- -

Two euAGAMOUS genes control C-function in Medicago truncatula

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

Two euAGAMOUS genes control C-function in Medicago truncatula

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Serwatowska, Joanna es_ES
dc.contributor.author Roque Mesa, Edelin Marta es_ES
dc.contributor.author Gómez Mena, María Concepción es_ES
dc.contributor.author Constantin, Gabriela D. es_ES
dc.contributor.author Wen, Jiangqi es_ES
dc.contributor.author Mysore, Kirankumar S. es_ES
dc.contributor.author Lund, Ole S. es_ES
dc.contributor.author Johansen, Elisabeth es_ES
dc.contributor.author Beltran Porter, Jose Pio es_ES
dc.contributor.author Cañas Clemente, Luís Antonio es_ES
dc.date.accessioned 2016-01-13T13:10:17Z
dc.date.available 2016-01-13T13:10:17Z
dc.date.issued 2014-08
dc.identifier.issn 1932-6203
dc.identifier.uri http://hdl.handle.net/10251/59846
dc.description.abstract [EN] C-function MADS-box transcription factors belong to the AGAMOUS (AG) lineage and specify both stamen and carpel identity and floral meristem determinacy. In core eudicots, the AG lineage is further divided into two branches, the euAG and PLE lineages. Functional analyses across flowering plants strongly support the idea that duplicated AG lineage genes have different degrees of subfunctionalization of the C-function. The legume Medicago truncatula contains three C-lineage genes in its genome: two euAG genes (MtAGa and MtAGb) and one PLENA-like gene (MtSHP). This species is therefore a good experimental system to study the effects of gene duplication within the AG subfamily. We have studied the respective functions of each euAG genes in M. truncatula employing expression analyses and reverse genetic approaches. Our results show that the M. truncatula euAG- and PLENA-like genes are an example of subfunctionalization as a result of a change in expression pattern. MtAGa and MtAGb are the only genes showing a full C-function activity, concomitant with their ancestral expression profile, early in the floral meristem, and in the third and fourth floral whorls during floral development. In contrast, MtSHP expression appears late during floral development suggesting it does not contribute significantly to the C-function. Furthermore, the redundant MtAGa and MtAGb paralogs have been retained which provides the overall dosage required to specify the C-function in M. truncatula. es_ES
dc.description.sponsorship This work was funded by grants BIO2009-08134 and BIO2012-39849-C02-01 from the Spanish Ministry of Economy and Competitiveness and the Ramon y Cajal Program (RYC-2007-00627 to CGM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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 AGAMOUS (AG) es_ES
dc.subject Legume Medicago truncatula es_ES
dc.title Two euAGAMOUS genes control C-function in Medicago truncatula es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1371/journal.pone.0103770
dc.relation.projectID info:eu-repo/grantAgreement/MICINN//BIO2009-08134/ES/Mejora Del Valor Nutritivo De La Alfalfa (Medicago Sativa L.) Mediante Ingenieria Genetica/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MINECO//BIO2012-39849-C02-01/ES/AISLAMIENTO Y CARACTERIZACION DE GENES QUE CONTROLAN CARACTERES DE INTERES AGRONOMICO EN LA ALFALFA (MEDICAGO SATIVA L.). DESARROLLO DE HERRAMIENTAS BIOTECNOLOGICAS./ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/MEC//RYC-2007-00627/ES/RYC-2007-00627/ 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.description.bibliographicCitation Serwatowska, J.; Roque Mesa, EM.; Gómez Mena, MC.; Constantin, GD.; Wen, J.; Mysore, KS.; Lund, OS.... (2014). Two euAGAMOUS genes control C-function in Medicago truncatula. PLoS ONE. 9(8):103770-1-103770-12. https://doi.org/10.1371/journal.pone.0103770 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.1371/journal.pone.0103770 es_ES
