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Laboratory of Plant-Microbe Interactions - LIPM

Laboratory of Plant-Microbe Interactions

Publications - Endosymbiotic infection and nodule development

Publications (5 last years)

  • Ribeiro CW, Baldacci-Cresp F, Pierre O, Larousse M, Benyamina S, Lambert A, Hopkins J, Castella C, Cazareth J, Alloing G, Boncompagni E, Couturier J, Mergaert P, Gamas P, Rouhier N, Montrichard F, Frendo P. 2017.  Regulation of Differentiation of Nitrogen-Fixing Bacteria by Microsymbiont Targeting of Plant Thioredoxin s1. Curr Biol  27:250-256. doi: 10.1016/j.cub.2016.11.013. 
    PubMed
  • Zanetti ME, Rípodas C, Niebel A. 2016. Plant NF-Y transcription factors: Key players in plant-microbe interactions, root development and adaptation to stress. Biochim Biophys Acta doi: 10.1016/j.bbagrm.2016.11.007.
    PubMed
  • Satgé C, Moreau S, Sallet E, Lefort G, Auriac MC, Remblière C, Cottret L, Gallardo K, Noirot C, Jardinaud MF, Gamas P. 2016. Reprogramming of DNA methylation is critical for nodule development in Medicago truncatula. Nat Plants 2:16166. doi: 10.1038/nplants.2016.166.
    PubMed
  • Fonouni-Farde C, Tan S, Baudin M, Brault M, Wen J, Mysore KS, Niebel A, Frugier F, Diet A. DELLA-mediated gibberellin signalling regulates Nod factor signalling and rhizobial infection. Nat Commun 7:12636. doi:10.1038/ncomms12636.
    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, 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 170:2312-24. doi:10.1104/pp.15.01694.
    PubMed
  • Boivin S, Kazmierczak T, Brault M, Wen J, Gamas P, Mysore KS, Frugier F. 2016. Different cytokinin CHK receptors regulate nodule initiation as well as later nodule developmental stages in Medicago truncatula. Plant Cell Environ doi: 10.1111/pce.12779.  
    PubMed
  • Jardinaud MF, Boivin S, Rodde N, Catrice O, Kisiala A, Lepage A, Moreau S, Roux B, Cottret L, Sallet E, Brault M, Emery RJ, Gouzy J, Frugier F, Gamas P. 2016. A laser dissection-RNAseq analysis highlights the activation of cytokinin pathways by Nod factors in the Medicago truncatula root epidermis. Plant Physiol 171:2256-76. doi: 10.1104/pp.16.00711.
    PubMed
  • Cerri MR, Frances L, Kelner A, Fournier J, Middleton PH, Auriac MC, Mysore KS, Wen J, Erard M, Barker DG, Oldroyd GE, de Carvalho-Niebel F. 2016. The Symbiosis-Related ERN Transcription Factors Act in Concert to Coordinate Rhizobial Host Root Infection. Plant Physiol 171:1037-54. doi: 10.1104/pp.16.00230.
    PubMed
  • Chabaud M, Gherbi H, Pirolles E, Vaissayre V, Fournier J, Moukouanga D, Franche C, Bogusz D, Tisa LS, Barker DG, Svistoonoff S. 2016. Chitinase-resistant hydrophilic symbiotic factors secreted by Frankia activate both Ca2+ spiking and NIN gene expression in the actinorhizal plant Casuarina glauca. New Phytol 209:86-93. doi: 10.1111/nph.13732. 
    PubMed
  • Vernié T, Kim J, Frances L, Ding Y, Sun J, Guan D, Niebel A, Gifford ML, de Carvalho-Niebel F, Oldroyd GE. 2015. The NIN Transcription Factor Coordinates Diverse Nodulation Programs in Different Tissues of the Medicago truncatula Root. Plant Cell 27:3410-3424. doi: 10.1105/tpc.15.00461. 
    PubMed
  • Roux B, Bolot S, Guy E, Denancé N, Lautier M, Jardinaud MF, Fischer-Le Saux M, Portier P, Jacques MA, Gagnevin L, Pruvost O, Lauber E, Arlat M, Carrère S, Koebnik R, Noël LD. 2015. Genomics and transcriptomics of Xanthomonas campestris species challenge the concept of core type III effectome. BMC Genomics 16:975. doi: 10.1186/s12864-015-2190-0. 
