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INRA
24, chemin de Borde Rouge –Auzeville – CS52627
31326 Castanet Tolosan CEDEX - France

Dernière mise à jour : Mai 2018

Menu LIPM INRA CNRS

Laboratory of Plant-Microbe Interactions - LIPM

Laboratory of Plant-Microbe Interactions

Publications - Symbiotic signalling

Publications

  • Girardin A, Wang T, Ding Y, Keller J, Buendia L, Gaston M, Ribeyre C, Gasciolli V, Auriac MC, Vernié T, Bendahmane A, Ried MK, Parniske M, Vandenbussche M, Schorderet M, Reinhardt D, Delaux PM, Bono JJ and Lefebvre B. 2019. LCO receptors involved in arbuscular mycorrhiza are functional for rhizobia perception in legumes. Current Biol, in press
  • Carrère S, Verdenaud M, Gough C, Gouzy J, Gamas P. 2019. LeGOO: An Expertized Knowledge Database for the Model Legume Medicago truncatula. Plant Cell Physiol, in press
  • Buendia L, Ribeyre C, Bensmihen S, Lefebvre B. 2019. Brachypodium distachyon tar2lhypo mutant shows reduced root developmental response to symbiotic signal but increased arbuscular mycorrhiza. Plant Signal Behav 14: e1651608.
    PubMed
  • Sorroche F, Walch M, Zou L, Rengel D, Maillet F, Gibelin-Viala C, Poinsot V, Chervin C, Masson-Boivin C, Gough C, Batut J, Garnerone AM. 2019. Endosymbiotic Sinorhizobium meliloti modulate Medicago root susceptibility to secondary infection via ethylene. New Phytol, 223:1505-1515.
    PubMed
  • Gibelin-Viala C, Amblard E, Puech-Pages V, Bonhomme M, Garcia M, Bascaules-Bedin A, Fliegmann J, Wen J, Mysore KS, le Signor C, Jacquet C, Gough C. 2019 The Medicago truncatula LysM receptor-like kinase LYK9 plays a dual role in immunity and the arbuscular mycorrhizal symbiosis. New Phytol, 223:1516-1529.
    PubMed
  • Buendia L., Maillet F., O’Connor D., van de-Kerkhove Q., Danoun S., Gough C., Lefebvre B. and Bensmihen S. 2019. LCOs promote lateral root formation and modify auxin homeostasis in Brachypodium distachyon. New Phytol, 221: 2190-2202
    PubMed
  • Buendia L., Girardin A., Wang T., Cottret L. and Lefebvre B. 2018 LysM Receptor-Like Kinase and LysM Receptor-Like Protein Families: An Update on Phylogeny and Functional Characterization. Front. Plant Sci. 9:1531
    PubMed
  • Buhian W.P. and Bensmihen S. 2018. Nod Factor Regulation of Phytohormone Signaling and Homeostasis During Rhizobia-Legume Symbiosis. Front. Plant Sci. 9:1247
    PubMed
  • Herrbach V., Maillet F. and Bensmihen S. 2018. Adapting the Lateral Root-Inducible System to Medicago truncatula. Methods Mol Biol. 1761:77-83
    PubMed
  • Sevin-Pujol A., Sicard M., Rosenberg C., Auriac M.C., Lepage A., Niebel A., Gough C. and Bensmihen S. 2018. Development of a GAL4-VP16/UAS trans-activation system for tissue specific expression in Medicago truncatula. PLoS One. 12:e0188923
    PubMed
  • Gough C., Cottret L., Lefebvre B. and Bono JJ. 2018. Evolutionary History of Plant LysM Receptor Proteins Related to Root Endosymbiosis. Front Plant Sci. 9:923
    PubMed
  • Lefebvre B. 2017. Arbuscular mycorrhiza: A new role for N-acetylglucosamine. Nature Plants 3, 17085
    PubMed
