Skip to main content
NCBI home page
Cell Cycle logoLink to Cell Cycle
. 2013 Feb 15;12(4):618–624. doi: 10.4161/cc.23513

A knockout screen for protein kinases required for the proper meiotic segregation of chromosomes in the fission yeast Schizosaccharomyces pombe

Ines Kovacikova 1,2, Silvia Polakova 1, Zsigmond Benko 1, Lubos Cipak 1,3, Lijuan Zhang 1, Cornelia Rumpf 1, Eva Miadokova 2, Juraj Gregan 1,2,*
PMCID: PMC3594262  PMID: 23370392

Abstract

The reduction of chromosome number during meiosis is achieved by two successive rounds of chromosome segregation after just single round of DNA replication. To identify novel proteins required for the proper segregation of chromosomes during meiosis, we analyzed the consequences of deleting Schizosaccharomyces pombe genes predicted to encode protein kinases that are not essential for cell viability. We show that Mph1, a member of the Mps1 family of spindle assembly checkpoint kinases, is required to prevent meiosis I homolog non-disjunction. We also provide evidence for a novel function of Spo4, the fission yeast ortholog of Dbf4-dependent Cdc7 kinase, in regulating the length of anaphase II spindles. In the absence of Spo4, abnormally elongated anaphase II spindles frequently overlap and thus destroy the linear order of nuclei in the ascus. Our observation that the spo4Δ mutant phenotype can be partially suppressed by inhibiting Cdc2-as suggests that dysregulation of the activity of this cyclin-dependent kinase may cause abnormal elongation of anaphase II spindles in spo4Δ mutant cells.

Keywords: protein kinase, chromosome segregation, meiosis, fission yeast, anaphase, spindle

Introduction

Reversible protein phosphorylation has been established as the major regulatory mechanism in the cell.1,2 Genome-wide surveys of protein kinases and phosphatases have been instrumental in characterizing novel proteins involved in various processes, including mitosis and meiosis.3-6 The fission yeast Schizosaccharomyces pombe is an excellent model organism for studying eukaryotic biology. There are more than one hundred predicted protein kinases encoded by the S. pombe genome, and some of them are known to play key roles in meiotic chromosome segregation.7-14 However, a systematic approach to analyze the role of S. pombe protein kinases in chromosome segregation during meiosis has not been conducted. While studies of S. pombe protein kinases that are essential for cell growth require the use of mutant strains carrying conditional alleles,15 non-essential protein kinases can be analyzed using knockout alleles.6 In our current study, we systematically analyze the role of non-essential S. pombe protein kinases in meiotic chromosome segregation. We focus on two protein kinases that show meiotic defects, namely Mph1 kinase, a member of the Mps1 family of spindle assembly checkpoint kinases and Spo4 kinase, the fission yeast ortholog of Dbf4-dependent Cdc7 kinase.

Results

A screen for protein kinases required for the proper segregation of chromosomes during meiosis

To identify novel proteins required for the proper segregation of chromosomes during meiosis, we analyzed the consequences of deleting Schizosaccharomyces pombe genes predicted to encode protein kinases that are not essential for cell viability. According to the PomBase database, there are 96 non-essential S. pombe genes predicted to encode protein kinases.16 In this study, we aimed to analyze knockout alleles from at least two independent sources for a majority of the studied kinases. Therefore, we analyzed kinase knockout alleles created by Bimbo et al.6 or purchased from the Bioneer collection.17,18 In addition, we made 38 knockout alleles according to our protocol described in Gregan et al.19 (Table S1). We failed to obtain knockout alleles of ppk18 and ppk19. We confirmed that byr1Δ, byr2Δ, spk1Δ, ssp1Δ, ssp2Δ and sty1Δ mutant cells are sterile, which prevented us from analyzing meiotic chromosome segregation in these mutants.20-24 As previously described,25,26 we found that gad8Δ mutant cells are also defective in mating. However, we were able to find enough asci to score meiotic chromosome segregation in gad8Δ mutant cells.

To analyze chromosome segregation, we introduced knockout alleles into a haploid homothallic h90 strain where chromosome I or chromosome II was marked with GFP (lys1-GFP27 or cen2-GFP28). These strains generate cells of both mating types and undergo mating and meiosis on sporulation medium. We sporulated mutant cells, stained nuclei with Hoechst dye and scored segregation of GFP dots in asci. In selected mutant strains, we also stained fixed cells with Hoechst dye and antibodies against tubulin and GFP in order to investigate chromosome segregation directly in anaphase I and anaphase II cells. Of the 88 mutants analyzed, 81 had no apparent meiotic phenotype. Two mutants (bub1Δ and mph1Δ) showed strong defects in chromosome segregation during meiosis, and five mutants (hhp2Δ, ppk24Δ, mug27Δ, spo4Δ and atg1Δ) showed various meiotic defects, such as a weak missegregation phenotype, lagging chromosomes or asci with more than four DNA masses (data not shown). Meiotic defects in hhp2Δ, spo4Δ and mug27Δ mutant cells have previously been described.10,29-34 Atg1 is an evolutionarily conserved protein kinase that is required for autophagy, and a defect in sporulation has been described in Saccharomyces cerevisiae atg1Δ mutant cells.35 In fission yeast atg1Δ mutant cells we observed that spore viability, as determined by random spore analysis, was strongly reduced (8% spore viability) compared with wild-type cells (86% spore viability). The role of Ppk24 in meiosis is not known and will be interesting to analyze in the future.

