- Open Access
A genetic screen for replication initiation defective (rid) mutants in Schizosaccharomyces pombe
© Locovei et al; licensee BioMed Central Ltd. 2010
- Received: 18 June 2010
- Accepted: 27 August 2010
- Published: 27 August 2010
In fission yeast the intra-S phase and DNA damage checkpoints are activated in response to inhibition of DNA replication or DNA damage, respectively. The intra-S phase checkpoint responds to stalled replication forks leading to the activation of the Cds1 kinase that both delays cell cycle progression and stabilizes DNA replication forks. The DNA damage checkpoint, that operates during the G2 phase of the cell cycle delays mitotic progression through activation of the checkpoint kinase, Chk1. Delay of the cell cycle is believed to be essential to allow time for either replication restart (in S phase) or DNA damage repair (in G2). Previously, our laboratory showed that fission yeast cells deleted for the N-terminal half of DNA polymerase ε (Cdc20) are delayed in S phase, but surprisingly require Chk1 rather than Cds1 to maintain cell viability. Several additional DNA replication mutants were then tested for their dependency on Chk1 or Cds1 when grown under semi-permissive temperatures. We discovered that mutants defective in DNA replication initiation are sensitive only to loss of Chk1, whilst mutations that inhibit DNA replication elongation are sensitive to loss of both Cds1 and Chk1. To confirm that the Chk1-sensitive, Cds1-insensitive phenotype (rid phenotype) is specific to mutants defective in DNA replication initiation, we completed a genetic screen for cell cycle mutants that require Chk1, but not Cds1 to maintain cell viability when grown at semi-permissive temperatures. Our screen identified two mutants, rid1-1 and rid2-1, that are defective in Orc1 and Mcm4, respectively. Both mutants show defects in DNA replication initiation consistent with our hypothesis that the rid phenotype is replication initiation specific. In the case of Mcm4, the mutation has been mapped to a highly conserved region of the protein that appears to be required for DNA replication initiation, but not elongation. Therefore, we conclude that the cellular response to inhibition of DNA replication initiation is distinct from blocking DNA replication elongation, and this difference can be exploited to identify mutants specifically defective in DNA replication initiation.
- Helicase Activity
- Replication Initiation
- Maintain Cell Viability
- Wildtype Cell
- Subsequent Cell Cycle
Assembly of DNA replication complexes begins in early G1 following degradation of cyclin-dependent kinases at the conclusion of mitosis . The dramatic drop in CDK activity following anaphase promotes the binding of Mcm2-7 to origin DNA to form pre-replicative complexes or pre-RCs. Formation of the pre-RC requires both Cdc18/Cdc6 and Cdt1 proteins [2–4]. Once the pre-RC is assembled, activation of CDK (cyclin dependent kinase) and DDK (Dbf4-dependent kinase) at the beginning of S phase leads to the binding of additional replication proteins to origin DNA including DNA polymerase epsilon, Sld2, Sld3, Cdc45, and GINS forming the pre-initiation complex or pre-IC [5, 6]. Binding of DNA polymerase alpha is then required to allow synthesis of short primers that are then extended during S phase by DNA polymerase delta [7–10].
DDK and CDK are two serine kinases required for the onset of S phase. They target components of the pre-RC and pre-IC, respectively and are essential for initiation of DNA replication. It is believed that structural modifications to the pre-RC stimulated by DDK activity leads to Cdc45 binding to the MCM complex stimulating its helicase activity . Following the partial unwinding of DNA, CDK then targets two proteins, Sld2 and Sld3, promoting the assembly of the pre-IC and ultimately the onset of S phase [12, 13]. The Mcm2-7 complex is unique in that it appears to function both in the initiation of DNA replication ie. during formation of the pre-RC, as well as in DNA replication elongation as the putative DNA helicase [11, 14]. These two functions appear to be separable, since Mcm mutants defective in DNA replication elongation are still capable of binding chromatin and presumably establishing the pre-RC . Mcm proteins contain ATP binding sites but ATP hydrolysis is only required for replication elongation and not for chromatin binding .