dc.description.upvformatpinicio 103770-1 es_ES
dc.description.upvformatpfin 103770-12 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 9 es_ES
dc.description.issue 8 es_ES
dc.relation.senia 285898 es_ES
dc.identifier.pmid 25105497 en_EN
dc.identifier.pmcid PMC4126672 en_EN
dc.contributor.funder Ministerio de Economía y Competitividad
dc.contributor.funder Ministerio de Ciencia e Innovación
dc.contributor.funder Ministerio de Educación y Ciencia es_ES
dc.description.references Prunet, N., & Jack, T. P. (2013). Flower Development in Arabidopsis: There Is More to It Than Learning Your ABCs. Flower Development, 3-33. doi:10.1007/978-1-4614-9408-9_1 es_ES
dc.description.references Causier, B., Schwarz-Sommer, Z., & Davies, B. (2010). Floral organ identity: 20 years of ABCs. Seminars in Cell & Developmental Biology, 21(1), 73-79. doi:10.1016/j.semcdb.2009.10.005 es_ES
dc.description.references Irish, V. F. (2010). The flowering of Arabidopsis flower development. The Plant Journal, 61(6), 1014-1028. doi:10.1111/j.1365-313x.2009.04065.x es_ES
dc.description.references Heijmans, K., Morel, P., & Vandenbussche, M. (2012). MADS-box Genes and Floral Development: the Dark Side. Journal of Experimental Botany, 63(15), 5397-5404. doi:10.1093/jxb/ers233 es_ES
dc.description.references Bowman, J. L., Smyth, D. R., & Meyerowitz, E. M. (1989). Genes directing flower development in Arabidopsis. The Plant Cell, 1(1), 37-52. doi:10.1105/tpc.1.1.37 es_ES
dc.description.references Yanofsky, M. F., Ma, H., Bowman, J. L., Drews, G. N., Feldmann, K. A., & Meyerowitz, E. M. (1990). The protein encoded by the Arabidopsis homeotic gene agamous resembles transcription factors. Nature, 346(6279), 35-39. doi:10.1038/346035a0 es_ES
dc.description.references Bradley, D., Carpenter, R., Sommer, H., Hartley, N., & Coen, E. (1993). Complementary floral homeotic phenotypes result from opposite orientations of a transposon at the plena locus of antirrhinum. Cell, 72(1), 85-95. doi:10.1016/0092-8674(93)90052-r es_ES
dc.description.references Pinyopich, A., Ditta, G. S., Savidge, B., Liljegren, S. J., Baumann, E., Wisman, E., & Yanofsky, M. F. (2003). Assessing the redundancy of MADS-box genes during carpel and ovule development. Nature, 424(6944), 85-88. doi:10.1038/nature01741 es_ES
dc.description.references Liljegren, S. J., Ditta, G. S., Eshed, Y., Savidge, B., Bowman, J. L., & Yanofsky, M. F. (2000). SHATTERPROOF MADS-box genes control seed dispersal in Arabidopsis. Nature, 404(6779), 766-770. doi:10.1038/35008089 es_ES
dc.description.references Davies, B., Motte, P., Keck, E., Saedler, H., Sommer, H., & Schwarz-Sommer, Z. (1999). PLENA and FARINELLI: redundancy and regulatory interactions between two Antirrhinum MADS-box factors controlling flower development. The EMBO Journal, 18(14), 4023-4034. doi:10.1093/emboj/18.14.4023 es_ES
dc.description.references Kramer, E. M., Jaramillo, M. A., & Di Stilio, V. S. (2004). Patterns of Gene Duplication and Functional Evolution During the Diversification of the AGAMOUS Subfamily of MADS Box Genes in Angiosperms. Genetics, 166(2), 1011-1023. doi:10.1534/genetics.166.2.1011 es_ES
dc.description.references Becker, A. (2003). The major clades of MADS-box genes and their role in the development and evolution of flowering plants. Molecular Phylogenetics and Evolution, 29(3), 464-489. doi:10.1016/s1055-7903(03)00207-0 es_ES
dc.description.references Irish, V. F. (2003). The evolution of floral homeotic gene function. BioEssays, 25(7), 637-646. doi:10.1002/bies.10292 es_ES
