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Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis

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Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis

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Corrales, AR.; Carrillo, L.; Lasierra, P.; Nebauer, SG.; Dominguez-Figueroa, J.; Renau-Morata, B.; Pollmann, S.... (2017). Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis. Plant Cell & Environment. 40(5):748-764. https://doi.org/10.1111/pce.12894

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Título: Multifaceted role of cycling DOF factor 3 (CDF3) in the regulation of flowering time and abiotic stress responses in Arabidopsis
Autor: Corrales, Alba Rocío Carrillo, Laura Lasierra, Pilar Nebauer, Sergio G. Dominguez-Figueroa, Jose Renau-Morata, Begoña Pollmann, Stephan GRANELL RICHART, ANTONIO Molina, Rosa-Victoria Vicente-Carbajosa, Jesús Medina, Joaquín
Entidad UPV: Universitat Politècnica de València. Departamento de Producción Vegetal - Departament de Producció Vegetal
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
Fecha difusión:
Resumen:
[EN] DNA-binding with one finger (DOF)-type transcription factors are involved in many fundamental processes in higher plants, from responses to light and phytohormones to flowering time and seed maturation, but their ...[+]
Palabras clave: Arabidopsis , CDF , DOF , Drought stress , Flowering time , Gene expression , Low temperature stress , Nitrogen
Derechos de uso: Reserva de todos los derechos
Fuente:
Plant Cell & Environment. (issn: 0140-7791 )
DOI: 10.1111/pce.12894
Editorial:
Blackwell Publishing
Versión del editor: https://doi.org/10.1111/pce.12894
Código del Proyecto:
info:eu-repo/grantAgreement/INIA//2009-0004-C01/
info:eu-repo/grantAgreement/INIA//2012-0008-C01/
info:eu-repo/grantAgreement/MICINN//BIO2010-14871/ES/REDES REGULADORAS EN EL ORIGEN Y METABOLISMO DE LA SEMILLA/
info:eu-repo/grantAgreement/MINECO//BFU2013-49665-EXP/ES/AUMENTO EN LA CAPTURA DE ENERGÍA Y CARBONO EN SISTEMAS VEGETALES/
Agradecimientos:
We thank Dr Pablo Gonzalez-Melendi and Dr Jan Zouhar for technical handling of the confocal microscope and Dr Rafael Catala for the assistance with the low temperature stress assays. This work was supported by grants from ...[+]
Tipo: Artículo

References

Achard, P., Gong, F., Cheminant, S., Alioua, M., Hedden, P., & Genschik, P. (2008). The Cold-Inducible CBF1 Factor–Dependent Signaling Pathway Modulates the Accumulation of the Growth-Repressing DELLA Proteins via Its Effect on Gibberellin Metabolism. The Plant Cell, 20(8), 2117-2129. doi:10.1105/tpc.108.058941

Ahuja, I., de Vos, R. C. H., Bones, A. M., & Hall, R. D. (2010). Plant molecular stress responses face climate change. Trends in Plant Science, 15(12), 664-674. doi:10.1016/j.tplants.2010.08.002

Alonso, R., Oñate-Sánchez, L., Weltmeier, F., Ehlert, A., Diaz, I., Dietrich, K., … Dröge-Laser, W. (2009). A Pivotal Role of the Basic Leucine Zipper Transcription Factor bZIP53 in the Regulation of Arabidopsis Seed Maturation Gene Expression Based on Heterodimerization and Protein Complex Formation. The Plant Cell, 21(6), 1747-1761. doi:10.1105/tpc.108.062968 [+]
Achard, P., Gong, F., Cheminant, S., Alioua, M., Hedden, P., & Genschik, P. (2008). The Cold-Inducible CBF1 Factor–Dependent Signaling Pathway Modulates the Accumulation of the Growth-Repressing DELLA Proteins via Its Effect on Gibberellin Metabolism. The Plant Cell, 20(8), 2117-2129. doi:10.1105/tpc.108.058941