When DNA replication is blocked by either addition of inhibitors such as hydroxyurea or by DNA damage, a checkpoint control ensures that mitotic entry is delayed and that replication complexes are stabilized [16, 17]. In fission yeast, this checkpoint, called the intra-S phase checkpoint requires several proteins encoded by the rad, hus1, mrc1 and cds1 genes. Although Cds1 delays cell cycle progression by phosphorylating and inhibiting the Cdc25 phosphatase [18, 19], its most critical role for maintaining cell viability is to stabilize stalled replication complexes [20–22]. In the absence of Cds1, cells lose viability rapidly upon inhibition of DNA replication elongation, and this decrease in viability is not the result of cells entering mitosis prematurely. On the other hand, DNA damage during G2 leads to the activation of a distinct checkpoint that is also dependent on the expression of the rad and hus1 genes, but requires a unique adaptor protein Crb2, and the effector kinase Chk1 [23, 24]. Chk1 maintains cell viability by preventing premature entry into mitosis by directly phosphorylating and inhibiting Cdc25 .
Previously, our lab reported that cells deleted for the N-terminal half of DNA polymerase ε catalytic subunit (Cdc20) are viable, but have a significant S phase delay . Although we expected that this delay would be due to activation of the intra-S phase checkpoint, we were surprised to find that these cells require Chk1, but not Cds1 to maintain cell viability. Our hypothesis was that the Chk1 dependency, Cds1-independency of the DNA polymerase epsilon mutant reflected a unique role for this polymerase in the assembly of the pre-IC. We therefore tested several other DNA replication temperature-sensitive (ts) mutants for their sensitivity to the loss of either Cds1 or Chk1 when grown under semi-permissive conditions. Our results suggest that mutants defective in DNA replication initiation (referred to as rid mutants) require the checkpoint kinase Chk1 for viability, while those defective in the elongation step (referred to as red mutants) require Cds1 . To test our hypothesis further we have now completed a genetic screen for cell division cycle (cdc) mutants that are sensitive to the loss of Chk1, but not Cds1. This screen identified novel mutant alleles of cdc30/orp1 and cdc21/mcm4, two proteins that are essential for DNA replication initiation. Consistent with the screen being specific for initiation mutants we find that the mutation identified in Mcm4, which maps to a highly conserved region within the central MCM domain signature motif III (http://srs.ebi.ac.uk/srsbin/cgi-bin/wgetz?-e+[prints-AccNumber:PR01657), disrupts only its initiation function, whilst leaving its putative elongation function intact. Our results demonstrate that the rid mutant phenotype provides a powerful tool to identify mutants defective in the DNA replication initiation, and that the cellular response to inhibition of DNA replication initiation is distinct from the response to blocking DNA replication elongation.
Replication initiation (rid) mutants have unique checkpoint requirements
Previously, we showed that several mutants defective in DNA replication initiation are sensitive to the loss of chk1 + , but not cds1 + , see also Additional file 1, Table S1. In contrast, the viability of DNA replication elongation mutants was severely compromised in the absence of either Cds1 or Chk1 when grown at semi-permissive temperatures. We hypothesized that the Chk1-dependent, Cds1-independent phenotype is unique to replication initiation mutants and could be exploited in a genetic screen to identify mutants specifically defective in DNA replication initiation.
Developing a screen for rid mutants
Identification of rid1-1 and rid2-1 as novel alleles of cdc30/orc1 and cdc21/mcm4
The phenotype of the two rid mutants suggests defects in DNA synthesis
Chk1 activation in rid1-1 and rid2-1 mutants
Mrc1 is required in rid1-1 and rid2-1 mutants
Our analysis of other rid mutants has demonstrated that their viability is not only dependent on Chk1, but also requires Mrc1 [30–34]. These experiments revealed a function for Mrc1 that is independent of its role in activation of the intra-S phase checkpoint. We confirmed that the viability of rid1-1 and rid2-1 strains is also dependent on expression of Mrc1 (Figure 4B). As was observed for Δchk1, no viable double mutants containing rid2-1 and deletion of mrc1 could be obtained at 25°C. Consistent with our previous findings regarding initiation mutants, we also found that rid1-1 or rid2-1 were not hypersensitive to hydroxyurea (Figure 4C).
