Comparative functional genomics of the fission yeasts
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A combined analysis of genome sequence, structure, and expression gives insights into fission yeast biology.
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Yeast's primary function during the initial stage of liquid fermentation in fruit vinegar production is to convert sugars into ethanol and carbon dioxide, even under aerobic conditions.
“Yeast serves as a crucial microorganism during the initial stage of liquid fermentation in fruit vinegar production. Its primary function is to convert sugars into ethanol and carbon dioxide, even under aerobic conditions [45,46].”
From The Metabolic Pathways of Yeast and Acetic Acid Bacteria During Fruit Vinegar Fermentation and Their Influence on Flavor Development (2025) · cites this paper as [46]
The “Gene content reflects glucose-dependent lifestyle” section (page unavailable) says fission and budding yeasts can produce ethanol by aerobic fermentation of glucose. It does not address fruit vinegar production, the initial stage of liquid fermentation, or carbon dioxide production. (LLM, conf=0.88)
Experimental — accuracy not yet measuredThis group was not enriched for lncRNAs conserved in other fission yeast species.
“This group was not enriched for lncRNAs conserved in other fission yeast species (Rhind et al., 2011).”
From Quantitative Analysis of Fission Yeast Transcriptomes and Proteomes in Proliferating and Quiescent Cells (2012) · cites this paper as Rhind et al., 2011
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Cites
Exploring the metabolic and genetic control of gene expression on a genomic scale.
Derisi, J., Iyer, V., & Brown, P. (1997) · Science · doi:10.1126/science.278.5338.680 · Cited by 4,832 · see citing works
Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi
Volpe, T. A., Kidner, C. A., Hall, I. M., Teng, G., Grewal, S. I. S., & Martienssen, R. A. (2002) · Science · doi:10.1126/science.1074973 · Cited by 2,055 · see citing works
Self-citationSequencing and comparison of yeast species to identify genes and regulatory elements
Kellis, M., Patterson, N. J., Endrizzi, M. G., Birren, B. W., & Lander, E. S. (2003) · Nature · doi:10.1038/nature01644 · Cited by 1,731 · see citing works
Self-citationThe genome sequence of Schizosaccharomyces pombe
Wood, V., Gwilliam, R., Rajandream, M.-A., Lyne, M. H., Lyne, R., Stewart, A., SGOUROS, J. G., Peat, N., Hayles, J., Baker, S. G., et al. (2002) · Nature · doi:10.1038/nature724 · Cited by 1,650 · see citing works
Dynamic repertoire of a eukaryotic transcriptome surveyed at single-nucleotide resolution
Wilhelm, B. T., Marguerat, S., Watt, S. B., Schubert, F., Wood, V., Goodhead, I., Penkett, C. J., Rogers, J., & Bähler, J. (2008) · Nature · doi:10.1038/nature07002 · Cited by 974 · see citing works
Bidirectional promoters generate pervasive transcription in yeast
Xu, Z., Wei, W., Gagneur, J., Perocchi, F., Clauder‐Münster, S., Camblong, J., Guffanti, E., Stutz, F., Huber, W. K., & Steinmetz, L. M. (2009) · Nature · doi:10.1038/nature07728 · Cited by 926 · see citing works
Comprehensive comparative analysis of strand-specific RNA sequencing methods
Levin, J. Z., Yassour, M., Adiconis, X., Nusbaum, C., Thompson, D. A., Friedman, N., Gnirke, A., & Regev, A. (2010) · Nature Methods · doi:10.1038/nmeth.1491 · Cited by 753 · see citing works
Self-citationNatural history and evolutionary principles of gene duplication in fungi
Wapinski, I., Pfeffer, A., Friedman, N., & Regev, A. (2007) · Nature · doi:10.1038/nature06107 · Cited by 614 · see citing works
How did Saccharomyces evolve to become a good brewer?
Piškur, J., Rozpędowska, E., Poláková, S., Merico, A., & Compagno, C. (2006) · Trends in Genetics · doi:10.1016/j.tig.2006.02.002 · Cited by 514 · see citing works
The transcriptional program of meiosis and sporulation in fission yeast
Mata, J., Lyne, R., Burns, G., & Bähler, J. (2002) · Nature Genetics · doi:10.1038/ng951 · Cited by 480 · see citing works
Four mating‐type genes control sexual differentiation in the fission yeast.