Ahuja, I., de Vos, R. C. H., Bones, A. M., & Hall, R. D. (2010). Plant molecular stress responses face climate change. Trends in Plant Science, 15(12), 664-674. doi:10.1016/j.tplants.2010.08.002

Alonso, R., Oñate-Sánchez, L., Weltmeier, F., Ehlert, A., Diaz, I., Dietrich, K., … Dröge-Laser, W. (2009). A Pivotal Role of the Basic Leucine Zipper Transcription Factor bZIP53 in the Regulation of Arabidopsis Seed Maturation Gene Expression Based on Heterodimerization and Protein Complex Formation. The Plant Cell, 21(6), 1747-1761. doi:10.1105/tpc.108.062968

BEUVE, N., RISPAIL, N., LAINE, P., CLIQUET, J.-B., OURRY, A., & LE DEUNFF, E. (2004). Putative role of gamma -aminobutyric acid (GABA) as a long-distance signal in up-regulation of nitrate uptake in Brassica napus L. Plant, Cell and Environment, 27(8), 1035-1046. doi:10.1111/j.1365-3040.2004.01208.x

Blümel, M., Dally, N., & Jung, C. (2015). Flowering time regulation in crops — what did we learn from Arabidopsis? Current Opinion in Biotechnology, 32, 121-129. doi:10.1016/j.copbio.2014.11.023

Bouche, N., Fait, A., Bouchez, D., Moller, S. G., & Fromm, H. (2003). Mitochondrial succinic-semialdehyde dehydrogenase of the  -aminobutyrate shunt is required to restrict levels of reactive oxygen intermediates in plants. Proceedings of the National Academy of Sciences, 100(11), 6843-6848. doi:10.1073/pnas.1037532100

Catala, R., Medina, J., & Salinas, J. (2011). Integration of low temperature and light signaling during cold acclimation response in Arabidopsis. Proceedings of the National Academy of Sciences, 108(39), 16475-16480. doi:10.1073/pnas.1107161108

Chaves, M. M., Flexas, J., & Pinheiro, C. (2008). Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Annals of Botany, 103(4), 551-560. doi:10.1093/aob/mcn125

Chen, H., Hwang, J. E., Lim, C. J., Kim, D. Y., Lee, S. Y., & Lim, C. O. (2010). Arabidopsis DREB2C functions as a transcriptional activator of HsfA3 during the heat stress response. Biochemical and Biophysical Research Communications, 401(2), 238-244. doi:10.1016/j.bbrc.2010.09.038

Claussen, W. (2005). Proline as a measure of stress in tomato plants. Plant Science, 168(1), 241-248. doi:10.1016/j.plantsci.2004.07.039

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

Corrales, A., Carrillo, L., Nebauer, S., Renau-Morata, B., Sánchez-Perales, M., Fernández-Nohales, P., … Medina, J. (2014). Salinity Assay in Arabidopsis. BIO-PROTOCOL, 4(16). doi:10.21769/bioprotoc.1216

Corrales, A.-R., Nebauer, S. G., Carrillo, L., Fernández-Nohales, P., Marqués, J., Renau-Morata, B., … Medina, J. (2014). Characterization of tomato Cycling Dof Factors reveals conserved and new functions in the control of flowering time and abiotic stress responses. Journal of Experimental Botany, 65(4), 995-1012. doi:10.1093/jxb/ert451

Davletova, S., Schlauch, K., Coutu, J., & Mittler, R. (2005). The Zinc-Finger Protein Zat12 Plays a Central Role in Reactive Oxygen and Abiotic Stress Signaling in Arabidopsis. Plant Physiology, 139(2), 847-856. doi:10.1104/pp.105.068254

DÉJARDIN, A., SOKOLOV, L. N., & KLECZKOWSKI, L. A. (1999). Sugar/osmoticum levels modulate differential abscisic acid-independent expression of two stress-responsive sucrose synthase genes in Arabidopsis. Biochemical Journal, 344(2), 503-509. doi:10.1042/bj3440503

