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Sir William Dunn School of Pathology, Oxford OX1 3RE, United Kingdom
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[Keywords: 5'–3' exonuclease; RNA polymerase I; S. cerevisiae; transcription termination]]
Received November 13, 2007; revised version accepted February 29, 2008.
). Knowledge of the molecular details that result in transcriptional initiation (e.g., through enhancer and promoter recognition) is now quite well advanced, especially for Pol II. However, the subsequent stages of the transcription cycle, elongation and termination, are less well described. In particular, the molecular process that switches each class of polymerase from processive elongation into termination is poorly understood but may differ significantly for each polymerase class. For Pol III, which copies relatively short genes, the mechanism of termination appears to be an intrinsic feature of the polymerase itself and especially the small subunit Rpc11p. Here simple sense-strand oligo(dT) sequences appear to define Pol III termination sites (Braglia et al. 2005). In marked contrast, the mechanism of Pol II termination is far more complex, being intimately connected to processing of the pre-mRNA. Thus capping, splicing, and cleavage/polyadenylation of the pre-mRNA all occur cotranscriptionally, mediated by mRNA processing factors that are known to interact directly or indirectly with the Pol II large subunit, the C-terminal domain (CTD) region, depending on its phosphorylation state (Orphanides and Reinberg 2002). Significantly, Pol II termination is dependent on pre-mRNA 3' end processing and requires a specific set of termination factors and complex genetic signals (Proudfoot 2004; Buratowski 2005). Additionally, Pol II termination requires at least some of the cleavage/polyadenylation factors that, as well as processing the pre-mRNA, may elicit structural or conformational changes to Pol II, somehow priming this molecular machine to terminate (Proudfoot 2004). Coupled to this, cleavage at the poly(A) signal generates a nascent RNA 3' product still attached to elongating Pol II. This RNA has an exposed, uncapped 5' terminus that is now susceptible to nuclear 5'–3' exonuclease degradation by Saccharomyces cerevisiae Rat1p (Kim et al. 2004b) or mammalian Xrn2 (West et al. 2004). Several studies have shown that this degradation process results in removal of the nascent RNA up to the elongating Pol II that then induces polymerase template release. This termination process has been dubbed the "torpedo" mechanism (Tollervey 2004). However, the relative importance of nuclease "torpedoes" over cleavage/poly(A) factors in eliciting Pol II termination remains an issue of active research and debate in the field (Luo et al. 2006; Kaneko et al. 2007). A further complexity of the Pol II termination process is that some specialized small genes, such as those encoding snRNA and snoRNA, in S. cerevisiae operate an ostensibly different termination mechanism involving an RNA-binding factor, Nab3p; a CTD-binding factor, Nrd1p; as well as a large protein containing a helicase domain called Sen1p (Steinmetz et al. 2001; Kim et al. 2006). It is possible that some or all of these factors may also act to promote termination on specific classes of Pol II genes encoding polyadenylated mRNAs (Steinmetz et al. 2006).
