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De novo European eel transcriptome provides insights into the evolutionary history of duplicated genes in teleost lineages

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De novo European eel transcriptome provides insights into the evolutionary history of duplicated genes in teleost lineages

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dc.contributor.author Rozenfeld, Christoffer es_ES
dc.contributor.author Blanca Postigo, José Miguel es_ES
dc.contributor.author Gallego Albiach, Victor es_ES
dc.contributor.author García-Carpintero, Víctor es_ES
dc.contributor.author Herranz-Jusdado, Juan Germán es_ES
dc.contributor.author Pérez Igualada, Luz María es_ES
dc.contributor.author Asturiano, Juan F. es_ES
dc.contributor.author Cañizares Sales, Joaquín es_ES
dc.contributor.author Peñaranda, D.S. es_ES
dc.date.accessioned 2021-01-28T04:31:51Z
dc.date.available 2021-01-28T04:31:51Z
dc.date.issued 2019-06-12 es_ES
dc.identifier.issn 1932-6203 es_ES
dc.identifier.uri http://hdl.handle.net/10251/160081
dc.description.abstract [EN] Paralogues pairs are more frequently observed in eels (Anguilla sp.) than in other teleosts. The paralogues often show low phylogenetic distances; however, they have been assigned to the third round of whole genome duplication (WGD), shared by all teleosts (3R), due to their conserved synteny. The apparent contradiction of low phylogenetic difference and 3R conserved synteny led us to study the duplicated gene complement of the freshwater eels. With this aim, we assembled de novo transcriptomes of two highly relevant freshwater eel species: The European (Anguilla anguilla) and the Japanese eel (Anguilla japonica). The duplicated gene complement was analysed in these transcriptomes, and in the genomes and transcriptomes of other Actinopterygii species. The study included an assessment of neutral genetic divergence (4dTv), synteny, and the phylogenetic origins and relationships of the duplicated gene complements. The analyses indicated a high accumulation of duplications (1217 paralogue pairs) among freshwater eel genes, which may have originated in a WGD event after the Elopomorpha lineage diverged from the remaining teleosts, and thus not at the 3R. However, very similar results were observed in the basal Osteoglossomorpha and Clupeocephala branches, indicating that the specific genomic regions of these paralogues may still have been under tetrasomic inheritance at the split of the teleost lineages. Therefore, two potential hypotheses may explain the results: i) The freshwater eel lineage experienced an additional WGD to 3R, and ii) Some duplicated genomic regions experienced lineage specific rediploidization after 3R in the ancestor to freshwater eels. The supporting/opposing evidence for both hypotheses is discussed. es_ES
dc.description.sponsorship This study received funding from the project REPRO-TEMP (AGL2013-41646-R) funded by the Spanish Ministry of Economy and Competitiveness, and from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No 642893 (IMPRESS), which also included the predoctoral contracts of CR and JGHJ. VG has a postdoctoral grant from the Spanish Ministry of Science, Innovation and Universities (MICIU; Programa Juan de la Cierva-Incorporacion; IJCI-2017-34200). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. es_ES
dc.language Inglés es_ES
dc.publisher Public Library of Science es_ES