Dubois, M., Skirycz, A., Claeys, H., Maleux, K., Dhondt, S., De Bodt, S., … Inzé, D. (2013). ETHYLENE RESPONSE FACTOR6 Acts as a Central Regulator of Leaf Growth under Water-Limiting Conditions in Arabidopsis. Plant Physiology, 162(1), 319-332. doi:10.1104/pp.113.216341

Farrant, J. M., & Moore, J. P. (2011). Programming desiccation-tolerance: from plants to seeds to resurrection plants. Current Opinion in Plant Biology, 14(3), 340-345. doi:10.1016/j.pbi.2011.03.018

Fornara, F., Montaigu, A., Sánchez‐Villarreal, A., Takahashi, Y., Ver Loren van Themaat, E., Huettel, B., … Coupland, G. (2015). The GI – CDF module of Arabidopsis affects freezing tolerance and growth as well as flowering. The Plant Journal, 81(5), 695-706. doi:10.1111/tpj.12759

Fornara, F., Panigrahi, K. C. S., Gissot, L., Sauerbrunn, N., Rühl, M., Jarillo, J. A., & Coupland, G. (2009). Arabidopsis DOF Transcription Factors Act Redundantly to Reduce CONSTANS Expression and Are Essential for a Photoperiodic Flowering Response. Developmental Cell, 17(1), 75-86. doi:10.1016/j.devcel.2009.06.015

Fowler, S. (1999). GIGANTEA: a circadian clock-controlled gene that regulates photoperiodic flowering in Arabidopsis and encodes a protein with several possible membrane-spanning domains. The EMBO Journal, 18(17), 4679-4688. doi:10.1093/emboj/18.17.4679

Galmés, J., Medrano, H., & Flexas, J. (2007). Photosynthetic limitations in response to water stress and recovery in Mediterranean plants with different growth forms. New Phytologist, 175(1), 81-93. doi:10.1111/j.1469-8137.2007.02087.x

Gill, S. S., & Tuteja, N. (2010). Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry, 48(12), 909-930. doi:10.1016/j.plaphy.2010.08.016

Gilmour, S. J., Fowler, S. G., & Thomashow, M. F. (2004). Arabidopsis Transcriptional Activators CBF1, CBF2, and CBF3 have Matching Functional Activities. Plant Molecular Biology, 54(5), 767-781. doi:10.1023/b:plan.0000040902.06881.d4

Gong, P., Zhang, J., Li, H., Yang, C., Zhang, C., Zhang, X., … Ye, Z. (2010). Transcriptional profiles of drought-responsive genes in modulating transcription signal transduction, and biochemical pathways in tomato. Journal of Experimental Botany, 61(13), 3563-3575. doi:10.1093/jxb/erq167

Gould, P. D., Locke, J. C. W., Larue, C., Southern, M. M., Davis, S. J., Hanano, S., … Hall, A. (2006). The Molecular Basis of Temperature Compensation in the Arabidopsis Circadian Clock. The Plant Cell, 18(5), 1177-1187. doi:10.1105/tpc.105.039990

Han, Q., Kang, G., & Guo, T. (2013). Proteomic analysis of spring freeze-stress responsive proteins in leaves of bread wheat (Triticum aestivum L.). Plant Physiology and Biochemistry, 63, 236-244. doi:10.1016/j.plaphy.2012.12.002

Hernando-Amado, S., González-Calle, V., Carbonero, P., & Barrero-Sicilia, C. (2012). The family of DOF transcription factors in Brachypodium distachyon: phylogenetic comparison with rice and barley DOFs and expression profiling. BMC Plant Biology, 12(1), 202. doi:10.1186/1471-2229-12-202