Kelly, M., Burke, J. F., Smith, M., Klar, A. J. S., & Beach, D. (1988) · The EMBO Journal · doi:10.1002/j.1460-2075.1988.tb02973.x · Cited by 388 · see citing works
Conserved nucleosome positioning defines replication originsPreprint
Eaton, M. L., Galani, K., Kang, S., Bell, S. P., & MacAlpine, D. M. (2010) · Genes & Development · doi:10.1101/gad.1913210 · Cited by 384 · see citing works
Lantermann, A. B., Straub, T., Strålfors, A., Yuan, G., Ekwall, K., & Korber, P. (2010) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.1741 · Cited by 242 · see citing works
Self-citationRNAi-dependent formation of heterochromatin and its diverse functions
Grewal, S. I. S. (2010) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2010.02.003 · Cited by 236 · see citing works
Control of DNA synthesis genes in fission yeast by the cell-cycle gene cdclO+
Lowndes, N. F., Mclnerny, C. J., Johnson, A. L., Fantes, P. A., & Johnston, L. H. (1992) · Nature · doi:10.1038/355449a0 · Cited by 230 · see citing works
Carbohydrate and energy-yielding metabolism in non-conventional yeasts: Figure 1
Flores, C., Rodrı́guez, C., Petit, T., & Gancedo, C. (2000) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2000.tb00553.x · Cited by 227 · see citing works
Heterochromatin Integrity Affects Chromosome Reorganization After Centromere Dysfunction
Ishii, K., Ogiyama, Y., Chikashige, Y., Soejima, S., Masuda, F., Kakuma, T., Hiraoka, Y., & Takahashi, K. (2008) · Science · doi:10.1126/science.1158699 · Cited by 202 · see citing works
Grewal, S. I. S., & Klar, A. J. S. (1997) · Genetics · doi:10.1093/genetics/146.4.1221 · Cited by 180 · see citing works
Host genome surveillance for retrotransposons by transposon-derived proteins
Cam, H. P., Noma, K.-I., Ebina, H., Levin, H. L., & Grewal, S. I. S. (2007) · Nature · doi:10.1038/nature06499 · Cited by 168 · see citing works
Self-citationCell type switching by DNA transposition in fission yeast
Beach, D. (1983) · Nature · doi:10.1038/305682a0 · Cited by 143 · see citing works
Histone H2A.Z cooperates with RNAi and heterochromatin factors to suppress antisense RNAs
Zofall, M., Fischer, T., Zhang, K., Zhou, M., Cui, B., Veenstra, T. D., & Grewal, S. I. S. (2009) · Nature · doi:10.1038/nature08321 · Cited by 141 · see citing works
Yassour, M., Pfiffner, J., Levin, J. Z., Adiconis, X., Gnirke, A., Nusbaum, C., Thompson, D. A., Friedman, N., & Regev, A. (2010) · Genome biology · doi:10.1186/gb-2010-11-8-r87 · Cited by 136 · see citing works
Self-citationCasola, C., Hucks, D., & Feschotte, C. (2007) · Molecular Biology and Evolution · doi:10.1093/molbev/msm221 · Cited by 129 · see citing works
TER1, the RNA subunit of fission yeast telomerase
Leonardi, J., Box, J. A., Bunch, J. T., & Baumann, P. (2007) · Nature Structural & Molecular Biology · doi:10.1038/nsmb1343 · Cited by 123 · see citing works
Self-citationFishel, B. R., Amstutz, H., Baum, M. P., Carbon, J. A., & Clarke, L. (1988) · Molecular and Cellular Biology · doi:10.1128/mcb.8.2.754-763.1988 · Cited by 112 · see citing works
Evolutionary dynamics of transposable elements at the centromere
Wong, L. H., & Choo, K. H. A. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.09.011 · Cited by 111 · see citing works
RNase-sensitive DNA modification(s) initiates S. pombe mating-type switchingPreprint
Vengrova, S., & Dalgaard, J. Z. (2004) · Genes & Development · doi:10.1101/gad.289404 · Cited by 104 · see citing works
Self-citationDynamic transcriptome of Schizosaccharomyces pombe shown by RNA-DNA hybrid mapping
Dutrow, N., Nix, D. A., Holt, D. G., Milash, B. A., Dalley, B. K., Westbroek, E. M., Parnell, T. J., & Cairns, B. R. (2008) · Nature Genetics · doi:10.1038/ng.196 · Cited by 103 · see citing works
Arcangioli, B., & Klar, A. J. S. (1991) · The EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07853.x · Cited by 101 · see citing works
Carbohydrate and energy-yielding metabolism in non-conventional yeasts
Flores, C. (2000) · FEMS Microbiology Reviews · doi:10.1016/s0168-6445(00)00037-1 · Cited by 100 · see citing works
Centromeres of the fission yeast Schizosaccharomyces pombe are highly variable genetic loci.
