The DOI matches its Crossref record; 59 of the 59 references it cites were found in a registry or an index.
Natural history and evolutionary principles of gene duplication in fungi
Abstract
Gene duplication and loss is a powerful source of functional innovation. However, the general principles that govern this process are still largely unknown. With the growing number of sequenced genomes, it is now possible to examine these events in a comprehensive and unbiased manner. Here, we develop a procedure that resolves the evolutionary history of all genes in a large group of species. We apply our procedure to seventeen fungal genomes to create a genome-wide catalogue of gene trees that determine precise orthology and paralogy relations across these species. We show that gene duplication and loss is highly constrained by the functional properties and interacting partners of genes. In particular, stress-related genes exhibit many duplications and losses, whereas growth-related genes show selection against such changes. Whole-genome duplication circumvents this constraint and relaxes the dichotomy, resulting in an expanded functional scope of gene duplication. By characterizing the functional fate of duplicate genes we show that duplicated genes rarely diverge with respect to biochemical function, but typically diverge with respect to regulatory control. Surprisingly, paralogous modules of genes rarely arise, even after whole-genome duplication. Rather, gene duplication may drive the modularization of functional networks through specialization, thereby disentangling cellular systems.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Evolution of genetic signaling and regulatory systems usually proceeds through gene duplication and loss with concomitant processes of neofunctionalization and subfunctionalization leading to functional changes”
From Mitochondrial retrograde control of transcription evolves with respiratory stress, metabolic adaptation, and virulence in budding yeasts (2026) · cites this paper as Wapinski et al. 2007
Citations
Cites
The neighbor-joining method: a new method for reconstructing phylogenetic trees.
Saitou, N., & Nei, M. (1987) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040454 · Cited by 59,959
MUSCLE: multiple sequence alignment with high accuracy and high throughput
Edgar, R. C. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh340 · Cited by 44,662
Gene Ontology: tool for the unification of biology
Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., Davis, A. P., Dolinski, K., Dwight, S. S., Eppig, J. T., et al. (2000) · Nature Genetics · doi:10.1038/75556 · Cited by 43,206
PHYLIP-Phylogeny inference package (Version 3.2)
Felsenstein, J. (1989) · Cladistics · Cited by 17,682
Improved tools for biological sequence comparison.
Pearson, W. R., & Lipman, D. J. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.8.2444 · Cited by 11,227
Ohno, S. (1970) · doi:10.1007/978-3-642-86659-3 · Cited by 7,833
The rapid generation of mutation data matrices from protein sequences
Jones, D. T., Taylor, W. R., & Thornton, J. M. (1992) · Computer applications in the biosciences · doi:10.1093/bioinformatics/8.3.275 · Cited by 7,003
The COG database: an updated version includes eukaryotes