The mutant rid2-1 is defective in DNA replication initiation, but not elongation
At 25°C, rid2-1 has a cell cycle time nearly double that of wild-type cells that was further increased by treatment with HU. Therefore, in order to examine two complete cell cycles following HU block and release, we needed to extend the time-course following release to 24 hrs. For controls, we examined the cell cycle timing for wild-type cells and for the DNA replication initiation mutant cdc20 (encoding DNA polymerase epsilon), and the DNA replication elongation mutant, cdc27 (encoding a subunit of DNA polymerase delta) at permissive (wt, cdc20, cdc27), semi-permissive (wt), or non-permissive temperatures (cdc20 and cdc27). To demonstrate the expected phenotype for initiation and elongation mutants following HU block and releases, cdc20 and cdc27 cells were grown at 25°C and treated with HU to arrest cells in early S phase. Cells were then shifted to the non-permissive temperature of 36°C for 1 hr prior to release from HU. Cells defective in DNA polymerase epsilon (cdc20) divided once before arresting in the subsequent cell cycle (Figure 5B, open squares). This phenotype is consistent with cdc20 cells being defective in DNA replication initiation. In contrast, cdc27 cells that are defective in DNA replication elongation fail to divide, and arrest with an elongated cell phenotype consistent with DNA replication being blocked immediately following release from HU (Figure 5B, open triangles). For the experiments involving wt cells and rid2-1, cells were first grown overnight at the permissive temperature of 25°C and HU was added for 4 hours to arrest cells in early S phase. Prior to release from HU, half of the cells were shifted to the higher temperature of 33°C while the other half was kept at 25°C. Cells were then filtered and washed with pre-warmed media (25°C or 33°C), and re-suspended in fresh media containing no HU. Cell number was then monitored every hour for approximately 24hrs (or 12 hrs for the wt control). As expected, we found that wild-type cells doubled in approximately 5 hrs (a delay attributable to the HU treatment) and quickly returned to the normal cell cycle time of approximately 2-2.5 hrs during subsequent cell divisions (Figure 5C, open squares). As expected, at 25°C, wt cells have a generation time approximately twice as long as cells grown at the higher temperature of 33°C (Figure 5C, filled squares). Interestingly, for rid2-1, no significant cell cycle delay is observed following release from HU at the higher temperature of 33°C (Figure 5C, open triangles) when compared to cells released at the lower temperature of 25°C (Figure 5C, filled triangles), consistent with rid2-1 having a negligible effect on DNA replication elongation. However, a strong cell cycle delay is observed for rid2-1 cells at 33°C during the subsequent cell cycle. Whereas at 25°C, rid2-1 completes the second cell doubling at approximately 15 hrs, at 33°C, cell division does not occur until approximately 24 hrs. Therefore, these results are consistent with rid2-1 having a significant defect in DNA replication initiation, whilst having little or no effect on DNA replication elongation, as predicted on the basis of its checkpoint phenotype.
In this report we have shown that mutants defective for DNA replication initiation require Chk1, but not Cds1 to maintain cell viability. We refer to this phenotype as the rid phenotype (for replication initiation defective). In contrast, the viability of mutants defective in DNA replication elongation ie. cdc6, cdc27, is dependent on the checkpoint kinase Cds1. We conducted a genetic screen for mutants that display the rid phenotype and isolated two mutants, rid1-1 and rid2-1. Sequencing confirmed that these mutants contain point mutations in two initiation proteins, Orc1 and Mcm4, respectively. These data are consistent with our screen being highly selective for the isolation of mutants specifically defective in DNA replication initiation. This implies that the cellular response to blocking DNA replication initiation is distinct from the cellular response to inhibiting DNA replication elongation. We have also found that although Cds1 is not essential in mutants defective in DNA replication initiation, the observed dependency on Mrc1 suggests a novel role for this protein in the stabilization of replication forks when initiation is impaired. Mrc1 was originally discovered in both fission yeast and budding yeast as a protein that mediates the activation of Cds1 (Rad53 in S. cerevisiae) at stalled replication forks [35–37]. The orthologous protein, Claspin, has a similar role in animal cells [38–41]. Mrc1 has also been shown to be a part of a protein complex that associates with unperturbed replication forks and is believed to have a role in both the stabilization of DNA replication complexes and the coupling of the MCM helicase to DNA polymerase epsilon [5, 42–45]. Still other reports suggest that Mrc1 has a role in sister chromatid cohesion [46, 47], and telomere capping [48–50]. Based on our analysis of Chk1 activation in rid mutants in the absence of Mrc1 we believe that Mrc1 has no role in checkpoint signaling in response to replication initiation defects. However, the dependency of rid mutant viability on the presence of Mrc1 strongly argues that the normal replication function(s) of Mrc1 are essential in mutants defective in DNA replication initiation. It is not yet clear whether this reflects its putative role in replication fork stabilization, coupling of the helicase to DNA polymerase or to some other yet unidentified replication function. Moreover, Mrc1 is known to form a complex with at least two additional proteins, Swi1 and Swi3, that could directly interact with the initiation complex and potentially regulate its activity [34, 51].