dc.description.references Zahn, L. M., Leebens-Mack, J. H., Arrington, J. M., Hu, Y., Landherr, L. L., dePamphilis, C. W., … Ma, H. (2006). Conservation and divergence in the AGAMOUS subfamily of MADS-box genes: evidence of independent sub- and neofunctionalization events. Evolution <html_ent glyph=«@amp;» ascii=«&amp;»/> Development, 8(1), 30-45. doi:10.1111/j.1525-142x.2006.05073.x es_ES
dc.description.references Ferrandiz, C. (2000). Negative Regulation of the SHATTERPROOF Genes by FRUITFULL During Arabidopsis Fruit Development. Science, 289(5478), 436-438. doi:10.1126/science.289.5478.436 es_ES
dc.description.references Ma, H., Yanofsky, M. F., & Meyerowitz, E. M. (1991). AGL1-AGL6, an Arabidopsis gene family with similarity to floral homeotic and transcription factor genes. Genes & Development, 5(3), 484-495. doi:10.1101/gad.5.3.484 es_ES
dc.description.references Savidge, B., Rounsley, S. D., & Yanofsky, M. F. (1995). Temporal relationship between the transcription of two Arabidopsis MADS box genes and the floral organ identity genes. The Plant Cell, 7(6), 721-733. doi:10.1105/tpc.7.6.721 es_ES
dc.description.references Colombo, M., Brambilla, V., Marcheselli, R., Caporali, E., Kater, M. M., & Colombo, L. (2010). A new role for the SHATTERPROOF genes during Arabidopsis gynoecium development. Developmental Biology, 337(2), 294-302. doi:10.1016/j.ydbio.2009.10.043 es_ES
dc.description.references Fourquin, C., & Ferrándiz, C. (2012). Functional analyses of AGAMOUS family members in Nicotiana benthamiana clarify the evolution of early and late roles of C-function genes in eudicots. The Plant Journal, 71(6), 990-1001. doi:10.1111/j.1365-313x.2012.05046.x es_ES
dc.description.references Kapoor, M., Tsuda, S., Tanaka, Y., Mayama, T., Okuyama, Y., Tsuchimoto, S., & Takatsuji, H. (2002). Role of petuniapMADS3in determination of floral organ and meristem identity, as revealed by its loss of function. The Plant Journal, 32(1), 115-127. doi:10.1046/j.1365-313x.2002.01402.x es_ES
dc.description.references Pan, I. L., McQuinn, R., Giovannoni, J. J., & Irish, V. F. (2010). Functional diversification of AGAMOUS lineage genes in regulating tomato flower and fruit development. Journal of Experimental Botany, 61(6), 1795-1806. doi:10.1093/jxb/erq046 es_ES
dc.description.references Pnueli, L., Hareven, D., Rounsley, S. D., Yanofsky, M. F., & Lifschitz, E. (1994). Isolation of the tomato AGAMOUS gene TAG1 and analysis of its homeotic role in transgenic plants. The Plant Cell, 6(2), 163-173. doi:10.1105/tpc.6.2.163 es_ES
dc.description.references Dreni, L., & Kater, M. M. (2013). MADSreloaded: evolution of theAGAMOUSsubfamily genes. New Phytologist, 201(3), 717-732. doi:10.1111/nph.12555 es_ES
dc.description.references Brunner, A. M. (2000). Plant Molecular Biology, 44(5), 619-634. doi:10.1023/a:1026550205851 es_ES
dc.description.references Perl-Treves, R., Kahana, A., Rosenman, N., Xiang, Y., & Silberstein, L. (1998). Expression of Multiple AGAMOUS-Like Genes in Male and Female Flowers of Cucumber (Cucumis sativus L.). Plant and Cell Physiology, 39(7), 701-710. doi:10.1093/oxfordjournals.pcp.a029424 es_ES
dc.description.references Yu, D., Kotilainen, M., Pöllänen, E., Mehto, M., Elomaa, P., Helariutta, Y., … Teeri, T. H. (1999). Organ identity genes and modified patterns of flower development in Gerbera hybrida (Asteraceae). The Plant Journal, 17(1), 51-62. doi:10.1046/j.1365-313x.1999.00351.x es_ES
dc.description.references Dong, Z., Zhao, Z., Liu, C., Luo, J., Yang, J., Huang, W., … Luo, D. (2005). Floral Patterning in Lotus japonicus. Plant Physiology, 137(4), 1272-1282. doi:10.1104/pp.104.054288 es_ES
