Comparative Functional Genomics of the Fission Yeasts

Exploring the metabolic and genetic control of gene expression on a genomic scale.

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Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi

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Sequencing and comparison of yeast species to identify genes and regulatory elements

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The genome sequence of Schizosaccharomyces pombe

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Dynamic repertoire of a eukaryotic transcriptome surveyed at single-nucleotide resolution

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Bidirectional promoters generate pervasive transcription in yeast

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Comprehensive comparative analysis of strand-specific RNA sequencing methods

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Natural history and evolutionary principles of gene duplication in fungi

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How did Saccharomyces evolve to become a good brewer?

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The transcriptional program of meiosis and sporulation in fission yeast

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Centromere deletion in Cryptococcus deuterogattii leads to neocentromere formation and chromosome fusions

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Essential function of Aco2, a fusion protein of aconitase and mitochondrial ribosomal protein bL21, in mitochondrial translation in fission yeast

Jung, S. J., Seo, Y., Lee, K.-C., Lee, D., & Roe, J. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.02.015 · Cited by 26

Posttranscriptional Regulation of Cell-Cell Interaction Protein-Encoding Transcripts by Zfs1p in Schizosaccharomyces pombe

Wells, M. L., Huang, W., Li, L., Gerrish, K. E., Fargo, D. C., Ozsolak, F., & Blackshear, P. J. (2012) · Molecular and Cellular Biology · doi:10.1128/mcb.00325-12 · Cited by 24

Evolution of Telomeres in Schizosaccharomyces pombe and Its Possible Relationship to the Diversification of Telomere Binding Proteins

Sepšiová, R., Nečasová, I., Willcox, S., Procházková, K., Gorilák, P., Nosek, J., Hofr, C., Griffith, J. D., & Tomáška, Ľ. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154225 · Cited by 25

Schizosaccharomyces japonicus Yeast Poised to Become a Favorite Experimental Organism for Eukaryotic Research

Klar, A. J. S. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.007187 · Cited by 25

Fission yeast: in shape to divide

Hachet, O., Bendezú, F. O., & Martin, S. G. (2012) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2012.10.001 · Cited by 25

The Ras1-Cdc42 pathway is involved in hyphal development of Schizosaccharomyces japonicus

Nozaki, S., Furuya, K., & Niki, H. (2018) · FEMS Yeast Research · doi:10.1093/femsyr/foy031 · Cited by 22

Nucleosomal signatures impose nucleosome positioning in coding and noncoding sequences in the genomePreprint

González, S., García, A., Vázquez, E., Serrano, R., Sánchez, M., Quintales, L. A. M., & Antequera, F. (2016) · Genome Research · doi:10.1101/gr.207241.116 · Cited by 25

Centrochromatin of Fungi

Friedman, S., & Freitag, M. (2017) · Progress in molecular and subcellular biology · doi:10.1007/978-3-319-58592-5_4 · Cited by 24

Optimization of energy production and central carbon metabolism in a non-respiring eukaryote

Alam, S., Gu, Y., Reichert, P., Bähler, J., & Oliferenko, S. (2023) · Current Biology · doi:10.1016/j.cub.2023.04.046 · Cited by 24

Divergence of mitotic strategies in fission yeasts

Gu, Y., Yam, C., & Oliferenko, S. (2012) · Nucleus · doi:10.4161/nucl.19514 · Cited by 24

Prevalent and distinct spliceosomal 3′-end processing mechanisms for fungal telomerase RNA

Qi, X., Rand, D. P., Podlevsky, J. D., Li, Y., Mosig, A., Stadler, P. F., & Chen, J. J. ‐. (2015) · Nature Communications · doi:10.1038/ncomms7105 · Cited by 22

A Matter of Scale and Dimensions: Chromatin of Chromosome Landmarks in the Fungi

Erlendson, A. A., Friedman, S., & Freitag, M. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0054-2017 · Cited by 26

Diverse transposable element landscapes in pathogenic and nonpathogenic yeast models: the value of a comparative perspective

Maxwell, P. H. (2020) · Mobile DNA · doi:10.1186/s13100-020-00215-x · Cited by 23

H2A.Z marks antisense promoters and has positive effects on antisense transcript levels in budding yeast

