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Lotus japonicus NOOT-BOP-COCH-LIKE1 is essential for nodule, nectary, leaf and flower development

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Lotus japonicus NOOT-BOP-COCH-LIKE1 is essential for nodule, nectary, leaf and flower development

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Magne, K.; George, J.; Berbel Tornero, A.; Broquet, B.; Madueño Albi, F.; Andersen, S.; Ratet, P. (2018). Lotus japonicus NOOT-BOP-COCH-LIKE1 is essential for nodule, nectary, leaf and flower development. The Plant Journal. 94(5):880-894. https://doi.org/10.1111/tpj.13905

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Título: Lotus japonicus NOOT-BOP-COCH-LIKE1 is essential for nodule, nectary, leaf and flower development
Autor: Magne, K. George, J. Berbel Tornero, Ana Broquet, B. Madueño Albi, Francisco Andersen, S. Ratet, P.
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] The NOOT-BOP-COCH-LIKE (NBCL) genes are orthologs of Arabidopsis thaliana BLADE-ON-PETIOLE1/2. The NBCLs are developmental regulators essential for plant shaping, mainly through the regulation of organ boundaries, the ...[+]
Palabras clave: NOOT-BOP-COCH-LIKE genes , Determinate nodule , Nodule identity , Nectary glands , Flower development , Leaf patterning , Lotus japonicus , Organogenesis
Derechos de uso: Reserva de todos los derechos
Fuente:
The Plant Journal. (issn: 0960-7412 )
DOI: 10.1111/tpj.13905
Editorial:
Blackwell Publishing
Versión del editor: https://doi.org/10.1111/tpj.13905
Código del Proyecto:
info:eu-repo/grantAgreement/ANR//ANR-14-CE19-0003/FR/The plant NOOT genes are guards for the symbiotic organ identity and abscission capacity/NOOT/
Agradecimientos:
This work was supported by the CNRS and by the grants ANR-14-CE19-0003 (NOOT) from the Agence National de la Recherche (ANR) to PR. This work has benefited from the facilities and expertise of the Servicio de Microscopia ...[+]
Tipo: Artículo

References

Aida, M., & Tasaka, M. (2006). Genetic control of shoot organ boundaries. Current Opinion in Plant Biology, 9(1), 72-77. doi:10.1016/j.pbi.2005.11.011

Aida, M., & Tasaka, M. (2006). Morphogenesis and Patterning at the Organ Boundaries in the Higher Plant Shoot Apex. Plant Molecular Biology, 60(6), 915-928. doi:10.1007/s11103-005-2760-7

Aida, M., Ishida, T., Fukaki, H., Fujisawa, H., & Tasaka, M. (1997). Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant. The Plant Cell, 9(6), 841-857. doi:10.1105/tpc.9.6.841 [+]
Aida, M., & Tasaka, M. (2006). Genetic control of shoot organ boundaries. Current Opinion in Plant Biology, 9(1), 72-77. doi:10.1016/j.pbi.2005.11.011

Aida, M., & Tasaka, M. (2006). Morphogenesis and Patterning at the Organ Boundaries in the Higher Plant Shoot Apex. Plant Molecular Biology, 60(6), 915-928. doi:10.1007/s11103-005-2760-7

Aida, M., Ishida, T., Fukaki, H., Fujisawa, H., & Tasaka, M. (1997). Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant. The Plant Cell, 9(6), 841-857. doi:10.1105/tpc.9.6.841

AKASAKA, Y. (1998). Morphological Alterations and Root Nodule Formation inAgrobacterium rhizogenes-mediated Transgenic Hairy Roots of Peanut (Arachis hypogaeaL.). Annals of Botany, 81(2), 355-362. doi:10.1006/anbo.1997.0566

Benlloch, R., Berbel, A., Ali, L., Gohari, G., Millán, T., & Madueño, F. (2015). Genetic control of inflorescence architecture in legumes. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.00543

Berbel, A., Ferrándiz, C., Hecht, V., Dalmais, M., Lund, O. S., Sussmilch, F. C., … Madueño, F. (2012). VEGETATIVE1 is essential for development of the compound inflorescence in pea. Nature Communications, 3(1). doi:10.1038/ncomms1801