Pol I transcription displays many close parallels with that of Pol II. Transcription elongation, as with Pol II, is coupled to pre-rRNA processing. This can be visualized by EM analysis of rDNA captured by the "Miller Spreading" technique, which shows characteristic "Christmas tree" structures representative of multiple Pol I elongation complexes transcribing the rDNA template in tandem (French et al. 2003). Nascent pre-rRNAs display RNA:protein complex particles associated with the 5' termini of progressively lengthening pre-rRNA, still attached to the Pol I:rDNA template. This complex contains RNA processing activities that cotranscriptionally cleave and degrade the transcript, thus generating mature rRNA (Dragon et al. 2002). The mechanism of Pol I transcriptional termination has also been investigated extensively, especially by using in vitro systems. In both yeast and mammals, a DNA-binding protein, Reb1p in S. cerevisiae and TTF1 in mouse, is shown to interact with specific DNA sequences in the spacer sequence downstream from the Pol I transcription unit (Grummt et al. 1986; Kuhn et al. 1990; Lang and Reeder 1993). This DNA-bound protein was shown to pause Pol I elongation, which then promoted transcriptional termination at a pyrimidine-rich "release" sequence just upstream of the terminator-bound Reb1p (Lang et al. 1994; Jeong et al. 1995). In mammals, Pol I transcript release at this position is facilitated by a specific release factor (Jansa et al. 1998; Jansa and Grummt 1999). While this mechanism may account for Pol I termination in purified in vitro systems, the in vivo picture is more complex. Several additional Pol I termination factors have been described more recently that suggest that the Pol I termination mechanism may be more complex than anticipated. In particular, the inessential Rpa12p small subunit of Pol I is required for both Pol I elongation and termination based on transcription run on (TRO) analysis of an rpa12 gene deletion strain (Prescott et al. 2004). This suggests a direct involvement of Pol I itself in the termination process. The endoribonuclease III protein Rnt1p, which is known to generate the initial 3' end cleavage of the pre-rRNA, is also required for efficient Pol I termination (Prescott et al. 2004). The requirement of Rnt1p for Pol I termination points to the possibility that a 5'–3' exonuclease degradation process may act on the remaining nascent transcript, still attached to Pol I, and so promote termination by a torpedo-like mechanism.
We have re-evaluated the torpedo mechanism for Pol II termination and tested if Pol I also employs a related mechanism. While we confirm that both Rpa12p and Rnt1p are indeed required for Pol I termination, we also show that Rat1p 5'–3' exonuclease is required. However, for both Pol II and Pol I termination, inactivation of Rat1p alone is insufficient to display a full termination defect. Instead, by combining Rat1p and Sen1p inactivation, we observe more severe termination defects. These data therefore point to the cooperation of these proteins in mediating efficient Pol II and Pol I termination. Consequently, we predict that each polymerase uses a torpedo mechanism to define the end of its transcription cycle.
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Results |
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We began these studies by re-evaluating the roles of previously defined Pol I termination factors. The well-documented involvement of Reb1p was first tested by measuring its occupancy on chromatin associated with S. cerevisiae Pol I and Pol II promoters, as well as the Pol I termination region. Chromatin immunoprecipitation (ChIP) experiments were performed (Fig. 1A,B) on strains containing either genetically HA-tagged Pol I Rpa14p subunit or Reb1p. Strong ChIP signals (Fig. 1A,B, gray bars) were detected across the Pol I 35S gene for the Rpa14p-tagged strain, but were at near background levels upstream of the Pol I promoter (Fig. 1A,B, US 5S primers) as well as downstream from the well-defined Pol I terminator region (Fig. 1A,B, cf. primer signals 2 + 3 and 4, 6 + 7). As expected, no significant signal was detected for the SIN3 Pol II promoter. In contrast, strong Reb1p signals (Fig. 1B, black bars) were detected over known Reb1p-binding site regions in the Pol I rDNA and Pol II SIN3 promoters. Significantly, only background signals were detected in the Pol I terminator region (Fig. 1A,B, primers 2 + 3), even though a Reb1p-binding site has been defined in this region at least in vitro (Kulkens et al. 1989; Morrow et al. 1989). We therefore predict that while Reb1p may associate transiently with the Pol I terminator region in such a manner that it is not detectable by ChIP, more stable interactions as observed for the rDNA and SIN3 promoters do not occur with chromatin at this position. To rule out potential artifact effects of the HA tag on Reb1p binding or epitope masking, we repeated the ChIP analysis using a Reb1p polyclonal antibody. However, again the ChIP signal was only detected over the Pol I promoter but not the terminator region (data not shown).