Tatusov, R. L., Fedorova, N. D., Jackson, J. D., Jacobs, A. R., Kiryutin, B., Koonin, E. V., Krylov, D. M., Mazumder, R., Mekhedov, S., Nikolskaya, A. N., et al. (2003) · BMC Bioinformatics · doi:10.1186/1471-2105-4-41 · Cited by 4,410
Proteome survey reveals modularity of the yeast cell machinery
Gavin, A., Aloy, P., Grandi, P., Krause, R., Böesche, M., Marzioch, M., Rau, C., Jensen, L. J., Bastuck, S., Dümpelfeld, B., et al. (2006) · Nature · doi:10.1038/nature04532 · Cited by 2,570
Functional Discovery via a Compendium of Expression Profiles
Hughes, T. R., Marton, M. J., Jones, A. R., Roberts, C. J., Stoughton, R. B., Armour, C. D., Bennett, H. A., Coffey, E. M., Dai, H. A., He, Y. D., et al. (2000) · Cell · doi:10.1016/s0092-8674(00)00015-5 · Cited by 2,534
Flagged first, then by citations
Research works printed but not linked: 1
- Arnaud, M. B. C. M. et al. Candida Genome Database 〈 http://www.candidagenome.org 〉 (2006)
Cited by
Sorted by citations
Items 401–500 of 614
Sellerio, A. L., Bassetti, B., Isambert, H., & Lagomarsino, M. C. (2008) · Molecular BioSystems · doi:10.1039/b815339f · Cited by 14
Evolutionary conservation of sequence motifs at sites of protein modification
Li, S., & Dohlman, H. G. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104617 · Cited by 12
Removing Noise from Gene Trees
Doroftei, A., & El-Mabrouk, N. (2011) · Lecture notes in computer science · doi:10.1007/978-3-642-23038-7_8 · Cited by 13
Hao, Y., Washburn, J. D., Rosenthal, J., Nielsen, B., Lyons, E. H., Edger, P. P., Pires, J. C., & Conant, G. C. (2018) · Genome Biology and Evolution · doi:10.1093/gbe/evy061 · Cited by 14
Cromar, G. L., Zhao, A., Xiong, X., Swapna, L. S., Loughran, N. B., Song, H., & Parkinson, J. (2016) · Database · doi:10.1093/database/baw013 · Cited by 16
Relationship between gene duplicability and diversifiability in the topology of biochemical networks
Guo, Z., Jiang, W. G., Lages, N., Borcherds, W. M., & Wang, D. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-577 · Cited by 13
Probing the Extent of Randomness in Protein Interaction Networks
Ivanic, J., Wallqvist, A., & Jaques Reifman, A. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000114 · Cited by 13
Modularity and Dissipation in Evolution of Macromolecular Structures, Functions, and Networks
Caetano‐Anollés, G., Yafremava, L. S., & Mittenthal, J. E. (2010) · Wiley eBooks · doi:10.1002/9780470570418.ch20 · Cited by 13
Kawaguchi, Y. W., Tsuchikane, Y., Tanaka, K., Taji, T., Suzuki, Y., Toyoda, A., Itô, M., Watano, Y., Nishiyama, T., Sekimoto, H., et al. (2023) · Genome Biology and Evolution · doi:10.1093/gbe/evad115 · Cited by 12
Partial Decay of Thiamine Signal Transduction Pathway Alters Growth Properties of Candida glabrata
Iosue, C. L., Attanasio, N., Shaik, N. F., Neal, E. M., Leone, S. G., Cali, B. J., Peel, M. T., Grannas, A. M., & Wykoff, D. D. (2016) · PLoS ONE · doi:10.1371/journal.pone.0152042 · Cited by 12
Zhang, H., Rokas, A., & Slot, J. C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041903 · Cited by 13
Gene Duplication and Phenotypic Changes in the Evolution of Mammalian Metabolic Networks
Bekaert, M., & Conant, G. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087115 · Cited by 12