Steiner, N. C., Hahnenberger, K. M., & Clarke, L. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.8.4578 · Cited by 96 · see citing works
Käufer, N. F. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.16.3003 · Cited by 96 · see citing works
Abe, H., & Shimoda, C. (2000) · Genetics · doi:10.1093/genetics/154.4.1497 · Cited by 96 · see citing works
CENP-B preserves genome integrity at replication forks paused by retrotransposon LTR
Zaratiegui, M., Vaughn, M. W., Irvine, D. V., Goto, D. B., Watt, S. B., Bähler, J., Arcangioli, B., & Martienssen, R. A. (2010) · Nature · doi:10.1038/nature09608 · Cited by 93 · see citing works
Self-citationForsburg, S. L. (1999) · Trends in Genetics · doi:10.1016/s0168-9525(99)01798-9 · Cited by 89 · see citing works
Organization of DNA replication origins in the fission yeast genome
Gómez, M., & Antequera, F. (1999) · The EMBO Journal · doi:10.1093/emboj/18.20.5683 · Cited by 87 · see citing works
Promoter-driven splicing regulation in fission yeast
Moldón, A., Malapeira, J., Gabrielli, N., Gogol, M., Gómez‐Escoda, B., Ivanova, T., Seidel, C. W., & Ayté, J. (2008) · Nature · doi:10.1038/nature07325 · Cited by 80 · see citing works
Uo, T., Yoshimura, T., Tanaka, N., Takegawa, K., & Esaki, N. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.7.2226-2233.2001 · Cited by 69 · see citing works
The Prevalence and Regulation of Antisense Transcripts in Schizosaccharomyces pombe
Ni, T., Tu, K., Wang, Z., Song, S., Wu, H., Xie, B., Scott, K. C., Grewal, S., Gao, Y., & Zhu, J. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015271 · Cited by 62 · see citing works
Matsuzawa, T., Ohashi, T., Hosomi, A., Tanaka, N., Tohda, H., & Takegawa, K. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-2586-3 · Cited by 60 · see citing works
Negative Control Contributes to an Extensive Program of Meiotic Splicing in Fission Yeast
Averbeck, N., Sunder, S., Sample, N., Wise, J. A., & Leatherwood, J. (2005) · Molecular Cell · doi:10.1016/j.molcel.2005.04.007 · Cited by 55 · see citing works
Self-citationThe pedigree pattern of mating-type switching in Schizosaccharomyces pombe
Egel, R. (1984) · Current Genetics · doi:10.1007/bf00417817 · Cited by 43 · see citing works
Singh, G., & Klar, A. J. S. (2002) · Genetics · doi:10.1093/genetics/162.2.591 · Cited by 29 · see citing works
Identification of a Novel Type of Spacer Element Required for Imprinting in Fission Yeast
Sayrac, S., Vengrova, S., Godfrey, E. L., & Dalgaard, J. Z. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001328 · Cited by 26 · see citing works
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Full-length transcriptome assembly from RNA-Seq data without a reference genome
Grabherr, M. G., Haas, B. J., Yassour, M., Levin, J. Z., Thompson, D. A., Amit, I., Adiconis, X., Fan, L., Raychowdhury, R., Zeng, Q., et al. (2011) · Nature Biotechnology · doi:10.1038/nbt.1883 · Cited by 20,770 · see citing works
Self-citationHaas, B. J., Papanicolaou, A., Yassour, M., Grabherr, M., Blood, P. D., Bowden, J., Couger, M. B., Eccles, D., Li, B., Lieber, M., et al. (2013) · Nature Protocols · doi:10.1038/nprot.2013.084 · Cited by 8,464 · see citing works
Self-citationDe novo assembly of bacterial transcriptomes from RNA-seq data
Tjaden, B. C. (2015) · Genome biology · doi:10.1186/s13059-014-0572-2 · Cited by 1,695 · see citing works
PhyloCSF: a comparative genomics method to distinguish protein coding and non-coding regionsPreprint
Lin, M. F., Jungreis, I., & Kellis, M. (2010) · Nature Precedings · doi:10.1093/bioinformatics/btr209 · Cited by 1,008 · see citing works
Self-citationMarguerat, S., Schmidt, A., Codlin, S., Chen, W., Aebersold, R., & Bähler, J. (2012) · Cell · doi:10.1016/j.cell.2012.09.019 · Cited by 571 · see citing works
Gene regulation by antisense transcription
Pelechano, V., & Steinmetz, L. M. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3594 · Cited by 636 · see citing works
Optimizing de novo transcriptome assembly from short-read RNA-Seq data: a comparative study
Zhao, Q.-Y., Wang, Y., Kong, Y.-M., Luo, D., Li, X., & Hao, P. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-s14-s2 · Cited by 479 · see citing works
Schep, A. N., Buenrostro, J. D., Denny, S. K., Schwartz, K., Sherlock, G., & Greenleaf, W. J. (2015) · Genome Research · doi:10.1101/gr.192294.115 · Cited by 375 · see citing works
Fungal evolution: diversity, taxonomy and phylogeny of the Fungi
Naranjo-Ortíz, M. A., & Gabaldón, T. (2019) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12550 · Cited by 401 · see citing works
Janbon, G., Ormerod, K. L., Paulet, D., Byrnes, E. J., Yadav, V., Chatterjee, G., Mullapudi, N., Hon, C.-C., Billmyre, R. B., Brunel, F., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004261 · Cited by 369 · see citing works
Self-citationProduction of recombinant proteins by yeast cells
Çelik, E., & Çalı́k, P. (2011) · Biotechnology Advances · doi:10.1016/j.biotechadv.2011.09.011 · Cited by 338 · see citing works
Ranzani, V., Rossetti, G., Panzeri, I., Arrigoni, A., Bonnal, R. J. P., Curti, S., Gruarin, P., Provasi, E., Sugliano, E., Marconi, M., et al. (2015) · Nature Immunology · doi:10.1038/ni.3093 · Cited by 332 · see citing works
Combining RNA-seq data and homology-based gene prediction for plants, animals and fungi
Keilwagen, J., Hartung, F., Paulini, M., Twardziok, S. O., & Grau, J. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2203-5 · Cited by 336 · see citing works
PomBase: a comprehensive online resource for fission yeast
Wood, V., Harris, M. A., McDowall, M. D., Rutherford, K., Vaughan, B. W., Staines, D. M., Aslett, M., Lock, A., Bahler, J., Kersey, P. J., et al. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr853 · Cited by 321 · see citing works
Why, when, and how did yeast evolve alcoholic fermentation?