  • Herrbach V., Chirinos X., Rengel D., Agbevenou K., Vincent R., Pateyron S., Huguet S., Balzergue S., Pasha A., Provart N., Gough C. and Bensmihen S. 2017. Nod factors potentiate auxin signaling for transcriptional regulation and lateral root formation in Medicago truncatula. J Exp Bot. 68:569-583
    PubMed
  • Fliegmann J., Jauneau A., Pichereaux C., Rosenberg C., Gasciolli V., Timmers A.C., Burlet-Schiltz O., Cullimore J. and Bono J.J. 2016. LYR3, a high-affinity LCO-binding protein of Medicago truncatula, interacts with LYK3, a key symbiotic receptor. FEBS Lett 590:1477-87
    PubMed
  •  Malkov N., Fliegmann J., Rosenberg C., Gasciolli V., Timmers A.C., Nurisso A., Cullimore J., Bono J.J. 2016. Molecular basis of lipo-chitooligosaccharide recognition by the lysin motif receptor-like kinase LYR3 in legumes. Biochem J 473:1369-78
    PubMed
  • Vernié T., Camut S., Camps C., Rembliere C., de Carvalho-Niebel F., Mbengue M., Timmers T., Gasciolli V., Thompson R., Le Signor C., Lefebvre B., Cullimore J. and Hervé C. 2016. PUB1 interacts with the receptor kinase DMI2 and negatively regulates rhizobial and arbuscular mycorrhizal symbioses through its ubiquitination activity in Medicago truncatula. Plant Physiol, 170: 2312-2324
    PubMed
  • Buendia L., Wang T., Girardin A.  and Lefebvre B. 2016 The LysM receptor-like kinase SlLYK10 regulates the arbuscular mycorrhizal symbiosis in tomato. New Phytol 210, 184-195.
    PubMed
  • Camps C., Jardinaud M.F., Rengel D., Carrère S., Hervé C., Debellé F., Gamas P., Bensmihen S. and Gough C. 2015. Combined genetic and transcriptomic analysis reveals three major signalling pathways activated by Myc-LCOs in Medicago truncatula. New Phytol. 208: 224-240.
    PubMed
  • Gonzalez A. A., Agbévénou K., Herrbach V., Gough C., Bensmihen S. Abscisic acid promotes pre-emergence stages of lateral root development in Medicago truncatula.Plant Signal Behav, 10(1):e977741.
    PubMed
  • Gough C, Jacquet C. 2013. Nod factor perception protein carries weight in biotic interactions. Trends Plant Sci 10:566-74.
    PubMed
  • Herrbach V, Remblière C, Gough C, Bensmihen S. 2013. Lateral root formation and patterning in Medicago truncatula. J Plant Physiol pii: S0176-1617(13)00362-3.
    PubMed
  • Fliegmann J., Canova S., Lachaud C., Uhlenbroich S., Gasciolli V., Pichereaux C., Rossignol M., Rosenberg C., Cumener M., Pitorre D., Lefebvre B., Gough C., Samain E., Fort S., Driguez H., Vauzeilles B., Beau J.M., Nurisso A., Imberty A., Cullimore J. and Bono J.J. 2013. Lipo-chitooligosaccharidic symbiotic signals are recognized by the LysM receptor like kinase LYR3 in the legume Medicago truncatula. ACS Chemical Biology 8: 1900-1906.
    PubMed
  • Pietraszewska-Bogiel A., Lefebvre B., Koini M.A., Klaus-Heisen D., Takken F.L.W., Geurts R., Cullimore J.V and Gadella T.W.J. 2013. Interaction of Medicago truncatula Lysin motif receptor-like kinases, NFP and LYK3, produced in Nicotiana benthamianaleaf induces a defence-like response. PlosOne 8(6):e65055.
    PubMed
  • Park C.J., Sharma R., Lefebvre B., Canlas P.E, and Ronald P.C. 2013. Endoplasmic reticulum-quality control component SDF2 is essential for XA21-mediated immunity in rice. Plant Science 210:53-60.
    PubMed
