Germinating fission yeast spores delay in G1 in response to UV irradiation
© Nilssen et al; licensee BioMed Central Ltd. 2004
Received: 25 March 2004
Accepted: 21 October 2004
Published: 21 October 2004
Checkpoint mechanisms prevent cell cycle transitions until previous events have been completed or damaged DNA has been repaired. In fission yeast, checkpoint mechanisms are known to regulate entry into mitosis, but so far no checkpoint inhibiting S phase entry has been identified.
We have studied the response of germinating Schizosaccharomyces pombe spores to UV irradiation in G1. When germinating spores are irradiated in early G1 phase, entry into S phase is delayed. We argue that the observed delay is caused by two separate mechanisms. The first takes place before entry into S phase, does not depend on the checkpoint proteins Rad3, Cds1 and Chk1 and is independent of Cdc2 phosphorylation. Furthermore, it is not dependent upon inhibiting the Cdc10-dependent transcription required for S phase entry, unlike a G1/S checkpoint described in budding yeast. We show that expression of Cdt1, a protein essential for initiation of DNA replication, is delayed upon UV irradiation. The second part of the delay occurs after entry into S phase and depends on Rad3 and Cds1 and is probably due to the intra-S checkpoint. If the germinating spores are irradiated in late G1, they enter S phase without delay and arrest in S phase, suggesting that the delay we observe upon UV irradiation in early G1 is not caused by nonspecific effects of UV irradiation.
We have studied the response of germinating S. pombe spores to UV irradiation in G1 and shown that S phase entry is delayed by a mechanism that is different from classical checkpoint responses. Our results point to a mechanism delaying expression of proteins required for S phase entry.
Checkpoint mechanisms are important for cell survival and genetic stability. They prevent cell cycle transitions until previous events have been completed or damaged DNA has been repaired . Checkpoint pathways and proteins are evolutionarily conserved from yeast to man, underlining their importance in maintaining genomic integrity. In fission yeast several checkpoint pathways monitor the status of the DNA and arrest the cell cycle in response to DNA damage or inhibition of DNA replication [2, 3] They include mechanisms to inhibit mitosis when the DNA is damaged (the G2/M checkpoint) or when S phase has not been completed (the S/M checkpoint) as well as a mechanism to inhibit ongoing DNA replication when the DNA is damaged (the intra-S checkpoint). Screens designed to reveal elements of the checkpoint pathways have led to the identification of the so-called checkpoint rad genes as well as crb2/rhp9, mrc1, chk1 and cds1 [4–13] The checkpoint rad genes consist of rad1, rad3, rad9, rad17, rad26 and hus1 (reviewed in (). Rad3 is a member of the phosphatidylinositol 3-kinase family of proteins and the closest mammalian homologue is the ATR (AT M and R ad3 related) protein [15, 16]. Rad3 forms a complex with Rad26 and this association is required for activation of Rad3 kinase activity in response to DNA damage or replication arrest [17, 18] The Rad1, Rad9 and Hus1 proteins have similarities to PCNA, the sliding clamp of the replicative DNA polymerase, and the three proteins may form a similar ring-shaped structure [19–21]. Rad17 has similarities to all five subunits of replication factor C , a complex which loads PCNA onto chromatin.
There are two known effector kinases downstream of the checkpoint Rad proteins, Chk1 and Cds1. Chk1 is phosphorylated in response to DNA damage induced in late S or G2 in a Rad3 dependent manner [12, 23, 24]. Phosphorylation of Chk1 leads to an increase of Chk1 kinase activity  and is often used as a convenient molecular marker for Chk1 dependent checkpoint activation. Cds1 is activated only in S phase as part of the intra-S and the S/M checkpoints [8, 26] Activation of either kinase leads to inhibition of Cdc2 activity by maintaining the inhibitory phosphorylation on Tyr15 [27–29].
Crb2 and Mrc1 act upstream of Chk1 and Cds1, respectively. Crb2 shares homology with the budding yeast RAD9 protein , which is involved in delaying entry into S phase upon DNA damage in G1 [30–32] In fission yeast, Crb2 is required both for activation of Chk1 and for subsequent inactivation of Chk1 for reentry into the cell cycle [10, 33] Mrc1 plays a parallel role by binding to and activating Cds1. Expression of Mrc1 is regulated in the cell cycle, thus linking Cds1 activation to S phase [6, 11].