Dashko, S., Zhou, N., Compagno, C., & Piškur, J. (2014) · FEMS Yeast Research · doi:10.1111/1567-1364.12161 · Cited by 313 · see citing works
Fairclough, S. R., Chen, Z., Kramer, E., Zeng, Q., Young, S., Robertson, H. M., Begović, E., Richter, D. J., Russ, C., Westbrook, M. J., et al. (2013) · Genome biology · doi:10.1186/gb-2013-14-2-r15 · Cited by 279 · see citing works
Self-citationRNAi and Heterochromatin AssemblyPreprint
Martienssen, R. A., & Moazed, D. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a019323 · Cited by 281 · see citing works
Self-citationAn Ancient Yeast for Young Geneticists: A Primer on the Schizosaccharomyces pombe Model System
Hoffman, C. S., Wood, V., & Fantes, P. A. (2015) · Genetics · doi:10.1534/genetics.115.181503 · Cited by 238 · see citing works
Testa, A. C., Hane, J. K., Ellwood, S. R., & Oliver, R. P. (2015) · BMC Genomics · doi:10.1186/s12864-015-1344-4 · Cited by 230 · see citing works
Russell, J. J., Theriot, J. A., Sood, P., Marshall, W. F., Landweber, L. F., Fritz‐Laylin, L. K., Polka, J., Oliferenko, S., Gerbich, T. M., Gladfelter, A. S., et al. (2017) · BMC Biology · doi:10.1186/s12915-017-0391-5 · Cited by 224 · see citing works
Martinez, D. A., Oliver, B. G. G., Gräser, Y., Goldberg, J. M., Li, W., Martinez-Rossi, N. M., Monod, M., Shelest, E., Barton, R., Birch, E., et al. (2012) · mBio · doi:10.1128/mbio.00259-12 · Cited by 227 · see citing works
Self-citationSurveillance of Nuclear Pore Complex Assembly by ESCRT-III/Vps4
Webster, B. M., Colombi, P., Jäger, J., & Lusk, C. P. (2014) · Cell · doi:10.1016/j.cell.2014.09.012 · Cited by 219 · see citing works
Hagman, A., Säll, T., Compagno, C., & Piskur, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068734 · Cited by 219 · see citing works
Carpinelli, E. C., Telatin, A., Vitulo, N., Forcato, C., D’Angelo, M., Schiavon, R., Vezzi, A., Giacometti, G. M., Morosinotto, T., & Valle, G. (2013) · Molecular Plant · doi:10.1093/mp/sst120 · Cited by 213 · see citing works
Ma, L., Chen, Z., Huang, D. W., Kutty, G., Ishihara, M., Wang, H., Abouelleil, A., Bishop, L. R., Davey, E., Deng, R., et al. (2016) · Nature Communications · doi:10.1038/ncomms10740 · Cited by 191 · see citing works
Self-citationJiang, R. H. Y., de Bruijn, I., Haas, B. J., Belmonte, R. C., Löbach, L., Christie, J. S., den Ackerveken, G. F. J. M. V., Bottin, A., Bulone, V., Díaz-Moreno, S. M., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003272 · Cited by 189 · see citing works
Self-citationLee, N. N., Chalamcharla, V. R., Reyes‐Turcu, F. E., Mehta, S. S., Zofall, M., Balachandran, V., Dhakshnamoorthy, J., Taneja, N., Yamanaka, S., Zhou, M., et al. (2013) · Cell · doi:10.1016/j.cell.2013.10.027 · Cited by 185 · see citing works
Evolutionary Role of Interspecies Hybridization and Genetic Exchanges in Yeasts
Morales, L., & Dujon, B. (2012) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00022-12 · Cited by 178 · see citing works
Epigenetic Regulation of Chromatin States inSchizosaccharomyces pombePreprint
Allshire, R. C., & Ekwall, K. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018770 · Cited by 174 · see citing works
Self-citationGenome Characterization of the Oleaginous Fungus Mortierella alpina
Wang, L., Chen, W., Feng, Y., Ren, Y., Gu, Z., Chen, H., Wang, H., Thomas, M. J., Zhang, B., Berquin, I. M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028319 · Cited by 173 · see citing works
Self-citationSchotanus, K., Soyer, J. L., Connolly, L., Grandaubert, J., Happel, P., Smith, K., Freitag, M., & Stukenbrock, E. H. (2015) · Epigenetics & Chromatin · doi:10.1186/s13072-015-0033-5 · Cited by 173 · see citing works
Functional Repurposing Revealed by Comparing S. pombe and S. cerevisiae Genetic Interactions
Frost, A. S., Elgort, M., Brandman, O., Ives, C., Collins, S. R., Miller-Vedam, L. E., Weibezahn, J., Hein, M. Y., Poser, I., Mann, M., et al. (2012) · Cell · doi:10.1016/j.cell.2012.04.028 · Cited by 161 · see citing works
Sandargo, B., Chepkirui, C., Cheng, T., Chaverra-Muñoz, L., Thongbai, B., Stadler, M., & Hüttel, S. (2019) · Biotechnology Advances · doi:10.1016/j.biotechadv.2019.01.011 · Cited by 151 · see citing works
Origin of Spliceosomal Introns and Alternative SplicingPreprint
Irimia, M., & Roy, S. W. (2014) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a016071 · Cited by 148 · see citing works