dc.description.references Hofer, J. M., & Noel Ellis, T. (2014). Developmental specialisations in the legume family. Current Opinion in Plant Biology, 17, 153-158. doi:10.1016/j.pbi.2013.11.014 es_ES
dc.description.references Fourquin, C., del Cerro, C., Victoria, F. C., Vialette-Guiraud, A., de Oliveira, A. C., & Ferrándiz, C. (2013). A Change in SHATTERPROOF Protein Lies at the Origin of a Fruit Morphological Novelty and a New Strategy for Seed Dispersal in Medicago Genus. Plant Physiology, 162(2), 907-917. doi:10.1104/pp.113.217570 es_ES
dc.description.references Hewitt EJ (1966) Sand and Water Culture Methods Used in the Study of Plant Nutrition. Farnham Royal, UK: Commonwealth Agricultural Bureau. es_ES
dc.description.references Cheng, X., Wang, M., Lee, H.-K., Tadege, M., Ratet, P., Udvardi, M., … Wen, J. (2013). An efficient reverse genetics platform in the model legumeMedicago truncatula. New Phytologist, 201(3), 1065-1076. doi:10.1111/nph.12575 es_ES
dc.description.references D’ Erfurth, I., Cosson, V., Eschstruth, A., Lucas, H., Kondorosi, A., & Ratet, P. (2003). Efficient transposition of theTnt1tobacco retrotransposon in the model legumeMedicago truncatula. The Plant Journal, 34(1), 95-106. doi:10.1046/j.1365-313x.2003.01701.x es_ES
dc.description.references Tadege, M., Ratet, P., & Mysore, K. S. (2005). Insertional mutagenesis: a Swiss Army knife for functional genomics of Medicago truncatula. Trends in Plant Science, 10(5), 229-235. doi:10.1016/j.tplants.2005.03.009 es_ES
dc.description.references Tadege, M., Wen, J., He, J., Tu, H., Kwak, Y., Eschstruth, A., … Mysore, K. S. (2008). Large-scale insertional mutagenesis using the Tnt1 retrotransposon in the model legume Medicago truncatula. The Plant Journal, 54(2), 335-347. doi:10.1111/j.1365-313x.2008.03418.x es_ES
dc.description.references Cheng, X., Wen, J., Tadege, M., Ratet, P., & Mysore, K. S. (2010). Reverse Genetics in Medicago truncatula Using Tnt1 Insertion Mutants. Plant Reverse Genetics, 179-190. doi:10.1007/978-1-60761-682-5_13 es_ES
dc.description.references Benlloch, R., d’ Erfurth, I., Ferrandiz, C., Cosson, V., Beltrán, J. P., Cañas, L. A., … Ratet, P. (2006). Isolation of mtpim Proves Tnt1 a Useful Reverse Genetics Tool in Medicago truncatula and Uncovers New Aspects of AP1-Like Functions in Legumes. Plant Physiology, 142(3), 972-983. doi:10.1104/pp.106.083543 es_ES
dc.description.references Larkin, M. A., Blackshields, G., Brown, N. P., Chenna, R., McGettigan, P. A., McWilliam, H., … Higgins, D. G. (2007). Clustal W and Clustal X version 2.0. Bioinformatics, 23(21), 2947-2948. doi:10.1093/bioinformatics/btm404 es_ES
dc.description.references Altschul, S. (1997). Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Research, 25(17), 3389-3402. doi:10.1093/nar/25.17.3389 es_ES
dc.description.references Tamura, K., Dudley, J., Nei, M., & Kumar, S. (2007). MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0. Molecular Biology and Evolution, 24(8), 1596-1599. doi:10.1093/molbev/msm092 es_ES
dc.description.references Dellaporta, S. L., Wood, J., & Hicks, J. B. (1983). A plant DNA minipreparation: Version II. Plant Molecular Biology Reporter, 1(4), 19-21. doi:10.1007/bf02712670 es_ES
dc.description.references Schmittgen, T. D., & Livak, K. J. (2008). Analyzing real-time PCR data by the comparative CT method. Nature Protocols, 3(6), 1101-1108. doi:10.1038/nprot.2008.73 es_ES
dc.description.references Constantin, G. D., Krath, B. N., MacFarlane, S. A., Nicolaisen, M., Elisabeth Johansen, I., & Lund, O. S. (2004). Virus-induced gene silencing as a tool for functional genomics in a legume species. The Plant Journal, 40(4), 622-631. doi:10.1111/j.1365-313x.2004.02233.x es_ES