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) containing engineered rDNA repeats that carry a 190-base-pair (bp) deletion in the Pol I termination region extending from just upstream of the Reb1p-binding site to downstream from a T-rich sequence region, including both a binding site for a second DNA-binding protein (Reb2p) (Morrow et al. 1989) and a so-called fail-safe terminator region (Reeder et al. 1999). Since URA3 was inserted into this deletion (to allow its selection), we used TRO oligonucleotide probes (3', 4', and 5') over URA3 to detect read-through Pol I transcripts (Fig. 1A). As shown with the isogenic wild-type strain (TAK314), Pol I termination occurs efficiently beyond the Reb1p-binding site region (Fig. 1C). However, in the deletion stain (TAK401), Pol I transcription extends into the antisense URA3 sequences, indicating a disruption to the Pol I termination process (Fig. 1C). These data confirm that the Pol I terminator region is indeed required for efficient Pol I termination. We finally attempted to address whether Reb1p itself is required for this termination process as predicted by in vitro experiments (Lang et al. 1994). We therefore engineered a yeast strain in which REB1 is tagged with a degron sequence to promote specific degradation of this protein when raised to a nonpermissive temperature (Supplemental Fig. 1A; Dohmen et al. 1994). However, even after 3 h of temperature shift, 
25% of the Reb1p, as compared with the amount of protein detected at the permissive temperature, was still detected in this strain. This suggests that strong selection acts to maintain minimal levels of this essential, pleiotropic transcription factor. TRO analysis of the Reb1p degron strain (showing fourfold reduction in Reb1p levels) did not reveal any significant loss of Pol I termination as compared with wild-type cells (Supplemental Fig. 1B).
Overall, these data suggest that Reb1p is unlikely to play a critical role in Pol I termination in vivo. Thus the absence of detectable Reb1p on Pol I terminator chromatin as well as the lack of any detectable termination defect of a fourfold reduction in Reb1p levels argues that the previous Pol I in vitro termination assays, which implicated Reb1p in this process (Lang and Reeder 1993; Lang et al. 1994), may have overlooked additional in vivo effects. However, it is also clear that the Pol I terminator sequence is required for Pol I termination to occur efficiently. Since this sequence is highly T-rich in the sense strand, it is possible that U-rich sequences as part of the nascent transcript in association with proteins bound to the template DNA may induce transcriptional pausing effects that could facilitate Pol I termination.
We next performed TRO analysis on strains deleted for either RPA12 or RNT1 (Fig. 1D). This shows a clear termination defect for both of these deletion mutant strains as compared with their isogenic wild types. While a strong termination defect for rpa12
was reported previously, the defect observed for the rnt1 strain was found previously to be less severe (Prescott et al. 2004). However, we note that in our current analysis, loss of Rnt1p appears to have almost as strong a termination defect as loss of Rpa12p. We predict that this experimental difference may reflect different growth conditions between these separate experiments.
Overall, these initial results confirm that both Rnt1p and Rpa12p play significant roles in Pol I termination. However, our experiments on the role of Reb1p in Pol I termination suggest that additional mechanisms are likely to operate in an in vivo situation.
Both Rat1p and Sen1p are required for Pol II termination at the CYC1 and PMA1 genes
Previous studies in yeast and mammals have demonstrated the involvement of 5'–3' exonucleases in Pol II termination of genes encoding polyadenylated mRNA. However, in these studies, the effect of deleting RAT1 on Pol II termination was often relatively minor, causing only twofold to threefold read-through of Pol II beyond the normal site of termination (Kim et al. 2004b). We therefore sought to identify other factors that might cooperate with Rat1p in the Pol II termination process. An attractive candidate was the DEAD-box helicase Sen1p (Ursic et al. 1997), since this protein is a known component of the alternative Pol II termination pathway also involving the RNA-binding protein Nab3p and Pol II CTD-binding protein Nrd1p (Steinmetz et al. 2001). It seemed plausible that Sen1p, through its RNA helicase activity, could act to expose the downstream RNA product generated by cleavage and polyadenylation and so facilitate Rat1p-mediated degradation of the nascent, Pol II-associated transcript.
