A genome–wide screen to identify genes controlling the rate of entry into mitosis in fission yeast

References

• Kim DU, Hayles J, Kim D, Wood V, Park HO, Won M, Yoo HS, Duhig T, Nam M, Palmer G, et al. Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe. Nat Biotechnol 2010; 28:617-23; PMID:20473289; http://dx.doi.org/10.1038/nbt.1628
   PubMed Web of Science ®Google Scholar
• Giaever G, Chu AM, Ni L, Connelly C, Riles L, Veronneau S, Dow S, Lucau-Danila A, Anderson K, Andre B, et al. Functional profiling of the Saccharomyces cerevisiae genome. Nature 2002; 418:387-91; PMID:12140549; http://dx.doi.org/10.1038/nature00935
   PubMed Web of Science ®Google Scholar
• Winzeler EA, Shoemaker DD, Astromoff A, Liang H, Anderson K, Andre B, Bangham R, Benito R, Boeke JD, Bussey H, et al. Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. Science 1999; 285:901-6; PMID:10436161; http://dx.doi.org/10.1126/science.285.5429.901
   PubMed Web of Science ®Google Scholar
• Hayles J, Wood V, Jeffery L, Hoe KL, Kim DU, Park HO, Salas-Pino S, Heichinger C, Nurse P. A genome-wide resource of cell cycle and cell shape genes of fission yeast. Open biology 2013; 3:130053; PMID:23697806; http://dx.doi.org/10.1098/rsob.130053
   PubMed Web of Science ®Google Scholar
• Pau G, Walter T, Neumann B, Heriche JK, Ellenberg J, Huber W. Dynamical modelling of phenotypes in a genome-wide RNAi live-cell imaging assay. BMC Bioinformatics 2013; 14:308; PMID:24131777; http://dx.doi.org/10.1186/1471-2105-14-308
   PubMed Web of Science ®Google Scholar
• Lee J, Nam S, Hwang SB, Hong M, Kwon JY, Joeng KS, Im SH, Shim J, Park MC. Functional genomic approaches using the nematode Caenorhabditis elegans as a model system. J Biochem Mol Biol 2004; 37:107-13; PMID:14761308; http://dx.doi.org/10.5483/BMBRep.2004.37.1.107
   PubMedGoogle Scholar
• Bjorklund M, Taipale M, Varjosalo M, Saharinen J, Lahdenpera J, Taipale J. Identification of pathways regulating cell size and cell-cycle progression by RNAi. Nature 2006; 439:1009-13; PMID:16496002; http://dx.doi.org/10.1038/nature04469
   PubMed Web of Science ®Google Scholar
• Neumann B, Walter T, Heriche JK, Bulkescher J, Erfle H, Conrad C, Rogers P, Poser I, Held M, Liebel U, et al. Phenotypic profiling of the human genome by time-lapse microscopy reveals cell division genes. Nature 2010; 464:721-7; PMID:20360735; http://dx.doi.org/10.1038/nature08869
   PubMed Web of Science ®Google Scholar
• Gonczy P, Echeverri C, Oegema K, Coulson A, Jones SJ, Copley RR, Duperon J, Oegema J, Brehm M, Cassin E, et al. Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III. Nature 2000; 408:331-6; PMID:11099034; http://dx.doi.org/10.1038/35042526
   PubMed Web of Science ®Google Scholar
• Billmann M, Horn T, Fischer B, Sandmann T, Huber W, Boutros M. A genetic interaction map of cell cycle regulators. Mol Biol Cell 2016; 27:1397-407; PMID:26912791; http://dx.doi.org/10.1091/mbc.E15-07-0467
   PubMed Web of Science ®Google Scholar
• Fraser AG, Kamath RS, Zipperlen P, Martinez-Campos M, Sohrmann M, Ahringer J. Functional genomic analysis of C. elegans chromosome I by systematic RNA interference. Nature 2000; 408:325-30; PMID:11099033; http://dx.doi.org/10.1038/35042517
   PubMed Web of Science ®Google Scholar
• Somma MP, Ceprani F, Bucciarelli E, Naim V, De Arcangelis V, Piergentili R, Palena A, Ciapponi L, Giansanti MG, Pellacani C, et al. Identification of Drosophila mitotic genes by combining co-expression analysis and RNA interference. PLoS Genet 2008; 4:e1000126; PMID:18797514; http://dx.doi.org/10.1371/journal.pgen.1000126
   PubMed Web of Science ®Google Scholar
• Bonatti S, Simili M, Abbondandola A. Isolation of temperature sensitive mutants of Schizosaccharomyces pombe. J Bact 1972; 109:484-91; PMID:4110142
