173 research outputs found

    Modelización espacial de trips (insecta: thysanoptera) en el cultivo de aguacate (persea americana)

    Get PDF
    SE LOGRÓ ESTABLECER MEDIANTE MODELIZACIÓN ESPACIAL LA DISTRIBUCIÓN DE LAS POBLACIONES DE TRIPS EN AGUACATE EN EL ESTADO DE MÉXICO.México es el principal productor y exportador de aguacate en el mundo. Los trips son considerados una de las principales plagas de este cultivo, ya que se alimentan del fruto pequeño y forman crestas o protuberancias, las cuales al crecer el fruto son más visibles, y este pierde valor económico. Además de este daño, las heridas causadas por los trips son el principal causante para que entre la enfermedad denominada roña de fruto. Las alternativas de control de los trips han carecido de eficacia debido, entre otras causas, a que se desconoce su distribución espacial dentro de las huertas de aguacate. Este trabajo tuvo por objetivo determinar la distribución espacial de las poblaciones de trips en aguacate mediante el uso de técnicas de estadística espacial que condujeron a la generación de mapas por medio del “krigeado”. Los resultados demostraron que las poblaciones de trips presentan una distribución de tipo agregada, que fue corroborada por los mapas de densidad. Las infestaciones se distribuyeron en el 100 % de la superficie de las dos parcelas experimentales, lo cual resulta interesante para dirigir las medidas de control sobre áreas específicas de infestación. Se logró determinar estabilidad espacial y temporal a corto plazo de las poblaciones de trips

    Alimentos funcionales para cerdos al destete

    Get PDF
    A functional food is a compound that, being or not a nutrient, has a positive effect on one or several functions in the organism, producing well-being in the animal. The following compounds are considered functional foods: prebiotics, probiotics, symbiotics, antioxidants, secondary products of plant metabolism, structural lipids, polyunsaturated fatty acids, fat metabolism byproducts, bioactive peptides, fi ber, vitamins and minerals. Prebiotics, probiotics and symbiotics are modifi ers of the intestinal microfl ora increasing mainly lactobacilli and bifi dobacteria populations and reducing pathogenic bacteria. Lactobacilli and bifi - dobacteria use oligosaccharides and fructo-oligosaccharides arriving at the colon, producing fatty acids and freeing minerals to be absorbed and utilized by the host. Prebiotics are partially-digestible oligosaccharides; probiotics are microorganisms (mainly lactobacilli and bifi dobacteria); and symbiotics are a mixture of probiotics and prebiotics. During the weaning period, piglets face dramatic changes in feeding management and environment, affecting feed intake and, at the same time, affecting digestive functions resulting in lower growth and higher incidence of disease, mainly diarrhea. Functional food may be an alternative to reduce the effects of weaning on growth performance and health of piglets, to diminish or to avoid gastrointestinal problems during weaning, preventing the proliferation of pathogenic bacteria, and improving digestive functions. All these may help to withdraw antibiotics from piglet feed

    The Arabidopsis Transcription Factor CDF3 Is Involved in Nitrogen Responses and Improves Nitrogen Use Efficiency in Tomato

    Get PDF
    Nitrate is an essential macronutrient and a signal molecule that regulates the expression of multiple genes involved in plant growth and development. Here, we describe the participation of Arabidopsis DNA binding with one finger (DOF) transcription factor CDF3 in nitrate responses and shows that CDF3 gene is induced under nitrate starvation. Moreover, knockout cdf3 mutant plants exhibit nitrate-dependent lateral and primary root modifications, whereas CDF3 overexpression plants show increased biomass and enhanced root development under both nitrogen poor and rich conditions. Expression analyses of 35S::CDF3 lines reveled that CDF3 regulates the expression of an important set of nitrate responsive genes including, glutamine synthetase-1, glutamate synthase-2, nitrate reductase-1, and nitrate transporters NRT2.1, NRT2.4, and NRT2.5 as well as carbon assimilation genes like PK1 and PEPC1 in response to N availability. Consistently, metabolite profiling disclosed that the total amount of key N metabolites like glutamate, glutamine, and asparagine were higher in CDF3-overexpressing plants, but lower in cdf3-1 in N limiting conditions. Moreover, overexpression of CDF3 in tomato increased N accumulation and yield efficiency under both optimum and limiting N supply. These results highlight CDF3 as an important regulatory factor for the nitrate response, and its potential for improving N use efficiency in crops

