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ACAULIS5 Is Required for Cytokinin Accumulation and Function During Secondary Growth of Populus Trees

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ACAULIS5 Is Required for Cytokinin Accumulation and Function During Secondary Growth of Populus Trees

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Milhinhos, A.; Bollhoner, B.; Blazquez Rodriguez, MA.; Novak, O.; Miguel, CM.; Tuominen, H. (2020). ACAULIS5 Is Required for Cytokinin Accumulation and Function During Secondary Growth of Populus Trees. Frontiers in Plant Science. 11:1-11. https://doi.org/10.3389/fpls.2020.601858

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Título: ACAULIS5 Is Required for Cytokinin Accumulation and Function During Secondary Growth of Populus Trees
Autor: Milhinhos, Ana Bollhoner, Benjamin BLAZQUEZ RODRIGUEZ, MIGUEL ANGEL Novak, Ondrej Miguel, Celia M. Tuominen, Hannele
Entidad UPV: 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] In the primary root and young hypocotyl of Arabidopsis, ACAULIS5 promotes translation of SUPPRESSOR OF ACAULIS51 (SAC51) and thereby inhibits cytokinin biosynthesis and vascular cell division. In this study, the ...[+]
Palabras clave: ACAULIS5 , Cytokinin , POPACAULIS5 , Polyamine , Populus tremula x Populus tremuloides , Thermospermine , Wood development , Xylem
Derechos de uso: Reconocimiento (by)
Fuente:
Frontiers in Plant Science. (eissn: 1664-462X )
DOI: 10.3389/fpls.2020.601858
Editorial:
Frontiers Media SA
Versión del editor: https://doi.org/10.3389/fpls.2020.601858
Código del Proyecto:
info:eu-repo/grantAgreement/FCT//CEEC%2FIND%2F00175%2F2017/
...[+]
info:eu-repo/grantAgreement/FCT//CEEC%2FIND%2F00175%2F2017/
info:eu-repo/grantAgreement/MSMT//CZ.02.1.01%2F0.0%2F0.0%2F16_019%2F0000827/CZ/Plants as a tool for sustainable global development/
info:eu-repo/grantAgreement/FCT//UIDB%2F04551%2F2020/
info:eu-repo/grantAgreement/MINECO//BFU2016-80621-P/ES/ANÁLISIS EVOLUTIVO DE UN 'HUB' FUNCIONAL EN PLANTAS/
info:eu-repo/grantAgreement/Swedish Research Council Formas//232-2009-1698/
info:eu-repo/grantAgreement/VR//621-2013-4949/
info:eu-repo/grantAgreement/VINNOVA//2016-00504/
info:eu-repo/grantAgreement/Knut and Alice Wallenberg Foundation//2016-0341/
info:eu-repo/grantAgreement/BioISI//UIDB%2F04046%2F2020/
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Agradecimientos:
This research was supported by the Swedish Research Council Formas (grant no. 232-2009-1698), the Swedish Research Council VR (grant no. 621-2013-4949), Vinnova (grant no. 201600504), Knut and Alice Wallenberg Foundation ...[+]
Tipo: Artículo

References

Agusti, J., Herold, S., Schwarz, M., Sanchez, P., Ljung, K., Dun, E. A., … Greb, T. (2011). Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proceedings of the National Academy of Sciences, 108(50), 20242-20247. doi:10.1073/pnas.1111902108

Antoniadi, I., Plačková, L., Simonovik, B., Doležal, K., Turnbull, C., Ljung, K., & Novák, O. (2015). Cell-Type-Specific Cytokinin Distribution within the Arabidopsis Primary Root Apex. The Plant Cell, 27(7), 1955-1967. doi:10.1105/tpc.15.00176

Baima, S., Forte, V., Possenti, M., Peñalosa, A., Leoni, G., Salvi, S., … Morelli, G. (2014). Negative Feedback Regulation of Auxin Signaling by ATHB8/ACL5–BUD2 Transcription Module. Molecular Plant, 7(6), 1006-1025. doi:10.1093/mp/ssu051 [+]
Agusti, J., Herold, S., Schwarz, M., Sanchez, P., Ljung, K., Dun, E. A., … Greb, T. (2011). Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proceedings of the National Academy of Sciences, 108(50), 20242-20247. doi:10.1073/pnas.1111902108