In these experiments, we initially used the well-defined Pol II terminator of the CYC1 gene (Birse et al. 1998). Yeast strains were generated with either single or double conditional (temperature-sensitive) mutations in RAT1 and SEN1, and each was transformed with a GAL1-CYC1-containing plasmid (Birse et al. 1998). TRO was performed on these four strains (wild type, rat1-1, sen1-1, and rat1-1 sen1-1) using a series of single-stranded M13 probes extending over and 3' to the CYC1 gene (Fig. 2A). Note that the convergent gene UTR1 is not transcribed in this plasmid as its promoter is absent. Also, the endogenous CYC1-UTR1 locus is expressed at very low levels (Alen et al. 2002) and so does not significantly contribute to the observed run on signals. Figure 2B shows representative TRO data for the four yeast strains, obtained by probing over the plasmid-borne CYC1 gene. Quantitation of these TRO data is shown below by normalizing to the value obtained for probe 1 within the CYC1 gene. While wild type gives the expected strong termination pattern indicated by high signals for probes 1 and 2, lower signal for probe 3 and background signals for probes 4–6, both the single mutant strains rat1-1 and sen1-1, show similar levels of increased read-through transcription. Importantly the combined rat1-1 sen1-1 strain gave higher read-through transcription levels, indicating that the double mutation has an additive effect over the single mutations. These data were reproduced in multiple, independent experiments and gave closely similar transcription profiles.
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). In both the single rat1-1 and sen1-1 mutant strains, significantly more Pol II signal was detected with PCR primers p7 and p9, indicative of Pol II termination defects. We also observe with rat1-1 that there appears to be some depletion of Pol II signal over the 3' end of the gene (p5 and p6), which may reflect enhanced pausing in this mutant background. Strikingly, with the double rat1-1 sen1-1 strain, even higher levels of Pol II were detectable downstream from the normal termination region. We note that a small increase in Pol II occupancy is detected for the inactive negative control gene MUC1 in both the sen1-1 and rat1-1 sen1-1 mutant strains (Fig. 3B). This may reflect read-through transcription from adjacent gene loci. The RT–PCR analysis of PMA1 read-through transcripts with the same four strains showed broadly similar results (Fig. 3C). While the wild-type strain gave little detectable signal beyond the second poly(A) signal, both rat1-1 and the double rat1-1 sen1-1 strains gave high levels of read-through transcripts reading into downstream LEU1. The sen1-1 strain gave lower, though significant, levels of read-through transcript. Since this RT–PCR analysis measures total cellular RNA levels, we predict that inactivation of Rat1p will increase read-through transcript levels both through loss of transcript degradation as well as loss of Pol II termination. Our results on PMA1 in these mutant strains broadly matches those obtained with CYC1. We therefore conclude that Rat1p and Sen1p cooperate to promote efficient Pol II termination on both genes.
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Both Rat1p and Sen1p are required for fully efficient Pol II termination, at least for the two tested Pol II genes, CYC1 and PMA1 (Figs. 2, 3). We therefore sought to establish a potential role for these two proteins in Pol I termination. As a first approach, we wished to determine if Rat1p and Sen1p are detectable on rDNA chromatin. We therefore used yeast strains with TAP tags on their endogenous RAT1 or SEN1 genes. We then performed ChIP analysis for the presence of Rat1p and Sen1p by immuno-selecting TAP-associated chromatin and clearly detected the presence of both proteins across rDNA genes (Fig. 4A,B). We presume that Rat1p and Sen1p are associated with active rDNA repeats, as the silenced rDNA repeats are likely to be inaccessible. Rat1p appears to display some signal across the whole locus but with a signal peak over region 4, just beyond the normal position of Pol I termination. Similarly, Sen1p is detectable across the rDNA cluster with a peak of signal directly over the termination region. As a control, Rat1p and Sen1p were also detected over the CYC1 gene, and here again Rat1p gave a strong 3' but relatively weak 5' signal, while Sen1p gave more even, positive signals over both tested CYC1 regions. We conclude from these ChIP analyses that Rat1p and Sen1p are indeed associated with rDNA chromatin in such a manner that they may potentially play direct roles in Pol I transcription elongation and/or termination. In the case of Sen1p, previous reports have noted the widespread association of Sen1p with Pol II genes consistent with our present data (Steinmetz et al. 2006).