Mph1 is required for the proper segregation of homologs during meiosis I

Our screening revealed two mutants (bub1Δ and mph1Δ) that showed a strong meiotic missegregation phenotype. We focused on mph1Δ because meiotic chromosome segregation in the bub1Δ mutant has been previously described.11,36 Mph1 (the fission yeast MPS1 homolog) is an evolutionarily conserved protein kinase required for the spindle assembly checkpoint (SAC).37-42 Analysis of cen2-GFP dots in the mature asci of strains carrying homozygous cen2-GFP indicated homolog non-disjunction at meiosis I in mph1Δ cells (Fig. 1A). To analyze chromosome segregation directly in anaphase I cells, we fixed and stained cells with antibodies against tubulin and GFP. We observed lagging chromosomes (5% of anaphase I cells) and homolog non-disjunction in mph1Δ cells (Fig. 1B). Analysis of cells in which only one copy of chromosome II was marked by cen2-GFP (heterozygous cen2-GFP) suggested that there were no major defects in the segregation of sister chromatids during meiosis I and meiosis II in mph1Δ cells (data not shown). We thus conclude that Mph1 is required for efficient homolog disjunction during meiosis I.

graphic file with name cc-12-618-g1.jpg

Open in a new tab

Figure 1. Mph1 is required for the proper segregation of recombined homologous chromosomes during meiosis I. (A) The meiotic segregation of chromosome II was scored in a wild-type h90 cen2-GFP strain (JG12618) and an h90 cen2-GFP strain carrying the knockout allele of mph1 (mph1Δ) (JG15607). Cells were stained with Hoechst and examined under the fluorescence microscope. Chromosome segregation was scored in at least 100 asci. (B) The strains described in (A) were fixed and immunostained for tubulin and GFP. DNA was visualized by Hoechst staining. A total of 100 anaphase I cells were examined under a fluorescence microscope, and the segregation of chromosome II, marked by cen2-GFP, was scored.

Spo4/Spo6 and Spo5 are required to prevent the abnormal extension of anaphase II spindles

The Dbf4-dependent Cdc7 kinase is essential for DNA replication in most eukaryotes.43,44 The fission yeast S. pombe possesses two complexes homologous to Cdc7-Dbf4. While the Hsk1/Dfp1 complex is required for DNA replication during mitosis and meiosis, the Spo4/Spo6 complex is meiosis-specific and dispensable for DNA replication, but it is required for progression of the second meiotic division.33,34 A recent report showing the role of S. cerevisiae Cdc7 kinase in setting up mono-orientation of sister kinetochores during the first meiotic division prompted us to carefully analyze chromosome segregation in spo4Δ and spo6Δ mutants.45

We asked if S. pombe Spo4 kinase and its regulatory subunit Spo6 are required for segregation of sister centromeres during meiosis. Consistent with previous reports,33,34 we observed that most of the spo4Δ and spo6Δ meiotic cells arrested at the binucleate stage, probably due to fragmentation of meiosis II spindles. However, a small number of cells underwent both meiotic divisions. We scored the segregation of sister centromeres in a strain with only one copy of chromosome I marked with GFP (lys1-GFP).27 S. pombe produces linear asci in which the order of spores reflects the descent of nuclei from the two meiotic divisions.46 This allows detection of the missegregation of sister centromeres by scoring lys1-GFP in mature asci. In about 40% of spo4Δ and spo6Δ asci with four nuclei, lys1-GFP dots occupied both halves of the ascus, which is indicative of missegregation of sister centromeres during meiosis I (equational meiosis I) (Fig. 2A). Segregation of sister centromeres to opposite poles during meiosis I could be caused by the precocious loss of sister-chromatid cohesion. However, we found no evidence of a cohesion defect by monitoring cut3-GFP dots in spo4Δ cells arrested in late prophase I by a mei4Δ mutation (Fig. S1). To investigate more directly the behavior of sister centromeres, we analyzed the segregation of lys1-GFP in fixed cells stained with antibodies against tubulin and GFP. Surprisingly, we could not detect any missegregation in spo4Δ or spo6Δ cells when we analyzed lys1-GFP in anaphase I and anaphase II cells (Fig. 2B).). In rare cases, sister lys1-GFP sequences segregated to opposite halves. We attribute this to recombination taking place between a centromere and the lys1 locus. Interestingly, we observed abnormally elongated anaphase II spindles in both spo4Δ and spo6Δ mutant cells. These elongated spindles overlapped and thereby indicated that corresponding nuclei that separated during meiosis II were no longer adjacent (Fig. 3). Live cell imaging showed that the abnormal elongation of spindles in the spo4Δ mutant cells pushed sister nuclei apart and thus destroyed the linear order of nuclei in the ascus, such that the two spores at one end of the ascus contained non-sister nuclei (Fig. 4). This abnormal expansion of meiosis II spindles is likely due to the absence of Spo4 kinase activity because only wild-type spo4, not the “kinase-dead” spo4K95A allele, rescued this phenotype (Figs. 2A and 3). We also observed that anaphase II was longer in spo4Δ mutant cells (21.5 min +/− 5.1) as compared with wild-type cells (9.3 min +/− 2.3), suggesting that Spo4 is required for the timely completion of anaphase II.

graphic file with name cc-12-618-g2.jpg

Open in a new tab

Figure 2. Segregation of sister centromeres in spo4Δ and spo6Δ meiotic cells. (A) The wild-type strain h− lys1-GFP (wt) (JG11338) and h− lys1-GFP strains carrying knockout alleles of spo4 (spo4Δ) (JG14885) or spo6 (spo6Δ) (JG14888) were crossed to h+ strains of the same genotype but lacking lys1-GFP (JG11339, JG14872 and JG14879, respectively). Similarly, strains carrying a knockout allele of spo4 transformed with a plasmid carrying either a wild-type allele of spo4 (spo4Δ spo4+) (JG14911) or a “kinase-dead” allele of spo4 (spo4Δ spo4K95A) (JG14913) were crossed to h+ strains of the same genotype but lacking lys1-GFP (JG14903 and JG14907, respectively). Cells were sporulated and stained with Hoechst. Segregation of chromosome I was scored in at least 100 asci. (B) The strains described in (A) were fixed and stained with antibodies against tubulin and GFP. DNA was visualized by Hoechst staining. Cells were examined under a fluorescence microscope and segregation of chromosome I, marked by lys1-GFP, was scored in 100 anaphase I or anaphase II cells.