Antoniadi, I., Plačková, L., Simonovik, B., Doležal, K., Turnbull, C., Ljung, K., & Novák, O. (2015). Cell-Type-Specific Cytokinin Distribution within the Arabidopsis Primary Root Apex. The Plant Cell, 27(7), 1955-1967. doi:10.1105/tpc.15.00176

Baima, S., Forte, V., Possenti, M., Peñalosa, A., Leoni, G., Salvi, S., … Morelli, G. (2014). Negative Feedback Regulation of Auxin Signaling by ATHB8/ACL5–BUD2 Transcription Module. Molecular Plant, 7(6), 1006-1025. doi:10.1093/mp/ssu051

Bollhöner, B., Jokipii-Lukkari, S., Bygdell, J., Stael, S., Adriasola, M., Muñiz, L., … Tuominen, H. (2017). The function of two type II metacaspases in woody tissues of Populus trees. New Phytologist, 217(4), 1551-1565. doi:10.1111/nph.14945

Chang, S., Puryear, J., & Cairney, J. (1993). A simple and efficient method for isolating RNA from pine trees. Plant Molecular Biology Reporter, 11(2), 113-116. doi:10.1007/bf02670468

Clay, N. K., & Nelson, T. (2005). Arabidopsis thickvein Mutation Affects Vein Thickness and Organ Vascularization, and Resides in a Provascular Cell-Specific Spermine Synthase Involved in Vein Definition and in Polar Auxin Transport. Plant Physiology, 138(2), 767-777. doi:10.1104/pp.104.055756

De Rybel, B., Adibi, M., Breda, A. S., Wendrich, J. R., Smit, M. E., Novák, O., … Weijers, D. (2014). Integration of growth and patterning during vascular tissue formation in Arabidopsis. Science, 345(6197). doi:10.1126/science.1255215

Endo, S., Iwamoto, K., & Fukuda, H. (2017). Overexpression and cosuppression of xylem-related genes in an early xylem differentiation stage-specific manner by the AtTED4 promoter. Plant Biotechnology Journal, 16(2), 451-458. doi:10.1111/pbi.12784

Etchells, J. P., Provost, C. M., & Turner, S. R. (2012). Plant Vascular Cell Division Is Maintained by an Interaction between PXY and Ethylene Signalling. PLoS Genetics, 8(11), e1002997. doi:10.1371/journal.pgen.1002997

Fischer, U., Kucukoglu, M., Helariutta, Y., & Bhalerao, R. P. (2019). The Dynamics of Cambial Stem Cell Activity. Annual Review of Plant Biology, 70(1), 293-319. doi:10.1146/annurev-arplant-050718-100402

Hanzawa, Y., Takahashi, T., & Komeda, Y. (1997). ACL5: an Arabidopsis gene required for internodal elongation after flowering. The Plant Journal, 12(4), 863-874. doi:10.1046/j.1365-313x.1997.12040863.x

Hanzawa, Y. (2000). ACAULIS5, an Arabidopsis gene required for stem elongation, encodes a spermine synthase. The EMBO Journal, 19(16), 4248-4256. doi:10.1093/emboj/19.16.4248

Imai, A., Hanzawa, Y., Komura, M., Yamamoto, K. T., Komeda, Y., & Takahashi, T. (2006). The dwarf phenotype of the Arabidopsis acl5 mutant is suppressed by a mutation in an upstream ORF of a bHLH gene. Development, 133(18), 3575-3585. doi:10.1242/dev.02535

Imai, A., Komura, M., Kawano, E., Kuwashiro, Y., & Takahashi, T. (2008). A semi-dominant mutation in the ribosomal protein L10 gene suppresses the dwarf phenotype of theacl5mutant inArabidopsis thaliana. The Plant Journal, 56(6), 881-890. doi:10.1111/j.1365-313x.2008.03647.x