dc.description.references Wesley, S. V., Helliwell, C. A., Smith, N. A., Wang, M., Rouse, D. T., Liu, Q., … Waterhouse, P. M. (2001). Construct design for efficient, effective and high-throughput gene silencing in plants. The Plant Journal, 27(6), 581-590. doi:10.1046/j.1365-313x.2001.01105.x es_ES
dc.description.references Guerineau F, Mullineaux P (1993) Plant transformation and expression vectors. In: Croy R, editor. Plant Molecular Biology. Oxford, UK: Bios Scientific Publishers, Academic Press. pp. 121–147. es_ES
dc.description.references Clough, S. J., & Bent, A. F. (1998). Floral dip: a simplified method forAgrobacterium-mediated transformation ofArabidopsis thaliana. The Plant Journal, 16(6), 735-743. doi:10.1046/j.1365-313x.1998.00343.x es_ES
dc.description.references Benlloch, R., Roque, E., Ferrándiz, C., Cosson, V., Caballero, T., Penmetsa, R. V., … Madueño, F. (2009). Analysis of B function in legumes: PISTILLATA proteins do not require the PI motif for floral organ development inMedicago truncatula. The Plant Journal, 60(1), 102-111. doi:10.1111/j.1365-313x.2009.03939.x es_ES
dc.description.references Roque, E., Serwatowska, J., Cruz Rochina, M., Wen, J., Mysore, K. S., Yenush, L., … Cañas, L. A. (2012). Functional specialization of duplicated AP3-like genes inMedicago truncatula. The Plant Journal, 73(4), 663-675. doi:10.1111/tpj.12068 es_ES
dc.description.references Flanagan, C. A., Hu, Y., & Ma, H. (1996). Specific expression of the AGL1 MADS-box gene suggests regulatory functions in Arabidopsis gynoecium and ovule development. The Plant Journal, 10(2), 343-353. doi:10.1046/j.1365-313x.1996.10020343.x es_ES
dc.description.references Sieburth, L. E., & Meyerowitz, E. M. (1997). Molecular dissection of the AGAMOUS control region shows that cis elements for spatial regulation are located intragenically. The Plant Cell, 9(3), 355-365. doi:10.1105/tpc.9.3.355 es_ES
dc.description.references Busch, M. A. (1999). Activation of a Floral Homeotic Gene in Arabidopsis. Science, 285(5427), 585-587. doi:10.1126/science.285.5427.585 es_ES
dc.description.references Moyroud, E., Minguet, E. G., Ott, F., Yant, L., Posé, D., Monniaux, M., … Parcy, F. (2011). Prediction of Regulatory Interactions from Genome Sequences Using a Biophysical Model for the Arabidopsis LEAFY Transcription Factor. The Plant Cell, 23(4), 1293-1306. doi:10.1105/tpc.111.083329 es_ES
dc.description.references Grønlund, M., Constantin, G., Piednoir, E., Kovacev, J., Johansen, I. E., & Lund, O. S. (2008). Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata. Virus Research, 135(2), 345-349. doi:10.1016/j.virusres.2008.04.005 es_ES
dc.description.references Mandel, M. A., Bowman, J. L., Kempin, S. A., Ma, H., Meyerowitz, E. M., & Yanofsky, M. F. (1992). Manipulation of flower structure in transgenic tobacco. Cell, 71(1), 133-143. doi:10.1016/0092-8674(92)90272-e es_ES
dc.description.references Mizukami, Y., & Ma, H. (1992). Ectopic expression of the floral homeotic gene AGAMOUS in transgenic Arabidopsis plants alters floral organ identity. Cell, 71(1), 119-131. doi:10.1016/0092-8674(92)90271-d es_ES
dc.description.references Cannon, S. B., Sterck, L., Rombauts, S., Sato, S., Cheung, F., Gouzy, J., … Young, N. D. (2006). Legume genome evolution viewed through the Medicago truncatula and Lotus japonicus genomes. Proceedings of the National Academy of Sciences, 103(40), 14959-14964. doi:10.1073/pnas.0603228103 es_ES
dc.description.references Young, N. D., & Bharti, A. K. (2012). Genome-Enabled Insights into Legume Biology. Annual Review of Plant Biology, 63(1), 283-305. doi:10.1146/annurev-arplant-042110-103754 es_ES
dc.description.references Jager, M. (2003). MADS-Box Genes in Ginkgo biloba and the Evolution of the AGAMOUS Family. Molecular Biology and Evolution, 20(5), 842-854. doi:10.1093/molbev/msg089 es_ES