Zou, H.-F., Zhang, Y.-Q., Wei, W., Chen, H.-W., Song, Q.-X., Liu, Y.-F., … Chen, S.-Y. (2012). The transcription factor AtDOF4.2 regulates shoot branching and seed coat formation in Arabidopsis. Biochemical Journal, 449(2), 373-388. doi:10.1042/bj20110060

Hussain, S. S., Kayani, M. A., & Amjad, M. (2011). Transcription factors as tools to engineer enhanced drought stress tolerance in plants. Biotechnology Progress, 27(2), 297-306. doi:10.1002/btpr.514

Imaizumi, T. (2005). FKF1 F-Box Protein Mediates Cyclic Degradation of a Repressor of CONSTANS in Arabidopsis. Science, 309(5732), 293-297. doi:10.1126/science.1110586

Ingram, J., & Bartels, D. (1996). THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS. Annual Review of Plant Physiology and Plant Molecular Biology, 47(1), 377-403. doi:10.1146/annurev.arplant.47.1.377

Jarillo, J. A., Del Olmo, I., Gómez-Zambrano, A., Lázaro, A., López-González, L., Miguel, E., … Piñeiro, M. (2008). Photoperiodic control of flowering time: a review. Spanish Journal of Agricultural Research, 6(S1), 221. doi:10.5424/sjar/200806s1-391

Izaurralde, E. (1997). The asymmetric distribution of the constituents of the Ran system is essential for transport into and out of the nucleus. The EMBO Journal, 16(21), 6535-6547. doi:10.1093/emboj/16.21.6535

Karimi, M., Depicker, A., & Hilson, P. (2007). Recombinational Cloning with Plant Gateway Vectors. Plant Physiology, 145(4), 1144-1154. doi:10.1104/pp.107.106989

Kim, S. Y., & Nam, K. H. (2010). Physiological roles of ERD10 in abiotic stresses and seed germination of Arabidopsis. Plant Cell Reports, 29(2), 203-209. doi:10.1007/s00299-009-0813-0

Kiyosue, T., Yamaguchi-Shinozaki, K., & Shinozaki, K. (1994). Cloning of cDNAs for genes that are early-responsive to dehydration stress (ERDs) inArabidopsis thaliana L.: identification of three ERDs as HSP cognate genes. Plant Molecular Biology, 25(5), 791-798. doi:10.1007/bf00028874

Kurai, T., Wakayama, M., Abiko, T., Yanagisawa, S., Aoki, N., & Ohsugi, R. (2011). Introduction of the ZmDof1 gene into rice enhances carbon and nitrogen assimilation under low-nitrogen conditions. Plant Biotechnology Journal, 9(8), 826-837. doi:10.1111/j.1467-7652.2011.00592.x

Liu, Q., Kasuga, M., Sakuma, Y., Abe, H., Miura, S., Yamaguchi-Shinozaki, K., & Shinozaki, K. (1998). Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis. The Plant Cell, 10(8), 1391. doi:10.2307/3870648

Matsui, A., Ishida, J., Morosawa, T., Mochizuki, Y., Kaminuma, E., Endo, T. A., … Seki, M. (2008). Arabidopsis Transcriptome Analysis under Drought, Cold, High-Salinity and ABA Treatment Conditions using a Tiling Array. Plant and Cell Physiology, 49(8), 1135-1149. doi:10.1093/pcp/pcn101

Medina, J., Bargues, M., Terol, J., Pérez-Alonso, M., & Salinas, J. (1999). The Arabidopsis CBF Gene Family Is Composed of Three Genes Encoding AP2 Domain-Containing Proteins Whose Expression Is Regulated by Low Temperature but Not by Abscisic Acid or Dehydration. Plant Physiology, 119(2), 463-470. doi:10.1104/pp.119.2.463

Messerli, G., Partovi Nia, V., Trevisan, M., Kolbe, A., Schauer, N., Geigenberger, P., … Zeeman, S. C. (2007). Rapid Classification of Phenotypic Mutants of Arabidopsis via Metabolite Fingerprinting. Plant Physiology, 143(4), 1484-1492. doi:10.1104/pp.106.090795