Self-citationRNAi triggered by specialized machinery silences developmental genes and retrotransposons
Yamanaka, S., Mehta, S. S., Reyes‐Turcu, F. E., Zhuang, F., Fuchs, R. T., Rong, Y. S., Robb, G. B., & Grewal, S. I. S. (2012) · Nature · doi:10.1038/nature11716 · Cited by 148 · see citing works
Approaches to Fungal Genome Annotation
Haas, B. J., Zeng, Q., Pearson, M. D., Cuomo, C. A., & Wortman, J. R. (2011) · Mycology: An International Journal on Fungal Biology · doi:10.1080/21501203.2011.606851 · Cited by 142 · see citing works
Self-citationPrevalence of transcription factors in ascomycete and basidiomycete fungi
Todd, R. B., Zhou, M., Ohm, R. A., Leeggangers, H. A. C. F., Visser, L., & de Vries, R. P. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-214 · Cited by 134 · see citing works
Hutchins, E. D., Markov, G. J., Eckalbar, W. L., George, R. M., King, J. M., Tokuyama, M. A., Geiger, L. A., Emmert, N., Ammar, M. J., Allen, A. N., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105004 · Cited by 139 · see citing works
Grützmann, K., Szafranski, K., Pohl, M., Voigt, K., Petzold, A., & Schuster, S. (2013) · DNA Research · doi:10.1093/dnares/dst038 · Cited by 139 · see citing works
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Dujon, B., & Louis, E. J. (2017) · Genetics · doi:10.1534/genetics.116.199216 · Cited by 127 · see citing works
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Cheng, B., Furtado, A., & Henry, R. J. (2017) · GigaScience · doi:10.1093/gigascience/gix086 · Cited by 116 · see citing works
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Iglesias, N., Paulo, J. A., Tatarakis, A., Wang, X., Edwards, A., Bhanu, N. V., Garcia, B. A., Haas, W., Gygi, S. P., & Moazed, D. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.10.018 · Cited by 107 · see citing works
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Malina, C., Yu, R., Björkeroth, J., Kerkhoven, E. J., & Nielsen, J. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2112836118 · Cited by 106 · see citing works
Genome Sequencing of the Plant Pathogen Taphrina deformans , the Causal Agent of Peach Leaf Curl
Cissé, O. H., Almeida, J. M. G. C. F., Fonseca, Á., Kumar, A. A., Salojärvi, J., Overmyer, K., Hauser, P. M., & Pagni, M. (2013) · mBio · doi:10.1128/mbio.00055-13 · Cited by 102 · see citing works
Genome-wide identification and characterization of replication origins by deep sequencing
Xu, J. L., Yanagisawa, Y., Tsankov, A. M., Hart, C. E., Aoki, K., Kommajosyula, N., Steinmann, K. E., Bochicchio, J., Russ, C., Regev, A., et al. (2012) · Genome biology · doi:10.1186/gb-2012-13-4-r27 · Cited by 100 · see citing works
Self-citationFowler, K. R., Sasaki, M., Milman, N., Keeney, S., & Smith, G. R. (2014) · Genome Research · doi:10.1101/gr.172122.114 · Cited by 99 · see citing works
Ard, R., Tong, P., & Allshire, R. C. (2014) · Nature Communications · doi:10.1038/ncomms6576 · Cited by 98 · see citing works
Self-citationPomBase 2015: updates to the fission yeast database
McDowall, M. D., Harris, M. A., Lock, A., Rutherford, K., Staines, D. M., Bähler, J., Kersey, P. J., Oliver, S. G., & Wood, V. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1040 · Cited by 95 · see citing works
Determinants of RNA metabolism in the Schizosaccharomyces pombe genome
Eser, P., Wachutka, L., Maier, K. C., Demel, C., Boroni, M., Iyer, S., Cramer, P., & Gagneur, J. (2016) · Molecular Systems Biology · doi:10.15252/msb.20156526 · Cited by 81 · see citing works
Transposon integration enhances expression of stress response genes
Feng, G., Leem, Y.-E., & Levin, H. L. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1185 · Cited by 86 · see citing works
Self-citationTel1ATM and Rad3ATR kinases promote Ccq1-Est1 interaction to maintain telomeres in fission yeast
Moser, B. A., Chang, Y.-T., Kosti, J., & Nakamura, T. (2011) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2187 · Cited by 83 · see citing works
The structure, function, and evolution of plant centromeresPreprint
Naish, M., & Henderson, I. R. (2024) · Genome Research · doi:10.1101/gr.278409.123 · Cited by 86 · see citing works
Genome architecture is a selectable trait that can be maintained by antagonistic pleiotropy