In addition to the G2/M, S/M and intra-S checkpoints, three papers have reported the existence of G1 checkpoints that inhibit mitosis when the cells are arrested in G1 using cell cycle mutants. Arrest at the cdc10 arrest point was shown to depend on Chk1  and Rum1 . Arrest of orp1 mutant cells depends on the checkpoint Rad proteins and on Chk1 . It should be noted that neither of these cell cycle mutants is able to replicate their DNA at the restrictive temperature, and failure of the checkpoints responsible for cell cycle arrest results in aberrant entry into mitosis and not into S phase.
A G1/S checkpoint has so far not been detected in S. pombe. The drop of CDK activity at the M/G1 transition allows the assembly of the pre-Replication Complex, preRC, which is the first step leading to initiation of S phase. The preRC consists of the ORC (Origin Recognition Complex), Cdc18, Cdt1 and the MCM proteins. Expression of Cdc18 and Cdt1 is cell cycle regulated, thus providing one of the means to regulate initiation of S phase [37, 38] Once the preRC is assembled, the chromatin is competent to replicate, but replication is not initiated until other replication proteins are loaded, and two kinases, Cdc2 and Hsk1, are activated. It has been shown both in fission yeast and in Xenopus that the intra-S phase checkpoint cannot be engaged until polα-primase is loaded and replication begins [39, 40] This observation poses the question whether the cells have any means to respond to DNA damage sustained in G1.
G1 in fission yeast is very short under standard laboratory growth conditions, rendering the investigation of a G1/S checkpoint(s) difficult. However, G1 might be much extended in the natural habitat of S. pombe due to poor nutrient availability. We decided to use several approaches to synchronise the cells and/or to extend G1. Recently we reported the existence of a mechanism that delays entry into S phase when cycling cells are UV-irradiated in G1, using cdc10 and cdc25 mutants to synchronise the cells or growing the cells in medium where G1 is extended .
Here we show that germinating S. pombe spores delay entry into S phase upon UV irradiation in early but not late G1. We demonstrate that there is a G1/S delay that is not dependent on any of the known checkpoint proteins and does not target Cdc2 phosphorylation. We argue that the delay is due to a novel mechanism that leads to delayed expression of Cdt1 and possibly other replication proteins.
Entry into S phase is delayed by UV irradiation
Spores made from diploid cells were allowed to germinate for 3.5 h at 30°C before UV irradiation. At this time point, 1 – 2 hours before S phase entry, the spores showed visible signs of germination by phase contrast microscopy. The dose of UV light was 1200 J/m2, which gave a cell survival of about 30% in wild type cells (data not shown). At the time of irradiation, the majority of germinating spores had a 1C DNA content. The timing of S phase was measured, by flow cytometry, as an increase in cellular DNA content from 1C to 2C. The decrease of the 1C population was plotted against time, and the graphs for unirradiated control and UV irradiated cells were compared at the point where 50% of the cells had 1C DNA content.
Length of the delay in the investigated mutants
Length of the 1C delay (min)(*)
Average length of the 1C delay (min)
wt early irradiation
70, 80, 90, 60, 80
wt late irradiation
40, 20, 45, 15
90, 55, 70
55, 45, 25
<10, <10, <10
The cells delay with low levels of Cdt1
Cdt1 expression and Cdc2 phosphorylation are delayed upon UV irradiation
Length of the delay (min)(*)
Average length of the delay (min)
Rum1 is required for part of the delay
Rum1 expression is cell cycle regulated such that it is only expressed in G1 . We investigated Rum1 levels in germinated spores UV irradiated as described above and samples of irradiated and control cells were removed for analysis by flow cytometry and by immunoblotting. Rum1 expression was induced at 30 minutes in both cultures, but was maintained to a higher extent and longer in the irradiated cells (Fig. 3B). Both increased expression of Rum1 and the requirement for Rum1 for part of the delay demonstrate that part of the delay takes place in G1.
Is the 1C delay checkpoint dependent?
Given that caffeine can inhibit Rad3 related kinases, we investigated whether the G1/S delay is also abolished in rad3 mutant cells. Irradiated rad3 germinating spores delayed with a 1C DNA content for 30 minutes, in contrast to the 76 minute delay of wild type cells (Fig. 4B, Table 1).
We have investigated whether the other checkpoint Rad proteins are involved in the G1/S delay. rad26, rad1, rad9, hus1, and rad17 spores were germinated and UV irradiated as described above. Figure 4C (and Table 1) shows that rad26, rad1, rad9, hus1 and rad17 cells delay much less than wild type cells do (35–50 versus 76 min). We conclude that Rad26, Rad1, Rad9, Hus1 and Rad17 are required for at least a part of the 1C delay.