Gu, M., Naiyachit, Y., Wood, T., & Millar, C. B. (2015) · BMC Genomics · doi:10.1186/s12864-015-1247-4 · Cited by 26

Heterogeneous rates of genome rearrangement contributed to the disparity of species richness in Ascomycota

Rajeh, A. A., Lv, J., & Lin, Z. (2018) · BMC Genomics · doi:10.1186/s12864-018-4683-0 · Cited by 23

Unexpected insertion of carrier DNA sequences into the fission yeast genome during CRISPR–Cas9 mediated gene deletion

Longmuir, S., Akhtar, N., & MacNeill, S. A. (2019) · BMC Research Notes · doi:10.1186/s13104-019-4228-x · Cited by 22

Patterns of Conservation and Diversification in the Fungal Polarization Network

Diepeveen, E. T., Gehrmann, T., Pourquié, V., Abeel, T., & Laan, L. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy121 · Cited by 22

Functional profiling of long intergenic non-coding RNAs in fission yeast

Rodríguez‐López, M., Anver, S., Cotobal, C., Kamrad, S., Małecki, M., Correia‐Melo, C., Hoti, M., Townsend, S., Marguerat, S., Pong, S. K., et al. (2021) · eLife · doi:10.7554/elife.76000 · Cited by 20

A high-quality reference genome for the fission yeast Schizosaccharomyces osmophilus

Jia, G., Zhang, W. C., Liang, Y., Liu, X.-H., Rhind, N., Pidoux, A. L., Brysch‐Herzberg, M., & Du, L. (2023) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkad028 · Cited by 21

Role of Non-coding RNAs in Fungal Pathogenesis and Antifungal Drug Responses

Dhingra, S. (2020) · Current Clinical Microbiology Reports · doi:10.1007/s40588-020-00151-7 · Cited by 21

The Fission Yeast Mating-Type Switching Motto: “One-for-Two” and “Two-for-One”

Arcangioli, B., & Gangloff, S. (2023) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00008-21 · Cited by 21

The Transcription Factors Atf1 and Pcr1 Are Essential for Transcriptional Induction of the Extracellular Maltase Agl1 in Fission Yeast

Kato, H., Kira, S., & Kawamukai, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080572 · Cited by 21

Identification and Functional Analysis of the erh1+ Gene Encoding Enhancer of Rudimentary Homolog from the Fission Yeast Schizosaccharomyces pombe

Krzyzanowski, M. K., Kozłowska, E., & Kozlowski, P. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049059 · Cited by 21

Asymmetric diversification of mating pheromones in fission yeast

Seike, T., Shimoda, C., & Niki, H. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000101 · Cited by 21

The AP‐2 complex is required for proper temporal and spatial dynamics of endocytic patches in fission yeast

de León, N., Hoya, M., Curto, M.-Á., Moro, S., Yanguas, F., Doncel, C., & Valdivieso, M. ‐. (2016) · Molecular Microbiology · doi:10.1111/mmi.13327 · Cited by 19

Detection of splice isoforms and rare intermediates using multiplexed primer extension sequencing

Xu, H., Fair, B. J., Dwyer, Z. W., Gildea, M. A., & Pleiss, J. A. (2018) · Nature Methods · doi:10.1038/s41592-018-0258-x · Cited by 25

The Long Terminal Repeat Retrotransposons Tf1 and Tf2 of Schizosaccharomyces pombe

Esnault, C., & Levin, H. L. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mdna3-0040-2014 · Cited by 19

Interconnections Between RNA-Processing Pathways Revealed by a Sequencing-Based Genetic Screen for Pre-mRNA Splicing Mutants in Fission Yeast

Larson, A., Fair, B. J., & Pleiss, J. A. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.027508 · Cited by 20

Schizosaccharomyces lindneri sp. nov., a fission yeast occurring in honey

Brysch‐Herzberg, M., Jia, G., Sipiczki, M., Seidel, M., Li, W., Assali, I., & Du, L. (2023) · Yeast · doi:10.1002/yea.3857 · Cited by 19

Long Non-coding RNA

Gullerová, M. (2015) · Springer eBooks · doi:10.1007/978-1-4939-3070-8_4 · Cited by 22