graphic file with name cc-12-618-g3.jpg

Open in a new tab

Figure 3. The anaphase II spindles are abnormally expanded in spo4Δ and spo6Δ mutant cells. A wild-type h90 strain and h90 strains carrying either a knockout allele of spo4 (spo4Δ) (JG14875), or a knockout allele of spo6 (spo6Δ) (JG14882) or a knockout allele of spo4 transformed with a plasmid carrying either a wild-type allele of spo4 (spo4Δ spo4+) (JG14906) or a “kinase-dead” allele of spo4 (spo4Δ spo4K95A) (JG14910) were sporulated, fixed and stained with antibodies against tubulin and GFP. DNA was visualized by Hoechst staining. The length of meiosis II spindles was determined in 100 zygotes.

graphic file with name cc-12-618-g4.jpg

Open in a new tab

Figure 4. Live-cell analysis of anaphase II spindles in spo4∆ cells. The wild-type strain h− mCherry-atb2 hta2-TagBFP (wt) (JG16499) (A) or the h− mCherry-atb2 hta2-BFP strain carrying a knockout allele of spo4 (spo4Δ) (JG16662) (B) was crossed to h+ strains of the same genotype (JG16486 and JG16663, respectively). Cells were sporulated and spindle elongation during meiosis II was analyzed by live cell imaging. The numbers indicate time in minutes. Anaphase II spindles were analyzed in four spo4Δ and eight wild-type cells.

spo4Δ and spo6Δ mutant cells are sporulation-defective, and we speculated that processes involved in spore formation might affect the spindle length and timing of anaphase II. We therefore decided to test if other sporulation-deficient mutants show abnormal elongation of anaphase II spindles. Interestingly, we observed abnormally elongated anaphase II spindles in spo5Δ mutant cells (Fig. S2). Spo5 is a putative RNA-binding protein required for spore formation, but its molecular function is not known.47,48 It will be interesting to analyze other sporulation-deficient mutants to gain more insight into the possible link between sporulation and the mechanisms governing anaphase II.

We next attempted to understand why spo4Δ and spo6Δ mutant cells fail to maintain the proper length of anaphase II spindles. Although molecular mechanisms that regulate the length of anaphase II spindles are poorly characterized, tight regulation of cyclin-dependent protein kinase (CDK) activity is known to be essential for progression through several stages of the cell cycle, including anaphase.14,49 Cells expressing non-degradable cyclin B have prolonged anaphase B, and chromosomes segregate much further than in wild-type cells.50 We therefore speculated that dysregulation of CDK activity may cause abnormal elongation of anaphase II spindles in spo4Δ and spo6Δ mutant cells. To test this possibility, we introduced a conditional analog-sensitive allele of cdc2 (cdc2-as) (Fig. S3),51 which encodes the fission yeast CDK, into spo4Δ cells. Whereas approximately 60% of spo4Δ asci with four nuclei contained cen2-GFP dots in both halves of the ascus, we observed a reduction to just 31% in cells where Cdc2-as was inhibited by adding inhibitor (Fig. 5). We observed a partial suppression of the spo4Δ mutant phenotype by cdc2-as, even in the absence of inhibitor, suggesting that Cdc2-as may not be fully functional. Thus, we conclude that inhibition of Cdc2-as by adding ATP-analog 1-NM-PP1 partially suppresses the mutant phenotype of spo4Δ cells.

graphic file with name cc-12-618-g5.jpg

Open in a new tab

Figure 5. Inactivation of Cdc2-as partially suppresses the mutant phenotype of spo4Δ cells. The h− cen2-GFP strain carrying either a knockout allele of spo4 (spo4Δ) (JG14873) or a knockout allele of spo4 and an analog-sensitive allele of cdc2 (spo4Δ cdc2-as) (JG16848) were crossed to h+ strains of the same genotype but lacking cen2-GFP (JG14872 and JG16858, respectively) and plated on PMG-N plates. After 24–43 h of incubation at 25°C cells were washed with water and incubated in a liquid PMG-N medium with or without inhibitor (5µM 1-NM-PP1) at 25°C for 4–7 h. Cells were stained with Hoechst to visualize DNA and segregation of cen2-GFP was scored in at least 50 asci.

Taken together, we conclude that Spo4 and Spo6 are dispensable for proper segregation of chromosomes during meiosis I, but Spo4 kinase activity is required to prevent the abnormal elongation of spindles during meiosis II. Our observation that the spo4Δ mutant phenotype can be partially suppressed by inhibiting Cdc2-as suggests that dysregulating the activity of this cyclin-dependent kinase may cause the abnormal elongation of anaphase II spindles in spo4Δ mutant cells.

Discussion

The strategy of knocking out selected groups of genes has proven to be an efficient way to identify key regulators of meiotic chromosome segregation. In fission yeast, such a strategy led to the identification of the protector of centromeric cohesion (Sgo1) and new proteins required for meiotic recombination (Rec24, Rec25, Rec27, Mde2 and Dil1).52-55 Our current study is focused on a systematic analysis of S. pombe genes predicted to encode protein kinases that are not essential for cell viability. This analysis uncovered new proteins required for the proper segregation of recombined homologous chromosomes during meiosis I (Mph1) and required to maintain the proper length of anaphase II spindles (Spo4, Spo5 and Spo6).

Mph1 is a member of the Mps1 family of protein kinases required for the spindle assembly checkpoint (SAC).37-42 Although the stringency of the SAC may be reduced during meiosis I,56-58 cells lacking a functional spindle assembly checkpoint enter anaphase I precociously, which does not allow sufficient time for recombined homologous chromosomes to complete their normal partitioning to opposite spindle poles59 and leads to the occurrence of homolog non-disjunction events in meiosis I.36,59-61 Although homolog non-disjunction during meiosis I can be caused by various defects, such as a failure to undergo meiotic recombination or defective sister-chromatid cohesion along chromosome arms, it is likely that the homolog non-disjunction phenotype observed in mph1Δ cells is due to a precocious entry into anaphase I.