Emergent Complexity in Myosin V-Based Organelle Inheritance
Mast, F. D., Rachubinski, R. A., & Dacks, J. B. (2011) · Molecular Biology and Evolution · doi:10.1093/molbev/msr264 · Cited by 12
Identifying Cis-Regulatory Changes Involved in the Evolution of Aerobic Fermentation in Yeasts
Lin, Z., Wang, T., Tsai, B.-S., Wu, F.-T., Yu, F.-J., Tseng, Y.-J., Sung, H., & Li, W. (2013) · Genome Biology and Evolution · doi:10.1093/gbe/evt067 · Cited by 12
High-Throughput Identification ofCis-Regulatory Rewiring Events in Yeast
Sarda, S., & Hannenhalli, S. S. (2015) · Molecular Biology and Evolution · doi:10.1093/molbev/msv203 · Cited by 12
A Phylogenetic Approach Finds Abundant Interlocus Gene Conversion in Yeast
Ji, X., Griffing, A. R., & Thorne, J. L. (2016) · Molecular Biology and Evolution · doi:10.1093/molbev/msw114 · Cited by 12
10 Evolution of Genes for Secondary Metabolism in Fungi
Teichert, I., & Nowrousian, M. (2011) · Springer eBooks · doi:10.1007/978-3-642-19974-5_10 · Cited by 12
Hase, T., Niimura, Y., & Tanaka, H. (2010) · BMC Evolutionary Biology · doi:10.1186/1471-2148-10-358 · Cited by 12
Network Centrality Analysis in Fungi Reveals Complex Regulation of Lost and Gained Genes
Coulombe‐Huntington, J., & Xia, Y. (2017) · PLoS ONE · doi:10.1371/journal.pone.0169459 · Cited by 11
Miao, B., Xiao, Q., Chen, W., Li, Y., & Wang, Z. (2018) · BMC Genomics · doi:10.1186/s12864-018-4661-6 · Cited by 10
Discovering local patterns of co - evolution: computational aspects and biological examples
Tuller, T., Felder, Y., & Kupiec, M. (2010) · BMC Bioinformatics · doi:10.1186/1471-2105-11-43 · Cited by 11
Revealing Mammalian Evolutionary Relationships by Comparative Analysis of Gene Clusters
Song, G., Riemer, C., Dickins, B., Kim, H. L., Zhang, L., Zhang, Y., Hsu, C.-H., Hardison, R. C., Program, N. C. S., Green, E. D., et al. (2012) · Genome Biology and Evolution · doi:10.1093/gbe/evs032 · Cited by 11
Intrinsic protein disorder reduces small-scale gene duplicability
Banerjee, S., Feyertag, F., & Alvarez‐Ponce, D. (2017) · DNA Research · doi:10.1093/dnares/dsx015 · Cited by 11
Multiple Optimal Reconciliations Under the Duplication-Loss-Coalescence Model
Du, H., Ong, Y. S., Knittel, M., Mawhorter, R., Liu, N., Gross, G., Tojo, R., Libeskind-Hadas, R., & Wu, Y.-C. (2019) · IEEE Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2019.2922337 · Cited by 11
López, J. G., Manea, F., & Mitrana, V. (2014) · Journal of Computer and System Sciences · doi:10.1016/j.jcss.2014.02.011 · Cited by 11
Evolution of the SH3 Domain Specificity Landscape in Yeasts
Verschueren, E., Spiess, M., Gkourtsa, A., Avula, T., Landgraf, C., Mancilla, V. E. T., Huber, A., Volkmer, R., Winsor, B., Serrano, L. G., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0129229 · Cited by 11
The Gene-Duplication Problem: Near-Linear Time Algorithms for NNI Based Local Searches
Bansal, M. S., & Eulenstein, O. (2008) · Springer eBooks · doi:10.1007/978-3-540-79450-9_3 · Cited by 11
Evolution of Genome Organization by Duplication and Loss: An Alignment Approach
Holloway, P., Swenson, K. M., Ardell, D. H., & El-Mabrouk, N. (2012) · Lecture notes in computer science · doi:10.1007/978-3-642-29627-7_10 · Cited by 10