Blázquez, M. A., Ferrándiz, C., Madueño, F., & Parcy, F. (2006). How Floral Meristems are Built. Plant Molecular Biology, 60(6), 855-870. doi:10.1007/s11103-006-0013-z

Brown, S. M., Oparka, K. J., Sprent, J. I., & Walsh, K. B. (1995). Symplastic transport in soybean root nodules. Soil Biology and Biochemistry, 27(4-5), 387-399. doi:10.1016/0038-0717(95)98609-r

Chen, Y., Chen, W., Li, X., Jiang, H., Wu, P., Xia, K., … Wu, G. (2013). Knockdown of LjIPT3 influences nodule development in Lotus japonicus. Plant and Cell Physiology, 55(1), 183-193. doi:10.1093/pcp/pct171

Cho, E., & Zambryski, P. C. (2011). ORGAN BOUNDARY1defines a gene expressed at the junction between the shoot apical meristem and lateral organs. Proceedings of the National Academy of Sciences, 108(5), 2154-2159. doi:10.1073/pnas.1018542108

Couzigou, J.-M., & Ratet, P. (2015). NOOT-Dependent Control of Nodule Identity: Nodule Homeosis and Merirostem Perturbation. Biological Nitrogen Fixation, 487-498. doi:10.1002/9781119053095.ch49

Couzigou, J.-M., Zhukov, V., Mondy, S., Abu el Heba, G., Cosson, V., Ellis, T. H. N., … Ratet, P. (2012). NODULE ROOT and COCHLEATA Maintain Nodule Development and Are Legume Orthologs of Arabidopsis BLADE-ON-PETIOLE Genes. The Plant Cell, 24(11), 4498-4510. doi:10.1105/tpc.112.103747

Couzigou, J.-M., Magne, K., Mondy, S., Cosson, V., Clements, J., & Ratet, P. (2015). The legume NOOT-BOP-COCH-LIKE genes are conserved regulators of abscission, a major agronomical trait in cultivated crops. New Phytologist, 209(1), 228-240. doi:10.1111/nph.13634

Czechowski, T., Stitt, M., Altmann, T., Udvardi, M. K., & Scheible, W.-R. (2005). Genome-Wide Identification and Testing of Superior Reference Genes for Transcript Normalization in Arabidopsis. Plant Physiology, 139(1), 5-17. doi:10.1104/pp.105.063743

Dong, Z., Zhao, Z., Liu, C., Luo, J., Yang, J., Huang, W., … Luo, D. (2005). Floral Patterning in Lotus japonicus. Plant Physiology, 137(4), 1272-1282. doi:10.1104/pp.104.054288

Ehrhardt, D., Atkinson, E., & Long. (1992). Depolarization of alfalfa root hair membrane potential by Rhizobium meliloti Nod factors. Science, 256(5059), 998-1000. doi:10.1126/science.10744524

Feng, X., Zhao, Z., Tian, Z., Xu, S., Luo, Y., Cai, Z., … Luo, D. (2006). Control of petal shape and floral zygomorphy in Lotus japonicus. Proceedings of the National Academy of Sciences, 103(13), 4970-4975. doi:10.1073/pnas.0600681103

Ferguson, B. J., & Reid, J. B. (2005). Cochleata: Getting to the Root of Legume Nodules. Plant and Cell Physiology, 46(9), 1583-1589. doi:10.1093/pcp/pci171

Ferraioli, S., Tatè, R., Rogato, A., Chiurazzi, M., & Patriarca, E. J. (2004). Development of Ectopic Roots from Abortive Nodule Primordia. Molecular Plant-Microbe Interactions®, 17(10), 1043-1050. doi:10.1094/mpmi.2004.17.10.1043

Franssen, H. J., Xiao, T. T., Kulikova, O., Wan, X., Bisseling, T., Scheres, B., & Heidstra, R. (2015). Root developmental programs shape the Medicago truncatula nodule meristem. Development, 142(17), 2941-2950. doi:10.1242/dev.120774