  • Rival P, Bono JJ, Gough C, Bensmihen S, Rosenberg C. 2013. Cell autonomous and non-cell autonomous control of rhizobial and mycorrhizal infection in Medicago truncatula. Plant Signal Behav 6;8(2).
    PubMed
  • Rival P, de Billy F, Bono JJ, Gough C, Rosenberg C, Bensmihen S. 2012. Epidermal and cortical roles of NFP and DMI3 in coordinating early steps of nodulation in Medicago truncatula. Development 139:3383-91.
    PubMed
  • Lefebvre B, Klaus-Heisen D, Pietraszewska-Bogiel A, Hervé C, Camut S, Auriac MC, Gasciolli V, Nurisso A, Gadella TW, Cullimore J. 2012. Role of N-glycosylation sites and CxC motifs in trafficking of Medicago truncatula Nod Factor Perception protein to plasma membrane. J Biol Chem 287 : 10812-10823.
    PubMed
  • Gobbato E, Marsh JF, Vernié T, Wang E, Maillet F, Kim J, Miller JB, Sun J, Bano SA, Ratet P, Mysore KS, Dénarié J, Schultze M, Oldroyd GE. 2012. A GRAS-type transcription factor with a specific function in mycorrhizal signaling. Curr Biol. 22(23):2236-41.
    PubMed
  • Czaja LF, Hogekamp C, Lamm P, Maillet F, Martinez EA, Samain E, Dénarié J, Küster H, Hohnjec N. 2012. Transcriptional responses toward diffusible signals from symbiotic microbes reveal MtNFP- and MtDMI3-dependent reprogramming of host gene expression by arbuscular mycorrhizal fungal lipochitooligosaccharides. Plant Physiol. 159(4):1671-85.
    PubMed
  • Bensmihen S, De Billy, F, Gough C. 2011. Contribution of NFP LysM domains to the recognition of Nod Factors during the Medicago truncatula/ Sinorhizobium meliloti symbiotic interaction. PLoSOne 6(11): 11.
    PubMed
  • Debellé F, Young ND, Oldroyd GE et al. 2011.  The Medicago genome provides insight into the evolution of rhizobial symbioses. Nature. 16;480(7378):520-4.
    PubMed
  • Gough, C. and Cullimore, J. 2011. Lipo-chitooligosaccharide signalling in endosymbiotic plant-microbe interactions. Mol. Plant-Microbe Interact. 24(8):867-878.
    PubMed
  • Herve, C., Lefebvre, B., Cullimore, J. 2011. How many E3 ubiquitin ligases are involved in the regulation of nodulation? Plant Signal. Behav 6(5):660-664.
    PubMed
  • Fliegmann, J., Uhlenbroich, S., Shinya, T., Martinez, Y., Lefebvre, B., Shibuya, N., Bono, J.J. 2011. Biochemical and phylogenetic analysis of CEBiP-like LysM domain-containing extracellular proteins in higher plants. Plant Phys. Biochem. 49(7):709-720.
    PubMed
  • Klaus-Heisen, D., Nurisso, A., Pietraszewska-Bogiel, A., Mbengue, M., Camut, S., Timmers, T., Pichereaux, C., Rossignol, M., Gadella, T.W.J., Imberty, A., Lefebvre, B., Cullimore, J.V. 2011. Structure-function similarities between a plant receptor-like kinase and the human interleukin-1 receptor-associated kinase-4. J Biol Chem 286: 11202-11210.
    PubMed
  • Maillet, F., Poinsot, V., André, O., Puech-Pagès, V., Haouy, A., Gueunier, M., Cromer, L., Giraudet, D., Formey, D., Niebel, A., Andres Martinez, E., Driguez, H., Bécard, G. and J. Dénarié. 2011. Fungal lipochitooligosaccharide symbiotic signals in arbuscular mycorrhiza. Nature, 469 : 58-63.
    PubMed