Dbf4-dependent Cdc7 kinase is essential for eukaryotic DNA replication during both mitosis and meiosis.44 In addition to its role in origin firing, Dbf4 is also required after S phase to ensure mono-orientation of sister kinetochores during the first meiotic division in the budding yeast S. cerevisiae.45 Our observation that Spo4, the fission yeast ortholog of Dbf4-dependent Cdc7 kinase, is not required for mono-orientation of sister kinetochores during meiosis I is not surprising, given that the Pcs1/Mde4 complex, the fission yeast counterpart of the budding yeast monopolin subcomplex Csm1/Lrs4, is also dispensable for the mono-orientation process.62 However, there are two orthologs of the Cdc7 kinase in the fission yeast S. pombe (Spo4 and Hsk1), and a possible involvement of the Hsk1 kinase in the mono-orientation of sister kinetochores during meiosis I remains to be tested. Unexpectedly, we discovered that Spo4 kinase activity is required to maintain the proper length of anaphase II spindles. The control of spindle length is critical for both mitosis and meiosis. However, the molecular mechanisms and proteins involved are poorly characterized. Spindle length depends on the coordinated actions of motor proteins and factors that control tubulin polymerization and depolymerization, such as MCAK, Klp2 and γ-tubulin.63-68 In mouse oocytes, the Mos-MAP kinase pathway has been shown to control spindle elongation during meiosis I.69 Interestingly, the phenotype of spo4Δ cells is similar to that of S. cerevisiae cells depleted for Cdc15. The MEN (mitotic exit network pathway) component Cdc15 is a protein kinase required for the formation of mature spores and for proper spindle disassembly after meiosis II.70 Finally, it has been shown that cells expressing non-degradable cyclin B have prolonged anaphase B.50 Indeed, our observation that the anaphase II spindle defect in spo4Δ cells can be partially suppressed by inhibiting the fission yeast cyclin-dependent kinase Cdc2 suggests that the activity of this cyclin-dependent kinase may be dysregulated in spo4Δ mutant cells. In the future, identifying the relevant Spo4 targets will be essential for elucidating the mechanism controlling the length of meiosis II spindles.

In summary, our current study, together with many previous reports (e.g., refs. 29 and 71-73), demonstrates that reversible protein phosphorylation and protein kinases play a major role in ensuring the proper segregation of chromosomes during meiosis. In the long run, greater knowledge of these processes may help us understand the origins of human meiotic aneuploidy, which can lead to miscarriages and genetic disorders such as Down syndrome.74

Materials and Methods

Strains and general methods

The genotypes of the yeast strains used in this study are listed in Table S2. Schizosaccharomyces pombe strains were maintained and grown using standard conditions.15,75,76 The transformation of S. pombe was performed using the lithium acetate method as previously described.19

To create plasmid pREP41-hta2-TagBFP-leu2 (p244), we used primers F gwTagBFP NheI (CGCGGCTAGCTCTGAATTGATTAAAGAGAATATGC) and R gwTagBFP XmaI (CGCGCCCGGGTTAGTTCAATTTGTGTCCTAACTTAG) to amplify gwTagBFP from Gateway®TagBFP-AS-C entry clone plasmid (Evrogen FP177). The amplified product containing gwTagBFP was digested with NheI restriction enzyme and ligated with NheI-digested hta2-containing PCR product amplified from the plasmid p245 using primers F H2A.2 XhoI (AAAACTCGAGATGTCTGGAGGTAAATCTGGTGGTA) and R H2A.2 NheI (AAAAGCTAGCAGCACCAGCACCGGCTCCGGCA). The ligated product was digested with XmaI and XhoI and ligated with pREP41 digested with the same restriction enzymes (XmaI and XhoI), thus creating pREP41-H2A.2-TagBFP. Primers F hom R SacI (AAACGAGCTCTCAACTCTCCGTAGAGTAT) and R hom R MluI (AAAAACGCGTCGAAATGTCTTATCTTGCCGCA) were used to amplify region near his7 locus from the plasmid p245, the PCR product was digested with MluI and SacI restriction enzymes and ligated with pREP41-hta2-TagBFP digested with the same restriction enzymes (MluI and SacI) (MluI and SacI digest removed ARS sequence from the pREP41-hta2-TagBFP plasmid). ApaI restriction enzyme was used to linearize the plasmid before transformation into yeast. The plasmid pREP41-hta2-TagBFP-leu2 (p244) was used to create strains JG16499, JG16486, JG16662 and JG16663.

Time-lapse fluorescence microscopy

Cells were grown on Edinburgh Minimal Medium (EMM)-leu plates overnight at 32°C and subsequently plated on PMG-N plates (24 h at 25°C) to induce meiosis. Cells were resuspended in liquid PMG-N and transferred to a glass-bottom microwell dish (MatTek, Ashland) coated with 1 μl of 2 mg/ml lectin BS-1 (Sigma-Aldrich). Fluorescence microscopy of live cells was performed using epifluorescence microscope Olympus Cell R system equipped with Olympus MT-20 150W mercury arc burner, Halogen Lamp 100W, Hamamatsu ORCA-ER CCD camera, 60x/1.42 PlanApoN oil immersion objective and standard filter sets: DAPI (excitation 381–392 nm, emission 420–460 nm) and CY3 (excitation BP547–572, emission 5669–623 nm). All the experiments were performed at 25°C. Three-dimensional time-lapse images of cells were taken with 7 optical Z-sections, with 1 μm z distance, 3 and 4 min intervals. Image and data analyses were performed in ImageJ.

The length of anaphase II was determined in four spo4Δ and eight wild-type cells using the above described Olympus Cell R system.