Mrc1 and Cds1, but not Crb2 and Chk1, are required for part of the delay
Crb2 and Mrc1 are required for activation of Chk1 and Cds1, respectively. We irradiated germinating crb2 and mrc1 spores . Consistent with the above findings, in mrc1 the delay was reduced to 50 minutes, while in crb2 the delay was not reduced compared to that in wild type cells (data not shown). We conclude that Mrc1 and Cds1 are required for part of the delay, while Crb2 and Chk1 are not required.
The arrested cells maintain Cdc2 in the unphosphorylated form
res2 mutant cells do not delay S phase entry after irradiation
Cdc10 dependent transcription is not inhibited during the delay
We have provided evidence for the existence of a mechanism in germinating fission yeast spores that delays entry into S phase upon UV irradiaton in early G1. Germinating wild type spores displayed a pronounced delay in entering S phase after UV irradiation. The delay was observed only when irradiation was carried out in early but not in late G1. We have investigated the dependence of the delay on classical checkpoint proteins and showed that they are required for some but not all of the delay with 1C DNA content. We argue that the observed delay is caused by two separate mechanisms, the first taking place before entry into S phase, and the second in early S phase (see below).
The delay in exit from the 1C population was demonstrated by means of flow cytometry, which does not allow us to distinguish between a G1/S and an early S delay. The following data represent strong evidence that part of the delay takes place before entry into S phase. First, the irradiated cells delay expression of Cdt1. In the absence of Cdt1 the cells cannot form preRCs and thus cannot initiate S phase. Second, the irradiated cells express Rum1 longer than unirradiated control cells. Since Rum1 expression is cell cycle regulated such that it is only expressed in G1, , this observation implies that the irradiated cells do delay in G1. Furthermore, the delay is shorter in a rum1 mutant, which presumably loses the G1 part of the delay. Third, mutants lacking Mrc1 or Cds1, which are essential for S-phase checkpoints reported so far in fission yeast , still delay for a significant length of time, pointing to the existence of a non-S mechanism . Fourth, cells delay with the Cdc2 kinase in an unphosphorylated state. Cdc2 is normally inhibited by phosphorylation on Tyr15 as DNA replication commences [35, 47], arguing that the cells arrest before S phase. Fifth, the delay is not observed in a res2 mutant, which can not turn off the Cdc10 dependent transcription signal. The finding that a mutation affecting expression of proteins crucial for preparation for S phase abolishes the delay argues that the wild type cells first stop in G1 and only later stop in S phase.
On the basis of these results we conclude that there is a UV-induced G1 delay, which is not checkpoint Rad dependent and is brought about by an as yet undescribed mechanism. This part of the total delay with 1C DNA content is ca 40 minutes, since rad, cds1 and mrc1 mutants delay 30–50 minutes and rum1Δ cells lose ca 40 minutes of the delay, compared to wild type cells. The remaining ca 40 minutes of the total delay requires the checkpoint Rads, Mrc1, Cds1 and Cdc2 is phosphorylated. We argue that this part of the delay is brought about by the intra-S checkpoint. However, the resolution of our experiments is not high enough to exclude the possibility that some of the checkpoint Rad- and Cds1-dependent part of the delay occurs in late G1. We consider this possibility unlikely for two reasons; first, previous work has shown that the role of Cds1 is specific for S phase  and second, we have shown in the current paper that if irradiation occurs later, the cells enter S phase without delay and delay in S phase.
Since the level of synchrony is low in germinating spores, we have not emphasised minor differences in the timing of S phase entry. In spite of poor synchrony, we deem germinating spores a good model system, since spore germination is a natural phenomenon, it involves an extended G1 period and we observed clear-cut effects. Furthermore, this model system allowed us to investigate the effects of a number of mutations that would have not been possible using synchronisation by other methods.
We have explored whether the G1/S delay is caused by a checkpoint mechanism. We have shown that caffeine abolishes the delay, but this is not entirely due to inhibition of Rad3 activity, since a rad3 mutation does not abolish all of the G1/S delay. Since we have not identified a checkpoint mutation which abolishes the delay, we attribute the effect of caffeine to another effect than the inhibition of checkpoint proteins. Interestingly, recent data suggest that caffeine inhibits checkpoint responses without inhibiting the ATR and ATM kinases in human cells [51, 52].
Previously, Rhind and Russell  showed that UV-irradiation during G1 delays passage through S-phase. However, this checkpoint arrests cells in S phase, requires Cds1 function and probably represents the intra-S checkpoint.
We have recently discovered a mechanism that delays entry into S phase in cells irradiated in early G1 in synchronised or in cycling cells  This inhibitory mechanism has several features in common with that described here. Both pathways are activated in early but not in late G1; both inhibit entry into S phase; both pathways are independent of classical checkpoint genes and of Cdc2 phosphorylation. These similarities argue that the G1/S mechanism demonstrated in germinating spores and in cycling cells is one and the same.