Cagliari, A., Turchetto‐Zolet, A. C., Maraschin, F. D. S., Loss, G., Margis, R., & Margis-Pinheiro, M. M. A. N. (2011) · InTech eBooks · doi:10.5772/23719 · Cited by 10
Subtelomeric Regions Promote Evolutionary Innovation of Gene Families in Yeast
Snoek, T., Voordeckers, K., & Verstrepen, K. J. (2013) · Springer eBooks · doi:10.1007/978-3-642-41566-1_3 · Cited by 9
Yang, E., Hulse‐Kemp, A. M., & Cai, J. J. (2012) · Evolutionary Bioinformatics · doi:10.4137/ebo.s10372 · Cited by 11
Lin, Z., & Li, W. (2010) · Molecular Biology and Evolution · doi:10.1093/molbev/msq324 · Cited by 10
Zhang, Y., Zhang, J., Gao, K., Lu, R., Cao, X., Yang, L., & Nie, G. (2023) · FEBS Open Bio · doi:10.1002/2211-5463.13594 · Cited by 11
Surm, J. M., Landau, M., Columbus-Shenkar, Y. Y., & Moran, Y. (2024) · Molecular Biology and Evolution · doi:10.1093/molbev/msae082 · Cited by 9
Functional genetic discovery of enzymes using full-scan mass spectrometry metabolomics
Caudy, A. A., Hanchard, J., Hsieh, A. H.-R., Shaan, S., & Rosebrock, A. P. (2018) · Biochemistry and Cell Biology · doi:10.1139/bcb-2018-0058 · Cited by 10
Loss of protein interactions and regulatory divergence in yeast whole-genome duplicates
Vinogradov, A. E., & Anatskaya, O. V. (2009) · Genomics · doi:10.1016/j.ygeno.2009.02.004 · Cited by 9
Pantzartzi, C. N., Drosopoulou, E., & Scouras, Z. G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073217 · Cited by 10
Evolution of transcriptional regulatory networks in yeast populations
Cavalieri, D. (2009) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.68 · Cited by 9
Rogers, J., Fishberg, A., Youngs, N., & Wu, Y.-C. (2017) · BMC Bioinformatics · doi:10.1186/s12859-017-1701-1 · Cited by 9
Nahas, J. V., Iosue, C. L., Shaik, N. F., Selhorst, K., He, B. Z., & Wykoff, D. D. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200303 · Cited by 8
Hill, R., Grey, M., Fedi, M. O., Smith, D., Canning, G., Ward, B. J., Irish, N., Smith, J., McMillan, V. E., Hammond, J., et al. (2025) · BMC Genomics · doi:10.1186/s12864-025-11432-0 · Cited by 6
Peters, A. E., Bavishi, A., Cho, H., & Choudhary, M. (2012) · BMC Research Notes · doi:10.1186/1756-0500-5-192 · Cited by 8
The evolutionary trajectory of mitochondrial carrier family during metazoan evolution
Gong, M., Li, J., Wang, M., Wang, J., Zen, K., & Zhang, C. (2010) · BMC Evolutionary Biology · doi:10.1186/1471-2148-10-282 · Cited by 8
Li, H., Shi, Q., Zhang, Z., Zeng, L., Qi, J., & Mā, H. (2016) · Journal of Systematics and Evolution · doi:10.1111/jse.12206 · Cited by 8
Lu, W.-J., Zhou, L., Gao, F.-X., Sun, Z., Li, Z., Liu, X., Li, S.-S., Wang, Y., & Gui, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102943 · Cited by 8
Benchouaia, M., Ripoche, H., Sissoko, M., Thiébaut, A., Merhej, J., Delaveau, T., Fasseu, L., Benaissa, S., Lorieux, G., Jourdren, L., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02689 · Cited by 8
Zeng, X., Li, H., Li, K., Yuan, R., Zhao, S., Li, J., Luo, J., Li, X., Mā, H., Wu, G., et al. (2020) · New Phytologist · doi:10.1111/nph.17053 · Cited by 8
Sources of Fungal Genetic Variation and Associating It with Phenotypic Diversity
Taylor, J. W., Branco, S., Gao, C. D., Hann-Soden, C., Montoya, L., Sylvain, I., & Gladieux, P. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch30 · Cited by 8