Gonzalez-Rizzo, S., Crespi, M., & Frugier, F. (2006). The Medicago truncatula CRE1 Cytokinin Receptor Regulates Lateral Root Development and Early Symbiotic Interaction with Sinorhizobium meliloti. The Plant Cell, 18(10), 2680-2693. doi:10.1105/tpc.106.043778

Gourion, B., Sulser, S., Frunzke, J., Francez-Charlot, A., Stiefel, P., Pessi, G., … Fischer, H.-M. (2009). The PhyR-σEcfGsignalling cascade is involved in stress response and symbiotic efficiency inBradyrhizobium japonicum. Molecular Microbiology, 73(2), 291-305. doi:10.1111/j.1365-2958.2009.06769.x

Gourlay, C. W., Hofer, J. M. I., & Ellis, T. H. N. (2000). Pea Compound Leaf Architecture Is Regulated by Interactions among the Genes UNIFOLIATA, COCHLEATA, AFILA, and TENDRIL-LESS. The Plant Cell, 12(8), 1279-1294. doi:10.1105/tpc.12.8.1279

Guether, M., Balestrini, R., Hannah, M., He, J., Udvardi, M. K., & Bonfante, P. (2009). Genome-wide reprogramming of regulatory networks, transport, cell wall and membrane biogenesis during arbuscular mycorrhizal symbiosis in Lotus japonicus. New Phytologist, 182(1), 200-212. doi:10.1111/j.1469-8137.2008.02725.x

Guinel, F. C. (2009). Getting around the legume nodule: I. The structure of the peripheral zone in four nodule types. Botany, 87(12), 1117-1138. doi:10.1139/b09-074

Ha, C. M. (2003). The BLADE-ON-PETIOLE 1 gene controls leaf pattern formation through the modulation of meristematic activity in Arabidopsis. Development, 130(1), 161-172. doi:10.1242/dev.00196

Ha, C. M., Jun, J. H., Nam, H. G., & Fletcher, J. C. (2004). BLADE-ON-PETIOLE1 Encodes a BTB/POZ Domain Protein Required for Leaf Morphogenesis in Arabidopsis thaliana. Plant and Cell Physiology, 45(10), 1361-1370. doi:10.1093/pcp/pch201

Ha, C. M., Jun, J. H., Nam, H. G., & Fletcher, J. C. (2007). BLADE-ON-PETIOLE1 and 2 Control Arabidopsis Lateral Organ Fate through Regulation of LOB Domain and Adaxial-Abaxial Polarity Genes. The Plant Cell, 19(6), 1809-1825. doi:10.1105/tpc.107.051938

Handberg, K., & Stougaard, J. (1992). Lotus japonicus, an autogamous, diploid legume species for classical and molecular genetics. The Plant Journal, 2(4), 487-496. doi:10.1111/j.1365-313x.1992.00487.x

Hepworth, S. R., & Pautot, V. A. (2015). Beyond the Divide: Boundaries for Patterning and Stem Cell Regulation in Plants. Frontiers in Plant Science, 6. doi:10.3389/fpls.2015.01052

Hepworth, S. R., Zhang, Y., McKim, S., Li, X., & Haughn, G. W. (2005). BLADE-ON-PETIOLE–Dependent Signaling Controls Leaf and Floral Patterning in Arabidopsis. The Plant Cell, 17(5), 1434-1448. doi:10.1105/tpc.104.030536

Hepworth, S. R., Klenz, J. E., & Haughn, G. W. (2005). UFO in the Arabidopsis inflorescence apex is required for floral-meristem identity and bract suppression. Planta, 223(4), 769-778. doi:10.1007/s00425-005-0138-3

Hibara, K., Karim, M. R., Takada, S., Taoka, K., Furutani, M., Aida, M., & Tasaka, M. (2006). Arabidopsis CUP-SHAPED COTYLEDON3 Regulates Postembryonic Shoot Meristem and Organ Boundary Formation. The Plant Cell, 18(11), 2946-2957. doi:10.1105/tpc.106.045716