Immanen, J., Nieminen, K., Duchens Silva, H., Rodríguez Rojas, F., Meisel, L. A., Silva, H., … Helariutta, Y. (2013). Characterization of cytokinin signaling and homeostasis gene families in two hardwood tree species: Populus trichocarpa and Prunus persica. BMC Genomics, 14(1). doi:10.1186/1471-2164-14-885

Immanen, J., Nieminen, K., Smolander, O.-P., Kojima, M., Alonso Serra, J., Koskinen, P., … Helariutta, Y. (2016). Cytokinin and Auxin Display Distinct but Interconnected Distribution and Signaling Profiles to Stimulate Cambial Activity. Current Biology, 26(15), 1990-1997. doi:10.1016/j.cub.2016.05.053

Kakehi, J.-I., Kawano, E., Yoshimoto, K., Cai, Q., Imai, A., & Takahashi, T. (2015). Mutations in Ribosomal Proteins, RPL4 and RACK1, Suppress the Phenotype of a Thermospermine-Deficient Mutant of Arabidopsis thaliana. PLOS ONE, 10(1), e0117309. doi:10.1371/journal.pone.0117309

Karimi, M., Inzé, D., & Depicker, A. (2002). GATEWAY™ vectors for Agrobacterium-mediated plant transformation. Trends in Plant Science, 7(5), 193-195. doi:10.1016/s1360-1385(02)02251-3

Knott, J. M., Römer, P., & Sumper, M. (2007). Putative spermine synthases fromThalassiosira pseudonanaandArabidopsis thalianasynthesize thermospermine rather than spermine. FEBS Letters, 581(16), 3081-3086. doi:10.1016/j.febslet.2007.05.074

Koncz, C., & Schell, J. (1986). The promoter of TL-DNA gene 5 controls the tissue-specific expression of chimaeric genes carried by a novel type of Agrobacterium binary vector. Molecular and General Genetics MGG, 204(3), 383-396. doi:10.1007/bf00331014

Larson, P. R. (1994). The Vascular Cambium. Springer Series in Wood Science. doi:10.1007/978-3-642-78466-8

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

Milhinhos, A., Prestele, J., Bollhöner, B., Matos, A., Vera-Sirera, F., Rambla, J. L., … Miguel, C. M. (2013). Thermospermine levels are controlled by an auxin-dependent feedback loop mechanism inPopulusxylem. The Plant Journal, 75(4), 685-698. doi:10.1111/tpj.12231

Milhinhos, A., Vera-Sirera, F., Blanco-Touriñán, N., Mari-Carmona, C., Carrió-Seguí, À., Forment, J., … Agustí, J. (2019). SOBIR1/EVR prevents precocious initiation of fiber differentiation during wood development through a mechanism involving BP and ERECTA. Proceedings of the National Academy of Sciences, 116(37), 18710-18716. doi:10.1073/pnas.1807863116

Muñiz, L., Minguet, E. G., Singh, S. K., Pesquet, E., Vera-Sirera, F., Moreau-Courtois, C. L., … Tuominen, H. (2008). ACAULIS5 controls Arabidopsis xylem specification through the prevention of premature cell death. Development, 135(15), 2573-2582. doi:10.1242/dev.019349

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

Nieminen, K., Immanen, J., Laxell, M., Kauppinen, L., Tarkowski, P., Dolezal, K., … Helariutta, Y. (2008). Cytokinin signaling regulates cambial development in poplar. Proceedings of the National Academy of Sciences, 105(50), 20032-20037. doi:10.1073/pnas.0805617106

Nilsson, O., Aldén, T., Sitbon, F., Anthony Little, C. H., Chalupa, V., Sandberg, G., & Olsson, O. (1992). Spatial pattern of cauliflower mosaic virus 35S promoter-luciferase expression in transgenic hybrid aspen trees monitored by enzymatic assay and non-destructive imaging. Transgenic Research, 1(5), 209-220. doi:10.1007/bf02524751