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Rat1p and Sen1p cooperate to promote efficient Pol I termination on rDNA genes
We next measured the profile of actively transcribing Pol I across rDNA genes in the wild-type, rat1-1, sen1-1, and rat1-1 sen1-1 strains using TRO analysis, and then confirmed these results by Pol I ChIP analysis. Each of these strains were subjected to a time course of growth at the restrictive temperature of 37°C and then analyzed by TRO. Single-stranded M13 probes 2–5 (Fig. 1A) across the Pol I termination region were used in this analysis. As shown in Figure 5A, while a slight increase in TRO signal over probes 4 and 5 was observed with the rat1-1 sen1-1 strain at 2.5 h of restrictive growth, a significant termination defect was visible at 3.5 h. Thus, threefold higher signal than wild type was detectable over downstream regions detected by probes 4 and 5. At the longest time point of 5 h, the single mutant rat1-1 strain also displayed a modest termination defect. In contrast, the double rat1-1 sen1-1 strain showed a somewhat reduced termination defect at this later time point, suggesting that alternative Pol I termination mechanisms become more significant.
These TRO analyses were validated by performing Pol I ChIP analysis (Fig. 5B) on all three mutant strain versus wild type, again using a time course of growth at the restrictive temperature. A clear increase in Pol I signal was detectable at the 3-h time point using spacer primers downstream from the Pol I termination region for the double rat1-1 sen1-1 mutant strain. Also, some increase in Pol I signal was detected, especially with primers 6 + 7 for the single rat1-1 mutant. These effects were maintained, although again at a slightly reduced level, for the longer 5-h time point of restrictive growth. The Pol II-transcribed gene ISY1 is also shown as a negative control.
Overall, our data demonstrate that Rat1p and Sen1p in combination play a significant role in promoting efficient Pol I termination, just as observed for Pol II termination. We therefore predict that efficient Pol I termination requires a combination of the previously described Reb1p-mediated termination mechanism as well as a torpedo mechanism.
rDNA spacer sequence Pol II transcripts do not influence Pol I termination
Two recent papers (Houseley et al. 2007; Vasiljeva et al. 2008) describe the presence of cryptic unstable transcripts (CUTs) transcribed by Pol II in the rDNA spacer region. These CUTs are detected readily only by inactivation of the exosome RNA degradation complex. One of these CUTs in particular is antisense to rRNA and is transcribed toward the Pol I gene, ending near the Pol I termination region. Furthermore, as with other yeast CUTs, the mechanism of Pol II termination employs the Nrd1p/Nab3p/Sen1p complex (Arigo et al. 2006; Vasiljeva et al. 2008). We wished to determine if this Pol II CUT that is close to the Pol I termination region plays a role in the Pol I torpedo-mediated termination mechanism. To achieve this, we selectively inhibited Pol II but not Pol I transcription during the TRO reaction by treating permeabilized cells with 
-amanitin. As shown in Figure 6A, we demonstrate that both the wild-type and mutant (rat1-1 sen1-1) TRO profiles on rDNA are unchanged with or without -amanitin treatment. Also, the strong reduction in Pol II TRO signal over the Pol II-transcribed gene (Fig. 6A, probe K1) following -amanitin treatment confirms that this drug treatment was effective in inhibiting Pol II.
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; Vasiljeva et al. 2008). We therefore reasoned that while inhibition of CUT synthesis by -amanitin treatment did not affect Pol I termination, the opposite effect of increasing CUT levels could result in some Pol I termination defect. However, as shown in Figure 6B, TRO analysis of the Pol I termination region revealed no detectable loss of Pol I termination efficiency with or without Sir2p. Overall, our analysis of the possible interplay between the Pol II-derived CUT and the adjacent Pol I termination region indicates that these two transcription units do not influence each other.