dc.relation.ispartof PLoS ONE es_ES
dc.rights Reconocimiento (by) es_ES
dc.subject.classification PRODUCCION ANIMAL es_ES
dc.subject.classification GENETICA es_ES
dc.title De novo European eel transcriptome provides insights into the evolutionary history of duplicated genes in teleost lineages es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1371/journal.pone.0218085 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/EC/H2020/642893/EU/Improved production strategies for endangered freshwater species./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MINECO//AGL2013-41646-R/ES/LA ANGUILA EUROPEA COMO MODELO PARA ESTUDIAR LA TEMPERATURA COMO MODULADOR DE LA MADURACION SEXUAL EN TELEOSTEOS. POTENCIAL APLICACION EN ACUICULTURA./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/AEI//IJCI-2017-34200/ES/AYUDAS JUAN DE LA CIERVA INCORPORACION/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto Universitario Mixto de Biología Molecular y Celular de Plantas - Institut Universitari Mixt de Biologia Molecular i Cel·lular de Plantes es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia es_ES
dc.contributor.affiliation Universitat Politècnica de València. Instituto de Ciencia y Tecnología Animal - Institut de Ciència i Tecnologia Animal es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Ciencia Animal - Departament de Ciència Animal es_ES
dc.description.bibliographicCitation Rozenfeld, C.; Blanca Postigo, JM.; Gallego Albiach, V.; García-Carpintero, V.; Herranz-Jusdado, JG.; Pérez Igualada, LM.; Asturiano, JF.... (2019). De novo European eel transcriptome provides insights into the evolutionary history of duplicated genes in teleost lineages. PLoS ONE. 14(6):1-25. https://doi.org/10.1371/journal.pone.0218085 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1371/journal.pone.0218085 es_ES
dc.description.upvformatpinicio 1 es_ES
dc.description.upvformatpfin 25 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 14 es_ES
dc.description.issue 6 es_ES
dc.identifier.pmid 31188893 es_ES
dc.identifier.pmcid PMC6561569 es_ES
dc.relation.pasarela S\388444 es_ES
dc.contributor.funder Ministerio de Economía y Empresa es_ES
dc.contributor.funder European Commission es_ES
dc.description.references Gu, X., Wang, Y., & Gu, J. (2002). Age distribution of human gene families shows significant roles of both large- and small-scale duplications in vertebrate evolution. Nature Genetics, 31(2), 205-209. doi:10.1038/ng902 es_ES
dc.description.references Cañestro, C., Albalat, R., Irimia, M., & Garcia-Fernàndez, J. (2013). Impact of gene gains, losses and duplication modes on the origin and diversification of vertebrates. Seminars in Cell & Developmental Biology, 24(2), 83-94. doi:10.1016/j.semcdb.2012.12.008 es_ES
dc.description.references Llorente, B., Malpertuy, A., Neuvéglise, C., de Montigny, J., Aigle, M., Artiguenave, F., … Dujon, B. (2000). Genomic Exploration of the Hemiascomycetous Yeasts: 18. Comparative analysis of chromosome maps and synteny withSaccharomyces cerevisiae. FEBS Letters, 487(1), 101-112. doi:10.1016/s0014-5793(00)02289-4 es_ES
dc.description.references Colbourne, J. K., Pfrender, M. E., Gilbert, D., Thomas, W. K., Tucker, A., Oakley, T. H., … Basu, M. K. (2011). The Ecoresponsive Genome of Daphnia pulex. Science, 331(6017), 555-561. doi:10.1126/science.1197761 es_ES