The role of Chk1 in maintaining the viability of rid mutants is likely to be its function in delaying the onset of mitosis, however we cannot exclude the possibility that Chk1 might have an additional function in directly stabilizing forks as has been recently observed in S. cerevisiae mutants lacking RAD53 and EXO1 .
In rid2-1, the mutation in Mcm4 resides in a highly conserved region of the protein called domain 4 of the MCM central homology region. No specific function has been attributed to this region of the protein that lies just outside but adjacent to the Walker A and Walker B motifs that are believed to bind ATP and be important MCM helicase activity . Based on our analysis of the rid2-1 mutant, we suggest that this mutation results in a specific defect in DNA replication initiation, but has little effect on the presumed function of Mcms in DNA replication elongation. Consistent with this hypothesis, rid2-1 shows normal cell cycle kinetics of DNA replication following release from an early S phase arrest imposed by treatment with hydroxyurea. Therefore, although Mcm proteins are required for both DNA replication initiation and elongation, the data is consistent with rid2-1 having defects only in its initiation function. With the exception of the degron mutants of Mcm4, which were specifically designed to test the role of Mcms in replication elongation, our results are similar to those reported for mcm mutants in S. cerevisiae and S. pombe that display no obvious defects in DNA replication elongation. In the case of Orc1, it is generally agreed that Orc1's primary role in DNA replication is to establish pre-RCs at the conclusion of mitosis, and therefore in this case, our screen has led to the identification of a bona-fide initiation protein. This of course does not exclude the possibility that Orc1 might have additional cellular functions outside of DNA replication, as has been recently reported for human Orc1 . The mutation in rid1-1 lies in the C-terminal portion of the protein in a region that has yet to be fully characterized.
Understanding the molecular events that lead to the initiation of DNA replication has been a central question for cell biologists for several decades. Recently, several reports have suggested that mutations in the genes that control this step might be associated with genetic instability and cancer. In particular, mutations in MCM4 in mice can lead to increased frequency of sporadic tumors . Moreover, several lines of research have suggested that Mcm proteins might provide important diagnostic markers for early detection of cancer [56–59]. Finally, inhibition of DNA replication might provide an attractive therapeutic strategy for the treatment of cancer, because recent studies have shown that tumor cell lines might be selectively sensitive to inhibition of DNA replication initiation [60–62].
While all previous evidence is consistent with Orc1 having a function in the initiation step of the DNA synthesis, studies on Mcm proteins, including Mcm4, support a dual function during replication, both during the initiation and the elongation stages. Mcm4 was found to interact with ORC components, Cdc18 and Cdc45, as well as with the other MCM complex components (11, 34-37). Mcm4 can be isolated as a heterotrimeric complex with Mcm6 and 7, also known as "the core MCM", that possesses in vitro helicase activity and is required for the proper formation of the heterohexameric MCM 2-7 complex (36, 37). Structurally, Mcm4, and all other Mcm subunits, have a central region of homology, known as the MCM domain. In this region, there are the consensus Walker A and B ATPase motifs which are required for nucleotide binding and ATPase activity. Therefore this domain is likely to be responsible for the putative helicase activity of the MCM complex (38-41).
The N-terminal region of Mcm4 presents several putative CDK-phosphorylation sites. Mutational analysis in Xenopus and S. pombe suggested that phosphorylation of these sites are important for the helicase activity regulation and prevention of re-replication [63–65]. Alignment of several Mcm4 molecules from diverse eukaryote systems showed that the G514E mutation in rid2-1 affects a small but very conserved sequence centrally located (in the MCM domain), about 40 amino-acids upstream of the Walker A motif. The G514E mutation lies in the third of five Mcm4 signature motifs that currently has no known function. The high degree of conservation in these signature motifs in many eukaryotes suggests an important yet not determined role for this region of the protein. Further work will be needed to fully understand how the mutation in rid2-1 can inhibit initiation of DNA replication. Here we provide a powerful genetic tool for the isolation of mutants defective in DNA replication initiation that should be helpful in identifying new genes required for initiation, as well as hypomorphic alleles of known initiation proteins that can be applied to further analysis of this critical step in cell division.