In budding yeast there is a G1 DNA damage checkpoint response that depends upon Mec1 [31, 32, 54], a homologue of the mammalian ATM/ATR and the fission yeast Rad3 protein. However, the budding yeast G1 checkpoint response depends on Rad53 [55, 56], whereas its homologue in S. pombe, Cds1, is not involved in the present pathway. The budding yeast G1/S checkpoint delays entry into S phase by phosphorylating and thereby downregulating Swi6, the homologue of Cdc10 . In contrast, in fission yeast Cdc10 dependent transcription is not delayed during the G1/S delay (Fig. 8).
Other possible mechanisms for the G1/S delay include inhibition of Cdc2 by Rum1 or an as yet unidentified mechanism such as preventing the formation of Cdc2-cyclin complexes or by restricting the availability of cyclins. We have shown that Rum1 is expressed during the delay and is required for the G1 delay. This observation does not imply that Rum1 is a direct target of the G1/S delay, but this remains an attractive possibility. Another possible mechanism for the delay is delaying expression of proteins required for the initiation of DNA replication. In particular, the findings that (1) irradiation in late G1 does not cause a delayed entry into S phase, (2) increased transcription of Cdc10 dependent genes in res2Δ overrides the delay, (3) transcription of Cdc10 dependent genes is not downregulated during the delay and (4) expression of Cdt1 is delayed, suggest that the G1/S delay is caused by delayed expression of Cdt1 and probably also of Cdc18 and Cig2. Since we have shown that transcription of Cdc10 regulated genes is not downregulated, the most likely mechanism of the delay is reduced translation rate of Cdt1 and possibly other proteins required for initiation of DNA replication.
We studied the response of Schizosaccharomyces pombe cells to UV irradiation in G1. We used germinating spores to exploit a natural phenomenon where the cells have a long G1. In this paper we provide evidence for the existence of a mechanism in fission yeast that delays entry into S phase upon UV irradiaton in early G1. The G1 delay is independent of classical checkpoint proteins and Cdc2 phosphorylation. Our results point to a mechanism that delays translation of proteins required for S phase entry.
Fission yeast strains and methods
All our strains are derivatives of the Schizosaccharomyces pombe L972h- strain. All basic growth and media conditions were as described .
Sporulation and spore germination
Diploids were made by interrupted mating of h+ and h- strains carrying the met3 or ade1 complementing markers. The rum1:::ura4+/rum1+ diploid was made by protoplast fusion since rum1Δ is sterile . All diploids, with the exceptions of res2Δ (which is deficient in meiosis ) and rum1Δ, were homozygous for the respective mutations. In case of these two mutants Δ/wild type ura4-D18/ura4-D18 diploids were sporulated and the spores were germinated in the absence of uracil. The diploids were sporulated in liquid malt extract medium at 30°C, then incubated with 3 μl/ml β-glucuronidase (Helix pomatia juice, Biosepra) at 30°C overnight. The spores were washed twice in water and resuspended in EMM2 supplemented with adenine and methionine for germination and UV irradiation.
Cells were irradiated with 254 nm UV light while rapidly stirred in a thin layer (3 mm) of liquid medium. The dose administered was measured with a radiometer (UVP instruments) and an exposure time of 4 minutes gave an incident dose of about 1100 J/m2. Cell survival was monitored by conventional plating on YE plates. The incident dose does not reflect the dose absorbed by the cells because UV light of this wavelength penetrates poorly into water. However, since irradiation conditions were constant, the incident dose was proportional to the absorbed dose.
Protein extracts and western blots
Protein extracts for western blotting were made by TCA extraction, as described previously . For western blot analysis the following antibodies were used: anti-phosphotyrosine Cdc2 (Sigma C0228) at a dilution of 1:400, anti-PSTAIRE against Cdc2 (Santa Cruz sc-53) at a dilution of 1:2000, anti-myc (PharMingen) at a dilution of 1:1000. The secondary antibodies were either HRP or AP conjugates, used at a dilution of 1/5000. Detection was performed using the enhanced chemiluminescence procedure (NEN ECL kit). Cdc2 and phosphorylated Cdc2 was measured using ECF detection (Amersham) and quantified with the Image Quant software.