dc.description.references Bailey, J. A., Gu, Z., Clark, R. A., Reinert, K., Samonte, R. V., Schwartz, S., … Eichler, E. E. (2002). Recent Segmental Duplications in the Human Genome. Science, 297(5583), 1003-1007. doi:10.1126/science.1072047 es_ES
dc.description.references Samonte, R. V., & Eichler, E. E. (2002). Segmental duplications and the evolution of the primate genome. Nature Reviews Genetics, 3(1), 65-72. doi:10.1038/nrg705 es_ES
dc.description.references David, L. (2003). Recent Duplication of the Common Carp (Cyprinus carpio L.) Genome as Revealed by Analyses of Microsatellite Loci. Molecular Biology and Evolution, 20(9), 1425-1434. doi:10.1093/molbev/msg173 es_ES
dc.description.references Jaillon, O., Aury, J.-M., Brunet, F., Petit, J.-L., Stange-Thomann, N., Mauceli, E., … Bernot, A. (2004). Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature, 431(7011), 946-957. doi:10.1038/nature03025 es_ES
dc.description.references Rondeau, E. B., Minkley, D. R., Leong, J. S., Messmer, A. M., Jantzen, J. R., von Schalburg, K. R., … Koop, B. F. (2014). The Genome and Linkage Map of the Northern Pike (Esox lucius): Conserved Synteny Revealed between the Salmonid Sister Group and the Neoteleostei. PLoS ONE, 9(7), e102089. doi:10.1371/journal.pone.0102089 es_ES
dc.description.references Albalat, R., & Cañestro, C. (2016). Evolution by gene loss. Nature Reviews Genetics, 17(7), 379-391. doi:10.1038/nrg.2016.39 es_ES
dc.description.references Hafeez, M., Shabbir, M., Altaf, F., & Abbasi, A. A. (2016). Phylogenomic analysis reveals ancient segmental duplications in the human genome. Molecular Phylogenetics and Evolution, 94, 95-100. doi:10.1016/j.ympev.2015.08.019 es_ES
dc.description.references Chain, F. J. J., Feulner, P. G. D., Panchal, M., Eizaguirre, C., Samonte, I. E., Kalbe, M., … Reusch, T. B. H. (2014). Extensive Copy-Number Variation of Young Genes across Stickleback Populations. PLoS Genetics, 10(12), e1004830. doi:10.1371/journal.pgen.1004830 es_ES
dc.description.references MABLE, B. K. (2004). ‘Why polyploidy is rarer in animals than in plants’: myths and mechanisms. Biological Journal of the Linnean Society, 82(4), 453-466. doi:10.1111/j.1095-8312.2004.00332.x es_ES
dc.description.references Otto, S. P., & Whitton, J. (2000). POLYPLOID INCIDENCE AND EVOLUTION. Annual Review of Genetics, 34(1), 401-437. doi:10.1146/annurev.genet.34.1.401 es_ES
dc.description.references Albertin, W., & Marullo, P. (2012). Polyploidy in fungi: evolution after whole-genome duplication. Proceedings of the Royal Society B: Biological Sciences, 279(1738), 2497-2509. doi:10.1098/rspb.2012.0434 es_ES
dc.description.references Schmutz, J., Cannon, S. B., Schlueter, J., Ma, J., Mitros, T., Nelson, W., … Jackson, S. A. (2010). Genome sequence of the palaeopolyploid soybean. Nature, 463(7278), 178-183. doi:10.1038/nature08670 es_ES
dc.description.references Del Pozo, J. C., & Ramirez-Parra, E. (2015). Whole genome duplications in plants: an overview fromArabidopsis. Journal of Experimental Botany, 66(22), 6991-7003. doi:10.1093/jxb/erv432 es_ES
dc.description.references Soltis, D. E., Visger, C. J., & Soltis, P. S. (2014). The polyploidy revolution then...and now: Stebbins revisited. American Journal of Botany, 101(7), 1057-1078. doi:10.3732/ajb.1400178 es_ES
dc.description.references Masterson, J. (1994). Stomatal Size in Fossil Plants: Evidence for Polyploidy in Majority of Angiosperms. Science, 264(5157), 421-424. doi:10.1126/science.264.5157.421 es_ES