   PubMed Web of Science ®Google Scholar
• Mitchison JM. The growth of single cells. I. Schizosaccharomyces pombe. Exp Cell Res 1957; 13:244-62; PMID:13480293; http://dx.doi.org/10.1016/0014-4827(57)90005-8
   PubMed Web of Science ®Google Scholar
• Nurse P. Genetic control of cell size at cell division in yeast. Nature 1975; 256:547-51; PMID:1165770; http://dx.doi.org/10.1038/256547a0
   PubMed Web of Science ®Google Scholar
• Nurse P, Thuriaux P, Nasmyth K. Genetic control of the cell division cycle in the fission yeast Schizosaccharomyces pombe. Mol Gen Genet 1976; 146:167-78; PMID:958201; http://dx.doi.org/10.1007/BF00268085
   PubMedGoogle Scholar
• Nurse P, Thuriaux P. Regulatory genes controlling mitosis in the fission yeast Schizosaccharomyces pombe. Genetics 1980; 96:627-37; PMID:7262540
   PubMed Web of Science ®Google Scholar
• Deutschbauer AM, Jaramillo DF, Proctor M, Kumm J, Hillenmeyer ME, Davis RW, Nislow C, Giaever G. Mechanisms of haploinsufficiency revealed by genome-wide profiling in yeast. Genetics 2005; 169:1915-25; PMID:15716499; http://dx.doi.org/10.1534/genetics.104.036871
   PubMed Web of Science ®Google Scholar
• Chuang CH, Wallace MD, Abratte C, Southard T, Schimenti JC. Incremental genetic perturbations to MCM2-7 expression and subcellular distribution reveal exquisite sensitivity of mice to DNA replication stress. PLoS Genet 2010; 6:e1001110; PMID:20838603; http://dx.doi.org/10.1371/journal.pgen.1001110
   PubMed Web of Science ®Google Scholar
• Hafen E, Dickson B, Brunner T, Raabe T. Genetic dissection of signal transduction mediated by the sevenless receptor tyrosine kinase in Drosophila. Philos Trans R Soc Lond B Biol Sci 1993; 340:273-8; PMID:8103929; http://dx.doi.org/10.1098/rstb.1993.0068
   PubMed Web of Science ®Google Scholar
• Springer M, Weissman JS, Kirschner MW. A general lack of compensation for gene dosage in yeast. Mol Syst Biol 2010; 6:368; PMID:20461075; http://dx.doi.org/10.1038/msb.2010.19
   PubMed Web of Science ®Google Scholar
• Torres EM, Springer M, Amon A. No current evidence for widespread dosage compensation in S. cerevisiae. elife 2016; 5.e10996.
   Web of Science ®Google Scholar
• Thuriaux P, Nurse P, Carter B. Mutants altered in the control co-ordinating cell division with cell growth in the fission yeast Schizosaccharomyces pombe. Mol Gen Genet 1978; 161:215-20; PMID:672898
   PubMedGoogle Scholar
• Nurse P. Universal control mechanism regulating onset of M-phase. Nature 1990; 344:503-8; PMID:2138713; http://dx.doi.org/10.1038/344503a0
   PubMed Web of Science ®Google Scholar
• Russell P, Nurse P. Negative regulation of mitosis by wee1+, a gene encoding a protein kinase homolog. Cell 1987; 49:559-67; PMID:3032459; http://dx.doi.org/10.1016/0092-8674(87)90458-2
   PubMed Web of Science ®Google Scholar
• Russell P, Nurse P. cdc25+ functions as an inducer in the mitotic control of fission yeast. Cell 1986; 45:145-53; PMID:3955656; http://dx.doi.org/10.1016/0092-8674(86)90546-5
   PubMed Web of Science ®Google Scholar
• Bean DM, Heimbach J, Ficorella L, Micklem G, Oliver SG, Favrin G. esyN: network building, sharing and publishing. PLoS One 2014; 9:e106035; PMID:25181461; http://dx.doi.org/10.1371/journal.pone.0106035
   PubMed Web of Science ®Google Scholar
• Bhatia P, Hachet O, Hersch M, Rincon SA, Berthelot-Grosjean M, Dalessi S, Basterra L, Bergmann S, Paoletti A, Martin SG. Distinct levels in Pom1 gradients limit Cdr2 activity and localization to time and position division. Cell Cycle 2014; 13:538-52; PMID:24316795; http://dx.doi.org/10.4161/cc.27411
   PubMed Web of Science ®Google Scholar
• Morgan D. Cell Cycle: Principles of Control. London: New Science Press, 2006.