Supplementary Material

Additional material
Click here for additional data file. (364.8KB, pdf)
cc-12-618-s01.pdf (364.8KB, pdf)

Acknowledgments

We would like to thank M. Sato, M. Yamamoto, C. Shimoda and M. Balasubramanian for providing plasmids and yeast strains and S. Loidl, Z. Cande, C. Kraft, Y. Watanabe, W. Zachariae and D. Zickler for helpful discussions. This work was supported by Austrian Science Fund grants P23609 and P21437 and HFSP grant RGY0069/2010. I.K. was supported by Slovak Academic Information Agency and S.P. was supported by EMBO long-term fellowship. L.C. was supported by the (European Community’s) Seventh Framework Programme (FP7/2007–2013) under grant agreement number PERG07-GA-2010–268167. J.G. was supported by the (European Community's) Seventh Framework Programme (FP7/2007–2013) under grant agreement number PCIG11-GA-2012-322300.

Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed.

Supplemental Materials

Supplemental materials may be found here:

www.landesbioscience.com/journals/cc/article/23513

Footnotes

References

  • 1.Krebs EG. Nobel Lecture. Protein phosphorylation and cellular regulation I. Biosci Rep. 1993;13:127–42. doi: 10.1007/BF01149958. [DOI] [PubMed] [Google Scholar]
  • 2.Fischer EH. Phosphorylase and the origin of reversible protein phosphorylation. Biol Chem. 2010;391:131–7. doi: 10.1515/bc.2010.011. [DOI] [PubMed] [Google Scholar]
  • 3.Carrassa L, Chilà R, Lupi M, Ricci F, Celenza C, Mazzoletti M, et al. Combined inhibition of Chk1 and Wee1: in vitro synergistic effect translates to tumor growth inhibition in vivo. Cell Cycle. 2012;11:2507–17. doi: 10.4161/cc.20899. [DOI] [PubMed] [Google Scholar]
  • 4.Bettencourt-Dias M, Giet R, Sinka R, Mazumdar A, Lock WG, Balloux F, et al. Genome-wide survey of protein kinases required for cell cycle progression. Nature. 2004;432:980–7. doi: 10.1038/nature03160. [DOI] [PubMed] [Google Scholar]
  • 5.Chen F, Archambault V, Kar A, Lio’ P, D’Avino PP, Sinka R, et al. Multiple protein phosphatases are required for mitosis in Drosophila. Curr Biol. 2007;17:293–303. doi: 10.1016/j.cub.2007.01.068. [DOI] [PubMed] [Google Scholar]
  • 6.Bimbó A, Jia Y, Poh SL, Karuturi RK, den Elzen N, Peng X, et al. Systematic deletion analysis of fission yeast protein kinases. Eukaryot Cell. 2005;4:799–813. doi: 10.1128/EC.4.4.799-813.2005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Cipak L, Hyppa RW, Smith GR, Gregan J. ATP analog-sensitive Pat1 protein kinase for synchronous fission yeast meiosis at physiological temperature. Cell Cycle. 2012;11:1626–33. doi: 10.4161/cc.20052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Guerra-Moreno A, Alves-Rodrigues I, Hidalgo E, Ayté J. Chemical genetic induction of meiosis in Schizosaccharomyces pombe. Cell Cycle. 2012;11:1621–5. doi: 10.4161/cc.20051. [DOI] [PubMed] [Google Scholar]
  • 9.Yamagishi Y, Honda T, Tanno Y, Watanabe Y. Two histone marks establish the inner centromere and chromosome bi-orientation. Science. 2010;330:239–43. doi: 10.1126/science.1194498. [DOI] [PubMed] [Google Scholar]
  • 10.Rumpf C, Cipak L, Dudas A, Benko Z, Pozgajova M, Riedel CG, et al. Casein kinase 1 is required for efficient removal of Rec8 during meiosis I. Cell Cycle. 2010;9:2657–62. doi: 10.4161/cc.9.13.12146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Vaur S, Cubizolles F, Plane G, Genier S, Rabitsch PK, Gregan J, et al. Control of Shugoshin function during fission-yeast meiosis. Curr Biol. 2005;15:2263–70. doi: 10.1016/j.cub.2005.11.034. [DOI] [PubMed] [Google Scholar]
  • 12.Hauf S, Biswas A, Langegger M, Kawashima SA, Tsukahara T, Watanabe Y. Aurora controls sister kinetochore mono-orientation and homolog bi-orientation in meiosis-I. EMBO J. 2007;26:4475–86. doi: 10.1038/sj.emboj.7601880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Tougan T, Kasama T, Ohtaka A, Okuzaki D, Saito TT, Russell P, et al. The Mek1 phosphorylation cascade plays a role in meiotic recombination of Schizosaccharomyces pombe. Cell Cycle. 2010;9:4688–702. doi: 10.4161/cc.9.23.14050. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Murakami H, Aiba H, Nakanishi M, Murakami-Tonami Y. Regulation of yeast forkhead transcription factors and FoxM1 by cyclin-dependent and polo-like kinases. Cell Cycle. 2010;9:3233–42. doi: 10.4161/cc.9.16.12599. [DOI] [PubMed] [Google Scholar]