dc.description.references Parisod, C., Holderegger, R., & Brochmann, C. (2010). Evolutionary consequences of autopolyploidy. New Phytologist, 186(1), 5-17. doi:10.1111/j.1469-8137.2009.03142.x es_ES
dc.description.references Blanc, G., & Wolfe, K. H. (2004). Widespread Paleopolyploidy in Model Plant Species Inferred from Age Distributions of Duplicate Genes[W]. The Plant Cell, 16(7), 1667-1678. doi:10.1105/tpc.021345 es_ES
dc.description.references Sémon, M., & Wolfe, K. H. (2007). Consequences of genome duplication. Current Opinion in Genetics & Development, 17(6), 505-512. doi:10.1016/j.gde.2007.09.007 es_ES
dc.description.references Inoue, J., Sato, Y., Sinclair, R., Tsukamoto, K., & Nishida, M. (2015). Rapid genome reshaping by multiple-gene loss after whole-genome duplication in teleost fish suggested by mathematical modeling. Proceedings of the National Academy of Sciences, 112(48), 14918-14923. doi:10.1073/pnas.1507669112 es_ES
dc.description.references Wolfe, K. H. (2001). Yesterday’s polyploids and the mystery of diploidization. Nature Reviews Genetics, 2(5), 333-341. doi:10.1038/35072009 es_ES
dc.description.references Kassahn, K. S., Dang, V. T., Wilkins, S. J., Perkins, A. C., & Ragan, M. A. (2009). Evolution of gene function and regulatory control after whole-genome duplication: Comparative analyses in vertebrates. Genome Research, 19(8), 1404-1418. doi:10.1101/gr.086827.108 es_ES
dc.description.references Wang, X., Jin, D., Wang, Z., Guo, H., Zhang, L., Wang, L., … Paterson, A. H. (2014). Telomere‐centric genome repatterning determines recurring chromosome number reductions during the evolution of eukaryotes. New Phytologist, 205(1), 378-389. doi:10.1111/nph.12985 es_ES
dc.description.references Glasauer, S. M. K., & Neuhauss, S. C. F. (2014). Whole-genome duplication in teleost fishes and its evolutionary consequences. Molecular Genetics and Genomics, 289(6), 1045-1060. doi:10.1007/s00438-014-0889-2 es_ES
dc.description.references Chester, M., Gallagher, J. P., Symonds, V. V., Cruz da Silva, A. V., Mavrodiev, E. V., Leitch, A. R., … Soltis, D. E. (2012). Extensive chromosomal variation in a recently formed natural allopolyploid species, Tragopogon miscellus (Asteraceae). Proceedings of the National Academy of Sciences, 109(4), 1176-1181. doi:10.1073/pnas.1112041109 es_ES
dc.description.references Gordon, J. L., Byrne, K. P., & Wolfe, K. H. (2011). Mechanisms of Chromosome Number Evolution in Yeast. PLoS Genetics, 7(7), e1002190. doi:10.1371/journal.pgen.1002190 es_ES
dc.description.references Dehal, P., & Boore, J. L. (2005). Two Rounds of Whole Genome Duplication in the Ancestral Vertebrate. PLoS Biology, 3(10), e314. doi:10.1371/journal.pbio.0030314 es_ES
dc.description.references Christoffels, A., Koh, E. G. L., Chia, J., Brenner, S., Aparicio, S., & Venkatesh, B. (2004). Fugu Genome Analysis Provides Evidence for a Whole-Genome Duplication Early During the Evolution of Ray-Finned Fishes. Molecular Biology and Evolution, 21(6), 1146-1151. doi:10.1093/molbev/msh114 es_ES
dc.description.references Vandepoele, K., De Vos, W., Taylor, J. S., Meyer, A., & Van de Peer, Y. (2004). Major events in the genome evolution of vertebrates: Paranome age and size differ considerably between ray-finned fishes and land vertebrates. Proceedings of the National Academy of Sciences, 101(6), 1638-1643. doi:10.1073/pnas.0307968100 es_ES
dc.description.references Leggatt, R. A., & Iwama, G. K. (2003). Occurrence of polyploidy in the fishes. Reviews in Fish Biology and Fisheries, 13(3), 237-246. doi:10.1023/b:rfbf.0000033049.00668.fe es_ES