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Discussion |
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). In particular, both polymerase systems rely on a torpedo-like mechanism to bring about efficient termination. It has been suggested (Kufel et al. 1999) that Rnt1p cleavage downstream from the 35S RNA transcript is the initial defining step for pre-rRNA processing that begins the complex series of RNA processing and modifying reactions that result in efficient 18S, 5.8S, and 25S rRNA synthesis. However, the mechanism of Pol I termination was predicted to be independent of these RNA processing reactions, depending solely on Reb1p-mediated pausing of elongating Pol I that in turn causes back-tracking of Pol I and its release by slippage on a close upstream pyrimidine-rich sequence (Lang et al. 1994). Our data now extend this simplistic model for Pol I termination to a mechanism that is coupled to both cleavage by Rnt1p and cotranscriptional degradation of the 3' transcript associated with Pol I still elongating into the rDNA spacer sequence (Fig. 7). In effect, we predict that both Pol I and Pol II employ a closely related torpedo mechanism to promote efficient polymerase release. Our new results do not exclude a role for Reb1p in Pol I termination. Although we do not detect Reb1p on chromatin around the normal termination site, it is known that Reb1p can specifically bind naked DNA at this site, since a conserved Reb1p consensus sequence is present here (Ganley et al. 2005) and clearly binds Reb1p in vitro (Lang and Reeder 1993). We predict that in vivo on a chromatin template, Reb1p interaction may be more transient. Indeed, we demonstrated recently a role for chromatin remodeling enzymes in Pol I termination (Jones et al. 2007), reflecting a need to alter chromatin structure over the termination region that may act to displace Reb1p from the template. A further structural complexity may relate to the presence of gene looping across the rDNA between promoter- and terminator-bound Reb1p. Such loops have been demonstrated in all tested Pol II-transcribed genes (O’Sullivan et al. 2004). Significantly, a recent analysis of murine rDNA demonstrates a loop conformation between the Pol I promoter and terminator sequences. Furthermore, the mouse homolog of Reb1p, TTF1, is implicated in the formation of this structure (Nemeth et al. 2008).
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, 2006; Arigo et al. 2006). However, the clear requirement of Sen1p for PMA1 termination (Fig. 3) argues that longer Pol II-transcribed genes may also require this activity. Whether Sen1p acts together with Nrd1p and Nab3p in this case remains to be established. The fact that Pol I termination also requires the combined actions of Rat1p and Sen1p argues that Sen1p may play a separate role from Nrd1p/Nab3p in Pol I- and some Pol II-transcribed genes. This appears especially likely as Nrd1p/Nab3p is known to interact with the Pol II CTD domain, which is absent from Pol I (Kuhn et al. 2007). A further connection between Sen1p and Pol I termination comes from the observed interaction between Sen1p and Rnt1p (Ursic et al. 2004). We propose that Sen1p helicase activity may act directly with Rat1p to expose the nascent transcript following Rnt1p cleavage [or poly(A) site cleavage] and so promotes more efficient Rat1p exonucleolytic degradation. Further in vitro analysis of Rat1p and Sen1p will be required to characterize this potential mechanism. Finally, it is worth considering the extraordinary complexity of the rDNA gene spacer repeat unit. Within each unit, all three—Pol I, Pol II, and Pol III—generate transcripts, 35S pre-rRNA, 5S RNA, and CUTs. Added to this array of three different gene classes, rDNA spacer sequence also contains a replication origin, a mitotic cohesion site, and a sequence that controls rDNA repeat copy number. This remarkable concentration of critical sequence elements must necessitate a clear delineation between each functional unit. The necessity for efficient Pol I termination is therefore likely to be of paramount importance.
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Materials and methods |
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The strains used in this study are presented in Supplemental Table 1.