  • 15.Cipak L, Zhang C, Kovacikova I, Rumpf C, Miadokova E, Shokat KM, et al. Generation of a set of conditional analog-sensitive alleles of essential protein kinases in the fission yeast Schizosaccharomyces pombe. Cell Cycle. 2011;10:3527–32. doi: 10.4161/cc.10.20.17792. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Wood V, Harris MA, McDowall MD, Rutherford K, Vaughan BW, Staines DM, et al. PomBase: a comprehensive online resource for fission yeast. Nucleic Acids Res. 2012;40(Database issue):D695–9. doi: 10.1093/nar/gkr853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Kim DU, Hayles J, Kim D, Wood V, Park HO, Won M, et al. Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe. Nat Biotechnol. 2010;28:617–23. doi: 10.1038/nbt.1628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Spirek M, Benko Z, Carnecka M, Rumpf C, Cipak L, Batova M, et al. S. pombe genome deletion project: an update. Cell Cycle. 2010;9:2399–402. doi: 10.4161/cc.9.12.11914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Gregan J, Rabitsch PK, Rumpf C, Novatchkova M, Schleiffer A, Nasmyth K. High-throughput knockout screen in fission yeast. Nat Protoc. 2006;1:2457–64. doi: 10.1038/nprot.2006.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Toda T, Shimanuki M, Yanagida M. Fission yeast genes that confer resistance to staurosporine encode an AP-1-like transcription factor and a protein kinase related to the mammalian ERK1/MAP2 and budding yeast FUS3 and KSS1 kinases. Genes Dev. 1991;5:60–73. doi: 10.1101/gad.5.1.60. [DOI] [PubMed] [Google Scholar]
  • 21.Nadin-Davis SA, Nasim A. A gene which encodes a predicted protein kinase can restore some functions of the ras gene in fission yeast. EMBO J. 1988;7:985–93. doi: 10.1002/j.1460-2075.1988.tb02905.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Wang Y, Xu HP, Riggs M, Rodgers L, Wigler M. byr2, a Schizosaccharomyces pombe gene encoding a protein kinase capable of partial suppression of the ras1 mutant phenotype. Mol Cell Biol. 1991;11:3554–63. doi: 10.1128/mcb.11.7.3554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Shiozaki K, Russell P. Conjugation, meiosis, and the osmotic stress response are regulated by Spc1 kinase through Atf1 transcription factor in fission yeast. Genes Dev. 1996;10:2276–88. doi: 10.1101/gad.10.18.2276. [DOI] [PubMed] [Google Scholar]
  • 24.Valbuena N, Moreno S. AMPK phosphorylation by Ssp1 is required for proper sexual differentiation in fission yeast. J Cell Sci. 2012;125:2655–64. doi: 10.1242/jcs.098533. [DOI] [PubMed] [Google Scholar]
  • 25.Matsuo T, Kubo Y, Watanabe Y, Yamamoto M. Schizosaccharomyces pombe AGC family kinase Gad8p forms a conserved signaling module with TOR and PDK1-like kinases. EMBO J. 2003;22:3073–83. doi: 10.1093/emboj/cdg298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Ikeda K, Morigasaki S, Tatebe H, Tamanoi F, Shiozaki K. Fission yeast TOR complex 2 activates the AGC-family Gad8 kinase essential for stress resistance and cell cycle control. Cell Cycle. 2008;7:358–64. doi: 10.4161/cc.7.3.5245. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Nabeshima K, Nakagawa T, Straight AF, Murray A, Chikashige Y, Yamashita YM, et al. Dynamics of centromeres during metaphase-anaphase transition in fission yeast: Dis1 is implicated in force balance in metaphase bipolar spindle. Mol Biol Cell. 1998;9:3211–25. doi: 10.1091/mbc.9.11.3211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Yamamoto A, Hiraoka Y. Monopolar spindle attachment of sister chromatids is ensured by two distinct mechanisms at the first meiotic division in fission yeast. EMBO J. 2003;22:2284–96. doi: 10.1093/emboj/cdg222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Ishiguro T, Tanaka K, Sakuno T, Watanabe Y. Shugoshin-PP2A counteracts casein-kinase-1-dependent cleavage of Rec8 by separase. Nat Cell Biol. 2010;12:500–6. doi: 10.1038/ncb2052. [DOI] [PubMed] [Google Scholar]
  • 30.Petronczki M, Matos J, Mori S, Gregan J, Bogdanova A, Schwickart M, et al. Monopolar attachment of sister kinetochores at meiosis I requires casein kinase 1. Cell. 2006;126:1049–64. doi: 10.1016/j.cell.2006.07.029. [DOI] [PubMed] [Google Scholar]
  • 31.Pérez-Hidalgo L, Rozalén AE, Martín-Castellanos C, Moreno S. Slk1 is a meiosis-specific Sid2-related kinase that coordinates meiotic nuclear division with growth of the forespore membrane. J Cell Sci. 2008;121:1383–92. doi: 10.1242/jcs.023812. [DOI] [PubMed] [Google Scholar]
  • 32.Yan H, Ge W, Chew TG, Chow JY, McCollum D, Neiman AM, et al. The meiosis-specific Sid2p-related protein Slk1p regulates forespore membrane assembly in fission yeast. Mol Biol Cell. 2008;19:3676–90. doi: 10.1091/mbc.E07-10-1060. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Nakamura T, Nakamura-Kubo M, Nakamura T, Shimoda C. Novel fission yeast Cdc7-Dbf4-like kinase complex required for the initiation and progression of meiotic second division. Mol Cell Biol. 2002;22:309–20. doi: 10.1128/MCB.22.1.309-320.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Nakamura T, Kishida M, Shimoda C. The Schizosaccharomyces pombe spo6+ gene encoding a nuclear protein with sequence similarity to budding yeast Dbf4 is required for meiotic second division and sporulation. Genes Cells. 2000;5:463–79. doi: 10.1046/j.1365-2443.2000.00343.x. [DOI] [PubMed] [Google Scholar]
  • 35.Briza P, Bogengruber E, Thür A, Rützler M, Münsterkötter M, Dawes IW, et al. Systematic analysis of sporulation phenotypes in 624 non-lethal homozygous deletion strains of Saccharomyces cerevisiae. Yeast. 2002;19:403–22. doi: 10.1002/yea.843. [DOI] [PubMed] [Google Scholar]