RNA preparation and blotting
Total RNA was isolated as described , resolved on formaldehyde agarose gels and blotted onto a nitrocellulose membrane (NitroPure, Osmonics). All blots were hybridized with 32P-labelled RNA probes, generated with T7 RNA polymerase (Riboprobe System T7 Kit, Promega). For cig2 and cdc18, the ORFs were inserted into pGEM-3 MCS to serve as template for producing the RNA probes. For cdt1, a PCR fragment of the ORF with T7 promoter sequence attached to the lower primer was used as template. Hybridisation was carried out using standard procedures and visualised by a STORM 860 Phosphoimager (Molecular Dynamics).
About 107 cells were spun down for each sample and fixed in 70% ethanol before storing at 4°C. Samples were processed for flow cytometry as described  and stained with Sytox Green (Molecular Probes S-7020) , and analysed with a Becton-Dickinson FACSCalibur. The fraction of 1C cells was quantified using the CellQuest software (BD Biosciences).
We would like to thank T. Carr, S. Moreno, H. Nishitani, P. Nurse and P. Russell for strains and antibodies and M. O. Haugli and J. A. Sandvik for technical assistance. Work in our laboratory is funded by The Norwegian Cancer Society, the Norwegian Research Council and the Astri and Birger Torsteds Legacy.
- Hartwell LH, Weinert TA: Checkpoints: controls that ensure the order of cell cycle events. Science. 1989, 246: 629-634.View ArticlePubMedGoogle Scholar
- Huberman JA: DNA damage and replication checkpoints in the fission yeast, Schizosaccharomyces pombe. Prog Nucleic Acid Res Mol Biol. 1999, 62: 369-395.View ArticlePubMedGoogle Scholar
- Caspari T, Carr AM: DNA structure checkpoint pathways in Schizosaccharomyces pombe. Biochimie. 1999, 81: 173-181. 10.1016/S0300-9084(99)80050-9.View ArticlePubMedGoogle Scholar
- al-Khodairy F, Fotou E, Sheldrick KS, Griffiths DJ, Lehmann AR, Carr AM: Identification and characterization of new elements involved in checkpoint and feedback controls in fission yeast. Mol Biol Cell. 1994, 5: 147-160.PubMed CentralView ArticlePubMedGoogle Scholar
- al-Khodairy F, Carr AM: DNA repair mutants defining G2 checkpoint pathways in Schizosaccharomyces pombe. EMBO J. 1992, 11: 1343-1350.PubMed CentralPubMedGoogle Scholar
- Alcasabas AA, Osborn AJ, Bachant J, Hu F, Werler PJ, Bousset K, Furuya K, Diffley JF, Carr AM, Elledge SJ: Mrc1 transduces signals of DNA replication stress to activate Rad53. Nat Cell Biol. 2001, 3: 958-965. 10.1038/ncb1101-958.View ArticlePubMedGoogle Scholar
- Enoch T, Carr AM, Nurse P: Fission yeast genes involved in coupling mitosis to completion of DNA replication. Genes Dev. 1992, 6: 2035-2046.View ArticlePubMedGoogle Scholar
- Murakami H, Okayama H: A kinase from fission yeast responsible for blocking mitosis in S phase. Nature. 1995, 374: 817-819. 10.1038/374817a0.View ArticlePubMedGoogle Scholar
- Rowley R, Subramani S, Young PG: Checkpoint controls in Schizosaccharomyces pombe: rad1. EMBO J. 1992, 11: 1335-1342.PubMed CentralPubMedGoogle Scholar
- Saka Y, Esashi F, Matsusaka T, Mochida S, Yanagida M: Damage and replication checkpoint control in fission yeast is ensured by interactions of Crb2, a protein with BRCT motif, with Cut5 and Chk1. Genes Dev. 1997, 11: 3387-3400.PubMed CentralView ArticlePubMedGoogle Scholar
- Tanaka K, Russell P: Mrc1 channels the DNA replication arrest signal to checkpoint kinase Cds1. Nat Cell Biol. 2001, 3: 966-972. 10.1038/ncb1101-966.View ArticlePubMedGoogle Scholar
- Walworth N, Davey S, Beach D: Fission yeast chk1 protein kinase links the rad checkpoint pathway to cdc2. Nature. 1993, 363: 368-371. 10.1038/363368a0.View ArticlePubMedGoogle Scholar