Mittler, R. (2006). Abiotic stress, the field environment and stress combination. Trends in Plant Science, 11(1), 15-19. doi:10.1016/j.tplants.2005.11.002

Mizoguchi, T., Wright, L., Fujiwara, S., Cremer, F., Lee, K., Onouchi, H., … Coupland, G. (2005). Distinct Roles of GIGANTEA in Promoting Flowering and Regulating Circadian Rhythms in Arabidopsis. The Plant Cell, 17(8), 2255-2270. doi:10.1105/tpc.105.033464

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

Murashige, T., & Skoog, F. (1962). A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures. Physiologia Plantarum, 15(3), 473-497. doi:10.1111/j.1399-3054.1962.tb08052.x

Nishiyama, R., Le, D. T., Watanabe, Y., Matsui, A., Tanaka, M., Seki, M., … Tran, L.-S. P. (2012). Transcriptome Analyses of a Salt-Tolerant Cytokinin-Deficient Mutant Reveal Differential Regulation of Salt Stress Response by Cytokinin Deficiency. PLoS ONE, 7(2), e32124. doi:10.1371/journal.pone.0032124

Noguero, M., Atif, R. M., Ochatt, S., & Thompson, R. D. (2013). The role of the DNA-binding One Zinc Finger (DOF) transcription factor family in plants. Plant Science, 209, 32-45. doi:10.1016/j.plantsci.2013.03.016

Novillo, F., Medina, J., & Salinas, J. (2007). Arabidopsis CBF1 and CBF3 have a different function than CBF2 in cold acclimation and define different gene classes in the CBF regulon. Proceedings of the National Academy of Sciences, 104(52), 21002-21007. doi:10.1073/pnas.0705639105

OliverosJ.C.(2007)Venny an interactive tool for comparing lists with Venn's diagrams.http://bioinfogp.cnb.csic.es/tools/venny/index.html.

Oñate-Sánchez, L., & Vicente-Carbajosa, J. (2008). DNA-free RNA isolation protocols for Arabidopsis thaliana, including seeds and siliques. BMC Research Notes, 1(1), 93. doi:10.1186/1756-0500-1-93

Osakabe, Y., Kajita, S., & Osakabe, K. (2011). Genetic engineering of woody plants: current and future targets in a stressful environment. Physiologia Plantarum, 142(2), 105-117. doi:10.1111/j.1399-3054.2011.01451.x

Park, D. H. (1999). Control of Circadian Rhythms and Photoperiodic Flowering by the Arabidopsis GIGANTEA Gene. Science, 285(5433), 1579-1582. doi:10.1126/science.285.5433.1579

Rajasekaran, L. R., Aspinall, D., & Paleg, L. G. (2000). Physiological mechanism of tolerance of Lycopersicon spp. exposed to salt stress. Canadian Journal of Plant Science, 80(1), 151-159. doi:10.4141/p99-003

Rizhsky, L., Liang, H., Shuman, J., Shulaev, V., Davletova, S., & Mittler, R. (2004). When Defense Pathways Collide. The Response of Arabidopsis to a Combination of Drought and Heat Stress. Plant Physiology, 134(4), 1683-1696. doi:10.1104/pp.103.033431

Rosso, M. G., Li, Y., Strizhov, N., Reiss, B., Dekker, K., & Weisshaar, B. (2003). An Arabidopsis thaliana T-DNA mutagenized population (GABI-Kat) for flanking sequence tag-based reverse genetics. Plant Molecular Biology, 53(1/2), 247-259. doi:10.1023/b:plan.0000009297.37235.4a

Rueda-López, M., Crespillo, R., Cánovas, F. M., & Ávila, C. (2008). Differential regulation of two glutamine synthetase genes by a single Dof transcription factor. The Plant Journal, 56(1), 73-85. doi:10.1111/j.1365-313x.2008.03573.x