  • 36.Bernard P, Maure JF, Javerzat JP. Fission yeast Bub1 is essential in setting up the meiotic pattern of chromosome segregation. Nat Cell Biol. 2001;3:522–6. doi: 10.1038/35074598. [DOI] [PubMed] [Google Scholar]
  • 37.He X, Jones MH, Winey M, Sazer S. Mph1, a member of the Mps1-like family of dual specificity protein kinases, is required for the spindle checkpoint in S. pombe. J Cell Sci. 1998;111:1635–47. doi: 10.1242/jcs.111.12.1635. [DOI] [PubMed] [Google Scholar]
  • 38.Musacchio A. Spindle assembly checkpoint: the third decade. Philos Trans R Soc Lond B Biol Sci. 2011;366:3595–604. doi: 10.1098/rstb.2011.0072. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Zich J, Sochaj AM, Syred HM, Milne L, Cook AG, Ohkura H, et al. Kinase activity of fission yeast Mph1 is required for Mad2 and Mad3 to stably bind the anaphase promoting complex. Curr Biol. 2012;22:296–301. doi: 10.1016/j.cub.2011.12.049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Shepperd LA, Meadows JC, Sochaj AM, Lancaster TC, Zou J, Buttrick GJ, et al. Phosphodependent recruitment of Bub1 and Bub3 to Spc7/KNL1 by Mph1 kinase maintains the spindle checkpoint. Curr Biol. 2012;22:891–9. doi: 10.1016/j.cub.2012.03.051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Yamagishi Y, Yang CH, Tanno Y, Watanabe Y. MPS1/Mph1 phosphorylates the kinetochore protein KNL1/Spc7 to recruit SAC components. Nat Cell Biol. 2012;14:746–52. doi: 10.1038/ncb2515. [DOI] [PubMed] [Google Scholar]
  • 42.Heinrich S, Windecker H, Hustedt N, Hauf S. Mph1 kinetochore localization is crucial and upstream in the hierarchy of spindle assembly checkpoint protein recruitment to kinetochores. J Cell Sci. 2012;125:4720–7. doi: 10.1242/jcs.110387. [DOI] [PubMed] [Google Scholar]
  • 43.Kearsey SE, Cotterill S. Enigmatic variations: divergent modes of regulating eukaryotic DNA replication. Mol Cell. 2003;12:1067–75. doi: 10.1016/S1097-2765(03)00441-6. [DOI] [PubMed] [Google Scholar]
  • 44.Masai H, Arai K. Cdc7 kinase complex: a key regulator in the initiation of DNA replication. J Cell Physiol. 2002;190:287–96. doi: 10.1002/jcp.10070. [DOI] [PubMed] [Google Scholar]
  • 45.Matos J, Lipp JJ, Bogdanova A, Guillot S, Okaz E, Junqueira M, et al. Dbf4-dependent CDC7 kinase links DNA replication to the segregation of homologous chromosomes in meiosis I. Cell. 2008;135:662–78. doi: 10.1016/j.cell.2008.10.026. [DOI] [PubMed] [Google Scholar]
  • 46.Leupold U. Die Vererbung von Homothallie und Heterothallie bei Schizosaccharomyces pombe. C R Trav Lab Carlsberg, Ser Physiol. 1950;24:381–480. [Google Scholar]
  • 47.Okuzaki D, Kasama T, Hirata A, Ohtaka A, Kakegawa R, Nojima H. Spo5 phosphorylation is essential for its own timely degradation and for successful meiosis in Schizosaccharomyces pombe. Cell Cycle. 2010;9:3751–60. doi: 10.4161/cc.9.18.12937. [DOI] [PubMed] [Google Scholar]
  • 48.Kasama T, Shigehisa A, Hirata A, Saito TT, Tougan T, Okuzaki D, et al. Spo5/Mug12, a putative meiosis-specific RNA-binding protein, is essential for meiotic progression and forms Mei2 dot-like nuclear foci. Eukaryot Cell. 2006;5:1301–13. doi: 10.1128/EC.00099-06. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Murakami H, Nurse P. DNA replication and damage checkpoints and meiotic cell cycle controls in the fission and budding yeasts. Biochem J. 2000;349:1–12. doi: 10.1042/0264-6021:3490001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Wheatley SP, Hinchcliffe EH, Glotzer M, Hyman AA, Sluder G, Wang Yl. CDK1 inactivation regulates anaphase spindle dynamics and cytokinesis in vivo. J Cell Biol. 1997;138:385–93. doi: 10.1083/jcb.138.2.385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Ohta M, Sato M, Yamamoto M. Spindle pole body components are reorganized during fission yeast meiosis. Mol Biol Cell. 2012;23:1799–811. doi: 10.1091/mbc.E11-11-0951. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Rabitsch KP, Gregan J, Schleiffer A, Javerzat JP, Eisenhaber F, Nasmyth K. Two fission yeast homologs of Drosophila Mei-S332 are required for chromosome segregation during meiosis I and II. Curr Biol. 2004;14:287–301. doi: 10.1016/j.cub.2004.01.051. [DOI] [PubMed] [Google Scholar]
  • 53.Gregan J, Rabitsch PK, Sakem B, Csutak O, Latypov V, Lehmann E, et al. Novel genes required for meiotic chromosome segregation are identified by a high-throughput knockout screen in fission yeast. Curr Biol. 2005;15:1663–9. doi: 10.1016/j.cub.2005.07.059. [DOI] [PubMed] [Google Scholar]
  • 54.Rumpf C, Cipak L, Novatchkova M, Li Z, Polakova S, Dudas A, et al. High-throughput knockout screen in Schizosaccharomyces pombe identifies a novel gene required for efficient homolog disjunction during meiosis I. Cell Cycle. 2010;9:1802–8. doi: 10.4161/cc.9.9.11526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Martín-Castellanos C, Blanco M, Rozalén AE, Pérez-Hidalgo L, García AI, Conde F, et al. A large-scale screen in S. pombe identifies seven novel genes required for critical meiotic events. Curr Biol. 2005;15:2056–62. doi: 10.1016/j.cub.2005.10.038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Hawley RS. Oogenesis: when most is good enough. Curr Biol. 2011;21:R288–90. doi: 10.1016/j.cub.2011.03.010. [DOI] [PubMed] [Google Scholar]