Cross-Regulation between Transposable Elements and Host DNA Replication

Zaratiegui, M. (2017) · Viruses · doi:10.3390/v9030057 · Cited by 19

Genome-wide Identification and Characterization of Natural Antisense Transcripts by Strand-specific RNA Sequencing in Ganoderma lucidum

Shao, J., Chen, H., Yang, D., Jiang, M., Zhang, H., Wu, B., Li, J., Yuan, L., & Liu, C. (2017) · Scientific Reports · doi:10.1038/s41598-017-04303-6 · Cited by 19

Distribution of methionine sulfoxide reductases in fungi and conservation of the free-methionine- R -sulfoxide reductase in multicellular eukaryotes

Hage, H., Rosso, M., & Tarrago, L. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.04.013 · Cited by 19

Functional and Structural Divergence of an Unusual LTR Retrotransposon Family in Plants

Gao, D., Jiménez-López, J. C., Iwata‐Otsubo, A., Gill, N., & Jackson, S. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0048595 · Cited by 18

Elevated Sporulation Efficiency in Fission Yeast Schizosaccharomyces japonicus Strains Isolated from Drosophila

Seike, T., Sakata, N., Matsuda, F., & Furusawa, C. (2021) · Journal of Fungi · doi:10.3390/jof7050350 · Cited by 18

Evolution of eukaryotic centromeres by drive and suppression of selfish genetic elements

Kumon, T., & Lampson, M. A. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.03.026 · Cited by 17

Genetic effects on molecular network states explain complex traits

Weith, M., Großbach, J., Clément‐Ziza, M., Gillet, L. C. J., Rodríguez‐López, M., Marguerat, S., Workman, C. T., Picotti, P., Bähler, J., Aebersold, R. H., et al. (2023) · Molecular Systems Biology · doi:10.15252/msb.202211493 · Cited by 16

A long terminal repeat retrotransposon of Schizosaccharomyces japonicus integrates upstream of RNA pol III transcribed genes

Guo, Y., Singh, P. K., & Levin, H. L. (2015) · Mobile DNA · doi:10.1186/s13100-015-0048-2 · Cited by 19

A conserved regulatory role for antisense RNA in meiotic gene expression in yeast

Chen, H.-M., & Neiman, A. M. (2011) · Current Opinion in Microbiology · doi:10.1016/j.mib.2011.09.010 · Cited by 18

The Schizosaccharomyces pombe AlkB homolog Abh1 exhibits AP lyase activity but no demethylase activity

Korvald, H., Falnes, P. Ø., Laerdahl, J. K., Bjørås, M., & Alseth, I. (2012) · DNA repair · doi:10.1016/j.dnarep.2012.01.014 · Cited by 18

Subnuclear relocalization and silencing of a chromosomal region by an ectopic ribosomal DNA repeat

Jakočiūnas, T., Jordö, M. D., Mebarek, M. A., Bünner, C. M., Verhein-Hansen, J., Oddershede, L. B., & Thon, G. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315581110 · Cited by 18

Genomics and evolution of Pneumocystis species

Cissé, O. H., & Hauser, P. M. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.08.015 · Cited by 19

Heh2/Man1 may be an evolutionarily conserved sensor of NPC assembly state

Borah, S., Thaller, D. J., Hakhverdyan, Z., Rodriguez, E. C., Isenhour, A. W., Rout, M. P., King, M. C., & Lusk, C. P. (2021) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-09-0584 · Cited by 18

DNA Sequences at a Glance

Pinho, A. J., Garcia, S. P., Pratas, D., & Ferreira, P. J. S. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0079922 · Cited by 18

Mating-Type Switching in Budding Yeasts, from Flip/Flop Inversion to Cassette Mechanisms

Wolfe, K. H., & Butler, G. (2022) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00007-21 · Cited by 17

Peroxisomal compartmentalization of amino acid biosynthesis reactions imposes an upper limit on compartment size

Gu, Y., Alam, S., & Oliferenko, S. (2023) · Nature Communications · doi:10.1038/s41467-023-41347-x · Cited by 17

Correlation of LNCR rasiRNAs Expression with Heterochromatin Formation during Development of the Holocentric Insect Spodoptera frugiperda