- Willson J, Wilson S, Warr N, Watts FZ: Isolation and characterization of the Schizosaccharomyces pombe rhp9 gene: A gene required for the DNA damage checkpoint but not the replication checkpoint. Nucleic Acids Res. 1997, 25: 2138-2145. 10.1093/nar/25.11.2138.PubMed CentralView ArticlePubMedGoogle Scholar
- O'Connell MJ, Walworth NC, Carr AM: The G2-phase DNA-damage checkpoint. Trends Cell Biol. 2000, 10: 296-303. 10.1016/S0962-8924(00)01773-6.View ArticlePubMedGoogle Scholar
- Bentley NJ, Holtzman DA, Flaggs G, Keegan KS, DeMaggio A, Ford JC, Hoekstra M, Carr AM: The Schizosaccharomyces pombe rad3 checkpoint gene. EMBO J. 1996, 15: 6641-6651.PubMed CentralPubMedGoogle Scholar
- Cimprich KA, Shin TB, Keith CT, Schreiber SL: cDNA cloning and gene mapping of a candidate human cell cycle checkpoint protein. Proc Natl Acad Sci U S A. 1996, 93: 2850-2855. 10.1073/pnas.93.7.2850.PubMed CentralView ArticlePubMedGoogle Scholar
- Wolkow TD, Enoch T: Fission yeast rad26 is a regulatory subunit of the rad3 checkpoint kinase. Mol Biol Cell. 2002, 13: 480-492. 10.1091/mbc.01-03-0104.PubMed CentralView ArticlePubMedGoogle Scholar
- Edwards RJ, Bentley NJ, Carr AM: A Rad3-Rad26 complex responds to DNA damage independently of other checkpoint proteins. Nat Cell Biol. 1999, 1: 393-398. 10.1038/15623.View ArticlePubMedGoogle Scholar
- Caspari T, Dahlen M, Kanter-Smoler G, Lindsay HD, Hofmann K, Papadimitriou K, Sunnerhagen P, Carr AM: Characterization of Schizosaccharomyces pombe Hus1: a PCNA-related protein that associates with Rad1 and Rad9. Mol Cell Biol. 2000, 20: 1254-1262. 10.1128/MCB.20.4.1254-1262.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Thelen MP, Venclovas C, Fidelis K: A sliding clamp model for the Rad1 family of cell cycle checkpoint proteins. Cell. 1999, 96: 769-770. 10.1016/S0092-8674(00)80587-5.View ArticlePubMedGoogle Scholar
- Venclovas C, Thelen MP: Structure-based predictions of Rad1, Rad9, Hus1 and Rad17 participation in sliding clamp and clamp-loading complexes. Nucleic Acids Res. 2000, 28: 2481-2493. 10.1093/nar/28.13.2481.PubMed CentralView ArticlePubMedGoogle Scholar
- Griffiths DJ, Barbet NC, McCready S, Lehmann AR, Carr AM: Fission yeast rad17: a homologue of budding yeast RAD24 that shares regions of sequence similarity with DNA polymerase accessory proteins. EMBO J. 1995, 14: 5812-5823.PubMed CentralPubMedGoogle Scholar
- Martinho RG, Lindsay HD, Flaggs G, DeMaggio AJ, Hoekstra MF, Carr AM, Bentley NJ: Analysis of Rad3 and Chk1 protein kinases defines different checkpoint responses. EMBO J. 1998, 17: 7239-7249. 10.1093/emboj/17.24.7239.PubMed CentralView ArticlePubMedGoogle Scholar
- Walworth NC, Bernards R: rad-dependent response of the chk1-encoded protein kinase at the DNA damage checkpoint. Science. 1996, 271: 353-356.View ArticlePubMedGoogle Scholar
- Capasso H, Palermo C, Wan S, Rao H, John UP, O'Connell MJ, Walworth NC: Phosphorylation activates Chk1 and is required for checkpoint-mediated cell cycle arrest. J Cell Sci. 2002, 115: 4555-4564. 10.1242/jcs.00133.View ArticlePubMedGoogle Scholar
- Lindsay HD, Griffiths DJ, Edwards RJ, Christensen PU, Murray JM, Osman F, Walworth N, Carr AM: S-phase-specific activation of Cds1 kinase defines a subpathway of the checkpoint response in Schizosaccharomyces pombe. Genes Dev. 1998, 12: 382-395.PubMed CentralView ArticlePubMedGoogle Scholar
- O'Connell MJ, Raleigh JM, Verkade HM, Nurse P: Chk1 is a wee1 kinase in the G2 DNA damage checkpoint inhibiting cdc2 by Y15 phosphorylation. EMBO J. 1997, 16: 545-554. 10.1093/emboj/16.3.545.PubMed CentralView ArticlePubMedGoogle Scholar