Høgslund, N., Radutoiu, S., Krusell, L., Voroshilova, V., Hannah, M. A., Goffard, N., … Stougaard, J. (2009). Dissection of Symbiosis and Organ Development by Integrated Transcriptome Analysis of Lotus japonicus Mutant and Wild-Type Plants. PLoS ONE, 4(8), e6556. doi:10.1371/journal.pone.0006556

JARVIS, B. D. W., PANKHURST, C. E., & PATEL, J. J. (1982). Rhizobium loti, a New Species of Legume Root Nodule Bacteria. International Journal of Systematic Bacteriology, 32(3), 378-380. doi:10.1099/00207713-32-3-378

Karim, M. R., Hirota, A., Kwiatkowska, D., Tasaka, M., & Aida, M. (2009). A Role for Arabidopsis PUCHI in Floral Meristem Identity and Bract Suppression. The Plant Cell, 21(5), 1360-1372. doi:10.1105/tpc.109.067025

Khan, M., Xu, M., Murmu, J., Tabb, P., Liu, Y., Storey, K., … Hepworth, S. R. (2011). Antagonistic Interaction of BLADE-ON-PETIOLE1 and 2 with BREVIPEDICELLUS and PENNYWISE Regulates Arabidopsis Inflorescence Architecture. Plant Physiology, 158(2), 946-960. doi:10.1104/pp.111.188573

Koch, B., & Evans, H. J. (1966). Reduction of Acetylene to Ethylene by Soybean Root Nodules. Plant Physiology, 41(10), 1748-1750. doi:10.1104/pp.41.10.1748

Krall, L., Wiedemann, U., Unsin, G., Weiss, S., Domke, N., & Baron, C. (2002). Detergent extraction identifies different VirB protein subassemblies of the type IV secretion machinery in the membranes of Agrobacterium tumefaciens. Proceedings of the National Academy of Sciences, 99(17), 11405-11410. doi:10.1073/pnas.172390699

Kumagai, H., & Kouchi, H. (2003). Gene Silencing by Expression of Hairpin RNA in Lotus japonicus Roots and Root Nodules. Molecular Plant-Microbe Interactions®, 16(8), 663-668. doi:10.1094/mpmi.2003.16.8.663

Levin, J. Z., & Meyerowitz, E. M. (1995). UFO: an Arabidopsis gene involved in both floral meristem and floral organ development. The Plant Cell, 7(5), 529-548. doi:10.1105/tpc.7.5.529

Long, J., & Barton, M. K. (2000). Initiation of Axillary and Floral Meristems in Arabidopsis. Developmental Biology, 218(2), 341-353. doi:10.1006/dbio.1999.9572

Małolepszy, A., Mun, T., Sandal, N., Gupta, V., Dubin, M., Urbański, D., … Andersen, S. U. (2016). The LORE 1 insertion mutant resource. The Plant Journal, 88(2), 306-317. doi:10.1111/tpj.13243

McKim, S. M., Stenvik, G.-E., Butenko, M. A., Kristiansen, W., Cho, S. K., Hepworth, S. R., … Haughn, G. W. (2008). The BLADE-ON-PETIOLE genes are essential for abscission zone formation in Arabidopsis. Development, 135(8), 1537-1546. doi:10.1242/dev.012807

Mun, T., Bachmann, A., Gupta, V., Stougaard, J., & Andersen, S. U. (2016). Lotus Base: An integrated information portal for the model legume Lotus japonicus. Scientific Reports, 6(1). doi:10.1038/srep39447

Norberg, M. (2005). The BLADE ON PETIOLE genes act redundantly to control the growth and development of lateral organs. Development, 132(9), 2203-2213. doi:10.1242/dev.01815

Okamoto, S., Yoro, E., Suzaki, T., & Kawaguchi, M. (2013). Hairy Root Transformation in Lotus japonicus. BIO-PROTOCOL, 3(12). doi:10.21769/bioprotoc.795

Oldroyd, G. E. D. (2013). Speak, friend, and enter: signalling systems that promote beneficial symbiotic associations in plants. Nature Reviews Microbiology, 11(4), 252-263. doi:10.1038/nrmicro2990