  • 57.Yin S, Sun XF, Schatten H, Sun QY. Molecular insights into mechanisms regulating faithful chromosome separation in female meiosis. Cell Cycle. 2008;7:2997–3005. doi: 10.4161/cc.7.19.6809. [DOI] [PubMed] [Google Scholar]
  • 58.Sebestova J, Danylevska A, Novakova L, Kubelka M, Anger M. Lack of response to unaligned chromosomes in mammalian female gametes. Cell Cycle. 2012;11:3011–8. doi: 10.4161/cc.21398. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Gilliland WD, Hughes SE, Cotitta JL, Takeo S, Xiang Y, Hawley RS. The multiple roles of mps1 in Drosophila female meiosis. PLoS Genet. 2007;3:e113. doi: 10.1371/journal.pgen.0030113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Shonn MA, McCarroll R, Murray AW. Requirement of the spindle checkpoint for proper chromosome segregation in budding yeast meiosis. Science. 2000;289:300–3. doi: 10.1126/science.289.5477.300. [DOI] [PubMed] [Google Scholar]
  • 61.Malmanche N, Owen S, Gegick S, Steffensen S, Tomkiel JE, Sunkel CE. Drosophila BubR1 is essential for meiotic sister-chromatid cohesion and maintenance of synaptonemal complex. Curr Biol. 2007;17:1489–97. doi: 10.1016/j.cub.2007.07.042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Gregan J, Riedel CG, Pidoux AL, Katou Y, Rumpf C, Schleiffer A, et al. The kinetochore proteins Pcs1 and Mde4 and heterochromatin are required to prevent merotelic orientation. Curr Biol. 2007;17:1190–200. doi: 10.1016/j.cub.2007.06.044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Inoué S. The role of microtubule assembly dynamics in mitotic force generation and functional organization of living cells. J Struct Biol. 1997;118:87–93. doi: 10.1006/jsbi.1996.3839. [DOI] [PubMed] [Google Scholar]
  • 64.Doubilet S, McKim KS. Spindle assembly in the oocytes of mouse and Drosophila--similar solutions to a problem. Chromosome Res. 2007;15:681–96. doi: 10.1007/s10577-007-1148-8. [DOI] [PubMed] [Google Scholar]
  • 65.O’Connell CB, Khodjakov AL. Cooperative mechanisms of mitotic spindle formation. J Cell Sci. 2007;120:1717–22. doi: 10.1242/jcs.03442. [DOI] [PubMed] [Google Scholar]
  • 66.Troxell CL, Sweezy MA, West RR, Reed KD, Carson BD, Pidoux AL, et al. pkl1(+)and klp2(+): Two kinesins of the Kar3 subfamily in fission yeast perform different functions in both mitosis and meiosis. Mol Biol Cell. 2001;12:3476–88. doi: 10.1091/mbc.12.11.3476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Ohi R, Burbank K, Liu Q, Mitchison TJ. Nonredundant functions of Kinesin-13s during meiotic spindle assembly. Curr Biol. 2007;17:953–9. doi: 10.1016/j.cub.2007.04.057. [DOI] [PubMed] [Google Scholar]
  • 68.Paluh JL, Nogales E, Oakley BR, McDonald K, Pidoux AL, Cande WZ. A mutation in gamma-tubulin alters microtubule dynamics and organization and is synthetically lethal with the kinesin-like protein pkl1p. Mol Biol Cell. 2000;11:1225–39. doi: 10.1091/mbc.11.4.1225. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Verlhac MH, Lefebvre C, Guillaud P, Rassinier P, Maro B. Asymmetric division in mouse oocytes: with or without Mos. Curr Biol. 2000;10:1303–6. doi: 10.1016/S0960-9822(00)00753-3. [DOI] [PubMed] [Google Scholar]
  • 70.Pablo-Hernando ME, Arnaiz-Pita Y, Nakanishi H, Dawson D, del Rey F, Neiman AM, et al. Cdc15 is required for spore morphogenesis independently of Cdc14 in Saccharomyces cerevisiae. Genetics. 2007;177:281–93. doi: 10.1534/genetics.107.076133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.McGuinness BE, Anger M, Kouznetsova A, Gil-Bernabé AM, Helmhart W, Kudo NR, et al. Regulation of APC/C activity in oocytes by a Bub1-dependent spindle assembly checkpoint. Curr Biol. 2009;19:369–80. doi: 10.1016/j.cub.2009.01.064. [DOI] [PubMed] [Google Scholar]
  • 72.Gutiérrez-Caballero C, Cebollero LR, Pendás AM. Shugoshins: from protectors of cohesion to versatile adaptors at the centromere. Trends Genet. 2012;28:351–60. doi: 10.1016/j.tig.2012.03.003. [DOI] [PubMed] [Google Scholar]
  • 73.Kerr GW, Sarkar S, Arumugam P. How to halve ploidy: lessons from budding yeast meiosis. Cell Mol Life Sci. 2012;69:3037–51. doi: 10.1007/s00018-012-0974-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Hassold T, Hall H, Hunt P. The origin of human aneuploidy: where we have been, where we are going. Hum Mol Genet 2007; 16 Spec No. 2:R203-8. [DOI] [PubMed]
  • 75.Sabatinos SA, Forsburg SL. Molecular genetics of Schizosaccharomyces pombe. Methods Enzymol. 2010;470:759–95. doi: 10.1016/S0076-6879(10)70032-X. [DOI] [PubMed] [Google Scholar]
  • 76.Dudas A, Ahmad S, Gregan J. Sgo1 is required for co-segregation of sister chromatids during achiasmate meiosis I. Cell Cycle. 2011;10:951–5. doi: 10.4161/cc.10.6.15032. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Additional material
Click here for additional data file. (364.8KB, pdf)
cc-12-618-s01.pdf (364.8KB, pdf)

Articles from Cell Cycle are provided here courtesy of Taylor & Francis

RESOURCES