Sakuma, Y., Maruyama, K., Osakabe, Y., Qin, F., Seki, M., Shinozaki, K., & Yamaguchi-Shinozaki, K. (2006). Functional Analysis of an Arabidopsis Transcription Factor, DREB2A, Involved in Drought-Responsive Gene Expression. The Plant Cell, 18(5), 1292-1309. doi:10.1105/tpc.105.035881

Sato, Y., & Yokoya, S. (2007). Enhanced tolerance to drought stress in transgenic rice plants overexpressing a small heat-shock protein, sHSP17.7. Plant Cell Reports, 27(2), 329-334. doi:10.1007/s00299-007-0470-0

Sawa, M., Nusinow, D. A., Kay, S. A., & Imaizumi, T. (2007). FKF1 and GIGANTEA Complex Formation Is Required for Day-Length Measurement in Arabidopsis. Science, 318(5848), 261-265. doi:10.1126/science.1146994

Scarpeci, T. E., Zanor, M. I., Mueller-Roeber, B., & Valle, E. M. (2013). Overexpression of AtWRKY30 enhances abiotic stress tolerance during early growth stages in Arabidopsis thaliana. Plant Molecular Biology, 83(3), 265-277. doi:10.1007/s11103-013-0090-8

Seki, M., Kamei, A., Yamaguchi-Shinozaki, K., & Shinozaki, K. (2003). Molecular responses to drought, salinity and frost: common and different paths for plant protection. Current Opinion in Biotechnology, 14(2), 194-199. doi:10.1016/s0958-1669(03)00030-2

Shelp, B. J., Mullen, R. T., & Waller, J. C. (2012). Compartmentation of GABA metabolism raises intriguing questions. Trends in Plant Science, 17(2), 57-59. doi:10.1016/j.tplants.2011.12.006

Shi, H., & Chan, Z. (2014). The cysteine2/histidine2-type transcription factor ZINC FINGER OF ARABIDOPSIS THALIANA 6 -activated C-REPEAT-BINDING FACTOR pathway is essential for melatonin-mediated freezing stress resistance in Arabidopsis. Journal of Pineal Research, 57(2), 185-191. doi:10.1111/jpi.12155

Shinozaki, K., & Yamaguchi-Shinozaki, K. (2006). Gene networks involved in drought stress response and tolerance. Journal of Experimental Botany, 58(2), 221-227. doi:10.1093/jxb/erl164

Shinozaki, K., Yamaguchi-Shinozaki, K., & Seki, M. (2003). Regulatory network of gene expression in the drought and cold stress responses. Current Opinion in Plant Biology, 6(5), 410-417. doi:10.1016/s1369-5266(03)00092-x

Skirycz, A., & Inzé, D. (2010). More from less: plant growth under limited water. Current Opinion in Biotechnology, 21(2), 197-203. doi:10.1016/j.copbio.2010.03.002

Snedden, W. A., Arazi, T., Fromm, H., & Shelp, B. J. (1995). Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase. Plant Physiology, 108(2), 543-549. doi:10.1104/pp.108.2.543

STITT, M., & KRAPP, A. (1999). The interaction between elevated carbon dioxide and nitrogen nutrition: the physiological and molecular background. Plant, Cell and Environment, 22(6), 583-621. doi:10.1046/j.1365-3040.1999.00386.x

Studart-Guimarães, C., Fait, A., Nunes-Nesi, A., Carrari, F., Usadel, B., & Fernie, A. R. (2007). Reduced Expression of Succinyl-Coenzyme A Ligase Can Be Compensated for by Up-Regulation of the γ-Aminobutyrate Shunt in Illuminated Tomato Leaves. Plant Physiology, 145(3), 626-639. doi:10.1104/pp.107.103101