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

    Full text link
    [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 relation with abiotic stress tolerance is largely unknown. Here, we identify the roles of CDF3, an Arabidopsis DOF gene in abiotic stress responses and developmental processes like flowering time. CDF3 is highly induced by drought, extreme temperatures and abscisic acid treatment. The CDF3 T-DNA insertion mutant cdf3-1 is much more sensitive to drought and low temperature stress, whereas CDF3 overexpression enhances the tolerance of transgenic plants to drought, cold and osmotic stress and promotes late flowering. Transcriptome analysis revealed that CDF3 regulates a set of genes involved in cellular osmoprotection and oxidative stress, including the stress tolerance transcription factors CBFs, DREB2A and ZAT12, which involve both gigantea-dependent and independent pathways. Consistently, metabolite profiling disclosed that the total amount of some protective metabolites including -aminobutyric acid, proline, glutamine and sucrose were higher in CDF3-overexpressing plants. Taken together, these results indicate that CDF3 plays a multifaceted role acting on both flowering time and abiotic stress tolerance, in part by controlling the CBF/DREB2A-CRT/DRE and ZAT10/12 modules.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 Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria (INIA; projects 2009-0004-C01, 2012-0008-C01), Spanish Ministry of Science and Innovation (projects BIO2010-1487, BFU2013-49665-EXP). A.R.C. and J.D.F. were supported by INIA pre-doctoral fellowshipsCorrales, 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.12894S748764405Achard, 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.108.058941Ahuja, 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.2010.08.002Alonso, 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.108.062968BEUVE, 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.xBlümel, 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.2014.11.023Bouche, 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.1037532100Catala, 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.1107161108Chaves, 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/mcn125Chen, 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.2010.09.038Claussen, W. (2005). Proline as a measure of stress in tomato plants. Plant Science, 168(1), 241-248. doi:10.1016/j.plantsci.2004.07.039Clough, 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.xCorrales, 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.1216Corrales, 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/ert451Davletova, 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.105.068254DÉJARDIN, 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/bj3440503Dubois, 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.113.216341Farrant, 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.2011.03.018Fornara, 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.12759Fornara, 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.2009.06.015Fowler, 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/18.17.4679Galmés, 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.xGill, 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.2010.08.016Gilmour, 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.d4Gong, 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/erq167Gould, 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.105.039990Han, 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.2012.12.002Hernando-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:10.1186/1471-2229-12-202Zou, 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/bj20110060Hussain, 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.514Imaizumi, 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.1110586Ingram, 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.47.1.377Jarillo, 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/200806s1-391Izaurralde, 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/16.21.6535Karimi, M., Depicker, A., & Hilson, P. (2007). Recombinational Cloning with Plant Gateway Vectors. Plant Physiology, 145(4), 1144-1154. doi:10.1104/pp.107.106989Kim, 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/s00299-009-0813-0Kiyosue, 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/bf00028874Kurai, 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.xLiu, 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:10.2307/3870648Matsui, 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/pcn101Medina, 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.119.2.463Messerli, 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.106.090795Mittler, R. (2006). Abiotic stress, the field environment and stress combination. Trends in Plant Science, 11(1), 15-19. doi:10.1016/j.tplants.2005.11.002Mizoguchi, 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.105.033464Munns, R., & Tester, M. (2008). Mechanisms of Salinity Tolerance. Annual Review of Plant Biology, 59(1), 651-681. doi:10.1146/annurev.arplant.59.032607.092911Murashige, 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.xNishiyama, 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.0032124Noguero, 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.2013.03.016Novillo, 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.0705639105OliverosJ.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:10.1186/1756-0500-1-93Osakabe, 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.xPark, D. H. (1999). Control of Circadian Rhythms and Photoperiodic Flowering by the Arabidopsis GIGANTEA Gene. Science, 285(5433), 1579-1582. doi:10.1126/science.285.5433.1579Rajasekaran, 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/p99-003Rizhsky, 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.103.033431Rosso, 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.0000009297.37235.4aRueda-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.xSakuma, 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.105.035881Sato, 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/s00299-007-0470-0Sawa, 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.1146994Scarpeci, 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/s11103-013-0090-8Seki, 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)00030-2Shelp, 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.2011.12.006Shi, 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.12155Shinozaki, 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/erl164Shinozaki, 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-xSkirycz, 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.2010.03.002Snedden, 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.108.2.543STITT, 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.xStudart-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.107.103101Supek, 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.0021800Suzuki, 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.xTaji, 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.xThomashow, 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.110.161794Toufighi, 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.xVogel, 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.xWang, 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.2004.03.006Yamaguchi-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.57.032905.105444Yanagisawa, 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/pce105Yanagisawa, S. (2002). The Dof family of plant transcription factors. Trends in Plant Science, 7(12), 555-560. doi:10.1016/s1360-1385(02)02362-2Yanagisawa, 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.0402267101Yanagisawa, 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.xYanagisawa, 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.10.1.75Yang, X., Srivastava, R., Howell, S. H., & Bassham, D. C. (2015). Activation of autophagy by unfolded proteins d