   Google Scholar
• McGrath DA, Balog ER, Koivomagi M, Lucena R, Mai MV, Hirschi A, Kellogg DR, Loog M, Rubin SM. Cks confers specificity to phosphorylation-dependent CDK signaling pathways. Nat Struct Mol Biol 2013; 20:1407-14; PMID:24186063; http://dx.doi.org/10.1038/nsmb.2707
   PubMed Web of Science ®Google Scholar
• Brambilla P, Ducommun B, Draetta G. Cdc2 protein kinase: interactions with cyclins and Suc1. Cold Spring Harbor symposia on quantitative biology 1991; 56:515-21; PMID:1840262; http://dx.doi.org/10.1101/SQB.1991.056.01.058
   PubMedGoogle Scholar
• Koivomagi M, Ord M, Iofik A, Valk E, Venta R, Faustova I, Kivi R, Balog ER, Rubin SM, Loog M. Multisite phosphorylation networks as signal processors for Cdk1. Nat Struct Mol Biol 2013; 20:1415-24; PMID:24186061; http://dx.doi.org/10.1038/nsmb.2706
   PubMed Web of Science ®Google Scholar
• Ha SH, Kim SY, Ferrell JE, Jr. The Prozone Effect Accounts for the Paradoxical Function of the Cdk-Binding Protein Suc1/Cks. Cell Rep 2016; 14:1408-21; PMID:26854218; http://dx.doi.org/10.1016/j.celrep.2016.01.033
   PubMed Web of Science ®Google Scholar
• Hayles J, Aves S, Nurse P. suc1 is an essential gene involved in both the cell cycle and growth in fission yeast. Embo J 1986; 5:3373-9; PMID:16453733
   PubMed Web of Science ®Google Scholar
• Martin SG, Berthelot-Grosjean M. Polar gradients of the DYRK-family kinase Pom1 couple cell length with the cell cycle. Nature 2009; 459:852-6; PMID:19474792; http://dx.doi.org/10.1038/nature08054
   PubMed Web of Science ®Google Scholar
• Moseley JB, Mayeux A, Paoletti A, Nurse P. A spatial gradient coordinates cell size and mitotic entry in fission yeast. Nature 2009; 459:857-60; PMID:19474789; http://dx.doi.org/10.1038/nature08074
   PubMed Web of Science ®Google Scholar
• Russell P, Nurse P. The mitotic inducer Nim1+ functions in a regulatory network of protein kinase homologs controlling the initiation of mitosis. Cell 1987; 49:569-76; PMID:3453113; http://dx.doi.org/10.1016/0092-8674(87)90459-4
   PubMed Web of Science ®Google Scholar
• Young PG, Fantes PA. Schizosaccharomyces pombe mutants affected in their division response to starvation. J Cell Sci 1987; 88 (Pt 3):295-304; PMID:3448096
   PubMed Web of Science ®Google Scholar
• Yu J, Zhao Y, Li Z, Galas S, Goldberg ML. Greatwall kinase participates in the Cdc2 autoregulatory loop in Xenopus egg extracts. Molecular cell 2006; 22:83-91; PMID:16600872; http://dx.doi.org/10.1016/j.molcel.2006.02.022
   PubMed Web of Science ®Google Scholar
• Mochida S, Maslen SL, Skehel M, Hunt T. Greatwall phosphorylates an inhibitor of protein phosphatase 2A that is essential for mitosis. Science 2010; 330:1670-3; PMID:21164013; http://dx.doi.org/10.1126/science.1195689
   PubMed Web of Science ®Google Scholar
• Chica N, Rozalen AE, Perez-Hidalgo L, Rubio A, Novak B, Moreno S. Nutritional Control of Cell Size by the Greatwall-Endosulfine-PP2A.B55 Pathway. Curr Biol 2016; 26:319-30; PMID:26776736; http://dx.doi.org/10.1016/j.cub.2015.12.035
   PubMed Web of Science ®Google Scholar
• Chua G, Lingner C, Frazer C, Young PG. The sal3(+) gene encodes an importin-beta implicated in the nuclear import of Cdc25 in Schizosaccharomyces pombe. Genetics 2002; 162:689-703; PMID:12399381
   PubMed Web of Science ®Google Scholar
• Nilsson J, Sengupta J, Frank J, Nissen P. Regulation of eukaryotic translation by the RACK1 protein: a platform for signalling molecules on the ribosome. EMBO reports 2004; 5:1137-41; PMID:15577927; http://dx.doi.org/10.1038/sj.embor.7400291
   PubMed Web of Science ®Google Scholar