Avelar, A. T., Perfeito, L., Gordo, I., & Ferreira, M. G. (2013) · Nature Communications · doi:10.1038/ncomms3235 · Cited by 83 · see citing works
Sakai, H., Naito, K., Ogiso‐Tanaka, E., Takahashi, Y., Iseki, K., Muto, C., Satou, K., Teruya, K., Shiroma, A., Shimoji, M., et al. (2015) · Scientific Reports · doi:10.1038/srep16780 · Cited by 83 · see citing works
Alings, F., Sarin, L. P., Fufezan, C., Drexler, H. C. A., & Leidel, S. A. (2014) · RNA · doi:10.1261/rna.048199.114 · Cited by 82 · see citing works
Reyes‐Turcu, F. E., & Grewal, S. I. S. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2011.12.004 · Cited by 81 · see citing works
Evolutionary principles of modular gene regulation in yeasts
Thompson, D. A., Roy, S., Chan, M., Styczynsky, M. P., Pfiffner, J., French, C., Socha, A., Thielke, A., Napolitano, S., Muller, P., et al. (2013) · eLife · doi:10.7554/elife.00603 · Cited by 78 · see citing works
Epigenetic mechanisms of drug resistance in fungi
Chang, Z., Yadav, V., Lee, S. C., & Heitman, J. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103253 · Cited by 81 · see citing works
Guida, A., Lindstädt, C., Maguire, S. L., Ding, C., Higgins, D. G., Corton, N. J., Berriman, M., & Butler, G. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-628 · Cited by 78 · see citing works
Thakur, J., & Sanyal, K. (2013) · Genome Research · doi:10.1101/gr.141614.112 · Cited by 78 · see citing works
The translational landscape of fission-yeast meiosis and sporulation
Duncan, C. D. S., & Mata, J. (2014) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2843 · Cited by 75 · see citing works
Brown, W. R., Liti, G., Rosa, C. A., James, S. A., Roberts, I. N., Robert, V., Jolly, N. P., Tang, W., Baumann, P., Green, C., et al. (2011) · G3 Genes Genomes Genetics · doi:10.1534/g3.111.001123 · Cited by 77 · see citing works
Self-citationFrancis, O., Han, F., & Adams, J. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075217 · Cited by 76 · see citing works
ESCRT-III/Vps4 Controls Heterochromatin-Nuclear Envelope Attachments
Pieper, G. H., Sprenger, S., Teis, D., & Oliferenko, S. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.01.028 · Cited by 75 · see citing works
Structural features of DNA that determine RNA polymerase II core promoter
Il’icheva, I. A., Khodikov, M. V., Poptsova, M. S., Nechipurenko, D. Y., Nechipurenko, Y. D., & Grokhovsky, S. L. (2016) · BMC Genomics · doi:10.1186/s12864-016-3292-z · Cited by 73 · see citing works
Phylogenomic evolutionary surveys of subtilase superfamily genes in fungi
Li, J., Gu, F., Wu, R., Yang, J., & Zhang, K. (2017) · Scientific Reports · doi:10.1038/srep45456 · Cited by 75 · see citing works
Awan, A. R., Manfredo, A., & Pleiss, J. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218353110 · Cited by 72 · see citing works
Sabouri, N., Capra, J. A., & Zakian, V. A. (2014) · BMC Biology · doi:10.1186/s12915-014-0101-5 · Cited by 72 · see citing works
Alternative Splicing and Subfunctionalization Generates Functional Diversity in Fungal Proteomes
Marshall, A. N., Montealegre, M. C., Jiménez-López, C., Lorenz, M. C., & van Hoof, A. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003376 · Cited by 71 · see citing works
Introduction to Fission Yeast as a Model SystemPreprint
Hayles, J., & Nurse, P. (2017) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top079749 · Cited by 67 · see citing works
Conserved rules govern genetic interaction degree across species
Koch, E. N., Costanzo, M., Bellay, J., Deshpande, R., Chatfield-Reed, K., Chua, G., D'Urso, G., Andrews, B. J., Boone, C., & Myers, C. L. (2012) · Genome Biology · doi:10.1186/gb-2012-13-7-r57 · Cited by 68 · see citing works
Functional and regulatory profiling of energy metabolism in fission yeast
Małecki, M., Bitton, D. A., Rodríguez‐López, M., Rallis, C., Calavia, N. G., Smith, G. C., & Bähler, J. (2016) · Genome biology · doi:10.1186/s13059-016-1101-2 · Cited by 60 · see citing works
Natural antisense transcripts in fungi
Donaldson, M. E., & Saville, B. J. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08125.x · Cited by 67 · see citing works
Fungal aquaporins: cellular functions and ecophysiological perspectives
Nehls, U., & Dietz, S. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6049-0 · Cited by 67 · see citing works
An Ancient Family of RNA-Binding Proteins: Still Important!