- Rhind N, Furnari B, Russell P: Cdc2 tyrosine phosphorylation is required for the DNA damage checkpoint in fission yeast. Genes Dev. 1997, 11: 504-511.View ArticlePubMedGoogle Scholar
- Rhind N, Russell P: Mitotic DNA damage and replication checkpoints in yeast. Curr Opin Cell Biol. 1998, 10: 749-758. 10.1016/S0955-0674(98)80118-X.PubMed CentralView ArticlePubMedGoogle Scholar
- Gerald JNF, Benjamin JM, Kron SJ: Robust G1 checkpoint arrest in budding yeast: dependence on DNA damage signaling and repair. J Cell Sci. 2002, 115: 1749-1757.PubMedGoogle Scholar
- Siede W, Friedberg AS, Friedberg EC: RAD9-dependent G1 arrest defines a second checkpoint for damaged DNA in the cell cycle of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A. 1993, 90: 7985-7989.PubMed CentralView ArticlePubMedGoogle Scholar
- Siede W, Friedberg AS, Dianova I, Friedberg EC: Characterization of G1 checkpoint control in the yeast Saccharomyces cerevisiae following exposure to DNA-damaging agents. Genetics. 1994, 138: 271-281.PubMed CentralPubMedGoogle Scholar
- Esashi F, Yanagida M: Cdc2 phosphorylation of Crb2 is required for reestablishing cell cycle progression after the damage checkpoint. Mol Cell. 1999, 4: 167-174. 10.1016/S1097-2765(00)80364-0.View ArticlePubMedGoogle Scholar
- Carr AM, Moudjou M, Bentley NJ, Hagan IM: The chk1 pathway is required to prevent mitosis following cell-cycle arrest at 'start'. Curr Biol. 1995, 5: 1179-1190. 10.1016/S0960-9822(95)00234-X.View ArticlePubMedGoogle Scholar
- Hayles J, Nurse P: A pre-start checkpoint preventing mitosis in fission yeast acts independently of p34cdc2 tyrosine phosphorylation. EMBO J. 1995, 14: 2760-2771.PubMed CentralPubMedGoogle Scholar
- Synnes M, Nilssen EA, Boye E, Grallert B: A novel chk1-dependent G1/M checkpoint in fission yeast. J Cell Sci. 2002, 115: 3609-3618. 10.1242/jcs.00004.View ArticlePubMedGoogle Scholar
- Nishitani H, Lygerou Z: Control of DNA replication licensing in a cell cycle. Genes to Cells. 2002, 7: 523-534. 10.1046/j.1365-2443.2002.00544.x.View ArticlePubMedGoogle Scholar
- Hideo N, Zoi L: Control of DNA replication licensing in a cell cycle. Genes to Cells. 2002, 7: 523-534. 10.1046/j.1365-2443.2002.00544.x.View ArticleGoogle Scholar
- Bhaumik D, Wang TSF: Mutational effect of fission yeast polalpha on cell cycle events. Mol Biol Cell. 1998, 9: 2107-2123.PubMed CentralView ArticlePubMedGoogle Scholar
- Michael WM, Ott R, Fanning E, Newport J: Activation of the DNA replication checkpoint through RNA synthesis by primase. Science. 2000, 289: 2133-2137. 10.1126/science.289.5487.2133.View ArticlePubMedGoogle Scholar
- Nilssen EA, Synnes M, Kleckner N, Grallert B, Boye E: Intra-G1 arrest in response to UV irradiation in fission yeast. PNAS. 2003, 100: 10758-10763. 10.1073/pnas.1833769100.PubMed CentralView ArticlePubMedGoogle Scholar
- Correa-Bordes J, Nurse P: p25 rum1 orders S phase and mitosis by acting as an inhibitor of the p34 cdc2 mitotic kinase. Cell. 1995, 83: 1001-1009. 10.1016/0092-8674(95)90215-5.View ArticlePubMedGoogle Scholar
- Correa-Bordes J, Gulli MP, Nurse P: p25rum1 promotes proteolysis of the mitotic B-cyclin p56cdc13 during G1 of the fission yeast cell cycle. EMBO J. 1997, 16: 4657-4664. 10.1093/emboj/16.15.4657.PubMed CentralView ArticlePubMedGoogle Scholar
- Moreno S, Nurse P: Regulation of progression through the G1 phase of the cell cycle by the rum1+ gene. Nature. 1994, 367: 236-242. 10.1038/367236a0.View ArticlePubMedGoogle Scholar
- Benito J, Martin-Castellanos C, Moreno S: Regulation of the G1 phase of the cell cycle by periodic stabilization and degradation of the p25rum1 CDK inhibitor. EMBO J. 1998, 17: 482-497. 10.1093/emboj/17.2.482.PubMed CentralView ArticlePubMedGoogle Scholar