• Shor B, Calaycay J, Rushbrook J, McLeod M. Cpc2/RACK1 is a ribosome-associated protein that promotes efficient translation in Schizosaccharomyces pombe. J Biol Chem 2003; 278:49119-28; PMID:12972434; http://dx.doi.org/10.1074/jbc.M303968200
   PubMed Web of Science ®Google Scholar
• McLeod M, Shor B, Caporaso A, Wang W, Chen H, Hu L. Cpc2, a fission yeast homologue of mammalian RACK1 protein, interacts with Ran1 (Pat1) kinase To regulate cell cycle progression and meiotic development. Mol Cell Biol 2000; 20:4016-27; PMID:10805744; http://dx.doi.org/10.1128/MCB.20.11.4016-4027.2000
   PubMed Web of Science ®Google Scholar
• Nunez A, Franco A, Soto T, Vicente J, Gacto M, Cansado J. Fission yeast receptor of activated C kinase (RACK1) ortholog Cpc2 regulates mitotic commitment through Wee1 kinase. J Biol Chem 2010; 285:41366-73; PMID:20974849; http://dx.doi.org/10.1074/jbc.M110.173815
   PubMed Web of Science ®Google Scholar
• Daga RR, Jimenez J. Translational control of the Cdc25 cell cycle phosphatase: a molecular mechanism coupling mitosis to cell growth. J Cell Sci 1999; 112 (Pt 18):3137-46; PMID:10462529
   PubMed Web of Science ®Google Scholar
• Suda M, Yamada S, Toda T, Miyakawa T, Hirata D. Regulation of Wee1 kinase in response to protein synthesis inhibition. FEBS letters 2000; 486:305-9; PMID:11119724; http://dx.doi.org/10.1016/S0014-5793(00)02299-7
   PubMed Web of Science ®Google Scholar
• Grallert B, Kearsey SE, Lenhard M, Carlson CR, Nurse P, Boye E, Labib K. A fission yeast general translation factor reveals links between protein synthesis and cell cycle controls. J Cell Sci 2000; 113 (Pt 8):1447-58; PMID:10725227
   PubMed Web of Science ®Google Scholar
• Forbes KC, Humphrey T, Enoch T. Suppressors of cdc25p overexpression identify two pathways that influence the G2/M checkpoint in fission yeast. Genetics 1998; 150:1361-75; PMID:9832516
   PubMed Web of Science ®Google Scholar
• Liu HY, Nefsky BS, Walworth NC. The Ded1 DEAD box helicase interacts with Chk1 and Cdc2. J Biol Chem 2002; 277:2637-43; PMID:11711540; http://dx.doi.org/10.1074/jbc.M109016200
   PubMed Web of Science ®Google Scholar
• Bilokapic S, Schwartz TU. 3D ultrastructure of the nuclear pore complex. Current opinion in cell biology 2012; 24:86-91; PMID:22244612; http://dx.doi.org/10.1016/j.ceb.2011.12.011
   PubMed Web of Science ®Google Scholar
• Asakawa H, Yang HJ, Yamamoto TG, Ohtsuki C, Chikashige Y, Sakata-Sogawa K, Tokunaga M, Iwamoto M, Hiraoka Y, Haraguchi T. Characterization of nuclear pore complex components in fission yeast Schizosaccharomyces pombe. Nucleus 2014; 5:149-62; PMID:24637836; http://dx.doi.org/10.4161/nucl.28487
   PubMed Web of Science ®Google Scholar
• Ibarra A, Hetzer MW. Nuclear pore proteins and the control of genome functions. Genes Dev 2015; 29:337-49; PMID:25691464; http://dx.doi.org/10.1101/gad.256495.114
   PubMed Web of Science ®Google Scholar
• Schrader N, Stelter P, Flemming D, Kunze R, Hurt E, Vetter IR. Structural basis of the nic96 subcomplex organization in the nuclear pore channel. Mol Cell 2008; 29:46-55; PMID:18206968; http://dx.doi.org/10.1016/j.molcel.2007.10.022
   PubMed Web of Science ®Google Scholar
• Vollmer B, Antonin W. The diverse roles of the Nup93/Nic96 complex proteins – structural scaffolds of the nuclear pore complex with additional cellular functions. Biol Chem 2014; 395:515-28; PMID:24572986; http://dx.doi.org/10.1515/hsz-2013-0285
   PubMed Web of Science ®Google Scholar
• Chen XQ, Du X, Liu J, Balasubramanian MK, Balasundaram D. Identification of genes encoding putative nucleoporins and transport factors in the fission yeast Schizosaccharomyces pombe: a deletion analysis. Yeast 2004; 21:495-509; PMID:15116432; http://dx.doi.org/10.1002/yea.1115
   PubMed Web of Science ®Google Scholar
