analyses that we performed, Not5 and Rrp41 would be the subunits within each complex that directly interact. Rrp42 was isolated in certain cases with Rrp41 and the Ccr4-Not complex and may be closely connected to Rrp41 within the exosome. This is certainly supported by the three dimensional interaction map derived by isolating exosome complexes directly from cells . It will be interesting to see whether an interaction between Rrp41 and Not5 can indeed be recapitulated in vitro.
In the case of the interactions between the Ccr4-Not complex and TRAMP, Mtr4, but none of the other subunits of TRAMP were identified by mass spectrometry in any of our purifications, suggesting that it is the most direct partner of the Ccr4-Not complex. Concerning which subunit of the Ccr4-Not complex may be the privileged partner of Mtr4, this is still an open question.
It is clear that none of our experiments have actually determined that the interactions between the Ccr4-Not complex and either the exosome or TRAMP are directly mediated by interactions between subunits of these different complexes. However we have no evidence for the presence of additional proteins in our purifications that might serve as adaptors and RNA is not required for the interactions. In vitro experiments will nevertheless be required to determine this more precisely.
This study has demonstrated an RNA-independent interaction between Not5 and the exosome, and between Mtr4 and the Ccr4-Not complex. It has also revealed the importance of certain Ccr4-Not complex subunits for co-purification of the nuclear exosome with its co-factor Mtr4. In parallel, non-coding nuclear RNAs whose turnover and/or processing needs the nuclear degradation machinery are also affected by the Ccr4-Not complex. An exciting implication of these findings is that the Ccr4-Not complex might be important to connect Mtr4 with the nuclear exosome for processing and/or degradation of their target RNAs.
Two subunits of the Ccr4-Not complex come out as particularly interesting in this functional association of the Ccr4-Not complex with the nuclear RNA degradation machinery. Not5, on one hand, co-purifies with the exosome, and its deletion is nearly lethal in cells lacking Rrp6. It might play a key role to bring the exosome to the Ccr4-Not complex. Caf40, on the other hand, is important for the integrity of the largest exosome-containing soluble structures and for the interaction between Rrp6 and Mtr4, but it competes for the interaction between Mtr4 and the other subunits of the Ccr4-Not complex. An exciting model (Fig. 9) is that the Caf40-Mtr4 interaction might be key to establish interactions between RNA-bound TRAMP, the Ccr4-Not complex and the nuclear exosome, but then also to transfer Mtr4 (and TRAMP) to the nuclear exosome, and to release it from the Ccr4-Not complex. In other words it might ensure dynamic interactions between all of these components. Our observation that the not5Δ rrp6Δ double mutant on one hand, and not5Δ caf40Δ double mutant on the other hand (unpublished data) have severe growth defects is compatible with the idea that Not5 and Caf40 might participate at different steps in the functional connection of TRAMP and the nuclear exosome.
Obviously, at present the mechanism by which the Ccr4-Not complex may be contributing to nuclear RNA expression with the nuclear exosome remains to be determined. Whether it may serve strictly as a platform allowing the appropriate assembly of the different partners, namely precursor RNA, nuclear exosome and TRAMP, or plays roles after processing, or even plays more direct roles for instance through the Ccr4 deadenylase, or by connecting nuclear events to the cytoplasm, really needs to be addressed. It will be interesting in a next step to confirm the roles attributed to Not5, Rrp41, Caf40 and Mtr4 in our model, and determine whether disruption of the proposed interactions will have an impact on nuclear exosome function. Finally, because it is becoming increasingly clear that unstable transcripts degraded by the nuclear exosome machinery contribute to regulate transcription, it will also be interesting to determine how much of the transcriptional phenotypes attributed to the Ccr4-Not complex might be indirectly due to inappropriate nuclear exosome function.
The strains used in this study are listed in Table 1. All media were standard, either YPD for glucose rich medium, or synthetic complete media when the presence of a plasmid was selected for. Single-step deletions or tagging were performed by PCR as described by Longtine . All of the strains were checked with a PCR reaction performed on genomic DNA extracts using a primer localized in the marker gene and a primer localized at the 5′ non-coding sequence of the target gene. All primers used are available upon request. Many new strains were created by crosses followed by sporulation and tetrad dissection. Plasmids expressing N-terminally tagged Not4 from the NOT4 promoter (pMAC684) and Caf40 from the SPT3 promoter (pMAC728) were made by PCR and homologous recombination, using the Drag and Drop system , and verified by sequencing.
For analysis of snoRNA steady-state levels, total cellular RNA was separated on an 8% polyacrylamide denaturing gel and electro-transferred to a nylon membrane in 0.5X TBE buffer. After cross-linking of the RNAs to the membrane by UV radiation, the membrane was hybridized with radio-labelled probes specific for the different mature or 3′extended snoRNAs or rRNA transcripts (sequences available upon request).