Ohashi-Ito, K., Saegusa, M., Iwamoto, K., Oda, Y., Katayama, H., Kojima, M., … Fukuda, H. (2014). A bHLH Complex Activates Vascular Cell Division via Cytokinin Action in Root Apical Meristem. Current Biology, 24(17), 2053-2058. doi:10.1016/j.cub.2014.07.050

Ragni, L., Nieminen, K., Pacheco-Villalobos, D., Sibout, R., Schwechheimer, C., & Hardtke, C. S. (2011). Mobile Gibberellin Directly Stimulates Arabidopsis Hypocotyl Xylem Expansion  . The Plant Cell, 23(4), 1322-1336. doi:10.1105/tpc.111.084020

Savidge, R. A. (1988). Auxin and ethylene regulation of diameter growth in trees. Tree Physiology, 4(4), 401-414. doi:10.1093/treephys/4.4.401

Sibout, R., Plantegenet, S., & Hardtke, C. S. (2008). Flowering as a Condition for Xylem Expansion in Arabidopsis Hypocotyl and Root. Current Biology, 18(6), 458-463. doi:10.1016/j.cub.2008.02.070

Smetana, O., Mäkilä, R., Lyu, M., Amiryousefi, A., Sánchez Rodríguez, F., Wu, M.-F., … Mähönen, A. P. (2019). High levels of auxin signalling define the stem-cell organizer of the vascular cambium. Nature, 565(7740), 485-489. doi:10.1038/s41586-018-0837-0

Sundell, D., Street, N. R., Kumar, M., Mellerowicz, E. J., Kucukoglu, M., Johnsson, C., … Hvidsten, T. R. (2017). AspWood: High-Spatial-Resolution Transcriptome Profiles Reveal Uncharacterized Modularity of Wood Formation in Populus tremula. The Plant Cell, 29(7), 1585-1604. doi:10.1105/tpc.17.00153

Svačinová, J., Novák, O., Plačková, L., Lenobel, R., Holík, J., Strnad, M., & Doležal, K. (2012). A new approach for cytokinin isolation from Arabidopsis tissues using miniaturized purification: pipette tip solid-phase extraction. Plant Methods, 8(1). doi:10.1186/1746-4811-8-17

Tiimonen, H., Häggman, H., Tsai, C.-J., Chiang, V., & Aronen, T. (2007). The seasonal activity and the effect of mechanical bending and wounding on the PtCOMT promoter in Betula pendula Roth. Plant Cell Reports, 26(8), 1205-1214. doi:10.1007/s00299-007-0331-x

Tuominen, H., Puech, L., Fink, S., & Sundberg, B. (1997). A Radial Concentration Gradient of Indole-3-Acetic Acid Is Related to Secondary Xylem Development in Hybrid Aspen. Plant Physiology, 115(2), 577-585. doi:10.1104/pp.115.2.577

Vera-Sirera, F., De Rybel, B., Úrbez, C., Kouklas, E., Pesquera, M., Álvarez-Mahecha, J. C., … Blázquez, M. A. (2015). A bHLH-Based Feedback Loop Restricts Vascular Cell Proliferation in Plants. Developmental Cell, 35(4), 432-443. doi:10.1016/j.devcel.2015.10.022

Vera-Sirera, F., Minguet, E. G., Singh, S. K., Ljung, K., Tuominen, H., Blázquez, M. A., & Carbonell, J. (2010). Role of polyamines in plant vascular development. Plant Physiology and Biochemistry, 48(7), 534-539. doi:10.1016/j.plaphy.2010.01.011

Xu, M., Zhang, B., Su, X., Zhang, S., & Huang, M. (2011). Reference gene selection for quantitative real-time polymerase chain reaction in Populus. Analytical Biochemistry, 408(2), 337-339. doi:10.1016/j.ab.2010.08.044

Zürcher, E., Tavor-Deslex, D., Lituiev, D., Enkerli, K., Tarr, P. T., & Müller, B. (2013). A Robust and Sensitive Synthetic Sensor to Monitor the Transcriptional Output of the Cytokinin Signaling Network in Planta      . Plant Physiology, 161(3), 1066-1075. doi:10.1104/pp.112.211763

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