• Tange Y, Hirata A, Niwa O. An evolutionarily conserved fission yeast protein, Ned1, implicated in normal nuclear morphology and chromosome stability, interacts with Dis3, Pim1/RCC1 and an essential nucleoporin. J Cell Sci 2002; 115:4375-85; PMID:12376568; http://dx.doi.org/10.1242/jcs.00135
   PubMed Web of Science ®Google Scholar
• Asakawa H, Mori C, Ohtsuki C, Iwamoto M, Hiraoka Y, Haraguchi T. Uncleavable Nup98-Nup96 is functional in the fission yeast Schizosaccharomyces pombe. FEBS open bio 2015; 5:508-14; PMID:26137436; http://dx.doi.org/10.1016/j.fob.2015.06.004
   PubMed Web of Science ®Google Scholar
• Hashizume C, Moyori A, Kobayashi A, Yamakoshi N, Endo A, Wong RW. Nucleoporin Nup62 maintains centrosome homeostasis. Cell Cycle 2013; 12:3804-16; PMID:24107630; http://dx.doi.org/10.4161/cc.26671
   PubMed Web of Science ®Google Scholar
• Laurell E, Beck K, Krupina K, Theerthagiri G, Bodenmiller B, Horvath P, Aebersold R, Antonin W, Kutay U. Phosphorylation of Nup98 by multiple kinases is crucial for NPC disassembly during mitotic entry. Cell 2011; 144:539-50; PMID:21335236; http://dx.doi.org/10.1016/j.cell.2011.01.012
   PubMed Web of Science ®Google Scholar
• Colombi P, Webster BM, Frohlich F, Lusk CP. The transmission of nuclear pore complexes to daughter cells requires a cytoplasmic pool of Nsp1. J Cell Biol 2013; 203:215-32; PMID:24165936; http://dx.doi.org/10.1083/jcb.201305115
   PubMed Web of Science ®Google Scholar
• Makio T, Lapetina DL, Wozniak RW. Inheritance of yeast nuclear pore complexes requires the Nsp1p subcomplex. J Cell Biol 2013; 203:187-96; PMID:24165935; http://dx.doi.org/10.1083/jcb.201304047
   PubMed Web of Science ®Google Scholar
• Kalverda B, Pickersgill H, Shloma VV, Fornerod M. Nucleoporins directly stimulate expression of developmental and cell-cycle genes inside the nucleoplasm. Cell 2010; 140:360-71; PMID:20144760; http://dx.doi.org/10.1016/j.cell.2010.01.011
   PubMed Web of Science ®Google Scholar
• Nazar RN. Ribosomal RNA processing and ribosome biogenesis in eukaryotes. IUBMB life 2004; 56:457-65; PMID:15545225; http://dx.doi.org/10.1080/15216540400010867
   PubMed Web of Science ®Google Scholar
• Terry LJ, Wente SR. Flexible gates: dynamic topologies and functions for FG nucleoporins in nucleocytoplasmic transport. Eukaryot Cell 2009; 8:1814-27; PMID:19801417; http://dx.doi.org/10.1128/EC.00225-09
   PubMed Web of Science ®Google Scholar
• Ribard C, Rochet M, Labedan B, Daignan-Fornier B, Alzari P, Scazzocchio C, Oestreicher N. Sub-families of alpha/beta barrel enzymes: a new adenine deaminase family. J Mol Biol 2003; 334:1117-31; PMID:14643670; http://dx.doi.org/10.1016/j.jmb.2003.10.005
   PubMed Web of Science ®Google Scholar
• Lin AL, Elford HL. Adenosine deaminase impairment and ribonucleotide reductase activity and levels in HeLa cells. J Biol Chem 1980; 255:8523-8; PMID:6997299
   PubMed Web of Science ®Google Scholar
• Jonna VR, Crona M, Rofougaran R, Lundin D, Johansson S, Brannstrom K, Sjoberg BM, Hofer A. Diversity in Overall Activity Regulation of Ribonucleotide Reductase. J Biol Chem 2015; 290:17339-48; PMID:25971975; http://dx.doi.org/10.1074/jbc.M115.649624
   PubMed Web of Science ®Google Scholar
• Fernandez Sarabia MJ, McInerny C, Harris P, Gordon C, Fantes P. The cell cycle genes cdc22+ and suc22+ of the fission yeast Schizosaccharomyces pombe encode the large and small subunits of ribonucleotide reductase. Mol Gen Genet 1993; 238:241-51; PMID:8479429
   PubMedGoogle Scholar
• Blackman FF. Optima and limiting factors. Ann Bot 1905; 19:281-98
   Google Scholar
• Kacser H, Burns JA. The control of flux. Biochemical Society transactions 1995; 23:341-66.