Large-scale tandem affinity purifications from wild-type or mutant cells were performed as previously described with 2 g of total protein extract  except that the NaCl concentration was 150 mM. Small-scale purifications with Tap-tagged proteins were essentially done the same way except that only 2 l of cells were grown, and 60 mg of protein extracts processed with the volumes scaled down. Elution with TEV protease was performed with 1 ml, of which 200 µl were directly analyzed after TCA precipitation on SDS-PAGE followed by coomassie staining and 50 µl were analyzed for western blotting.
For mass spectrometry analysis the sample preparation, gel separation and gel staining were performed according to the SWISS-2D-PAGE protocols. Briefly, the samples were separated on 4–12% SDS-PAGE gradient gels and stained using coomassie in keratin free conditions. The visualized bands were excised from the gel and treated for mass spectrometry fingerprint analysis as following: they were washed 15 min at RT with acetonitril 30%, incubated 35 min at 56°C in 1,4,-dithioerythritol 10 mM, followed by 30 min incubation in iodoacetamid 55 mM at room temperature in the dark. After one wash for 10 min with ammonium biocarbonate 50 mM pH 8.0 and two other washes of 10 min with acetonitril 30%, samples were then completely dried down in a vacuum centrifuge for 1 h. After sample rehydration in 20 µl of freshly prepared digestion buffer containing 6.25 ng/µl trypsin for 45 min on ice, digestion was allowed to proceed over night at 37°C. To extract the peptides from the gel digestion supernatant was recovered and pooled with two successive washes of 20 min using 40 µl trifluoroacetic acid (TFA) 1% and one wash using TFA 0.1%. The collected supernatants were lyophilized to remove salts and washed again with 35 µl TFA 0.1% before sample concentration to 2–5 µl. 1 µl was loaded on a MALDI plate and after matrix addition, sample acquisition was performed using the MALDI-Tof MS (VOYAGEUR CONTROL PANEL program) and peptides were submitted to fingerprinting analysis. The obtained spectra were finally analyzed using the DATA EXPLORER program and proteins were identified using the MASCOT SEARCH website. When not provided as supplementary data, all identified peptides and scores are available upon request.
100 ml of cells expressing myc6-tagged Not4 or HA7-tagged Caf40 from plasmids were collected at an OD600 of 1.0 and broken with glass beads in 0.5 ml of buffer A (150 mM potassium acetate pH 7.5, 20 mM TrisHCl pH 8.0, 5 mM MgCl2, 0.1% Triton X-100, 1 mM DTT, 0.5 mM PMSF, Roche Anti Protease tablets) and spun at 16'000 g for 30 min at 4°C. Lysates were brought to equivalent protein concentration and 30 µl of lysates were boiled with 30 µl of 2 times concentrated SDS-sample buffer and used as total extracts (TE). 0.4 ml of the lysates containing 5 mg of total protein were treated or not with RNAse A (final concentration 1 µg/ml) for 5 min at room temperature and then were incubated with 20 µl of Protein-G-magnetic beads overnight at 4°C with (IP) or without (IP0) antibodies against Mtr4. Beads were washed three times with 1 ml buffer A and boiled with 40 µl of 2 times concentrated SDS-sample buffer. To analyze the proteins co-immunoprecipitated with Mtr4, 20 µl of total extracts (TE) and 20 µl of immunoprecipitates (IP) were loaded on an SDS-PAGE gel followed by western blotting with antibodies against the tag. To analyze the efficiency of RNAse A treatment, RNA was extracted from total extracts and loaded on a 1% agarose gel stained by ethidium bromide.
For cells expressing Tap-tagged proteins, extracts were prepared in 40 mM Hepes pH 7.5, 1 mM EDTA, 20% glycerol, 150 mM potassium acetate, 100 mM potassium chloride and protease inhibitors. 2 mg of extracts in 210 µl buffer were incubated overnight at 4°C with 40 µl of magnetic beads coupled to protein G equilibrated in the same buffer with or without 1 µl of antibody against CBP. After washing, the proteins were eluted from the beads in 20 µl of 2 times concentrated SDS-sample buffer.
Total protein extracts (5 mg) were submitted to size separation on a 10 to 30% glycerol gradient in A200 buffer (200 mM potassium acetate, 20 mM Tris/HCl pH 8.0, 5 mM Mg acetate, 1 mM DTT). The gradients were spun at 4°C for 10 h at 20000 rpm in Beckmann Sw41 Ti rotor. 500 µl fractions were collected and proteins were extracted from 250 µl by 30 min precipitation in 10% TCA followed by resuspension in 30 µl of SDS loading buffer and 10 µl were analyzed by SDS-PAGE and western blotting. RNA was extracted from the other 250 µl by phenol chloroform extraction and ethanol precipitation and analyzed by migration on a 1% agarose gel.