    PubMed
  • Baudin M, Laloum T, Lepage A, Rípodas C, Ariel F, Frances L, Crespi M, Gamas P, Blanco FA, Zanetti ME, de Carvalho-Niebel F, Niebel A. 2015. A Phylogenetically Conserved Group of Nuclear Factor-Y Transcription Factors Interact to Control Nodulation in Legumes. Plant Physiol 169:2761-2773. doi:10.1104/pp.15.01144. 
    PubMed
  • Wang G, Roux B, Feng F, Guy E, Li L, Li N, Zhang X, Lautier M, Jardinaud MF, Chabannes M, Arlat M, Chen S, He C, Noël LD, Zhou JM. 2015. The Decoy Substrate of a Pathogen Effector and a Pseudokinase Specify Pathogen-Induced Modified-Self Recognition and Immunity in Plants. Cell Host Microbe 18:285-295. doi: 10.1016/j.chom.2015.08.004.
    PubMed
  • Alves-Carvalho S, Aubert G, Carrère S, Cruaud C, Brochot AL, Jacquin F, Klein A, Martin C, Boucherot K, Kreplak J, da Silva C, Moreau S, Gamas P, Wincker P, Gouzy J, Burstin J. 2015. Full-length de novo assembly of RNA-seq data in pea (Pisum sativum L.) provides a gene expression atlas and gives insights into root nodulation in this species. Plant J 84:1-19. doi: 10.1111/tpj.12967.
    PubMed
  • Venkateshwaran M, Jayaraman D, Chabaud M, Genre A, Balloon AJ, Maeda J, Forshey K, den Os D, Kwiecien NW, Coon JJ, Barker DG, Ané JM. 2015. A role for the mevalonate pathway in early plant symbiotic signaling. Proc Natl Acad Sci U S A. 112:9781-9786. doi: 10.1073/pnas.1413762112.
    PubMed
  • Clavijo F, Diedhiou I, Vaissayre V, Brottier L, Acolatse J, Moukouanga D, Crabos A, Auguy F, Franche C, Gherbi H, Champion A, Hocher V, Barker D, Bogusz D, Tisa LS, Svistoonoff S. 2015. The Casuarina NIN gene is transcriptionally activated throughout Frankia root infection as well as in response to bacterial diffusible signals. New Phytol 208:887-903. doi: 10.1111/nph.13506.
    PubMed
  • Camps C, Jardinaud MF, Rengel D, Carrère S, Hervé C, Debellé F, Gamas P, Bensmihen S, 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. doi: 10.1111/nph.13427. 
    PubMed
  • Fournier J, Teillet A, Chabaud M, Ivanov S, Genre A, Limpens E, de Carvalho-Niebel F, Barker DG. 2015. Remodeling of the infection chamber before infection thread formation reveals a two-step mechanism for rhizobial entry into the host legume root hair. Plant Physiol 167:1233-1242. doi:10.1104/pp.114.253302. 
    PubMed
  • Laloum, T., Baudin, M., Frances, L., Lepage, A., Billault-Penneteau, B., Cerri, M.R., Ariel, F., Jardinaud, M-F., Gamas, P., de Carvalho-Niebel F,. and Niebel A. 2014. Two CCAAT box-binding transcription factors redundantly control early steps of legume-rhizobia endosymbiosis. Plant J 79:757-68. doi: 10.1111/tpj.12587.  
    PubMed
  • Formey, D., Sallet, E., Lelandais-Brière, C., Ben, C., Bustos-Sanmamed, P., Niebel, A., Frugier, F., Combier, J., Debellé, F., Hartmann, C., Poulain, J., Gavory, F., Wincker, P., Roux, C., Gentzbittel, L., Gouzy, J., Crespi, M. 2014. The small RNA diversity from Medicago truncatula roots under biotic interactions evidences the environmental plasticity of the miRNAome. Genome Biol. 15:457. 
    PubMed
  • Xiao, T. T., Schilderink, S., Moling, S., Deinum, E.E., Kondorosi, E., Franssen, H., Kulikova, O., Niebel, A., and Bisseling, T. 2014. Fate map of Medicago truncatula root nodules. Development 141:3517-28. doi: 10.1242/dev.110775. 
