- -

A cross population between D. kaki and D. virginiana shows high variability for saline tolerance and improved salt stress tolerance

RiuNet: Repositorio Institucional de la Universidad Politécnica de Valencia

Compartir/Enviar a

Citas

Estadísticas

  • Estadisticas de Uso

A cross population between D. kaki and D. virginiana shows high variability for saline tolerance and improved salt stress tolerance

Mostrar el registro sencillo del ítem

Ficheros en el ítem

dc.contributor.author Gil Muñoz, Francisco es_ES
dc.contributor.author Pérez-Pérez, Juan Gabriel es_ES
dc.contributor.author Quiñones, Ana es_ES
dc.contributor.author Primo-Capella, Amparo es_ES
dc.contributor.author Cebolla Cornejo, Jaime es_ES
dc.contributor.author FORNER GINER, MARIA ANGELES es_ES
dc.contributor.author BADENES CATALA, MARISA es_ES
dc.contributor.author Naval Merino, María del Mar es_ES
dc.date.accessioned 2021-06-12T03:33:28Z
dc.date.available 2021-06-12T03:33:28Z
dc.date.issued 2020-02-25 es_ES
dc.identifier.issn 1932-6203 es_ES
dc.identifier.uri http://hdl.handle.net/10251/167857
dc.description.abstract [EN] Persimmon (Diospyros kaki Thunb.) production is facing important problems related to climate change in the Mediterranean areas. One of them is soil salinization caused by the decrease and change of the rainfall distribution. In this context, there is a need to develop cultivars adapted to the increasingly challenging soil conditions. In this study, a backcross between (D. kaki x D. virginiana) x D. kaki was conducted, to unravel the mechanism involved in salinity tolerance of persimmon. The backcross involved the two species most used as rootstock for persimmon production. Both species are clearly distinct in their level of tolerance to salinity. Variables related to growth, leaf gas exchange, leaf water relations and content of nutrients were significantly affected by saline stress in the backcross population. Water flow regulation appears as a mechanism of salt tolerance in persimmon via differences in water potential and transpiration rate, which reduces ion entrance in the plant. Genetic expression of eight putative orthologous genes involved in different mechanisms leading to salt tolerance was analyzed. Differences in expression levels among populations under saline or control treatment were found. The 'High affinity potassium transporter' (HKT1-like) reduced its expression levels in the roots in all studied populations. Results obtained allowed selection of tolerant rootstocks genotypes and describe the hypothesis about the mechanisms involved in salt tolerance in persimmon that will be useful for breeding salinity tolerant rootstocks. es_ES
dc.description.sponsorship This study was funded by the IVIA and the European Funds for Regional Development. F. G.M.was funded by a PhD fellowship from the European Social Fund and the Generalitat Valenciana (ACIF/2016/115). 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 Salinity es_ES
dc.subject Leaves es_ES
dc.subject Membrane proteins es_ES
dc.subject Photosynthesis es_ES
dc.subject Proline es_ES
dc.subject Gene expression es_ES
dc.subject Osmotic shock es_ES
dc.subject Principal Component Analysis es_ES
dc.subject.classification GENETICA es_ES
dc.title A cross population between D. kaki and D. virginiana shows high variability for saline tolerance and improved salt stress tolerance es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1371/journal.pone.0229023 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/GVA//ACIF%2F2016%2F115/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia es_ES
dc.description.bibliographicCitation Gil Muñoz, F.; Pérez-Pérez, JG.; Quiñones, A.; Primo-Capella, A.; Cebolla Cornejo, J.; Forner Giner, MA.; Badenes Catala, M.... (2020). A cross population between D. kaki and D. virginiana shows high variability for saline tolerance and improved salt stress tolerance. PLoS ONE. 15(2):1-27. https://doi.org/10.1371/journal.pone.0229023 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion https://doi.org/10.1371/journal.pone.0229023 es_ES
dc.description.upvformatpinicio 1 es_ES
dc.description.upvformatpfin 27 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 15 es_ES
dc.description.issue 2 es_ES
dc.identifier.pmid 32097425 es_ES
dc.identifier.pmcid PMC7041798 es_ES
dc.relation.pasarela S\403820 es_ES
dc.contributor.funder European Social Fund es_ES
dc.contributor.funder Generalitat Valenciana es_ES
dc.contributor.funder European Regional Development Fund es_ES
dc.contributor.funder Institut Valencià d'Investigacions Agràries es_ES
dc.description.references Visconti, F., de Paz, J. M., Bonet, L., Jordà, M., Quiñones, A., & Intrigliolo, D. S. (2015). Effects of a commercial calcium protein hydrolysate on the salt tolerance of Diospyros kaki L. cv. «Rojo Brillante» grafted on Diospyros lotus L. Scientia Horticulturae, 185, 129-138. doi:10.1016/j.scienta.2015.01.028 es_ES
dc.description.references Forner-Giner, M. A., & Ancillo, G. (2013). Breeding Salinity Tolerance in Citrus Using Rootstocks. Salt Stress in Plants, 355-376. doi:10.1007/978-1-4614-6108-1_14 es_ES
dc.description.references Visconti, F., Intrigliolo, D. S., Quiñones, A., Tudela, L., Bonet, L., & de Paz, J. M. (2017). Differences in specific chloride toxicity to Diospyros kaki cv. «Rojo Brillante» grafted on D. lotus and D. virginiana. Scientia Horticulturae, 214, 83-90. doi:10.1016/j.scienta.2016.11.025 es_ES
dc.description.references INCESU, M., CIMEN, B., YESILOGLU, T., & YILMAZ, B. (2014). Growth and Photosynthetic Response of Two Persimmon Rootstocks (Diospyros kaki and D. virginiana) under Different Salinity Levels. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 42(2), 386-391. doi:10.15835/nbha4229471 es_ES
dc.description.references De Paz, J. M., Visconti, F., Chiaravalle, M., & Quiñones, A. (2016). Determination of persimmon leaf chloride contents using near-infrared spectroscopy (NIRS). Analytical and Bioanalytical Chemistry, 408(13), 3537-3545. doi:10.1007/s00216-016-9430-2 es_ES
dc.description.references Gil-Muñoz, F., Peche, P. M., Climent, J., Forner, M. A., Naval, M. M., & Badenes, M. L. (2018). Breeding and screening persimmon rootstocks for saline stress tolerance. Acta Horticulturae, (1195), 105-110. doi:10.17660/actahortic.2018.1195.18 es_ES
dc.description.references Besada, C., Gil, R., Bonet, L., Quiñones, A., Intrigliolo, D., & Salvador, A. (2016). Chloride stress triggers maturation and negatively affects the postharvest quality of persimmon fruit. Involvement of calyx ethylene production. Plant Physiology and Biochemistry, 100, 105-112. doi:10.1016/j.plaphy.2016.01.006 es_ES
dc.description.references Acosta-Motos, J., Ortuño, M., Bernal-Vicente, A., Diaz-Vivancos, P., Sanchez-Blanco, M., & Hernandez, J. (2017). Plant Responses to Salt Stress: Adaptive Mechanisms. Agronomy, 7(1), 18. doi:10.3390/agronomy7010018 es_ES
dc.description.references Munns, R., & Tester, M. (2008). Mechanisms of Salinity Tolerance. Annual Review of Plant Biology, 59(1), 651-681. doi:10.1146/annurev.arplant.59.032607.092911 es_ES
dc.description.references Sibole, J. V., Cabot, C., Poschenrieder, C., & Barceló, J. (2003). Ion allocation in two different salt-tolerant MediterraneanMedicagospecies. Journal of Plant Physiology, 160(11), 1361-1365. doi:10.1078/0176-1617-00811 es_ES
dc.description.references CRAIG PLETT, D., & MØLLER, I. S. (2010). Na+transport in glycophytic plants: what we know and would like to know. Plant, Cell & Environment, 33(4), 612-626. doi:10.1111/j.1365-3040.2009.02086.x es_ES
dc.description.references SHAPIRA, O., KHADKA, S., ISRAELI, Y., SHANI, U., & SCHWARTZ, A. (2009). Functional anatomy controls ion distribution in banana leaves: significance of Na+seclusion at the leaf margins. Plant, Cell & Environment, 32(5), 476-485. doi:10.1111/j.1365-3040.2009.01941.x es_ES
dc.description.references Huang, C. X., & Van Steveninck, R. F. M. (1989). Maintenance of Low Cl− Concentrations in Mesophyll Cells of Leaf Blades of Barley Seedlings Exposed to Salt Stress. Plant Physiology, 90(4), 1440-1443. doi:10.1104/pp.90.4.1440 es_ES
dc.description.references Karley, A. J., Leigh, R. A., & Sanders, D. (2000). Differential Ion Accumulation and Ion Fluxes in the Mesophyll and Epidermis of Barley. Plant Physiology, 122(3), 835-844. doi:10.1104/pp.122.3.835 es_ES
dc.description.references Karley, A. J., Leigh, R. A., & Sanders, D. (2000). Where do all the ions go? The cellular basis of differential ion accumulation in leaf cells. Trends in Plant Science, 5(11), 465-470. doi:10.1016/s1360-1385(00)01758-1 es_ES
dc.description.references JAMES, R. A., MUNNS, R., VON CAEMMERER, S., TREJO, C., MILLER, C., & CONDON, T. (A. G. . (2006). Photosynthetic capacity is related to the cellular and subcellular partitioning of Na+, K+and Cl-in salt-affected barley and durum wheat. Plant, Cell and Environment, 29(12), 2185-2197. doi:10.1111/j.1365-3040.2006.01592.x es_ES
dc.description.references Zekri, M., & Parsons, L. R. (1989). Growth and root hydraulic conductivity of several citrus rootstocks under salt and polyethylene glycol stresses. Physiologia Plantarum, 77(1), 99-106. doi:10.1111/j.1399-3054.1989.tb05984.x es_ES
dc.description.references Joly, R. J. (1989). Effects of Sodium Chloride on the Hydraulic Conductivity of Soybean Root Systems. Plant Physiology, 91(4), 1262-1265. doi:10.1104/pp.91.4.1262 es_ES
dc.description.references Maurel, C., Verdoucq, L., Luu, D.-T., & Santoni, V. (2008). Plant Aquaporins: Membrane Channels with Multiple Integrated Functions. Annual Review of Plant Biology, 59(1), 595-624. doi:10.1146/annurev.arplant.59.032607.092734 es_ES
dc.description.references Johanson, U., Karlsson, M., Johansson, I., Gustavsson, S., Sjövall, S., Fraysse, L., … Kjellbom, P. (2001). The Complete Set of Genes Encoding Major Intrinsic Proteins in Arabidopsis Provides a Framework for a New Nomenclature for Major Intrinsic Proteins in Plants. Plant Physiology, 126(4), 1358-1369. doi:10.1104/pp.126.4.1358 es_ES
dc.description.references Carmen Martínez-Ballesta, M., Aparicio, F., Pallás, V., Martínez, V., & Carvajal, M. (2003). Influence of saline stress on root hydraulic conductance and PIP expression inArabidopsis. Journal of Plant Physiology, 160(6), 689-697. doi:10.1078/0176-1617-00861 es_ES
dc.description.references Boursiac, Y., Chen, S., Luu, D.-T., Sorieul, M., van den Dries, N., & Maurel, C. (2005). Early Effects of Salinity on Water Transport in Arabidopsis Roots. Molecular and Cellular Features of Aquaporin Expression. Plant Physiology, 139(2), 790-805. doi:10.1104/pp.105.065029 es_ES
dc.description.references López-Pérez, L., Martínez-Ballesta, M. del C., Maurel, C., & Carvajal, M. (2009). Changes in plasma membrane lipids, aquaporins and proton pump of broccoli roots, as an adaptation mechanism to salinity. Phytochemistry, 70(4), 492-500. doi:10.1016/j.phytochem.2009.01.014 es_ES
dc.description.references Rodríguez-Gamir, J., Ancillo, G., Legaz, F., Primo-Millo, E., & Forner-Giner, M. A. (2012). Influence of salinity on pip gene expression in citrus roots and its relationship with root hydraulic conductance, transpiration and chloride exclusion from leaves. Environmental and Experimental Botany, 78, 163-166. doi:10.1016/j.envexpbot.2011.12.027 es_ES
dc.description.references Chaumont, F., & Tyerman, S. D. (2014). Aquaporins: Highly Regulated Channels Controlling Plant Water Relations. Plant Physiology, 164(4), 1600-1618. doi:10.1104/pp.113.233791 es_ES
dc.description.references Amtmann, A., & Sanders, D. (1998). Mechanisms of Na+ Uptake by Plant Cells. Advances in Botanical Research, 75-112. doi:10.1016/s0065-2296(08)60310-9 es_ES
dc.description.references TESTER, M. (2003). Na+ Tolerance and Na+ Transport in Higher Plants. Annals of Botany, 91(5), 503-527. doi:10.1093/aob/mcg058 es_ES
dc.description.references Qiu, Q.-S., Barkla, B. J., Vera-Estrella, R., Zhu, J.-K., & Schumaker, K. S. (2003). Na+/H+ Exchange Activity in the Plasma Membrane of Arabidopsis. Plant Physiology, 132(2), 1041-1052. doi:10.1104/pp.102.010421 es_ES
dc.description.references Shi, H., Quintero, F. J., Pardo, J. M., & Zhu, J.-K. (2002). The Putative Plasma Membrane Na+/H+ Antiporter SOS1 Controls Long-Distance Na+ Transport in Plants. The Plant Cell, 14(2), 465-477. doi:10.1105/tpc.010371 es_ES
dc.description.references Zhu, J.-K., Liu, J., & Xiong, L. (1998). Genetic Analysis of Salt Tolerance in Arabidopsis: Evidence for a Critical Role of Potassium Nutrition. The Plant Cell, 10(7), 1181-1191. doi:10.1105/tpc.10.7.1181 es_ES
dc.description.references Liu, J., & Zhu, J.-K. (1998). A Calcium Sensor Homolog Required for Plant Salt Tolerance. Science, 280(5371), 1943-1945. doi:10.1126/science.280.5371.1943 es_ES
dc.description.references Halfter, U., Ishitani, M., & Zhu, J.-K. (2000). The Arabidopsis SOS2 protein kinase physically interacts with and is activated by the calcium-binding protein SOS3. Proceedings of the National Academy of Sciences, 97(7), 3735-3740. doi:10.1073/pnas.97.7.3735 es_ES
dc.description.references Liu, J., Ishitani, M., Halfter, U., Kim, C.-S., & Zhu, J.-K. (2000). The Arabidopsis thaliana SOS2 gene encodes a protein kinase that is required for salt tolerance. Proceedings of the National Academy of Sciences, 97(7), 3730-3734. doi:10.1073/pnas.97.7.3730 es_ES
dc.description.references Hrabak, E. M., Chan, C. W. M., Gribskov, M., Harper, J. F., Choi, J. H., Halford, N., … Harmon, A. C. (2003). The Arabidopsis CDPK-SnRK Superfamily of Protein Kinases. Plant Physiology, 132(2), 666-680. doi:10.1104/pp.102.011999 es_ES
dc.description.references Shi, H., Ishitani, M., Kim, C., & Zhu, J.-K. (2000). The Arabidopsis thaliana salt tolerance gene SOS1 encodes a putative Na+/H+ antiporter. Proceedings of the National Academy of Sciences, 97(12), 6896-6901. doi:10.1073/pnas.120170197 es_ES
dc.description.references Qiu, Q.-S., Guo, Y., Dietrich, M. A., Schumaker, K. S., & Zhu, J.-K. (2002). Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3. Proceedings of the National Academy of Sciences, 99(12), 8436-8441. doi:10.1073/pnas.122224699 es_ES
dc.description.references Quintero, F. J., Ohta, M., Shi, H., Zhu, J.-K., & Pardo, J. M. (2002). Reconstitution in yeast of the Arabidopsis SOS signaling pathway for Na+ homeostasis. Proceedings of the National Academy of Sciences, 99(13), 9061-9066. doi:10.1073/pnas.132092099 es_ES
dc.description.references Quan, R., Lin, H., Mendoza, I., Zhang, Y., Cao, W., Yang, Y., … Guo, Y. (2007). SCABP8/CBL10, a Putative Calcium Sensor, Interacts with the Protein Kinase SOS2 to Protect Arabidopsis Shoots from Salt Stress. The Plant Cell, 19(4), 1415-1431. doi:10.1105/tpc.106.042291 es_ES
dc.description.references Quintero, F. J., Martinez-Atienza, J., Villalta, I., Jiang, X., Kim, W.-Y., Ali, Z., … Pardo, J. M. (2011). Activation of the plasma membrane Na/H antiporter Salt-Overly-Sensitive 1 (SOS1) by phosphorylation of an auto-inhibitory C-terminal domain. Proceedings of the National Academy of Sciences, 108(6), 2611-2616. doi:10.1073/pnas.1018921108 es_ES
dc.description.references Ji, H., Pardo, J. M., Batelli, G., Van Oosten, M. J., Bressan, R. A., & Li, X. (2013). The Salt Overly Sensitive (SOS) Pathway: Established and Emerging Roles. Molecular Plant, 6(2), 275-286. doi:10.1093/mp/sst017 es_ES
dc.description.references Isayenkov, S. V., & Maathuis, F. J. M. (2019). Plant Salinity Stress: Many Unanswered Questions Remain. Frontiers in Plant Science, 10. doi:10.3389/fpls.2019.00080 es_ES
dc.description.references Evans, A. R., Hall, D., Pritchard, J., & Newbury, H. J. (2011). The roles of the cation transporters CHX21 and CHX23 in the development of Arabidopsis thaliana. Journal of Experimental Botany, 63(1), 59-67. doi:10.1093/jxb/err271 es_ES
dc.description.references Uozumi, N., Kim, E. J., Rubio, F., Yamaguchi, T., Muto, S., Tsuboi, A., … Schroeder, J. I. (2000). The Arabidopsis HKT1 Gene Homolog Mediates Inward Na+ Currents in Xenopus laevis Oocytes and Na+ Uptake in Saccharomyces cerevisiae  . Plant Physiology, 122(4), 1249-1260. doi:10.1104/pp.122.4.1249 es_ES
dc.description.references Mäser, P., Eckelman, B., Vaidyanathan, R., Horie, T., Fairbairn, D. J., Kubo, M., … Schroeder, J. I. (2002). Altered shoot/root Na+ distribution and bifurcating salt sensitivity in Arabidopsis by genetic disruption of the Na+ transporter AtHKT1. FEBS Letters, 531(2), 157-161. doi:10.1016/s0014-5793(02)03488-9 es_ES
dc.description.references Berthomieu, P. (2003). Functional analysis of AtHKT1 in Arabidopsis shows that Na+ recirculation by the phloem is crucial for salt tolerance. The EMBO Journal, 22(9), 2004-2014. doi:10.1093/emboj/cdg207 es_ES
dc.description.references Rus, A., Lee, B., Muñoz-Mayor, A., Sharkhuu, A., Miura, K., Zhu, J.-K., … Hasegawa, P. M. (2004). AtHKT1 Facilitates Na+ Homeostasis and K+ Nutrition in Planta. Plant Physiology, 136(1), 2500-2511. doi:10.1104/pp.104.042234 es_ES
dc.description.references Sunarpi, Horie, T., Motoda, J., Kubo, M., Yang, H., Yoda, K., … Uozumi, N. (2005). Enhanced salt tolerance mediated by AtHKT1 transporter-induced Na+ unloading from xylem vessels to xylem parenchyma cells. The Plant Journal, 44(6), 928-938. doi:10.1111/j.1365-313x.2005.02595.x es_ES
dc.description.references Huang, S., Spielmeyer, W., Lagudah, E. S., James, R. A., Platten, J. D., Dennis, E. S., & Munns, R. (2006). A Sodium Transporter (HKT7) Is a Candidate forNax1, a Gene for Salt Tolerance in Durum Wheat. Plant Physiology, 142(4), 1718-1727. doi:10.1104/pp.106.088864 es_ES
dc.description.references Byrt, C. S., Platten, J. D., Spielmeyer, W., James, R. A., Lagudah, E. S., Dennis, E. S., … Munns, R. (2007). HKT1;5-Like Cation Transporters Linked to Na+ Exclusion Loci in Wheat, Nax2 and Kna1. Plant Physiology, 143(4), 1918-1928. doi:10.1104/pp.106.093476 es_ES
dc.description.references Garciadeblás, B., Senn, M. E., Bañuelos, M. A., & Rodríguez-Navarro, A. (2003). Sodium transport and HKT transporters: the rice model. The Plant Journal, 34(6), 788-801. doi:10.1046/j.1365-313x.2003.01764.x es_ES
dc.description.references Huang, S., Spielmeyer, W., Lagudah, E. S., & Munns, R. (2008). Comparative mapping of HKT genes in wheat, barley, and rice, key determinants of Na+ transport, and salt tolerance. Journal of Experimental Botany, 59(4), 927-937. doi:10.1093/jxb/ern033 es_ES
dc.description.references Horie, T., Costa, A., Kim, T. H., Han, M. J., Horie, R., Leung, H.-Y., … Schroeder, J. I. (2007). Rice OsHKT2;1 transporter mediates large Na+ influx component into K+-starved roots for growth. The EMBO Journal, 26(12), 3003-3014. doi:10.1038/sj.emboj.7601732 es_ES
dc.description.references Almeida, P., Katschnig, D., & de Boer, A. (2013). HKT Transporters—State of the Art. International Journal of Molecular Sciences, 14(10), 20359-20385. doi:10.3390/ijms141020359 es_ES
dc.description.references Cellier, F., Conéjéro, G., Ricaud, L., Luu, D. T., Lepetit, M., Gosti, F., & Casse, F. (2004). Characterization ofAtCHX17, a member of the cation/H+exchangers, CHX family, fromArabidopsis thalianasuggests a role in K+homeostasis. The Plant Journal, 39(6), 834-846. doi:10.1111/j.1365-313x.2004.02177.x es_ES
dc.description.references Song, C.-P., Guo, Y., Qiu, Q., Lambert, G., Galbraith, D. W., Jagendorf, A., & Zhu, J.-K. (2004). A probable Na+(K+)/H+ exchanger on the chloroplast envelope functions in pH homeostasis and chloroplast development in Arabidopsis thaliana. Proceedings of the National Academy of Sciences, 101(27), 10211-10216. doi:10.1073/pnas.0403709101 es_ES
dc.description.references Padmanaban, S., Chanroj, S., Kwak, J. M., Li, X., Ward, J. M., & Sze, H. (2007). Participation of Endomembrane Cation/H+ Exchanger AtCHX20 in Osmoregulation of Guard Cells. Plant Physiology, 144(1), 82-93. doi:10.1104/pp.106.092155 es_ES
dc.description.references Szczerba, M. W., Britto, D. T., & Kronzucker, H. J. (2009). K+ transport in plants: Physiology and molecular biology. Journal of Plant Physiology, 166(5), 447-466. doi:10.1016/j.jplph.2008.12.009 es_ES
dc.description.references Brini, F., Gaxiola, R. A., Berkowitz, G. A., & Masmoudi, K. (2005). Cloning and characterization of a wheat vacuolar cation/proton antiporter and pyrophosphatase proton pump. Plant Physiology and Biochemistry, 43(4), 347-354. doi:10.1016/j.plaphy.2005.02.010 es_ES
dc.description.references Barragán, V., Leidi, E. O., Andrés, Z., Rubio, L., De Luca, A., Fernández, J. A., … Pardo, J. M. (2012). Ion Exchangers NHX1 and NHX2 Mediate Active Potassium Uptake into Vacuoles to Regulate Cell Turgor and Stomatal Function in Arabidopsis. The Plant Cell, 24(3), 1127-1142. doi:10.1105/tpc.111.095273 es_ES
dc.description.references Barbier-Brygoo, H., De Angeli, A., Filleur, S., Frachisse, J.-M., Gambale, F., Thomine, S., & Wege, S. (2011). Anion Channels/Transporters in Plants: From Molecular Bases to Regulatory Networks. Annual Review of Plant Biology, 62(1), 25-51. doi:10.1146/annurev-arplant-042110-103741 es_ES
dc.description.references Apse, M. P., Aharon, G. S., Snedden, W. A., & Blumwald, E. (1999). Salt Tolerance Conferred by Overexpression of a Vacuolar Na + /H + Antiport in Arabidopsis. Science, 285(5431), 1256-1258. doi:10.1126/science.285.5431.1256 es_ES
dc.description.references Gaxiola, R. A., Li, J., Undurraga, S., Dang, L. M., Allen, G. J., Alper, S. L., & Fink, G. R. (2001). Drought- and salt-tolerant plants result from overexpression of the AVP1 H+-pump. Proceedings of the National Academy of Sciences, 98(20), 11444-11449. doi:10.1073/pnas.191389398 es_ES
dc.description.references Callister, A. N., Arndt, S. K., & Adams, M. A. (2006). Comparison of four methods for measuring osmotic potential of tree leaves. Physiologia Plantarum, 127(3), 383-392. doi:10.1111/j.1399-3054.2006.00652.x es_ES
dc.description.references Bates, L. S., Waldren, R. P., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39(1), 205-207. doi:10.1007/bf00018060 es_ES
dc.description.references Gilliam, J. W. (1971). Rapid Measurement of Chlorine in Plant Materials. Soil Science Society of America Journal, 35(3), 512-513. doi:10.2136/sssaj1971.03615995003500030051x es_ES
dc.description.references Gambino, G., Perrone, I., & Gribaudo, I. (2008). A Rapid and effective method for RNA extraction from different tissues of grapevine and other woody plants. Phytochemical Analysis, 19(6), 520-525. doi:10.1002/pca.1078 es_ES
dc.description.references Akagi, T., Henry, I. M., Kawai, T., Comai, L., & Tao, R. (2016). Epigenetic Regulation of the Sex Determination Gene MeGI in Polyploid Persimmon. The Plant Cell, 28(12), 2905-2915. doi:10.1105/tpc.16.00532 es_ES
dc.description.references Andersen, C. L., Jensen, J. L., & Ørntoft, T. F. (2004). Normalization of Real-Time Quantitative Reverse Transcription-PCR Data: A Model-Based Variance Estimation Approach to Identify Genes Suited for Normalization, Applied to Bladder and Colon Cancer Data Sets. Cancer Research, 64(15), 5245-5250. doi:10.1158/0008-5472.can-04-0496 es_ES
dc.description.references Akagi, T., Ikegami, A., Tsujimoto, T., Kobayashi, S., Sato, A., Kono, A., & Yonemori, K. (2009). DkMyb4 Is a Myb Transcription Factor Involved in Proanthocyanidin Biosynthesis in Persimmon Fruit. Plant Physiology, 151(4), 2028-2045. doi:10.1104/pp.109.146985 es_ES