Stanojčić, S., Gimenez, S., Permal, E., Cousserans, F., Quesneville, H., Fournier, P., & d’Alençon, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024746 · Cited by 16

Remarkably Simple Sequence Requirement of the M-Factor Pheromone ofSchizosaccharomyces pombe

Seike, T., Yamagishi, Y., Iio, H., Nakamura, T., & Shimoda, C. (2012) · Genetics · doi:10.1534/genetics.112.140483 · Cited by 17

Natural antisense transcript of Period2, Per2AS, regulates the amplitude of the mouse circadian clockPreprint

Mosig, R., Castaneda, A. N., Deslauriers, J. C., Frazier, L. P., He, K. L., Maghzian, N., Pokharel, A., Schrier, C. T., Zhu, L., Koike, N., et al. (2021) · Genes & Development · doi:10.1101/gad.343541.120 · Cited by 18

Separable roles for RNAi in regulation of transposable elements and viability in the fission yeast Schizosaccharomyces japonicus

Chapman, E., Taglini, F., & Bayne, E. H. (2022) · PLoS Genetics · doi:10.1371/journal.pgen.1010100 · Cited by 16

Uncoupling of Genomic and Epigenetic Signals in the Maintenance and Inheritance of Heterochromatin Domains in Fission Yeast

Wheeler, B. S., Ruderman, B. T., Willard, H. F., & Scott, K. C. (2011) · Genetics · doi:10.1534/genetics.111.137083 · Cited by 16

Proteome effects of genome-wide single gene perturbations

Öztürk, M., Freiwald, A., Cartano, J., Schmitt, R., Dejung, M., Luck, K., Al‐Sady, B., Braun, S. J., Levin, M., & Butter, F. (2022) · Nature Communications · doi:10.1038/s41467-022-33814-8 · Cited by 16

Tor Signaling Regulates Transcription of Amino Acid Permeases through a GATA Transcription Factor Gaf1 in Fission Yeast

Ma, Y., Ma, N., Liu, Q., Qi, Y., Manabe, R., & Furuyashiki, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144677 · Cited by 16

HIV-1 Natural Antisense Transcription and Its Role in Viral Persistence

Li, R., Sklutuis, R., Groebner, J. L., & Romerio, F. (2021) · Viruses · doi:10.3390/v13050795 · Cited by 16

Schizosaccharomyces japonicus: A Distinct Dimorphic Yeast among the Fission YeastsPreprint

Aoki, K., Furuya, K., & Niki, H. (2017) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top082651 · Cited by 16

Specification of DNA Replication Origins and Genomic Base Composition in Fission Yeasts

Mojardín, L., Vázquez, E., & Antequera, F. (2013) · Journal of Molecular Biology · doi:10.1016/j.jmb.2013.09.023 · Cited by 15

Kinetochore assembly and heterochromatin formation occur autonomously in Schizosaccharomyces pombe

Brown, W. R., Thomas, G., Lee, N., Blythe, M., Liti, G., Warringer, J., & Loose, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1216934111 · Cited by 15

Hybrid sterility of the yeast Schizosaccharomyces pombe: Genetic genus and many species in statu nascendi?

Naumov, G. I., Kondratieva, V. I., & Naumova, E. S. (2015) · Microbiology · doi:10.1134/s0026261715010099 · Cited by 15

Fitness Landscape of the Fission Yeast Genome

Grech, L., Jeffares, D. C., Sadée, C., Rodríguez‐López, M., Bitton, D. A., Hoti, M., Biagosch, C., Aravani, D., Speekenbrink, M., Illingworth, C. J. R., et al. (2019) · Molecular Biology and Evolution · doi:10.1093/molbev/msz113 · Cited by 14

Diverse mating phenotypes impact the spread of wtf meiotic drivers in Schizosaccharomyces pombe

Hernández, J. F. L., Helston, R. M., Lange, J. J., Billmyre, R. B., Schaffner, S. H., Eickbush, M. T., McCroskey, S., & Zanders, S. E. (2021) · eLife · doi:10.7554/elife.70812 · Cited by 15

Increase in cellular triacylglycerol content and emergence of large ER-associated lipid droplets in the absence of CDP-DG synthase function