dc.description.references Johansen, B., Pedersen, L. B., Skipper, M., & Frederiksen, S. (2002). MADS-box gene evolution—structure and transcription patterns. Molecular Phylogenetics and Evolution, 23(3), 458-480. doi:10.1016/s1055-7903(02)00032-5 es_ES
dc.description.references Rutledge, R., Regan, S., Nicolas, O., Fobert, P., Côté, C., Bosnich, W., … Stewart, D. (1998). Characterization of an AGAMOUS homologue from the conifer black spruce ( Picea mariana ) that produces floral homeotic conversions when expressed in Arabidopsis. The Plant Journal, 15(5), 625-634. doi:10.1046/j.1365-313x.1998.00250.x es_ES
dc.description.references Parcy, F., Nilsson, O., Busch, M. A., Lee, I., & Weigel, D. (1998). A genetic framework for floral patterning. Nature, 395(6702), 561-566. doi:10.1038/26903 es_ES
dc.description.references Causier, B., Bradley, D., Cook, H., & Davies, B. (2009). Conserved intragenic elements were critical for the evolution of the floral C-function. The Plant Journal, 58(1), 41-52. doi:10.1111/j.1365-313x.2008.03759.x es_ES
dc.description.references Airoldi, C. A., & Davies, B. (2012). Gene Duplication and the Evolution of Plant MADS-box Transcription Factors. Journal of Genetics and Genomics, 39(4), 157-165. doi:10.1016/j.jgg.2012.02.008 es_ES
dc.description.references Giménez, E., Pineda, B., Capel, J., Antón, M. T., Atarés, A., Pérez-Martín, F., … Lozano, R. (2010). Functional Analysis of the Arlequin Mutant Corroborates the Essential Role of the ARLEQUIN/TAGL1 Gene during Reproductive Development of Tomato. PLoS ONE, 5(12), e14427. doi:10.1371/journal.pone.0014427 es_ES
dc.description.references Kater, M. M., Colombo, L., Franken, J., Busscher, M., Masiero, S., Van Lookeren Campagne, M. M., & Angenent, G. C. (1998). Multiple AGAMOUS Homologs from Cucumber and Petunia Differ in Their Ability to Induce Reproductive Organ Fate. The Plant Cell, 10(2), 171-182. doi:10.1105/tpc.10.2.171 es_ES
dc.description.references Tsuchimoto, S., van der Krol, A. R., & Chua, N. H. (1993). Ectopic expression of pMADS3 in transgenic petunia phenocopies the petunia blind mutant. The Plant Cell, 5(8), 843-853. doi:10.1105/tpc.5.8.843 es_ES
dc.description.references Airoldi, C. A., Bergonzi, S., & Davies, B. (2010). Single amino acid change alters the ability to specify male or female organ identity. Proceedings of the National Academy of Sciences, 107(44), 18898-18902. doi:10.1073/pnas.1009050107 es_ES
dc.description.references Causier, B., Castillo, R., Zhou, J., Ingram, R., Xue, Y., Schwarz-Sommer, Z., & Davies, B. (2005). Evolution in Action: Following Function in Duplicated Floral Homeotic Genes. Current Biology, 15(16), 1508-1512. doi:10.1016/j.cub.2005.07.063 es_ES
dc.description.references Birchler, J. A., & Veitia, R. A. (2007). The Gene Balance Hypothesis: From Classical Genetics to Modern Genomics. The Plant Cell, 19(2), 395-402. doi:10.1105/tpc.106.049338 es_ES
dc.description.references Birchler, J. A., & Veitia, R. A. (2009). The gene balance hypothesis: implications for gene regulation, quantitative traits and evolution. New Phytologist, 186(1), 54-62. doi:10.1111/j.1469-8137.2009.03087.x es_ES
dc.description.references Edger, P. P., & Pires, J. C. (2009). Gene and genome duplications: the impact of dosage-sensitivity on the fate of nuclear genes. Chromosome Research, 17(5), 699-717. doi:10.1007/s10577-009-9055-9 es_ES
dc.description.references Freeling, M. (2006). Gene-balanced duplications, like tetraploidy, provide predictable drive to increase morphological complexity. Genome Research, 16(7), 805-814. doi:10.1101/gr.3681406 es_ES


Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem