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BvCOLD1: A novel aquaporin from sugar beet (Beta vulgaris L.) involved in boron homeostasis and abiotic stress

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BvCOLD1: A novel aquaporin from sugar beet (Beta vulgaris L.) involved in boron homeostasis and abiotic stress

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Porcel, R.; Bustamante-González, AJ.; Ros, R.; Serrano Salom, R.; Mulet, JM. (2018). BvCOLD1: A novel aquaporin from sugar beet (Beta vulgaris L.) involved in boron homeostasis and abiotic stress. Plant Cell & Environment. 41(12):2844-2857. https://doi.org/10.1111/pce.13416

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Title: BvCOLD1: A novel aquaporin from sugar beet (Beta vulgaris L.) involved in boron homeostasis and abiotic stress
Author: Porcel, R Bustamante-González, Antonio Javier Ros, Roc Serrano Salom, Ramón Mulet, José Miguel
UPV Unit: Universitat Politècnica de València. Instituto Universitario de Conservación y Mejora de la Agrodiversidad Valenciana - Institut Universitari de Conservació i Millora de l'Agrodiversitat Valenciana
Universitat Politècnica de València. Departamento de Biotecnología - Departament de Biotecnologia
Issued date:
Abstract:
[EN] In this report we have identified BvCOLD1, a novel aquaporin from sugar beet (Beta vulgaris) which is only conserved in the Chenopodioideae family. BvCOLD1 is expressed in all plant organs investigated and ...[+]
Subjects: Aquaporina , Estrés abiótico , Boro , Remolacha
Copyrigths: Reserva de todos los derechos
Source:
Plant Cell & Environment. (issn: 0140-7791 )
DOI: 10.1111/pce.13416
Publisher:
Blackwell Publishing
Publisher version: https://doi.org/10.1111/pce.13416
Project ID:
info:eu-repo/grantAgreement/MINECO//BIO2014-61826-EXP/ES/OPTIMIZACION PARA USO A ESCALA INDUSTRIAL DE UN SISTEMA PARA LA EXPRESION SELECTIVA DE COMPUESTOS HETEROLOGOS EN CLOROPLASTOS MEDIADO POR NON-CODING RNAS/
info:eu-repo/grantAgreement/MINECO//AGL2013-47886-R/ES/CARACTERIZACION DE LA RESPUESTA A ESTRES MULTIPLE REGULADA POR NCRNAS EN CUCURBITACEAS. BASES PARA EL DISEÑO DE ESTRATEGIAS INTEGRALES PARA LA PROTECCION DE CULTIVOS¿/
info:eu-repo/grantAgreement/UPV//PAID-06-10-1496/
info:eu-repo/grantAgreement/MINECO//BIO2016-77776-P/ES/DESCIFRANDO LA REGULACION DE TRANSPORTADORES DE POTASIO EN PLANTAS Y LEVADURAS/
Thanks:
Ministerio de Economia y Competitividad, Grant/Award Number: BIO2016-77776-P; Secretaria de Estado de Investigacion, Desarrollo e Innovacion, Grant/Award Number: AGL2013-47886-R; Direccion General Investigacion Cientifica; ...[+]
Type: Artículo

References

Aroca, R., Amodeo, G., Fernández-Illescas, S., Herman, E. M., Chaumont, F., & Chrispeels, M. J. (2004). The Role of Aquaporins and Membrane Damage in Chilling and Hydrogen Peroxide Induced Changes in the Hydraulic Conductance of Maize Roots. Plant Physiology, 137(1), 341-353. doi:10.1104/pp.104.051045

Biancardi, E. (2005). Genetics and Breeding of Sugar Beet. doi:10.1201/9781482280296

Bienert, G. P., Møller, A. L. B., Kristiansen, K. A., Schulz, A., Møller, I. M., Schjoerring, J. K., & Jahn, T. P. (2006). Specific Aquaporins Facilitate the Diffusion of Hydrogen Peroxide across Membranes. Journal of Biological Chemistry, 282(2), 1183-1192. doi:10.1074/jbc.m603761200 [+]
Aroca, R., Amodeo, G., Fernández-Illescas, S., Herman, E. M., Chaumont, F., & Chrispeels, M. J. (2004). The Role of Aquaporins and Membrane Damage in Chilling and Hydrogen Peroxide Induced Changes in the Hydraulic Conductance of Maize Roots. Plant Physiology, 137(1), 341-353. doi:10.1104/pp.104.051045

Biancardi, E. (2005). Genetics and Breeding of Sugar Beet. doi:10.1201/9781482280296

Bienert, G. P., Møller, A. L. B., Kristiansen, K. A., Schulz, A., Møller, I. M., Schjoerring, J. K., & Jahn, T. P. (2006). Specific Aquaporins Facilitate the Diffusion of Hydrogen Peroxide across Membranes. Journal of Biological Chemistry, 282(2), 1183-1192. doi:10.1074/jbc.m603761200

Bissoli, G., Niñoles, R., Fresquet, S., Palombieri, S., Bueso, E., Rubio, L., … Serrano, R. (2012). Peptidyl-prolyl cis-trans isomerase ROF2 modulates intracellular pH homeostasis in Arabidopsis. The Plant Journal, 70(4), 704-716. doi:10.1111/j.1365-313x.2012.04921.x

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

Brown, P. H., Bellaloui, N., Wimmer, M. A., Bassil, E. S., Ruiz, J., Hu, H., … Römheld, V. (2002). Boron in Plant Biology. Plant Biology, 4(2), 205-223. doi:10.1055/s-2002-25740

Camacho-Cristóbal, J. J., Rexach, J., & González-Fontes, A. (2008). Boron in Plants: Deficiency and Toxicity. Journal of Integrative Plant Biology, 50(10), 1247-1255. doi:10.1111/j.1744-7909.2008.00742.x

Cava, F., de Pedro, M. A., Blas-Galindo, E., Waldo, G. S., Westblade, L. F., & Berenguer, J. (2008). Expression and use of superfolder green fluorescent protein at high temperatures in vivo: a tool to study extreme thermophile biology. Environmental Microbiology, 10(3), 605-613. doi:10.1111/j.1462-2920.2007.01482.x

Dell, B., & Huang, L. (1997). Plant and Soil, 193(2), 103-120. doi:10.1023/a:1004264009230

Dewar, A. M., May, M. J., Woiwod, I. P., Haylock, L. A., Champion, G. T., Garner, B. H., … Pidgeon, J. D. (2003). A novel approach to the use of genetically modified herbicide tolerant crops for environmental benefit. Proceedings of the Royal Society of London. Series B: Biological Sciences, 270(1513), 335-340. doi:10.1098/rspb.2002.2248

Dohm, J. C., Minoche, A. E., Holtgräwe, D., Capella-Gutiérrez, S., Zakrzewski, F., Tafer, H., … Himmelbauer, H. (2013). The genome of the recently domesticated crop plant sugar beet (Beta vulgaris). Nature, 505(7484), 546-549. doi:10.1038/nature12817

Duncan, D. B. (1955). Multiple Range and Multiple F Tests. Biometrics, 11(1), 1. doi:10.2307/3001478

Evans, E., & Messerschmidt, U. (2017). Review: Sugar beets as a substitute for grain for lactating dairy cattle. Journal of Animal Science and Biotechnology, 8(1). doi:10.1186/s40104-017-0154-8

Food and Agriculture Organization of the United Nations 2015 World agricultural statistics = Statistiques agricoles mondiales = Estadísticas agricolas mundiales

Gietz, D., Jean, A. S., Woods, R. A., & Schiestl, R. H. (1992). Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Research, 20(6), 1425-1425. doi:10.1093/nar/20.6.1425

Jahn, T. P., Møller, A. L. B., Zeuthen, T., Holm, L. M., Klaerke, D. A., Mohsin, B., … Schjoerring, J. K. (2004). Aquaporin homologues in plants and mammals transport ammonia. FEBS Letters, 574(1-3), 31-36. doi:10.1016/j.febslet.2004.08.004

KAY, R., CHAN, A., DALY, M., & MCPHERSON, J. (1987). Duplication of CaMV 35S Promoter Sequences Creates a Strong Enhancer for Plant Genes. Science, 236(4806), 1299-1302. doi:10.1126/science.236.4806.1299

Klebl, F., Wolf, M., & Sauer, N. (2003). A defect in the yeast plasma membrane urea transporter Dur3p is complemented by CpNIP1 , a Nod26-like protein from zucchini (Cucurbita pepo L.), and by Arabidopsis thaliana δ-TIP or γ-TIP. FEBS Letters, 547(1-3), 69-74. doi:10.1016/s0014-5793(03)00671-9

Kobayashi, M., Matoh, T., & Azuma, J. (1996). Two Chains of Rhamnogalacturonan II Are Cross-Linked by Borate-Diol Ester Bonds in Higher Plant Cell Walls. Plant Physiology, 110(3), 1017-1020. doi:10.1104/pp.110.3.1017

Livak, K. J., & Schmittgen, T. D. (2001). Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method. Methods, 25(4), 402-408. doi:10.1006/meth.2001.1262

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

Moliterni, V. M. C., Paris, R., Onofri, C., Orrù, L., Cattivelli, L., Pacifico, D., … Mandolino, G. (2015). Early transcriptional changes in Beta vulgaris in response to low temperature. Planta, 242(1), 187-201. doi:10.1007/s00425-015-2299-z

Mulet, J. M., Alemany, B., Ros, R., Calvete, J. J., & Serrano, R. (2004). Expression of a plant serine O-acetyltransferase inSaccharomyces cerevisiae confers osmotic tolerance and creates an alternative pathway for cysteine biosynthesis. Yeast, 21(4), 303-312. doi:10.1002/yea.1076

Muries, B., Faize, M., Carvajal, M., & Martínez-Ballesta, M. del C. (2011). Identification and differential induction of the expression of aquaporins by salinity in broccoli plants. Molecular BioSystems, 7(4), 1322. doi:10.1039/c0mb00285b

Noguchi, K., Yasumori, M., Imai, T., Naito, S., Matsunaga, T., Oda, H., … Fujiwara, T. (1997). bor1-1, an Arabidopsis thaliana Mutant That Requires a High Level of Boron. Plant Physiology, 115(3), 901-906. doi:10.1104/pp.115.3.901

Nozawa, A., Takano, J., Kobayashi, M., von Wirén, N., & Fujiwara, T. (2006). Roles of BOR1, DUR3, and FPS1 in boron transport and tolerance inSaccharomyces cerevisiae. FEMS Microbiology Letters, 262(2), 216-222. doi:10.1111/j.1574-6968.2006.00395.x

O’Neill, M. A., Warrenfeltz, D., Kates, K., Pellerin, P., Doco, T., Darvill, A. G., & Albersheim, P. (1996). Rhamnogalacturonan-II, a Pectic Polysaccharide in the Walls of Growing Plant Cell, Forms a Dimer That Is Covalently Cross-linked by a Borate Ester. Journal of Biological Chemistry, 271(37), 22923-22930. doi:10.1074/jbc.271.37.22923

Pang, Y., Li, L., Ren, F., Lu, P., Wei, P., Cai, J., … Wang, X. (2010). Overexpression of the tonoplast aquaporin AtTIP5;1 conferred tolerance to boron toxicity in Arabidopsis. Journal of Genetics and Genomics, 37(6), 389-397. doi:10.1016/s1673-8527(09)60057-6

Patankar, H. V., Al-Harrasi, I., Al-Yahyai, R., & Yaish, M. W. (2018). Identification of Candidate Genes Involved in the Salt Tolerance of Date Palm (Phoenix dactylifera L.) Based on a Yeast Functional Bioassay. DNA and Cell Biology, 37(6), 524-534. doi:10.1089/dna.2018.4159

Peiro, A., Izquierdo‐Garcia, A. C., Sanchez‐Navarro, J. A., Pallas, V., Mulet, J. M., & Aparicio, F. (2014). Patellins 3 and 6, two members of the P lant P atellin family, interact with the movement protein of A lfalfa mosaic virus and interfere with viral movement. Molecular Plant Pathology, 15(9), 881-891. doi:10.1111/mpp.12146

Porcel, R., Aroca, R., Azcón, R., & Ruiz-Lozano, J. M. (2006). PIP Aquaporin Gene Expression in Arbuscular Mycorrhizal Glycine max and Lactuca  sativa Plants in Relation to Drought Stress Tolerance. Plant Molecular Biology, 60(3), 389-404. doi:10.1007/s11103-005-4210-y

ROZEMA, J., BRUIN, J., & BROEKMAN, R. A. (1992). Effect of boron on the growth and mineral economy of some halophytes and non-halophytes. New Phytologist, 121(2), 249-256. doi:10.1111/j.1469-8137.1992.tb01111.x

Sayle, R. (1995). RASMOL: biomolecular graphics for all. Trends in Biochemical Sciences, 20(9), 374-376. doi:10.1016/s0968-0004(00)89080-5

Serrano, R., Montesinos, C., Gaxiola, R., Ríos, G., Forment, J., Leube, M., … Ros, R. (2003). FUNCTIONAL GENOMICS OF SALT TOLERANCE: THE YEAST OVEREXPRESSION APPROACH. Acta Horticulturae, (609), 31-38. doi:10.17660/actahortic.2003.609.2

Shorrocks, V. M. (1997). Plant and Soil, 193(2), 121-148. doi:10.1023/a:1004216126069

Soto, G., Alleva, K., Mazzella, M. A., Amodeo, G., & Muschietti, J. P. (2008). AtTIP1;3andAtTIP5;1, the only highly expressed Arabidopsis pollen-specific aquaporins, transport water and urea. FEBS Letters, 582(29), 4077-4082. doi:10.1016/j.febslet.2008.11.002

Sreedharan, S., Shekhawat, U. K. S., & Ganapathi, T. R. (2015). Constitutive and stress-inducible overexpression of a native aquaporin gene (MusaPIP2;6) in transgenic banana plants signals its pivotal role in salt tolerance. Plant Molecular Biology, 88(1-2), 41-52. doi:10.1007/s11103-015-0305-2

Su, Y., Liang, W., Liu, Z., Wang, Y., Zhao, Y., Ijaz, B., & Hua, J. (2017). Overexpression of GhDof1 improved salt and cold tolerance and seed oil content in Gossypium hirsutum. Journal of Plant Physiology, 218, 222-234. doi:10.1016/j.jplph.2017.07.017

Takano, J., Noguchi, K., Yasumori, M., Kobayashi, M., Gajdos, Z., Miwa, K., … Fujiwara, T. (2002). Arabidopsis boron transporter for xylem loading. Nature, 420(6913), 337-340. doi:10.1038/nature01139

Tanaka, M., & Fujiwara, T. (2007). Physiological roles and transport mechanisms of boron: perspectives from plants. Pflügers Archiv - European Journal of Physiology, 456(4), 671-677. doi:10.1007/s00424-007-0370-8

Tanaka, M., Wallace, I. S., Takano, J., Roberts, D. M., & Fujiwara, T. (2008). NIP6;1 Is a Boric Acid Channel for Preferential Transport of Boron to Growing Shoot Tissues in Arabidopsis. The Plant Cell, 20(10), 2860-2875. doi:10.1105/tpc.108.058628

Törnroth-Horsefield, S., Wang, Y., Hedfalk, K., Johanson, U., Karlsson, M., Tajkhorshid, E., … Kjellbom, P. (2005). Structural mechanism of plant aquaporin gating. Nature, 439(7077), 688-694. doi:10.1038/nature04316

Uraguchi, S. (2014). Generation of boron-deficiency-tolerant tomato by overexpressing an Arabidopsis thaliana borate transporter AtBOR1. Frontiers in Plant Science, 5. doi:10.3389/fpls.2014.00125

Vicent, I., Navarro, A., Mulet, J. M., Sharma, S., & Serrano, R. (2015). Uptake of inorganic phosphate is a limiting factor for Saccharomyces cerevisiae during growth at low temperatures. FEMS Yeast Research, 15(3). doi:10.1093/femsyr/fov008

Wallis, J. W., Chrebet, G., Brodsky, G., Rolfe, M., & Rothstein, R. (1989). A hyper-recombination mutation in S. cerevisiae identifies a novel eukaryotic topoisomerase. Cell, 58(2), 409-419. doi:10.1016/0092-8674(89)90855-6

Wieland, W. H., Lammers, A., Schots, A., & Orzáez, D. V. (2006). Plant expression of chicken secretory antibodies derived from combinatorial libraries. Journal of Biotechnology, 122(3), 382-391. doi:10.1016/j.jbiotec.2005.12.020

Wimmer, M. A., & Eichert, T. (2013). Review: Mechanisms for boron deficiency-mediated changes in plant water relations. Plant Science, 203-204, 25-32. doi:10.1016/j.plantsci.2012.12.012

Yu, G., Li, J., Sun, X., Liu, Y., Wang, X., Zhang, H., & Pan, H. (2017). Exploration for the Salinity Tolerance-Related Genes from Xero-Halophyte Atriplex canescens Exploiting Yeast Functional Screening System. International Journal of Molecular Sciences, 18(11), 2444. doi:10.3390/ijms18112444

Yuan, D., Li, W., Hua, Y., King, G. J., Xu, F., & Shi, L. (2017). Genome-Wide Identification and Characterization of the Aquaporin Gene Family and Transcriptional Responses to Boron Deficiency in Brassica napus. Frontiers in Plant Science, 8. doi:10.3389/fpls.2017.01336

Zabed, H., Faruq, G., Sahu, J. N., Azirun, M. S., Hashim, R., & Nasrulhaq Boyce, A. (2014). Bioethanol Production from Fermentable Sugar Juice. The Scientific World Journal, 2014, 1-11. doi:10.1155/2014/957102

Zhang, Q., Chen, H., He, M., Zhao, Z., Cai, H., Ding, G., … Xu, F. (2017). The boron transporterBnaC4.BOR1;1cis critical for inflorescence development and fertility under boron limitation inBrassica napus. Plant, Cell & Environment, 40(9), 1819-1833. doi:10.1111/pce.12987

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