All strains used in this study were derived from wildtype 972h- and 975h+. All genetic manipulations were performed as previously described .
Approximately 108 exponentially growing wildtype or Δcds1 cells were treated with nitrosoguanidine at a final concentration of 0.15 mg/ml. Aliquots of 107 cells were harvested at different times (0, 5, 10, 15, 20, 30, 45, 60 and 90 minutes) after treatment, were washed three times in Tris-maleate buffer pH6, once in YE and then resuspended in 1 ml YE and incubated at 25°C for four hours to allow recovery. Cells were counted and approximately1000 cells were plated in triplicate for each time-point and incubated at 25°C. After several days, the colonies arising on each plate were counted and a survival curve was plotted. Time 0 was presumed to represent 100% survival. For screening, cells from the 5 minute time-point (representing 50% survival) were plated on rich media plates at a density of approximately 2000 cells per plate and incubated at 25°C until colonies formed. To screen individual colonies for the cell division cycle (cdc) phenotype, colonies were replica-plated to YE plates containing phloxine B (a vital stain) and incubated at the elevated temperature of 36°C. The temperature-sensitive (ts) colonies (determined by their dark pink staining) were analyzed microscopically and the colonies displaying the cdc or elongated cell phenotype were selected as putative rid mutants.
Construction of double mutants
Double mutants were generated using standard procedures . Briefly, cells of different mating types (h+ and h-), were mixed on malt extract (ME) plates and incubated at 25°C for 2-3 days. Mature asci were then suspended in 1 ml sterile H2O. 5 μl of glusulase were added to the suspension and incubated overnight at 25°C, to allow digestion of the asci walls and to kill all vegetative cells. Spores were then washed twice with sterile H2O, plated at a density of 500 spores/plate on rich media (YE) plates and incubated at 25°C to allow spore germination and colony formation. Double mutants were identified after replica plating to confirm the presence of specific markers or phenotypes.
Viability test (synthetic lethality assessment)
Exponentially growing cultures (OD595 = 0.2 - 0.4) for each strain to be analyzed were adjusted to a density of 107 cells/ml that were then subjected to at least 5 rounds of a 5-fold serial dilution. For each strain, 5 μl of each diluted sample were spotted on YE plates from most concentrated to least concentrated. Plates were incubated at the indicated temperature (ranging between 25 to 36°C) for 4-7 days, or for the amount of time necessary to determine differences between the viability of the strains being tested. For this study, the semi-permissive temperature is defined as the temperature where the single ts mutant in the presence or absence of cds1 + is viable, but is sick or inviable in the absence of chk1 + .
Hydroxyurea sensitivity test
Cultures were prepared for each strain as described for the viability experiment. Spots were plated on YE plates containing 0, 2, 5, 7.5, and 10 mM HU, and plates were incubated at temperatures ranging from 25 to 36°C for 4-5 days, and colony formation was assessed.
Fixing cells for flow cytometry
Cells were harvested by centrifugation at 5000 g for 5 mins, washed once with sterile H2O, and re-suspended in 1 ml cold 70% ethanol. For flow cytometry analysis, 0.2 ml of cells in ethanol were centrifuged and re-suspended in re-hydration buffer (50 mM Na citrate containing 0.1 mg/ml RNAase A) and incubated at 37°C for 2 hours. Sytox green (Molecular Probes) was then added to a final concentration of 2 μm prior to analysis.
Fission yeast transformation
Exponentially growing cells (OD595 = 0.2-0.5) were harvested, washed once with sterile water, re-suspended at a density of 109 cells/ml in 0.1 M lithium acetate (pH 4.9) and dispensed in 100 μl aliquots into Eppendorf tubes. Cells were incubated at 25°C for 60 - 120 minutes. 1 μg of plasmid DNA in 15 μl TE (pH 7.5) was added to each aliquot and mixed, followed by the addition of 290 μl of 50% (w/v) PEG 4000, mixing and incubation at 25°C for 60 minutes. Cells were heat shocked at 43°C for 15 minutes. Tubes were cooled to room temperature for 10 minutes, and then cells were harvested by centrifugation, and re-suspended in 1 ml of 1/2 YE broth. The suspension was transferred to a 50 ml flask and diluted with 9 ml of 1/2 YE, followed by recovery at 25°C for 60 minutes. Cells were then concentrated in 1 ml of ½ YE and 100 ul aliquots were plated on selective agar plates.