Supek, F., Bošnjak, M., Škunca, N., & Šmuc, T. (2011). REVIGO Summarizes and Visualizes Long Lists of Gene Ontology Terms. PLoS ONE, 6(7), e21800. doi:10.1371/journal.pone.0021800

Suzuki, M., Kao, C.-Y., Cocciolone, S., & McCarty, D. R. (2002). Maize VP1 complements Arabidopsisabi3 and confers a novel ABA/auxin interaction in roots. The Plant Journal, 28(4), 409-418. doi:10.1046/j.1365-313x.2001.01165.x

Taji, T., Ohsumi, C., Iuchi, S., Seki, M., Kasuga, M., Kobayashi, M., … Shinozaki, K. (2002). Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in Arabidopsis thaliana. The Plant Journal, 29(4), 417-426. doi:10.1046/j.0960-7412.2001.01227.x

Thomashow, M. F. (2010). Molecular Basis of Plant Cold Acclimation: Insights Gained from Studying the CBF Cold Response Pathway: Figure 1. Plant Physiology, 154(2), 571-577. doi:10.1104/pp.110.161794

Toufighi, K., Brady, S. M., Austin, R., Ly, E., & Provart, N. J. (2005). The Botany Array Resource: e-Northerns, Expression Angling, and promoter analyses. The Plant Journal, 43(1), 153-163. doi:10.1111/j.1365-313x.2005.02437.x

Vogel, J. T., Zarka, D. G., Van Buskirk, H. A., Fowler, S. G., & Thomashow, M. F. (2004). Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis. The Plant Journal, 41(2), 195-211. doi:10.1111/j.1365-313x.2004.02288.x

Wang, W., Vinocur, B., Shoseyov, O., & Altman, A. (2004). Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends in Plant Science, 9(5), 244-252. doi:10.1016/j.tplants.2004.03.006

Yamaguchi-Shinozaki, K., & Shinozaki, K. (2006). TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES. Annual Review of Plant Biology, 57(1), 781-803. doi:10.1146/annurev.arplant.57.032905.105444

Yanagisawa, S. (2001). The Transcriptional Activation Domain of the Plant-Specific Dof1 Factor Functions in Plant, Animal, and Yeast Cells. Plant and Cell Physiology, 42(8), 813-822. doi:10.1093/pcp/pce105

Yanagisawa, S. (2002). The Dof family of plant transcription factors. Trends in Plant Science, 7(12), 555-560. doi:10.1016/s1360-1385(02)02362-2

Yanagisawa, S., Akiyama, A., Kisaka, H., Uchimiya, H., & Miwa, T. (2004). Metabolic engineering with Dof1 transcription factor in plants: Improved nitrogen assimilation and growth under low-nitrogen conditions. Proceedings of the National Academy of Sciences, 101(20), 7833-7838. doi:10.1073/pnas.0402267101

Yanagisawa, S., & Schmidt, R. J. (1999). Diversity and similarity among recognition sequences of Dof transcription factors. The Plant Journal, 17(2), 209-214. doi:10.1046/j.1365-313x.1999.00363.x

Yanagisawa, S., & Sheen, J. (1998). Involvement of Maize Dof Zinc Finger Proteins in Tissue-Specific and Light-Regulated Gene Expression. The Plant Cell, 10(1), 75-89. doi:10.1105/tpc.10.1.75

Yang, X., Srivastava, R., Howell, S. H., & Bassham, D. C. (2015). Activation of autophagy by unfolded proteins during endoplasmic reticulum stress. The Plant Journal, 85(1), 83-95. doi:10.1111/tpj.13091

Yoo, S.-D., Cho, Y.-H., & Sheen, J. (2007). Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis. Nature Protocols, 2(7), 1565-1572. doi:10.1038/nprot.2007.199

Zhu, J.-K. (2002). SALT ANDDROUGHTSTRESSSIGNALTRANSDUCTION INPLANTS. Annual Review of Plant Biology, 53(1), 247-273. doi:10.1146/annurev.arplant.53.091401.143329

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