    PubMed
  • Rípodas, C., Clúa, J., Battaglia, M., Baudin, M., Niebel, A., Zanetti, M.E., Blanco F. 2014. Transcriptional regulators of legume-rhizobia symbiosis: nuclear factors Ys and GRAS are two for tango. Plant Signal Behav. 9:e28847. 
    PubMed
  • Battaglia, M., Rípodas, C., Clúa, J., Baudin, M., Aguilar, O.M., Niebel, A., Zanetti, M.E., Blanco, F.A. 2014. A nuclear factor Y interacting protein of the GRAS family is required for nodule organogenesis, infection thread progression, and lateral root growth. Plant Physiol. 164(3):1430-42.  
    PubMed
  • Moreau, S., Fromentin, J., Vailleau, F., Vernié, T., Huguet, S., Balzergue, S., Frugier, F., Gamas, P., Jardinaud, M-F. 2014. The symbiotic transcription factor MtEFD and cytokinins are positively acting in the Medicago truncatula and Ralstonia solanacearum pathogenic interaction. New Phytol 201,1343-1357.
    PubMed
  • Roux, B., Rodde, N., Jardinaud, M.F., Timmers, T., Sauviac, L., Cottret, L., Carrère, S., Sallet, E., Courcelle, E., Moreau, S., Debellé, .F, Capela, D., de Carvalho-Niebel, F., Gouzy, J., Bruand, C., Gamas, P. 2014. An integrated analysis of plant and bacterial gene expression in symbiotic root nodules using laser capture microdissection coupled to RNA-seq. Plant J 77, 817-837.
    PubMed
  • Laporte, P., Lepage, A., Fournier, J., Catrice, O., Moreau, S., Jardinaud, M-F., Mun, J-H., Larrainzar, E., Cook, D., Gamas, P., Niebel, A. 2014. The CCAAT box-binding transcription factor MtNF-YA1 controls rhizobial infection. J Exp Bot 65, 481-494.  
    PubMed
  • Rey, T., Nars, A., Bonhomme, M., Bottin, A., Huguet, S., Balzergue, S., Jardinaud, M.F., Bono, J.J., Cullimore, J., Dumas, B., Gough, C., Jacquet, C. 2013. NFP, a LysM protein controlling Nod factor perception, also intervenes in Medicago truncatula resistance to pathogens. New Phytol 198, 875-886. 
    PubMed
  • Ben, C., Debellé, F., Berges, H., Bellec, A., Jardinaud, M.F., Anson, P., Huguet, T., Gentzbittel, L., Vailleau, F. 2013. MtQRRS1, an R-locus required for Medicago truncatula quantitative resistance to Ralstoniasolanacearum. New Phytol 199, 758-772. 
    PubMed
  • Balzergue, C., Chabaud, M., Barker, D.G., Bécard, G., S. F. Rochange. 2013. High phosphate reduces host ability to develop arbuscular mycorrhizal symbiosis without affecting root calcium spiking responses to the fungus. Front Plant Sci 4, 426. 
    PubMed
  • Nars, A., Lafitte, C., Chabaud, M., Drouillard, S., Mélida, H., Danoun, S., Le Costaouëc, T., Rey,  T., Benedetti, J. Bulone,  V., Barker,  D.G. Bono, J-J,  Dumas, B., Jacquet, C., Heux,  L.,  Fliegmann, J., Bottin, A. 2013. Aphanomyces euteiches Cell Wall Fractions Containing Novel Glucan-Chitosaccharides Induce Defense Genes and Nuclear Calcium Oscillations in the Plant Host Medicago truncatula. PLoS ONE 8(9), e75039.  
    PubMed
  • Sallet, E., Roux, B., Sauviac, L., Jardinaud, M-F., Carrère, S., Faraut, T., de Carvalho-Niebel, F., Gouzy, J., Gamas, P., Capela, D., Bruand, C,. Schiex, T. 2013. Next-generation annotation of prokaryotic genomes with EuGene-P: application to Sinorhizobium meliloti. DNA Res 20, 339-354. 