Discovery of Dynein and its Properties
Gibbons, I. R. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-382004-4.10001-9 · Cited by 8
Kaganovich, M., & Snyder, M. P. (2011) · Journal of Proteome Research · doi:10.1021/pr201065k · Cited by 8
Enrichment of homologs in insignificant BLAST hits by co-complex network alignment
Fokkens, L., Botelho, S. M., Boekhorst, J., & Snel, . (2010) · BMC Bioinformatics · doi:10.1186/1471-2105-11-86 · Cited by 8
Gene divergence and pathway duplication in the metabolic network of yeast and digital organisms
Gerlee, P., Lundh, T., Zhang, B., & Anderson, A. R. A. (2009) · Journal of The Royal Society Interface · doi:10.1098/rsif.2008.0514 · Cited by 8
Coestimation of Gene Trees and Reconciliations Under a Duplication-Loss-Coalescence Model
Zhang, B., & Wu, Y.-C. (2017) · Lecture notes in computer science · doi:10.1007/978-3-319-59575-7_18 · Cited by 8
Horizontal Gene Transfer in Fungi
Bredeweg, E., & Baker, S. (2020) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-030-29541-7_11 · Cited by 8
Sari, E., Enright, D. J., Ordoñez, M. E., Allison, S., Homyak, P. M., Wilkins, M. J., & Glassman, S. I. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2519152123 · Cited by 7
Yeast as a Window into Changes in Genome Complexity Due to Polyploidization
Hudson, C. M., & Conant, G. C. (2012) · Springer eBooks · doi:10.1007/978-3-642-31442-1_15 · Cited by 7
Using Trees to Capture Reticulate Evolution
Tofigh, A. A. (2009) · Cited by 7
Muñoz, A., MuĂąoz, D. S., Zimin, A. V., & Yorke, J. A. (2016) · BMC Genomics · doi:10.1186/s12864-016-3102-7 · Cited by 7
Evolutionary Analysis of Pectin Lyases of the Genus Colletotrichum
Lara-Márquez, A., Oyama, K., Zavala-Páramo, M. G., Villa-Rivera, M. G., Conejo-Saucedo, U., & Cano-Camacho, H. (2017) · Journal of Molecular Evolution · doi:10.1007/s00239-017-9812-x · Cited by 7
Architectural groups of a subtelomeric gene family evolve along distinct paths in Candida albicans
Dunn, M. J., Shazib, S. U. A., Simonton, E., Slot, J. C., & Anderson, M. Z. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkac283 · Cited by 7
Evolution of a domain conserved in microtubule-associated proteins of eukaryotes
Arvestad, L. (2008) · Advances and Applications in Bioinformatics and Chemistry · doi:10.2147/aabc.s3211 · Cited by 7
Inferring Gene Family Histories in Yeast Identifies Lineage Specific Expansions
Ames, R. M., Money, D., & Lovell, S. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099480 · Cited by 7
Gene cloning and expression analyses of WBC genes in the developing grapevine seeds
Tang, Y., Wang, Q., Xue, J., Li, Y., Li, R., van Nocker, S., Wang, Y., & Zhang, C. (2018) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(17)61827-6 · Cited by 7
Ramaiah, A., Nayak, S., Rakshit, S., Manson, A. L., Abeel, T., Shanmugam, S., Sahoo, P. N., John, A. J. U. K., Sundaramurthi, J. C., Narayanan, S., et al. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00195 · Cited by 7
Reagents for investigating MAPK signalling in model yeast species
Pincus, D., Benjamin, K. R., Burbulis, I. E., Tsong, A. E., & Resnekov, O. (2010) · Yeast · doi:10.1002/yea.1758 · Cited by 7
Experimental analysis of co-evolution within protein complexes: The yeast exosome as a model