dc.description.references COMBER, S. C. L., & SMITH, C. (2004). Polyploidy in fishes: patterns and processes. Biological Journal of the Linnean Society, 82(4), 431-442. doi:10.1111/j.1095-8312.2004.00330.x es_ES
dc.description.references Braasch, I., Gehrke, A. R., Smith, J. J., Kawasaki, K., Manousaki, T., Pasquier, J., … Catchen, J. (2016). The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons. Nature Genetics, 48(4), 427-437. doi:10.1038/ng.3526 es_ES
dc.description.references Bian, C., Hu, Y., Ravi, V., Kuznetsova, I. S., Shen, X., Mu, X., … Li, X. (2016). The Asian arowana (Scleropages formosus) genome provides new insights into the evolution of an early lineage of teleosts. Scientific Reports, 6(1). doi:10.1038/srep24501 es_ES
dc.description.references Lien, S., Koop, B. F., Sandve, S. R., Miller, J. R., Kent, M. P., Nome, T., … Davidson, W. S. (2016). The Atlantic salmon genome provides insights into rediploidization. Nature, 533(7602), 200-205. doi:10.1038/nature17164 es_ES
dc.description.references Blischak, P. D., Mabry, M. E., Conant, G. C., & Pires, J. C. (2018). Integrating Networks, Phylogenomics, and Population Genomics for the Study of Polyploidy. Annual Review of Ecology, Evolution, and Systematics, 49(1), 253-278. doi:10.1146/annurev-ecolsys-121415-032302 es_ES
dc.description.references Robertson, F. M., Gundappa, M. K., Grammes, F., Hvidsten, T. R., Redmond, A. K., Lien, S., … Macqueen, D. J. (2017). Lineage-specific rediploidization is a mechanism to explain time-lags between genome duplication and evolutionary diversification. Genome Biology, 18(1). doi:10.1186/s13059-017-1241-z es_ES
dc.description.references DUFOUR, S., WELTZIEN, F.-A., SEBERT, M.-E., LE BELLE, N., VIDAL, B., VERNIER, P., & PASQUALINI, C. (2005). Dopaminergic Inhibition of Reproduction in Teleost Fishes: Ecophysiological and Evolutionary Implications. Annals of the New York Academy of Sciences, 1040(1), 9-21. doi:10.1196/annals.1327.002 es_ES
dc.description.references Henkel, C. V., Burgerhout, E., de Wijze, D. L., Dirks, R. P., Minegishi, Y., Jansen, H. J., … van den Thillart, G. E. E. J. M. (2012). Primitive Duplicate Hox Clusters in the European Eel’s Genome. PLoS ONE, 7(2), e32231. doi:10.1371/journal.pone.0032231 es_ES
dc.description.references Lafont, A.-G., Rousseau, K., Tomkiewicz, J., & Dufour, S. (2016). Three nuclear and two membrane estrogen receptors in basal teleosts, Anguilla sp.: Identification, evolutionary history and differential expression regulation. General and Comparative Endocrinology, 235, 177-191. doi:10.1016/j.ygcen.2015.11.021 es_ES
dc.description.references Maugars, G., & Dufour, S. (2015). Demonstration of the Coexistence of Duplicated LH Receptors in Teleosts, and Their Origin in Ancestral Actinopterygians. PLOS ONE, 10(8), e0135184. doi:10.1371/journal.pone.0135184 es_ES
dc.description.references Morini, M., Pasquier, J., Dirks, R., van den Thillart, G., Tomkiewicz, J., Rousseau, K., … Lafont, A.-G. (2015). Duplicated Leptin Receptors in Two Species of Eel Bring New Insights into the Evolution of the Leptin System in Vertebrates. PLOS ONE, 10(5), e0126008. doi:10.1371/journal.pone.0126008 es_ES
dc.description.references Pasqualini, C., Weltzien, F.-A., Vidal, B., Baloche, S., Rouget, C., Gilles, N., … Dufour, S. (2009). Two Distinct Dopamine D2 Receptor Genes in the European Eel: Molecular Characterization, Tissue-Specific Transcription, and Regulation by Sex Steroids. Endocrinology, 150(3), 1377-1392. doi:10.1210/en.2008-0578 es_ES