He, Y., Yam, C., Pomraning, K., Chin, J. S. R., Yew, J. Y., Freitag, M., & Oliferenko, S. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-03-0832 · Cited by 15

RetroGREAT signaling: The lessons we learn from yeast

Bui, T. H. D., & Labedzka‐Dmoch, K. (2024) · IUBMB Life · doi:10.1002/iub.2775 · Cited by 14

Identifying RNA splicing factors using IFT genes in Chlamydomonas reinhardtii

Lin, H., Zhang, Z., Iomini, C., & Dutcher, S. K. (2018) · Open Biology · doi:10.1098/rsob.170211 · Cited by 14

Lipids and chromatin: a tale of intriguing connections shaping genomic landscapes

Ponce, M. L. S., Cobb, J. A., & Zaremberg, V. (2024) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.06.004 · Cited by 14

Centrophilic Retrotransposons of Plant Genomes

Bousios, A., Kakutani, T., & Henderson, I. R. (2025) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-083123-082220 · Cited by 16

Spd2 assists Spd1 in modulation of RNR architecture but does not regulate deoxynucleotide pools

Vejrup-Hansen, R., Fleck, O., Landvad, K., Fahnøe, U., Broendum, S. S., Schreurs, A., Kragelund, B. B., Carr, A. M., Holmberg, C., & Nielsen, O. (2014) · Journal of Cell Science · doi:10.1242/jcs.139816 · Cited by 14

Basic principles of yeast genomics, a personal recollection: Graphical Abstract Figure.

Dujon, B. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov047 · Cited by 14

Natural gene expression variation studies in yeast

Thompson, D. A., & Cubillos, F. A. (2016) · Yeast · doi:10.1002/yea.3210 · Cited by 15

Multi-Species Network Inference Improves Gene Regulatory Network Reconstruction for Early Embryonic Development in Drosophila

Joshi, A., Beck, Y., & Michoel, T. (2015) · Journal of Computational Biology · doi:10.1089/cmb.2014.0290 · Cited by 15

Zygosaccharomyces seidelii sp. nov. a new yeast species from the Maldives, and a revisit of the single-strain species debate

Brysch‐Herzberg, M., Wohlmann, E., & Fischer, R. (2019) · Antonie van Leeuwenhoek · doi:10.1007/s10482-019-01352-x · Cited by 14

The process of kinetochore assembly in yeasts

Roy, B., Varshney, N., Yadav, V., & Sanyal, K. (2012) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12019 · Cited by 14

Systematic Localization Study on Novel Proteins Encoded by Meiotically Up-Regulated ORFs in Fission Yeast

Ikebe, C., Konishi, M., Hirata, D., Matsusaka, T., & Toda, T. (2011) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.110558 · Cited by 14

Mediator Can Regulate Mitotic Entry and Direct Periodic Transcription in Fission Yeast

Bányai, G., López, M. D., Szilágyi, Z., & Gustafsson, C. M. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00819-14 · Cited by 16

A homeostatic mechanism rapidly corrects aberrant nucleocytoplasmic ratios maintaining nuclear size in fission yeast

Cantwell, H., & Nurse, P. (2019) · Journal of Cell Science · doi:10.1242/jcs.235911 · Cited by 14

Global Analysis of Gene Expression Profiles Provides Novel Insights into the Development and Evolution of the Large Crustacean Eriocheir Sinensis

Wang, J., Chen, X., He, F., Song, X., Huang, S., Yue, W., Chen, Y., Su, Z., & Wang, C. (2020) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2019.01.006 · Cited by 13

Investigating Host Induced Meiosis in a Fungal Plant Pathogen

J., B., E., M., & E., C. (2012) · InTech eBooks · doi:10.5772/30032 · Cited by 13

Schizosaccharomyces pombe Ofd2 Is a Nuclear 2-Oxoglutarate and Iron Dependent Dioxygenase Interacting with Histones

Korvald, H., Moe, A. M. M., Cederkvist, F. H., Thiede, B., Laerdahl, J. K., Bjørås, M., & Alseth, I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025188 · Cited by 13