dc.description.references Chambers, J. M., Cleveland, W. S., Kleiner, B., & Tukey, P. A. (2018). Graphical Methods for Data Analysis. doi:10.1201/9781351072304 es_ES
dc.description.references Flowers, T. J., & Colmer, T. D. (2008). Salinity tolerance in halophytes*. New Phytologist, 179(4), 945-963. doi:10.1111/j.1469-8137.2008.02531.x es_ES
dc.description.references Munns, R. (2002). Comparative physiology of salt and water stress. Plant, Cell & Environment, 25(2), 239-250. doi:10.1046/j.0016-8025.2001.00808.x es_ES
dc.description.references Brugnoli, E., & Lauteri, M. (1991). Effects of Salinity on Stomatal Conductance, Photosynthetic Capacity, and Carbon Isotope Discrimination of Salt-Tolerant (Gossypium hirsutum L.) and Salt-Sensitive (Phaseolus vulgaris L.) C3 Non-Halophytes. Plant Physiology, 95(2), 628-635. doi:10.1104/pp.95.2.628 es_ES
dc.description.references Koyro, H.-W. (2006). Effect of salinity on growth, photosynthesis, water relations and solute composition of the potential cash crop halophyte Plantago coronopus (L.). Environmental and Experimental Botany, 56(2), 136-146. doi:10.1016/j.envexpbot.2005.02.001 es_ES
dc.description.references Rahnama, A., James, R. A., Poustini, K., & Munns, R. (2010). Stomatal conductance as a screen for osmotic stress tolerance in durum wheat growing in saline soil. Functional Plant Biology, 37(3), 255. doi:10.1071/fp09148 es_ES
dc.description.references Zhu, X., Cao, Q., Sun, L., Yang, X., Yang, W., & Zhang, H. (2018). Stomatal Conductance and Morphology of Arbuscular Mycorrhizal Wheat Plants Response to Elevated CO2 and NaCl Stress. Frontiers in Plant Science, 9. doi:10.3389/fpls.2018.01363 es_ES
dc.description.references Horie, T., Sugawara, M., Okunou, K., Nakayama, H., Schroeder, J. I., Shinmyo, A., & Yoshida, K. (2008). Functions of HKT transporters in sodium transport in roots and in protecting leaves from salinity stress. Plant Biotechnology, 25(3), 233-239. doi:10.5511/plantbiotechnology.25.233 es_ES
dc.description.references Hazzouri, K. M., Khraiwesh, B., Amiri, K. M. A., Pauli, D., Blake, T., Shahid, M., … Masmoudi, K. (2018). Mapping of HKT1;5 Gene in Barley Using GWAS Approach and Its Implication in Salt Tolerance Mechanism. Frontiers in Plant Science, 9. doi:10.3389/fpls.2018.00156 es_ES
dc.description.references Han, Y., Yin, S., Huang, L., Wu, X., Zeng, J., Liu, X., … Zhang, G. (2018). A Sodium Transporter HvHKT1;1 Confers Salt Tolerance in Barley via Regulating Tissue and Cell Ion Homeostasis. Plant and Cell Physiology, 59(10), 1976-1989. doi:10.1093/pcp/pcy116 es_ES
dc.description.references Henderson, S. W., Baumann, U., Blackmore, D. H., Walker, A. R., Walker, R. R., & Gilliham, M. (2014). Shoot chloride exclusion and salt tolerance in grapevine is associated with differential ion transporter expression in roots. BMC Plant Biology, 14(1). doi:10.1186/s12870-014-0273-8 es_ES
dc.description.references Vitali, V., Bellati, J., Soto, G., Ayub, N. D., & Amodeo, G. (2015). Root hydraulic conductivity and adjustments in stomatal conductance: hydraulic strategy in response to salt stress in a halotolerant species. AoB Plants, 7, plv136. doi:10.1093/aobpla/plv136 es_ES
dc.subject.ods 02.- Poner fin al hambre, conseguir la seguridad alimentaria y una mejor nutrición, y promover la agricultura sostenible es_ES


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

Mostrar el registro sencillo del ítem