Synthetic growth phenotypes when deletions of RRP6 and the Ccr4-Not complex are combined. The indicated strains were grown at 30°C exponentially in high glucose for 24 hours, then diluted to an OD600 of 0.2 and followed for growth during the next 11 hours by measuring the OD600.
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Accumulation of heterogeneous U14 in mutants of the Ccr4-Not complex. A. Total cellular RNAs isolated from the indicated strains were analyzed by northern blot with a probe against mature U14. The position of mature and extended and polyadenylated U14 is indicated on the right of the blot. A low exposure of the blot was added as a bottom panel to be able to assess the relative levels of mature U14. B. Total cellular RNAs isolated from the indicated strains were analyzed by northern blot with probes against several 3prime-extended snoRNAs (U18, snR71 and U3). The positions of mature and extended snoRNAs are indicated on the right of the blot.
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Low unspecific background binding of proteins in the tandem affinity purification. Total protein extracts prepared from the indicated strains were subject to the tandem affinity purification protocol. The proteins eluted from the second column were separated by SDS-PAGE and the gel was stained with coomassie. Mass spectrometry analysis of the visible proteins did not reveal any Ccr4-Not complex or exosome subunit (data not shown).
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Analysis of RNA in glycerol gradient fractionation of total cell extracts. RNA was extracted from 250 microlitre of the glycerol gradient fractions obtained from wild-type cells expressing Tap-tagged Rrp41 (see Fig. 4C, top panel), and these fractions were then analyzed on a 1% agarose gel which was further stained with ethidium bromide to reveal abundant RNAs. The visible tRNAs, and the 18S and 25S rRNAs are indicated.
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Not5 co-immunoprecipitates with subunits of the exosome and TRAMP complexes. Total protein extracts were prepared from wild-type cells expressing Tap-tagged Rrp45, Rrp46, Mtr3, Rrp43, Rrp40, Rrp4 or Air2, namely from strains MY6425, MY6430, MY6428, MY6429, MY6423, MY5567 or MY7010. 2mg of total protein extracts was incubated with (IP) or without (IP0) antibodies against CBP. 50 mg of total extract (TE), equivalent volume of unbound extract (FT) and the immunoprecipitate were loaded on SDS-PAGE followed by western blotting with antibodies against Not5, which revealed both Not5 and the Tap-tagged proteins as indicated.
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RNA is required for the integrity of the largest Rrp41-containing complexes. 5 mg of total protein extracts prepared from wild-type cells expressing Tap-tagged Rrp41 and treated or not with RNAse A as indicated were loaded on a glycerol gradient. Proteins in the different fractions of the gradient were precipitated by TCA and analyzed by SDS-PAGE and western blotting for the presence of Tap-tagged Rrp41 with antibodies against CBP. This gradient was spun for 12 rather than 10 hours leading to greater sedimentation. Hence the first peak of Rrp41 sediments in fractions 10–13 rather than fractions 3–8 as in Fig. 4.
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Verification of RNA digestion for total cellular extracts treated with RNAse A. The RNA present in the total protein extracts prepared from not4delta or caf40delta cells expressing tagged Not4 or tagged Caf40 respectively, that were digested or not with RNAse A (see Fig. 7), was analyzed by migration on a 1% agarose gel stained with ethidium bromide.
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The results of the micro-array analyses for all of the snRNAs and snoRNAs present on the ChIPs are indicated, as well as a description of the types of snoRNAs as obtained from the yeast snoRNA database at US Amherst (http://people.biochem.umass.edu/fournierlab/snornadb/main.php).
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List of the peptides identified by mass spectrometry with scores for identified proteins.
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List of the peptides identified by mass spectrometry with scores for identified proteins.
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We thank Prof. Patrick Linder for oligonucleotides, antibodies against Mtr4 and a critical reading of this manuscript. We thank Prof. David Tollervey for the strain expressing Tap-tagged Csl4 and for antibodies against Rrp4 and Rrp43. Finally we thank Dr. Stapanka Vanacova for the strain expressing Tap-tagged Trf4. We would also like to thank Henrike Henye for her contribution to several key experiments.
Competing Interests: The authors have declared that no competing interests exist.
Funding: This work was supported by the Leenards Foundation, the Lucie and Ernst Schmidheiny Foundation and by grant 3100AO-100793 and 3100A0-120419/1 from the National Science Foundation, as well as by an IHP/Network European grant HPRN-CTG-2002-00261 supported by the Office Federal de l Education et de la Science, grant #02.0017, to M.A.C. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.