dc.description.references Pasquier, J., Lafont, A.-G., Jeng, S.-R., Morini, M., Dirks, R., van den Thillart, G., … Dufour, S. (2012). Multiple Kisspeptin Receptors in Early Osteichthyans Provide New Insights into the Evolution of This Receptor Family. PLoS ONE, 7(11), e48931. doi:10.1371/journal.pone.0048931 es_ES
dc.description.references Rozenfeld, C., Butts, I. A. E., Tomkiewicz, J., Zambonino-Infante, J.-L., & Mazurais, D. (2016). Abundance of specific mRNA transcripts impacts hatching success in European eel, Anguilla anguilla L. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 191, 59-65. doi:10.1016/j.cbpa.2015.09.011 es_ES
dc.description.references Morini, M., Peñaranda, D. S., Vílchez, M. C., Nourizadeh-Lillabadi, R., Lafont, A.-G., Dufour, S., … Pérez, L. (2017). Nuclear and membrane progestin receptors in the European eel: Characterization and expression in vivo through spermatogenesis. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 207, 79-92. doi:10.1016/j.cbpa.2017.02.009 es_ES
dc.description.references Ravi, V., & Venkatesh, B. (2018). The Divergent Genomes of Teleosts. Annual Review of Animal Biosciences, 6(1), 47-68. doi:10.1146/annurev-animal-030117-014821 es_ES
dc.description.references Peña-Llopis, S., & Brugarolas, J. (2013). Simultaneous isolation of high-quality DNA, RNA, miRNA and proteins from tissues for genomic applications. Nature Protocols, 8(11), 2240-2255. doi:10.1038/nprot.2013.141 es_ES
dc.description.references Andrews S. FastQC: A quality control tool for high throughput sequence data. 2010. p. http://www.bioinformatics.babraham.ac.uk/projects/ es_ES
dc.description.references Bolger, A. M., Lohse, M., & Usadel, B. (2014). Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics, 30(15), 2114-2120. doi:10.1093/bioinformatics/btu170 es_ES
dc.description.references Haas, B. J., Papanicolaou, A., Yassour, M., Grabherr, M., Blood, P. D., Bowden, J., … Regev, A. (2013). De novo transcript sequence reconstruction from RNA-seq using the Trinity platform for reference generation and analysis. Nature Protocols, 8(8), 1494-1512. doi:10.1038/nprot.2013.084 es_ES
dc.description.references Howe, K., Clark, M. D., Torroja, C. F., Torrance, J., Berthelot, C., Muffato, M., … Matthews, L. (2013). The zebrafish reference genome sequence and its relationship to the human genome. Nature, 496(7446), 498-503. doi:10.1038/nature12111 es_ES
dc.description.references Kai, W., Kikuchi, K., Tohari, S., Chew, A. K., Tay, A., Fujiwara, A., … Venkatesh, B. (2011). Integration of the Genetic Map and Genome Assembly of Fugu Facilitates Insights into Distinct Features of Genome Evolution in Teleosts and Mammals. Genome Biology and Evolution, 3, 424-442. doi:10.1093/gbe/evr041 es_ES
dc.description.references Schartl, M., Walter, R. B., Shen, Y., Garcia, T., Catchen, J., Amores, A., … Warren, W. C. (2013). The genome of the platyfish, Xiphophorus maculatus, provides insights into evolutionary adaptation and several complex traits. Nature Genetics, 45(5), 567-572. doi:10.1038/ng.2604 es_ES
dc.description.references Nomura, K., Fujiwara, A., Iwasaki, Y., Nishiki, I., Matsuura, A., Ozaki, A., … Tanaka, H. (2018). Genetic parameters and quantitative trait loci analysis associated with body size and timing at metamorphosis into glass eels in captive-bred Japanese eels (Anguilla japonica). PLOS ONE, 13(8), e0201784. doi:10.1371/journal.pone.0201784 es_ES