Oldroyd, G. E. D., & Downie, J. A. (2008). Coordinating Nodule Morphogenesis with Rhizobial Infection in Legumes. Annual Review of Plant Biology, 59(1), 519-546. doi:10.1146/annurev.arplant.59.032607.092839

Pate, J. S., Gunning, B. E. S., & Briarty, L. G. (1969). Ultrastructure and functioning of the transport system of the leguminous root nodule. Planta, 85(1), 11-34. doi:10.1007/bf00387658

Ping, J., Liu, Y., Sun, L., Zhao, M., Li, Y., She, M., … Ma, J. (2014). Dt2 Is a Gain-of-Function MADS-Domain Factor Gene That Specifies Semideterminacy in Soybean. The Plant Cell, 26(7), 2831-2842. doi:10.1105/tpc.114.126938

Quandt, H.-J. (1993). Transgenic Root Nodules ofVicia hirsuta:A Fast and Efficient System for the Study of Gene Expression in Indeterminate-Type Nodules. Molecular Plant-Microbe Interactions, 6(6), 699. doi:10.1094/mpmi-6-699

Roux, B., Rodde, N., Jardinaud, M.-F., Timmers, T., Sauviac, L., Cottret, L., … Gamas, P. (2014). An integrated analysis of plant and bacterial gene expression in symbiotic root nodules using laser-capture microdissection coupled to RNA sequencing. The Plant Journal, 77(6), 817-837. doi:10.1111/tpj.12442

Schultz, E. A., & Haughn, G. W. (1991). LEAFY, a Homeotic Gene That Regulates Inflorescence Development in Arabidopsis. The Plant Cell, 771-781. doi:10.1105/tpc.3.8.771

Sinharoy, S., & DasGupta, M. (2009). RNA Interference Highlights the Role of CCaMK in Dissemination of Endosymbionts in the Aeschynomeneae Legume Arachis. Molecular Plant-Microbe Interactions®, 22(11), 1466-1475. doi:10.1094/mpmi-22-11-1466

Soltis, D. E., Soltis, P. S., Morgan, D. R., Swensen, S. M., Mullin, B. C., Dowd, J. M., & Martin, P. G. (1995). Chloroplast gene sequence data suggest a single origin of the predisposition for symbiotic nitrogen fixation in angiosperms. Proceedings of the National Academy of Sciences, 92(7), 2647-2651. doi:10.1073/pnas.92.7.2647

Soyano, T., Kouchi, H., Hirota, A., & Hayashi, M. (2013). NODULE INCEPTION Directly Targets NF-Y Subunit Genes to Regulate Essential Processes of Root Nodule Development in Lotus japonicus. PLoS Genetics, 9(3), e1003352. doi:10.1371/journal.pgen.1003352

Suzaki, T., Yoro, E., & Kawaguchi, M. (2015). Leguminous Plants: Inventors of Root Nodules to Accommodate Symbiotic Bacteria. International Review of Cell and Molecular Biology, 111-158. doi:10.1016/bs.ircmb.2015.01.004

Takeda, S., Hanano, K., Kariya, A., Shimizu, S., Zhao, L., Matsui, M., … Aida, M. (2011). CUP-SHAPED COTYLEDON1 transcription factor activates the expression of LSH4 and LSH3, two members of the ALOG gene family, in shoot organ boundary cells. The Plant Journal, 66(6), 1066-1077. doi:10.1111/j.1365-313x.2011.04571.x

Tavakol, E., Okagaki, R., Verderio, G., Shariati J., V., Hussien, A., Bilgic, H., … Rossini, L. (2015). The Barley Uniculme4 Gene Encodes a BLADE-ON-PETIOLE-Like Protein That Controls Tillering and Leaf Patterning. Plant Physiology, 168(1), 164-174. doi:10.1104/pp.114.252882

Udvardi, M., & Poole, P. S. (2013). Transport and Metabolism in Legume-Rhizobia Symbioses. Annual Review of Plant Biology, 64(1), 781-805. doi:10.1146/annurev-arplant-050312-120235