- Moser BA, Brondello JM, Baber-Furnari B, Russell P: Mechanism of caffeine-induced checkpoint override in fission yeast. Mol Cell Biol. 2000, 20: 4288-4294. 10.1128/MCB.20.12.4288-4294.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Zarzov P, Decottignies A, Baldacci G, Nurse P: G1/S CDK is inhibited to restrain mitotic onset when DNA replication is blocked in fission yeast. EMBO J. 2002, 21: 3370-3376. 10.1093/emboj/cdf346.PubMed CentralView ArticlePubMedGoogle Scholar
- Aves SJ, Durkacz BW, Carr A, Nurse P: Cloning, sequencing and transcriptional control of the Schizosaccharomyces pombe cdc10 'start' gene. EMBO J. 1985, 4: 457-463.PubMed CentralPubMedGoogle Scholar
- Lowndes NF, McInerny CJ, Johnson AL, Fantes PA, Johnston LH: Control of DNA synthesis genes in fission yeast by the cell- cycle gene cdc10+. Nature. 1992, 355: 449-453. 10.1038/355449a0.View ArticlePubMedGoogle Scholar
- Baum B, Wuarin J, Nurse P: Control of S-phase periodic transcription in the fission yeast mitotic cycle. EMBO J. 1997, 16: 4676-4688. 10.1093/emboj/16.15.4676.PubMed CentralView ArticlePubMedGoogle Scholar
- Kaufmann WK, Heffernan TP, Beaulieu LM, Doherty S, Frank AR, Zhou Y, Bryant MF, Zhou T, Luche DD, Nikolaishvili-Feinberg N: Caffeine and human DNA metabolism: the magic and the mystery. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 2003, 532: 85-102. 10.1016/j.mrfmmm.2003.08.012.View ArticlePubMedGoogle Scholar
- Cortez D: Caffeine Inhibits Checkpoint Responses without Inhibiting the Ataxia-Telangiectasia-mutated (ATM) and ATM- and Rad3-related (ATR) Protein Kinases. J Biol Chem. 2003, 278: 37139-37145. 10.1074/jbc.M307088200.View ArticlePubMedGoogle Scholar
- Rhind N, Russell P: The Schizosaccharomyces pombe S-phase checkpoint differentiates between different types of DNA damage. Genetics. 1998, 149: 1729-1737.PubMed CentralPubMedGoogle Scholar
- Siede W, Allen JB, Elledge SJ, Friedberg EC: The Saccharomyces cerevisiae MEC1 gene, which encodes a homolog of the human ATM gene product, is required for G1 arrest following radiation treatment. J Bacteriol. 1996, 178: 5841-5843.PubMed CentralPubMedGoogle Scholar
- Allen JB, Zhou Z, Siede W, Friedberg EC, Elledge SJ: The SAD1/RAD53 protein kinase controls multiple checkpoints and DNA damage-induced transcription in yeast. Genes Dev. 1994, 8: 2401-2415.View ArticlePubMedGoogle Scholar
- Pellicioli A, Lucca C, Liberi G, Marini F, Lopes M, Plevani P, Romano A, Di Fiore P, Foiani M: Activation of Rad53 kinase in response to DNA damage and its effect in modulating phosphorylation of the lagging strand DNA polymerase. EMBO J. 1999, 18: 6561-6572. 10.1093/emboj/18.22.6561.PubMed CentralView ArticlePubMedGoogle Scholar
- Sidorova JM, Breeden LL: Rad53-dependent phosphorylation of Swi6 and down-regulation of CLN1 and CLN2 transcription occur in response to DNA damage in Saccharomyces cerevisiae. Genes Dev. 1997, 11: 3032-3045.PubMed CentralView ArticlePubMedGoogle Scholar
- Moreno S, Klar A, Nurse P: Molecular genetic analysis of fission yeast Schizosaccharomyces pombe. Methods Enzymol. 1991, 194: 795-823.View ArticlePubMedGoogle Scholar
- Zhu Y, Takeda T, Nasmyth K, Jones N: pct1+, which encodes a new DNA-binding partner of p85cdc10, is required for meiosis in the fission yeast Schizosaccharomyces pombe. Genes Dev. 1994, 8: 885-898.View ArticlePubMedGoogle Scholar
- Sazer S, Sherwood SW: Mitochondrial growth and DNA synthesis occur in the absence of nuclear DNA replication in fission yeast. J Cell Sci. 1990, 97: 509-516.PubMedGoogle Scholar
- The Forsburg Lab pombe Pages:Yeast Cell Cycle by Flow Cytometry. [http://pingu.salk.edu/fcm/protocols/ycc.html]
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