dc.description.references Simão, F. A., Waterhouse, R. M., Ioannidis, P., Kriventseva, E. V., & Zdobnov, E. M. (2015). BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics, 31(19), 3210-3212. doi:10.1093/bioinformatics/btv351 es_ES
dc.description.references Pertea, M., Kim, D., Pertea, G. M., Leek, J. T., & Salzberg, S. L. (2016). Transcript-level expression analysis of RNA-seq experiments with HISAT, StringTie and Ballgown. Nature Protocols, 11(9), 1650-1667. doi:10.1038/nprot.2016.095 es_ES
dc.description.references Li, H., & Durbin, R. (2010). Fast and accurate long-read alignment with Burrows–Wheeler transform. Bioinformatics, 26(5), 589-595. doi:10.1093/bioinformatics/btp698 es_ES
dc.description.references Li, L. (2003). OrthoMCL: Identification of Ortholog Groups for Eukaryotic Genomes. Genome Research, 13(9), 2178-2189. doi:10.1101/gr.1224503 es_ES
dc.description.references Capella-Gutierrez, S., Silla-Martinez, J. M., & Gabaldon, T. (2009). trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics, 25(15), 1972-1973. doi:10.1093/bioinformatics/btp348 es_ES
dc.description.references Lartillot, N., Lepage, T., & Blanquart, S. (2009). PhyloBayes 3: a Bayesian software package for phylogenetic reconstruction and molecular dating. Bioinformatics, 25(17), 2286-2288. doi:10.1093/bioinformatics/btp368 es_ES
dc.description.references Huerta-Cepas, J., Szklarczyk, D., Forslund, K., Cook, H., Heller, D., Walter, M. C., … Bork, P. (2015). eggNOG 4.5: a hierarchical orthology framework with improved functional annotations for eukaryotic, prokaryotic and viral sequences. Nucleic Acids Research, 44(D1), D286-D293. doi:10.1093/nar/gkv1248 es_ES
dc.description.references Finn, R. D., Clements, J., & Eddy, S. R. (2011). HMMER web server: interactive sequence similarity searching. Nucleic Acids Research, 39(suppl), W29-W37. doi:10.1093/nar/gkr367 es_ES
dc.description.references Alexa A, Rahnenfuhrer J. topGO: Enrichment analysis for gene ontology. 2016. p. R package version 2.29.0. es_ES
dc.description.references Kanehisa, M., Sato, Y., & Morishima, K. (2016). BlastKOALA and GhostKOALA: KEGG Tools for Functional Characterization of Genome and Metagenome Sequences. Journal of Molecular Biology, 428(4), 726-731. doi:10.1016/j.jmb.2015.11.006 es_ES
dc.description.references Burgerhout, E., Minegishi, Y., Brittijn, S. A., de Wijze, D. L., Henkel, C. V., Jansen, H. J., … van den Thillart, G. E. E. J. M. (2016). Changes in ovarian gene expression profiles and plasma hormone levels in maturing European eel ( Anguilla anguilla ); Biomarkers for broodstock selection. General and Comparative Endocrinology, 225, 185-196. doi:10.1016/j.ygcen.2015.08.006 es_ES
dc.description.references Ager-Wick, E., Dirks, R. P., Burgerhout, E., Nourizadeh-Lillabadi, R., de Wijze, D. L., Spaink, H. P., … Henkel, C. V. (2013). The Pituitary Gland of the European Eel Reveals Massive Expression of Genes Involved in the Melanocortin System. PLoS ONE, 8(10), e77396. doi:10.1371/journal.pone.0077396 es_ES
dc.description.references Minegishi, Y., Aoyama, J., Inoue, J. G., Miya, M., Nishida, M., & Tsukamoto, K. (2005). Molecular phylogeny and evolution of the freshwater eels genus Anguilla based on the whole mitochondrial genome sequences. Molecular Phylogenetics and Evolution, 34(1), 134-146. doi:10.1016/j.ympev.2004.09.003 es_ES


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