    A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.

    Get PDF
    We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120 controls of European descent from five studies followed by a replication strategy, which included 8,382 cases and 48,275 controls from 16 studies. In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. We confirmed four previously identified genome-wide associations on chromosomes 3q28, 4p16.3, 8q24.21 and 8q24.3, validated previous candidate associations for the GSTM1 deletion (P = 4 × 10⁻¹¹) and a tag SNP for NAT2 acetylation status (P = 4 × 10⁻¹¹), and found interactions with smoking in both regions. Our findings on common variants associated with bladder cancer risk should provide new insights into the mechanisms of carcinogenesis

    A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.

    Get PDF
    We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120 controls of European descent from five studies followed by a replication strategy, which included 8,382 cases and 48,275 controls from 16 studies. In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. We confirmed four previously identified genome-wide associations on chromosomes 3q28, 4p16.3, 8q24.21 and 8q24.3, validated previous candidate associations for the GSTM1 deletion (P = 4 × 10⁻¹¹) and a tag SNP for NAT2 acetylation status (P = 4 × 10⁻¹¹), and found interactions with smoking in both regions. Our findings on common variants associated with bladder cancer risk should provide new insights into the mechanisms of carcinogenesis

    Breast cancer risks associated with missense variants in breast cancer susceptibility genes

    Get PDF
    BACKGROUND: Protein truncating variants in ATM, BRCA1, BRCA2, CHEK2, and PALB2 are associated with increased breast cancer risk, but risks associated with missense variants in these genes are uncertain. METHODS: We analyzed data on 59,639 breast cancer cases and 53,165 controls from studies participating in the Breast Cancer Association Consortium BRIDGES project. We sampled training (80%) and validation (20%) sets to analyze rare missense variants in ATM (1146 training variants), BRCA1 (644), BRCA2 (1425), CHEK2 (325), and PALB2 (472). We evaluated breast cancer risks according to five in silico prediction-of-deleteriousness algorithms, functional protein domain, and frequency, using logistic regression models and also mixture models in which a subset of variants was assumed to be risk-associated. RESULTS: The most predictive in silico algorithms were Helix (BRCA1, BRCA2 and CHEK2) and CADD (ATM). Increased risks appeared restricted to functional protein domains for ATM (FAT and PIK domains) and BRCA1 (RING and BRCT domains). For ATM, BRCA1, and BRCA2, data were compatible with small subsets (approximately 7%, 2%, and 0.6%, respectively) of rare missense variants giving similar risk to those of protein truncating variants in the same gene. For CHEK2, data were more consistent with a large fraction (approximately 60%) of rare missense variants giving a lower risk (OR 1.75, 95% CI (1.47-2.08)) than CHEK2 protein truncating variants. There was little evidence for an association with risk for missense variants in PALB2. The best fitting models were well calibrated in the validation set. CONCLUSIONS: These results will inform risk prediction models and the selection of candidate variants for functional assays and could contribute to the clinical reporting of gene panel testing for breast cancer susceptibility