   Google Scholar
• Pardee AB. G1 events and regulation of cell proliferation. Science 1989; 246:603-8; PMID:2683075; http://dx.doi.org/10.1126/science.2683075
   PubMed Web of Science ®Google Scholar
• Nurse P, Bissett Y. Gene required in G1 for commitment to cell cycle and in G2 for control of mitosis in fission yeast. Nature 1981; 292:558-60; PMID:7254352; http://dx.doi.org/10.1038/292558a0
   PubMed Web of Science ®Google Scholar
• Johnston GC, Pringle JR, Hartwell LH. Coordination of growth with cell division in the yeast Saccharomyces cerevisiae. Exp Cell Res 1977; 105:79-98; PMID:320023; http://dx.doi.org/10.1016/0014-4827(77)90154-9
   PubMed Web of Science ®Google Scholar
• Evans T, Rosenthal ET, Youngblom J, Distel D, Hunt T. Cyclin: a protein specified by maternal mRNA in sea urchin eggs that is destroyed at each cleavage division. Cell 1983; 33:389-96; PMID:6134587; http://dx.doi.org/10.1016/0092-8674(83)90420-8
   PubMed Web of Science ®Google Scholar
• Reed SI, Dulic V, Lew DJ, Richardson HE, Wittenberg C. G1 control in yeast and animal cells. Ciba Found Symp 1992; 170:7-15; discussion −9; PMID:1483351
   PubMedGoogle Scholar
• Bitton DA, Wood V, Scutt PJ, Grallert A, Yates T, Smith DL, Hagan IM, Miller CJ. Augmented annotation of the Schizosaccharomyces pombe genome reveals additional genes required for growth and viability. Genetics 2011; 187:1207-17; PMID:21270388; http://dx.doi.org/10.1534/genetics.110.123497
   PubMed Web of Science ®Google Scholar
• Spirek M, Benko Z, Carnecka M, Rumpf C, Cipak L, Batova M, Marova I, Nam M, Kim DU, Park HO, et al. S. pombe genome deletion project: an update. Cell Cycle 2010; 9:2399-402; PMID:20519959; http://dx.doi.org/10.4161/cc.9.12.11914
   PubMed Web of Science ®Google Scholar
• Navarro FJ, Nurse P. A systematic screen reveals new elements acting at the G2/M cell cycle control. Gen Biol 2012; 13:R36; PMID:22624651; http://dx.doi.org/10.1186/gb-2012-13-5-r36
   PubMed Web of Science ®Google Scholar
• Graml V, Studera X, Lawson JL, Chessel A, Geymonat M, Bortfeld-Miller M, Walter T, Wagstaff L, Piddini E, Carazo-Salas RE. A genomic Multiprocess survey of machineries that control and link cell shape, microtubule organization, and cell-cycle progression. Dev Cell 2014; 31:227-39; PMID:25373780; http://dx.doi.org/10.1016/j.devcel.2014.09.005
   PubMed Web of Science ®Google Scholar
• Moreno S, Klar A, Nurse P. Molecular genetic analysis of fission yeast Schizosaccharomyces pombe. Methods Enzymol 1991; 194:795-823; PMID:2005825; http://dx.doi.org/10.1016/0076-6879(91)94059-L
   PubMed Web of Science ®Google 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 (Pt 3):509-16; PMID:2074269
   PubMed Web of Science ®Google Scholar
• Lyne R, Burns G, Mata J, Penkett CJ, Rustici G, Chen D, Langford C, Vetrie D, Bahler J. Whole-genome microarrays of fission yeast: characteristics, accuracy, reproducibility, and processing of array data. BMC genomics 2003; 4:27; PMID:12854975; http://dx.doi.org/10.1186/1471-2164-4-27
   PubMed Web of Science ®Google Scholar