Cloning of rid1-1 and rid2-1 mutated genes
Genomic DNA extraction from rid1-1 and rid2-1 strains: rid1-1 and rid2-1 liquid cultures were grown to stationary phase. Cells were harvested, re-suspended in 50 mM citrate/phosphate pH 5.6 40 mM EDTA pH 8.0 1.2 M sorbitol, followed by the addition of Zymolase and incubated at 37°C for 30-60 minutes. The cells were then pelleted briefly and resuspended in TE buffer 1% SDS and incubated at 65°C for 1 hr. 5 M potassium acetate was added, and the tube was kept on ice for 5 minutes. The resulting suspension was centrifuged at 12000 rpm for 15 minutes at 4°C, the supernatant was collected and the DNA was precipitated by addition of cold isopropanol and incubation at -20°C for 10 minutes. The tube was then centrifuged for 15 minutes at 4°C. The supernatant was discarded and the pellet was washed with 70% ETOH. The pellet was resuspended in TE buffer containing 50 μg/ml RNAse A and incubated at 65°C for 10 minutes. Two rounds of phenol/chloroform extraction were performed, followed by 3 M sodium acetate and cold 100% ethanol precipitation of DNA on ice for 10 minutes. The DNA was pelleted by centrifugation at 10000 rpm for 10 minutes, washed with 70% ETOH and dried at 37°C. The last step was the resuspension of genomic DNA in TE buffer containing RNAse A and incubating for 5 minutes at 37°C.
Primer design: The primers used for PCR amplification of the entire cdc21/mcm4 and cdc30/orp1 open reading frames were:
mcm4 Xho I-F: 5' CCGCTCGAGCGGTCTTTCTACACCCACCACGAG 3'
mcm4 Bam HI-R: 5' CGCGGATCCGCGGAATAATACCAGCTTATTCGC 3'
orp1Bam HI-F: 5' CGCGGATCCATGCCTAGAAGAAAGTCATTG 3'
orp1Xma I-R: 5' TCCCCCCGGGTTATGCTATCCCAGCAAGTTCC 3'
Cloning rid1-1 and rid2-1 in pCR Blunt vector: PCR amplification of rid1-1 (mutated cdc30/orp1 gene) and rid2-1 (mutated cdc21/mcm4 gene) was completed using the above primers and genomic DNA extracted using rid1-1 and rid2-1 strains as the template DNA. After checking the proper band size on a 0.8% agarose gel, the ligation was performed directly from the PCR product into a pCR-Blunt vector (Invitrogen Topo-Blunt kit).
Sequencing the rid1(cdc30/orp1) and rid2(cdc21/mcm4) gene
Primer design: Additional forward and reverse primers were designed for cdc30 and cdc21, spanning the entire gene lengths, spaced at every 600bp:
Other primers used were the M13 forward and reverse primers existing in the pCR-Blunt vector, flanking the cloning sites.
Sequencing and data analysis: Cloned DNA from each mutant were sequenced and aligned with the wildtype cdc30 + and cdc21 + sequences using the Clone Manager Suite 7 software to identify the site of the mutations in rid1-1 and rid2-1. The same software was used to translate and compare the amino acid sequences of wildtype and mutant Orc1 and Cdc21 proteins.
Exponentially growing cultures were treated with 12 mM HU for 4 hours, followed by HU wash by filtration under vacuum on Millipore membranes, with media warmed to the temperature to be used for shift. For each experiment, after wash, cells were shifted to the indicated temperatures, and aliquots were collected every 30 minutes for cell counting. The length of temperature exposure depended on the time needed for wt (used as control for each experiment and every temperature tested) and mutant strains to undergo two complete rounds of cell division. Samples were fixed in formal saline and then the number of cells in a fixed volume was counted using Sysmex K-1000, in triplicate, for each sample.
The authors would like to thank A. Carr, Y. Murakami, P. Nurse, S. Yamashita, M. Yanagida, N. Walworth and T. Wang for strains. We would also like to J. Huberman, F. Verde and S. Lemmon for helpful discussions. National Institutes of Health grant R01 CA-099034 supported G.D., L.Y. and A.M.L. A.M.L. was also a recipient of a graduate student fellowship from the American Heart Association.
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