Sandler, I., Medalia, O., & Aharoni, A. (2013) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.24360 · Cited by 7
OAF is a DAF-like gene that controls ovule development in plants
Li, Y.-C., Lin, J.-Y., Hsu, W., Kung, C.-T., Dai, S.-Y., Yang, J., Tan, C., & Yang, C. (2023) · Communications Biology · doi:10.1038/s42003-023-04864-5 · Cited by 6
Liu, J., Wei, Q., Zhao, Z., Qiang, F., Li, G., & Wu, G. (2024) · Plant and Cell Physiology · doi:10.1093/pcp/pcae054 · Cited by 6
DNA signals at isoform promoters
Dai, Z., Xiong, Y., & Dai, X. (2016) · Scientific Reports · doi:10.1038/srep28977 · Cited by 6
Huang, J. T., Liu, S., & Cook, D. E. (2023) · Physiological and Molecular Plant Pathology · doi:10.1016/j.pmpp.2023.102006 · Cited by 6
Cyert, M., Goldman, A. R., Roy, J., Bodenmiller, B., Wanka, S., Landry, C. R., & Aebersold, R. H. (2014) · The FASEB Journal · doi:10.1096/fasebj.28.1_supplement.586.3 · Cited by 6
Wang, Z., Huang, X.-Q., & Cloutier, S. (2009) · Functional & Integrative Genomics · doi:10.1007/s10142-009-0150-y · Cited by 6
The evolution of gene expression regulatory networks in yeasts
Lelandais, G., Goudot, C., & Devaux, F. (2011) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2011.05.014 · Cited by 6
Bansal, M. S., Alm, E. J., & Kellis, M. (2013) · Lecture notes in computer science · doi:10.1007/978-3-642-37195-0_1 · Cited by 6
Gene Expression Divergence is Coupled to Evolution of DNA Structure in Coding Regions
Dai, Z., & Dai, X. (2011) · PLoS Comput. Biol. · doi:10.1371/journal.pcbi.1002275 · Cited by 4
Fares, M. A., Sabater‐Muñoz, B., & Toft, C. (2017) · Genome Biology and Evolution · doi:10.1093/gbe/evx085 · Cited by 6
Progressive transcriptomic shifts in evolved yeast strains following gene knockout
Jiang, B., Xiao, C., & Liu, L. (2024) · iScience · doi:10.1016/j.isci.2024.111219 · Cited by 5
Daghino, S., Murat, C., Mita, S. D., Martino, E. M. D., & Perotto, S. (2025) · Mycorrhiza · doi:10.1007/s00572-025-01191-x · Cited by 5
Joshi, A., & Göttgens, B. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.02.013 · Cited by 5
Corréa, M., Lerat, E., Birmelé, É., Samson, F., Bouillon, B., Normand, K., & Rizzon, C. (2021) · Genome Biology and Evolution · doi:10.1093/gbe/evab062 · Cited by 11
Taming the Duplication-Loss-Coalescence Model with Integer Linear Programming
Paszek, J., Markin, A., Górecki, P., & Eulenstein, O. (2021) · Journal of Computational Biology · doi:10.1089/cmb.2021.0011 · Cited by 5
Protein innovation through template switching in the Saccharomyces cerevisiae lineage
Abraham, M., & Hazkani‐Covo, E. (2021) · Scientific Reports · doi:10.1038/s41598-021-01736-y · Cited by 5
From large-scale assays to mechanistic insights: computational analysis of interactions
Jaimovich, A., & Friedman, N. (2010) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2010.10.017 · Cited by 5
Ouangraoua, A., Swenson, K. M., & Chauve, C. (2010) · Lecture notes in computer science · doi:10.1007/978-3-642-16181-0_24 · Cited by 5
Slot, J. C., Hallstrom, K., Matheny, P. B., Hosaka, K., Mueller, G. M., Robertson, D. L., & Hibbett, D. S. (2009) · Fungal ecology · doi:10.1016/j.funeco.2009.10.001 · Cited by 5
Improvisation in evolution of genes and genomes: whose structure is it anyway?