Wells, M. L., Perera, L., & Blackshear, P. J. (2017) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.12.003 · Cited by 67 · see citing works
LaSSO, a strategy for genome-wide mapping of intronic lariats and branch points using RNA-seqPreprint
Bitton, D. A., Rallis, C., Jeffares, D. C., Smith, G. C., Chen, Y. Y. C., Codlin, S., Marguerat, S., & Bähler, J. (2014) · Genome Research · doi:10.1101/gr.166819.113 · Cited by 67 · see citing works
Eckalbar, W. L., Hutchins, E. D., Markov, G. J., Allen, A. N., Corneveaux, J. J., Lindblad‐Toh, K., Palma, F. D., Alföldi, J., Huentelman, M. J., & Kusumi, K. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-49 · Cited by 66 · see citing works
Determinants of Heterochromatic siRNA Biogenesis and Function
Yu, R., Jih, G. T., Iglesias, N., & Moazed, D. (2014) · Molecular Cell · doi:10.1016/j.molcel.2013.11.014 · Cited by 65 · see citing works
Takemata, N., & Ohta, K. (2016) · RNA Biology · doi:10.1080/15476286.2016.1248020 · Cited by 64 · see citing works
Atkinson, S. R., Marguerat, S., Bitton, D. A., Rodríguez‐López, M., Rallis, C., Lemay, J., Cotobal, C., Małecki, M., Smialowski, P., Mata, J., et al. (2018) · RNA · doi:10.1261/rna.065524.118 · Cited by 64 · see citing works
Schwer, B., Bitton, D. A., Sánchez, A. M., Bähler, J., & Shuman, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321842111 · Cited by 62 · see citing works
Saint, M., Bertaux, F., Tang, W., Sun, X.-M., Gamé, L., Köferle, A., Bähler, J., Shahrezaei, V., & Marguerat, S. (2019) · Nature Microbiology · doi:10.1038/s41564-018-0330-4 · Cited by 63 · see citing works
Loss of centromere function drives karyotype evolution in closely related Malassezia species
Sankaranarayanan, S. R., Ianiri, G., Coelho, M. A., Reza, M. H., Thimmappa, B. C., Ganguly, P., Vadnala, R. N., Sun, S., Siddharthan, R., Tellgren‐Roth, C., et al. (2020) · eLife · doi:10.7554/elife.53944 · Cited by 62 · see citing works
Evolutionary Invariant of the Structure of DNA Double Helix in RNAP II Core Promoters
Melikhova, A. V., Anashkina, A. A., & Il’icheva, I. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810873 · Cited by 60 · see citing works
Genetic instability in budding and fission yeast—sources and mechanisms
Skoneczna, A., Kaniak, A., & Skoneczny, M. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv028 · Cited by 57 · see citing works
Fungal genome sequencing: basic biology to biotechnology
Sharma, K. K. (2015) · Critical Reviews in Biotechnology · doi:10.3109/07388551.2015.1015959 · Cited by 59 · see citing works
Cissé, O. H., Pagni, M., & Hauser, P. M. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu155 · Cited by 60 · see citing works
Heinrich, S., Sewart, K., Windecker, H., Langegger, M., Schmidt, N., Hustedt, N., & Hauf, S. (2014) · EMBO Reports · doi:10.1002/embr.201338114 · Cited by 57 · see citing works
Seppälä, S., Wilken, S. E., Knop, D., Solomon, K., & O'Malley, M. A. (2017) · Metabolic Engineering · doi:10.1016/j.ymben.2017.09.008 · Cited by 57 · see citing works
RNAi keeps Atf1-bound stress response genes in check at nuclear poresPreprint
Woolcock, K., Stunnenberg, R., Gaidatzis, D., Hotz, H.-R., Emmerth, S., Barraud, P., & Bühler, M. (2012) · Genes & Development · doi:10.1101/gad.186866.112 · Cited by 57 · see citing works
Killer Meiotic Drive and Dynamic Evolution of the wtf Gene Family
Eickbush, M. T., Young, J. M., & Zanders, S. E. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz052 · Cited by 56 · see citing works
Roy, S., Wapinski, I. N., Pfiffner, J., French, C. E., Socha, A. L., Konieczka, J. H., Habib, N., Kellis, M., Thompson, D. A., & Regev, A. (2013) · Genome Research · doi:10.1101/gr.146233.112 · Cited by 55 · see citing works
Self-citationComparative analysis of alternative polyadenylation in S. cerevisiae and S. pombePreprint
Liu, X., Hoque, M., Larochelle, M., Lemay, J., Yurko, N., Manley, J., Bachand, F., & Tian, B. (2017) · Genome Research · doi:10.1101/gr.222331.117 · Cited by 56 · see citing works
- Authors
- Rhind, N., Chen, Z., Yassour, M., Thompson, D. A., Haas, B. J., Habib, N., Wapinski, I., Roy, S., Lin, M. F., Heiman, D. I., Young, S. K., Furuya, K., Guo, Y., Pidoux, A., Chen, H. M., Robbertse, B., Goldberg, J. M., Aoki, K., Bayne, E. H., Berlin, A. M., Desjardins, C. A., Dobbs, E., Dukaj, L., Fan, L., FitzGerald, M. G., French, C., Gujja, S., Hansen, K., Keifenheim, D., Levin, J. Z., Mosher, R. A., Müller, C. A., Pfiffner, J., Priest, M., Russ, C., Smialowska, A., Swoboda, P., Sykes, S. M., Vaughn, M., Vengrova, S., Yoder, R., Zeng, Q., Allshire, R., Baulcombe, D., Birren, B. W., Brown, W., Ekwall, K., Kellis, M., Leatherwood, J., Levin, H., Margalit, H., Martienssen, R., Nieduszynski, C. A., Spatafora, J. W., Friedman, N., Dalgaard, J. Z., Baumann, P., Niki, H., Regev, A., & Nusbaum, C.