A metabolic strategy to enhance long-term survival by Phx1 through stationary phase-specific pyruvate decarboxylases in fission yeast

Kim, J., Kim, E., López‐Maury, L., Bähler, J., & Roe, J. (2014) · Aging · doi:10.18632/aging.100682 · Cited by 13

Mating response and construction of heterothallic strains of the fission yeast Schizosaccharomyces octosporus

Seike, T., & Niki, H. (2017) · FEMS Yeast Research · doi:10.1093/femsyr/fox045 · Cited by 13

Rbm10 facilitates heterochromatin assembly via the Clr6 HDAC complex

Weigt, M., Gao, Q., Ban, H., He, H., Mastrobuoni, G., Kempa, S., Chen, W., & Li, F. (2021) · Epigenetics & Chromatin · doi:10.1186/s13072-021-00382-y · Cited by 13

Class-II dihydroorotate dehydrogenases from three phylogenetically distant fungi support anaerobic pyrimidine biosynthesis

Bouwknegt, J., Koster, C. C., Vos, A. M., Ortiz‐Merino, R. A., Wassink, M., Luttik, M. A. H., van den Broek, M. A., Hagedoorn, P., & Pronk, J. T. (2021) · Fungal Biology and Biotechnology · doi:10.1186/s40694-021-00117-4 · Cited by 13

Eukaryotic Pangenomes

Richard, G. (2020) · Springer eBooks · doi:10.1007/978-3-030-38281-0_12 · Cited by 14

Fungal Genomics for Energy and Environment

Grigoriev, I. V. (2013) · Soil biology · doi:10.1007/978-3-642-39339-6_2 · Cited by 13

Nsk1 ensures accurate chromosome segregation by promoting association of kinetochores to spindle poles during anaphase B

Buttrick, G. J., Meadows, J. C., Lancaster, T. C., Vanoosthuyse, V., Shepperd, L. A., Hoe, K., Kim, D.-U., Park, H.-O., Hardwick, K., & Millar, J. B. A. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-07-0608 · Cited by 12

Characterization and Prediction of Haploinsufficiency Using Systems-Level Gene Properties in Yeast

Norris, M., Lovell, S. C., & Delneri, D. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.008144 · Cited by 13

Identification of S-phase DNA damage-response targets in fission yeast reveals conservation of damage-response networks

Willis, N. A., Zhou, C., Elia, A. E. H., Murray, J. M., Carr, A. M., Elledge, S. J., & Rhind, N. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1525620113 · Cited by 15

Data provenance management for bioinformatics workflows using NoSQL database systems in a cloud computing environment

Hondo, F., Wercelens, P., da Silva, W. M. C., de Castro, K. R., Santana, I., Walter, M. E. M. T., Araújo, A., de Holanda, M. T., & Lifschitz, S. (2017) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm.2017.8217954 · Cited by 13

Genetic Analysis of Schizosaccharomyces pombePreprint

Ekwall, K., & Thon, G. (2017) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top079772 · Cited by 13

Genomic evidence for hybridization and introgression between blue peafowl and endangered green peafowl and molecular foundation of leucistic plumage of blue peafowl

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Selection for reduced translation costs at the intronic 5′ end in fungi

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Ccq1-Tpz1TPP1interaction facilitates telomerase and SHREC association with telomeres in fission yeast

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Assembly of Schizosaccharomyces cryophilus chromosomes and their comparative genomic analyses revealed principles of genome evolution of the haploid fission yeasts

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Structure and evolution of the 4-helix bundle domain of Zuotin, a J-domain protein co-chaperone of Hsp70

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Hyphal differentiation induced via a DNA damage checkpoint-dependent pathway engaged in crosstalk with nutrient stress signaling in Schizosaccharomyces japonicus

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A species-specific nucleosomal signature defines a periodic distribution of amino acids in proteins

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Challenges and solutions for analysing dual RNA ‐seq data for non‐model host–pathogen systems

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Establishment of centromere identity is dependent on nuclear spatial organization

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Molecular Biology of the Fission Yeast

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Fission yeast compared and contrasted

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An Ancient Yeast for Young Geneticists: A Primer on the Schizosaccharomyces pombe Model System

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The transcriptional program of meiosis and sporulation in fission yeast

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