Shakhnovich, B. E., & Shakhnovich, E. I. (2008) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2008.02.007 · Cited by 5
Law of genome evolution direction: Coding information quantity grows
Luo, L. (2009) · 物理学前沿:英文版 · doi:10.1007/s11467-009-0014-x · Cited by 5
A comparative evolutionary study of transcription networksPreprint
Sellerio, A. L., Bassetti, B., Isambert, H., & Lagomarsino, M. C. (2008) · arXiv (Cornell University) · doi:10.48550/arxiv.0805.2288 · Cited by 5
Discovering Local Patterns of Co-evolution
Felder, Y., & Tuller, T. (2008) · Lecture notes in computer science · doi:10.1007/978-3-540-87989-3_5 · Cited by 5
Phylogenomic Approach to the Evolutionary Dynamics of Gene Duplication in Birds
Organ, C. L., Rasmussen, M. D., Baldwin, M. W., Kellis, M., & Edwards, S. V. (2010) · Wiley eBooks · doi:10.1002/9780470619902.ch14 · Cited by 5
Sácký, J., Chaloupecká, A., Šantrůček, J., Kaňa, A., Leonhardt, T., Borovička, J., & Kotrba, P. (2025) · BioMetals · doi:10.1007/s10534-025-00721-6 · Cited by 4
The Pattern and Evolution of Looped Gene Bendability
Dai, Z., Xiong, Y., & Dai, X. (2013) · Molecular Biology and Evolution · doi:10.1093/molbev/mst188 · Cited by 4
Reconciliation With Nonbinary Gene Trees Revisited
Zheng, Y., & Zhang, L. (2017) · Journal of the ACM · doi:10.1145/3088512 · Cited by 4
Computational Tools: RNA Interference in Fungal Therapeutics
Jain, C. K., & Wadhwa, G. (2018) · Springer eBooks · doi:10.1007/978-981-10-7483-7_12 · Cited by 4
Iosue, C. L., Gulotta, A. P., Selhorst, K. B., Mody, A. C., Barbour, K. M., Marcotte, M. J., Bui, L. N., Leone, S. G., Lang, E. C., Hughes, G. H., et al. (2019) · G3 Genes Genomes Genetics · doi:10.1534/g3.119.400897 · Cited by 4
Király, A., Szabó, I. G., Emri, T., Leiter, É., & Pócsi, I. (2020) · Journal of Basic Microbiology · doi:10.1002/jobm.202000067 · Cited by 4
Heineike, B. M., & El‐Samad, H. (2021) · Frontiers in Fungal Biology · doi:10.3389/ffunb.2021.642336 · Cited by 4
Dubreuil, B., & Levy, E. D. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.626729 · Cited by 4
Species-specific effects of the introduction of Aspergillus nidulans gfdB in osmophilic aspergilli
Bodnár, V., Király, A., Orosz, E., Miskei, M., Emri, T., Karányi, Z., Leiter, É., de Vries, R. P., & Pócsi, I. (2023) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-023-12384-9 · Cited by 4
Root, Z. D., Allen, C., Gould, C. H., Brewer, M., Jandzík, D., & Medeiros, D. M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.809979 · Cited by 4
Metadata
- Authors
- Wapinski, I., Pfeffer, A., Friedman, N., & Regev, A.
- Affiliations
- Broad Institute (US)
- Harvard University (US)
- Hebrew University of Jerusalem (IL)
- Corresponding author
- Regev, Aviv
- Venue
- Nature
- Published
- 2007-09
- Volume
- 449
- Issue
- 7158
- Pages
- 54-61
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1992140809
- Cited by
- 614
- References
- 59
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 6 · 2023: 14 · 2022: 11 · 2021: 17 · 2020: 22 · 2019: 20 · 2018: 37 · 2017: 44 · 2016: 33 · 2015: 34 · 2014: 34 · 2013: 44 · 2012: 59
- FWCI
- 23.70
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- gene duplication, gene loss, fungi, Ascomycota, whole-genome duplication, orthology, paralogy, gene tree inference, functional innovation, stress-related genes, growth-related genes, Saccharomyces cerevisiae, Schizosaccharomyces pombe
- MeSH terms
- Algorithms, Ascomycota, Genes, Fungal, Phylogeny, Genome, Fungal, Gene Deletion, Gene Dosage, Evolution, Molecular, Genes, Duplicate, Gene Duplication
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review