- Affiliations
- Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, 364 Plantation Street, Worcester, MA 01605, USA.
- Broad Institute (US)
- Hebrew University of Jerusalem (IL)
- MIT Computer Science and Artificial Intelligence Laboratory (US)
- National Institute of Genetics (JP)
- National Institutes of Health (US)
- Wellcome Centre for Cell Biology (GB)
- Stony Brook University (US)
- Oregon State University (US)
- University of Massachusetts Chan Medical School (US)
- Cold Spring Harbor Laboratory (US)
- University of Cambridge (GB)
- University of Nottingham (GB)
- Södertörn University (SE)
- Karolinska Institutet (SE)
- University of Warwick (GB)
- Cold Spring Harbor Laboratory, 1 Bungtown Road, Cold Spring Harbor, NY 11724, USA.
- Stowers Institute for Medical Research (US)
- Corresponding author
- Yassour, Moran
- Thompson, Dawn A.
- Haas, Brian J.
- Habib, Naomi
- Wapinski, Ilan
- Roy, Sushmita
- Regev, Aviv
- Nusbaum, Chad
- ORCID
- Chen, Zehua
- Yassour, Moran
- Thompson, Dawn A.
- Haas, Brian J.
- Habib, Naomi
- Roy, Sushmita
- Lin, Michael F.
- Heiman, David I.
- Young, Sarah K.
- Furuya, Kanji
- Guo, Yabin
- Pidoux, Alison
- Robbertse, Barbara
- Goldberg, Jonathan M.
- Aoki, Keita
- Bayne, Elizabeth H.
- Desjardins, Christopher A.
- Dukaj, Livio
- FitzGerald, Michael G.
- French, Courtney
- Hansen, Klavs
- Levin, Joshua Z.
- Mosher, Rebecca A.
- Müller, Carolin A.
- Swoboda, Peter
- Vaughn, Matthew
- Zeng, Qiandong
- Allshire, Robin
- Baulcombe, David
- Birren, Bruce W.
- Brown, William
- Ekwall, Karl
- Kellis, Manolis
- Levin, Henry
- Margalit, Hanah
- Nieduszynski, Conrad A.
- Spatafora, Joseph W.
- Friedman, Nir
- Dalgaard, Jacob Z.
- Baumann, Peter
- Niki, Hironori
- Regev, Aviv
- Nusbaum, Chad
- Venue
- Science
- Published
- 2011-05-20
- Volume
- 332
- Issue
- 6032
- Pages
- 930-936
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3131103
- OpenAlex
- W2130412392
- Cited by
- 484
- References
- 44
- Citations by year
- 2026: 16 · 2025: 23 · 2024: 11 · 2023: 30 · 2022: 21 · 2021: 32 · 2020: 21 · 2019: 27 · 2018: 29 · 2017: 43 · 2016: 31 · 2015: 46 · 2014: 48 · 2013: 47 · 2012: 37
- FWCI
- 19.74
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Edinburgh Research Explorer (University of Edinburgh) (submittedVersion, other-oa)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- UEA Digital Repository (University of East Anglia) (submittedVersion)
- PMC
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (DP1OD003958)
- Biotechnology and Biological Sciences Research Council (BB/E023754/1)
- Japan Society for the Promotion of Science (22770178)
- National Human Genome Research Institute (U54HG003067, R01HG004037)
- National Institute of General Medical Sciences (R01GM069957, R01GM076396)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
- Keywords
- Schizosaccharomyces pombe, Schizosaccharomyces octosporus, Schizosaccharomyces japonicus, comparative genomics, antisense transcription, meiotic genes, trans-acting regulators, gene expression regulation, stress response, ethanol carbon source, Ascomycota
- MeSH terms
- Centromere, DNA Transposable Elements, Glucose, Meiosis, Molecular Sequence Data, Phylogeny, RNA, Fungal, Schizosaccharomyces, Species Specificity, Transcription Factors, Transcription, Genetic, Gene Expression Regulation, Fungal, RNA, Antisense, Genome, Fungal, Sequence Analysis, DNA, Evolution, Molecular, Gene Expression Profiling, RNA, Untranslated, Genomics, Schizosaccharomyces pombe Proteins, RNA, Small Interfering, Genes, Mating Type, Fungal, Regulatory Elements, Transcriptional, Molecular Sequence Annotation
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