  • Mbengue, M., Camut, S., de Carvalho-Niebel, F., Deslandes, L., Froidure, S., Klaus-Heisen, D., Moreau, S., Rivas, S., Timmers, T., Hervé, C., Cullimore, J., Lefebvre, B. 2010. The Medicago truncatula E3 ubiquitin ligase PUB1 interacts with the LYK3 symbiotic receptor and negatively regulates infection and nodulation. Plant Cell 22: 3474-3488.
    PubMed
  • Lefebvre, B., Timmers, T., Mbengue, M., Moreau, S., Hervé, C., Tóth, K., Bittencourt-Silvestre, J., Klaus, D., Deslandes, L., Godiard, L., Murray, J.D., Udvardi, M.K., Raffaele, S., Mongrand, S., Cullimore, J., Gamas, P., Niebel, A. and Ott, T. 2010. A remorin protein interacts with symbiotic receptors and regulates bacterial infection. Proc Natl Acad Sci U S A. 107: 2343-2348.
    PubMed
  • Arrighi, J.F., Godfroy, O., de Billy, F., Saurat, O., Jauneau, A., Gough, C. 2008. The RPG gene of Medicago truncatula controls Rhizobium-directed polar growth during infection. Proc Natl Acad Sci U S A. 105:9817-9822.
    PubMed
  • Lefebvre, B., Furt, F., Hartmann, M.A., Michaelson, L.V., Carde, J.P., Sargueil-Boiron, F., Rossignol, M., Napier, J.A., Cullimore, J., Bessoule, J.J., Mongrand, S. 2007. Characterization of lipid rafts from Medicago truncatula root plasma membranes: a proteomic study reveals the presence of a raft-associated redox system. Plant Phys. 144:402-418.
    PubMed
  • Hogg, B.V., Cullimore, J.V., Ranjeva, Bono, J.J. 2006. The DMI1 and DMI2 early symbiotic genes of Medicago truncatula are required for a high-affinity nodulation factor-binding site associated to a particulate fraction of roots. Plant Physiol. 140:365-73.
    PubMed
  • Mulder, L., Lefebvre, B., Cullimore, J.V., Imberty, A. 2006. LysM domains of Medicago truncatula NFP protein involved in Nod factor perception. Glycosylation state, molecular modelling and docking of chitooligosaccharides and Nod factors. Glycobiology 16: 801-809.
    PubMed
  • Oláh, B., Brière, C., Bécard, G., Dénarié, J., Gough, C. 2005. Nod factors and a diffusible factor from arbuscular mycorrhizal fungi stimulate lateral root formation in Medicago truncatula via the DMI1/DMI2 signalling pathway. Plant J. 44:195.
    PubMed
  • Lévy, J., Bres, C., Geurts, R., Chalhoub, B., Kulikova, O., Duc, G., Journet, E.P., Ané, J.M., Lauber, E., Bisseling, T., Dénarié, J., Rosenberg, C., Debellé, F. 2004. A Putative Ca²+ and Calmodulin-Dependent Protein Kinase Required for Bacterial and Fungal Symbioses. Science 303:1361-1364.
    PubMed
  • Ané, J.M., Kiss, G.B., Riely, B.K., Penmetsa, R.V., Oldroyd, G.E., Ayax, C., Lévy, J., Debellé, F., Baek, J.M., Kalo, P., Rosenberg, C., Roe, B.A., Long, S.R., Dénarié, J., Cook, D.R. 2004. MedicagotruncatulaDMI1 required for bacterial and fungal symbioses in legumes. Science. 303:1364-1367.
    PubMed
  • Catoira, R., Galera, C., de Billy, F., Penmetsa, R.V., Journet, E.P., Maillet, F., Rosenberg, C., Cook, D., Gough, C., Dénarié, J. 2000. Four genes of Medicagotruncatula controlling components of a Nod factor transduction pathway. Plant Cell 12: 1647-1666.
    PubMed
  • Wais, R. J., Galera, C., Oldroyd, G., Catoira, R., Penmetsa, R. V., Cook, D., Gough, C., Dénarié, J. and S. R. Long. 2000. Genetic analysis of calcium spiking responses in nodulation mutants of Medicago truncatula. Proc Natl Acad Sci U S A., 97: 13407-13412.
    PubMed