FD-4D, FD-4C, FD-4B, FD-4A, and the relative Pol I-tagged strains (Rpa14-3HA) were grown in YPD or minimal media at 25°C and transferred to 37°C as indicated. The Reb1-HA-degron strain was grown in YPD in the presence of G418 (200 µg/mL) at 25°C, then shifted at 37°C as indicated. All the other strains were grown in YPD at 30°C.
ChIP
The strains used for ChIP analyses were AS14, BY4742, Reb1-HA, rat1-1 Pol I-HA, sen1-1 Pol I-HA, rat1-1 sen1-1 Pol I-HA, wild-type Pol I-HA, wild-type SC0000, TAP-Rat1, and TAP-Sen1. Analysis was carried out as before (Jones et al. 2007) with the following modifications: The cross-linking time was 15 min (Fig. 1B) or 20 min (Fig. 4B), chromatin was sonicated using a Bioruptor, cross-links were reversed overnight with proteinase K, and DNA was purified using Qiagen minicolumns. The antibodies used for ChIP analysis were Anti-HA clone F7 (Santa Cruz Biotechnology) in Figures 1B and 5B and Anti-polII CTD antibody 8WG16 (Covance) in Figure 3B.
The ChIP analysis in Figure 4B was conducted essentially as described (Keogh and Buratowski 2004) with the following modifications: Cross-linking was carried out for 20 min at 25°C, and chromatin was sonicated using a Bioruptor. Immunoprecipitation (IP) was performed with IgG Sepharose 6 Fast Flow beads (Amersham), and elution was performed for 30 min at 65°C. Cross-links were reversed by adding Pronase (20 mg/mL) and incubating the samples for 1 h at 42°C and overnight at 65°C. DNA was purified using Qiagen minicolumns.
ChIP analysis was performed using real-time PCR with a Corbett Rotorgene system. Input, IP, and NO (no antibody control) samples were all run in triplicate to ensure data accuracy. PCR up to 45 cycles was carried out using the Qiagen QuantiTect SYBR Green PCR Master mix or Quantace SensiMix NoRef DNA Kit. Primers were used at 0.5 µM for each experiment. Fluorescent intensities were calculated by
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For TAP-tagged Rat1p and Sen1p ChIPs (Fig. 4B), IP signals were divided by the relative input and the fold enrichment is expressed relative to the isogenic nontagged strain.
Average data sets are presented. Error bars reflect the SD of average signal obtained between two and four independent experiments.
The coordinates of the PCR primers used are shown in Supplemental Table 3.
TRO analysis
TRO analysis and probes for rDNA, CYC1, and pTEF:KANR (K1) were all described previously (Birse et al. 1998; Alen et al. 2002; Morillon et al. 2003; Jones et al. 2007), and locations of the probes used are shown in Figures 1A, 2A, and 4A. Signals were plotted as a percentage of probe 2 for rDNA or normalized to the probe 1 signal for CYC1 to allow for direct comparison between wild-type and several mutant strains. For the TRO analysis of TAK401 and TAK314 strains, 120-bp-long oligo probes (2, 3, 4, 5, 3', 4', and 5') were used (Supplemental Table 2), and the signals obtained were normalized toward the A content of the probes. For TRO on CYC1 and rDNA representative data are presented based on multiple experiments.
RT–PCR
Standard conditions were used. In outline, total RNA was isolated from logarithmically growing yeast strains after indicated temperature shift times. cDNA was synthesized by RT primed with specific RT primers (p5R and p8-11R in Fig. 3C; p1–6 in Fig. 4C) and PCR-amplified by Taq polymerase for 30 cycles with indicated PCR primers. For both RT–PCR analyses (Figs. 3C, 4C), no genomic DNA contamination was confirmed by –RT controls. The locations of the RT and PCR primers are shown in Figures 3A and 4A, and their sequences are in Supplemental Table 4.
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Footnotes |
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E-MAIL Nicholas.proudfoot{at}path.ox.ac.uk; FAX 44-1865-275556.
Supplemental material is available at http://www.genesdev.org.
Article is online at http://www.genesdev.org/cgi/doi/10.1101/gad.463408.
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