    The impact of coding germline variants on contralateral breast cancer risk and survival

    Get PDF
    Evidence linking coding germline variants in breast cancer (BC)-susceptibility genes other than BRCA1, BRCA2, and CHEK2 with contralateral breast cancer (CBC) risk and breast cancer-specific survival (BCSS) is scarce. The aim of this study was to assess the association of protein-truncating variants (PTVs) and rare missense variants (MSVs) in nine known (ATM, BARD1, BRCA1, BRCA2, CHEK2, PALB2, RAD51C, RAD51D, and TP53) and 25 suspected BC-susceptibility genes with CBC risk and BCSS. Hazard ratios (HRs) and 95% confidence intervals (CIs) were estimated with Cox regression models. Analyses included 34,401 women of European ancestry diagnosed with BC, including 676 CBCs and 3,449 BC deaths; the median follow-up was 10.9 years. Subtype analyses were based on estrogen receptor (ER) status of the first BC. Combined PTVs and pathogenic/likely pathogenic MSVs in BRCA1, BRCA2, and TP53 and PTVs in CHEK2 and PALB2 were associated with increased CBC risk [HRs (95% CIs): 2.88 (1.70–4.87), 2.31 (1.39–3.85), 8.29 (2.53–27.21), 2.25 (1.55–3.27), and 2.67 (1.33–5.35), respectively]. The strongest evidence of association with BCSS was for PTVs and pathogenic/likely pathogenic MSVs in BRCA2 (ER-positive BC) and TP53 and PTVs in CHEK2 [HRs (95% CIs): 1.53 (1.13–2.07), 2.08 (0.95–4.57), and 1.39 (1.13–1.72), respectively, after adjusting for tumor characteristics and treatment]. HRs were essentially unchanged when censoring for CBC, suggesting that these associations are not completely explained by increased CBC risk, tumor characteristics, or treatment. There was limited evidence of associations of PTVs and/or rare MSVs with CBC risk or BCSS for the 25 suspected BC genes. The CBC findings are relevant to treatment decisions, follow-up, and screening after BC diagnosis.</p

    Incorporating progesterone receptor expression into the PREDICT breast prognostic model

    Get PDF
    Background: Predict Breast (www.predict.nhs.uk) is an online prognostication and treatment benefit tool for early invasive breast cancer. The aim of this study was to incorporate the prognostic effect of progesterone receptor (PR) status into a new version of PREDICT and to compare its performance to the current version (2.2).Method: The prognostic effect of PR status was based on the analysis of data from 45,088 European patients with breast cancer from 49 studies in the Breast Cancer Association Consortium. Cox proportional hazard models were used to estimate the hazard ratio for PR status. Data from a New Zealand study of 11,365 patients with early invasive breast cancer were used for external validation. Model calibration and discrimination were used to test the model performance.Results: Having a PR-positive tumour was associated with a 23% and 28% lower risk of dying from breast cancer for women with oestrogen receptor (ER)-negative and ER-positive breast cancer, respectively. The area under the ROC curve increased with the addition of PR status from 0.807 to 0.809 for patients with ER-negative tumours (p = 0.023) and from 0.898 to 0. 902 for patients with ER-positive tumours (p = 2.3 x 10(-6)) in the New Zealand cohort. Model calibration was modest with 940 observed deaths compared to 1151 predicted.Conclusion: The inclusion of the prognostic effect of PR status to PREDICT Breast has led to an improvement of model performance and more accurate absolute treatment benefit predic-tions for individual patients. Further studies should determine whether the baseline hazard function requires recalibration. (C) 2022 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).Peer reviewe
    corecore