Van de Velde, W., Guerra, J. C. P., Keyser, A. D., De Rycke, R., Rombauts, S., Maunoury, N., … Goormachtig, S. (2006). Aging in Legume Symbiosis. A Molecular View on Nodule Senescence in Medicago truncatula. Plant Physiology, 141(2), 711-720. doi:10.1104/pp.106.078691

Verdier, J., Torres-Jerez, I., Wang, M., Andriankaja, A., Allen, S. N., He, J., … Udvardi, M. K. (2013). Establishment of theLotus japonicusGene Expression Atlas (LjGEA) and its use to explore legume seed maturation. The Plant Journal, 74(2), 351-362. doi:10.1111/tpj.12119

WALSH, K. B., McCULLY, M. E., & CANNY, M. J. (1989). Vascular transport and soybean nodule function: nodule xylem is a blind alley, not a throughway. Plant, Cell and Environment, 12(4), 395-405. doi:10.1111/j.1365-3040.1989.tb01955.x

Wang, Q., Hasson, A., Rossmann, S., & Theres, K. (2015). Divide et impera : boundaries shape the plant body and initiate new meristems. New Phytologist, 209(2), 485-498. doi:10.1111/nph.13641

Weng, L., Tian, Z., Feng, X., Li, X., Xu, S., Hu, X., … Yang, J. (2011). Petal Development in Lotus japonicus. Journal of Integrative Plant Biology, 53(10), 770-782. doi:10.1111/j.1744-7909.2011.01072.x

Werner, G. D. A., Cornwell, W. K., Sprent, J. I., Kattge, J., & Kiers, E. T. (2014). A single evolutionary innovation drives the deep evolution of symbiotic N2-fixation in angiosperms. Nature Communications, 5(1). doi:10.1038/ncomms5087

Wopereis, J., Pajuelo, E., Dazzo, F. B., Jiang, Q., Gresshoff, P. M., de Bruijn, F. J., … Szczyglowski, K. (2000). Short root mutant of Lotus japonicus with a dramatically altered symbiotic phenotype. The Plant Journal, 23(1), 97-114. doi:10.1046/j.1365-313x.2000.00799.x

Wu, X.-M., Yu, Y., Han, L.-B., Li, C.-L., Wang, H.-Y., Zhong, N.-Q., … Xia, G.-X. (2012). The Tobacco BLADE-ON-PETIOLE2 Gene Mediates Differentiation of the Corolla Abscission Zone by Controlling Longitudinal Cell Expansion. Plant Physiology, 159(2), 835-850. doi:10.1104/pp.112.193482

Xu, M., Hu, T., McKim, S. M., Murmu, J., Haughn, G. W., & Hepworth, S. R. (2010). Arabidopsis BLADE-ON-PETIOLE1 and 2 promote floral meristem fate and determinacy in a previously undefined pathway targeting APETALA1 and AGAMOUS-LIKE24. The Plant Journal, 63(6), 974-989. doi:10.1111/j.1365-313x.2010.04299.x

Xu, C., Park, S. J., Van Eck, J., & Lippman, Z. B. (2016). Control of inflorescence architecture in tomato by BTB/POZ transcriptional regulators. Genes & Development, 30(18), 2048-2061. doi:10.1101/gad.288415.116

Yaxley, J. (2001). Leaf and Flower Development in Pea (Pisum sativum L.): Mutants cochleata andunifoliata. Annals of Botany, 88(2), 225-234. doi:10.1006/anbo.2001.1448

Žádníková, P., & Simon, R. (2014). How boundaries control plant development. Current Opinion in Plant Biology, 17, 116-125. doi:10.1016/j.pbi.2013.11.013

Zhang, S., Sandal, N., Polowick, P. L., Stiller, J., Stougaard, J., & Fobert, P. R. (2003). Proliferating Floral Organs (Pfo ), a Lotus japonicus gene required for specifying floral meristem determinacy and organ identity, encodes an F-box protein. The Plant Journal, 33(4), 607-619. doi:10.1046/j.1365-313x.2003.01660.x

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