    PubMed
  • Verdier, J., Lalanne, D., Pelletier, S., Torres-Jerez, I., Righetti, K., Bandyopadhyay, K., Leprince, O., Chatelain, E., Ly Vu, B., Gouzy, J., Gamas, P., Udvardi, M., Buitink, J. 2013. A regulatory network-based approach dissects late maturation processes related to the acquisition of desiccation tolerance and longevity of Medicago truncatula seeds. Plant Physiol 163, 757-774. 
    PubMed
  • Genre, A., Chabaud, M., Balzergue, C., Puech-Pagès, V., Novero, M., Rey, T., Fournier, J., Rochange, S., Bécard, G., Bonfante, P. and Barker, D.G. 2013. Short-chain chitin oligomers from arbuscular mycorrhizal fungi trigger nuclear Ca2+ spiking in Medicago truncatula roots and their production is enhanced by strigolactone. New Phytol 198, 179-189.  
    PubMed
  • Laloum, T., De Mita, S., Gamas, P., Baudin, M. and Niebel, A. 2013. CCAAT-box binding transcription factors in plants: Y so many? Trends Plant Sci 18, 157-166.  
    PubMed
  • Cerri, M. R., Frances, L., Laloum T., Auriac M.-C., Niebel A., Oldroyd G.E., Barker D.G., Fournier J., de Carvalho-Niebel F. 2012. Medicago truncatula ERN transcription factors: regulatory interplay with NSP1/NSP2 GRAS factors and expression dynamics throughout rhizobial infection. Plant Physiol 160, 2155-2172.  
    PubMed
  • Lauressergues, D., Delaux, P.-M., Formey, D., Lelandais-Brière, C., Fort, S., Cottaz, S., Bécard, G., Niebel, A., Roux, C., Combier, J-P. 2012. The microRNA miR171h modulates arbuscular mycorrhizal colonization of Medicago truncatula by targeting NSP2. Plant J 72, 512-522.  
    PubMed
  • Ariel, F., Brault-Hernandez, M., Laffont, C., Huault, E., Brault, M., Plet, J., Moison, M., Blanchet, S., Ichanté, J.L., Chabaud, M., Carrere, S., Crespi, M., Chan, R.L., Frugier, F. 2012. Two direct targets of cytokinin signaling regulate symbiotic nodulation in Medicago truncatula. Plant Cell 24, 3838-52. 
    PubMed
  • Sieberer, B.J., Chabaud, M., Fournier, J., Timmers, T., Barker, D.G. 2012. A switch in Ca(2+) spiking signature is concomitant with endosymbiotic microbe entry into cortical root cells of Medicago truncatula. Plant J 69, 822-830.  
    PubMed
  • Ovchinnikova, E., Journet, E.P., Chabaud, M., Cosson, V., Ratet, P., Duc, G., Fedorova, E., Liu, W., Op den Camp, R., Zhukov, V., Tikhonovich, I., Borisov, A., Bisseling, T., Limpens, E. 2011. IPD3 controls the formation of nitrogen-fixing symbiosomes in pea and Medicago Spp. Mol Plant Microbe Interact 24,1333-1344. 
    PubMed
  • Godiard, L., Lepage, A., Moreau, S., Laporte, D., Verdenaud, M., Timmers, T., Gamas, P. 2011. MtbHLH1, a bHLH transcription factor involved in Medicago truncatula nodule vascular patterning and nodule to plant metabolic exchanges. New Phytol 191, 391-404. 
    PubMed
  • Chabaud, M., Genre, A., Sieberer, B.J., Faccio, A., Fournier, J., Novero, M., Barker, D.G. and Bonfante, P. 2011. Arbuscular mycorrhizal hyphopodia and germinated spore exudates trigger calcium spiking in the legume and non-legume root epidermis. New Phytol 189, 347-55. 
    PubMed
  • Moreau, S., Verdenaud, M., Ott, T., Letort, S., de Billy, F., Niebel, A., Gouzy, J., de Carvalho-Niebel, F. and Gamas, P. 2011. Transcription reprogramming during root nodule development in Medicago truncatula. PloS ONE 6(1), e16463. 
    PubMed
  • Maillet, F., Poinsot, V., André, O., Puech-Pagès, V., Haouy, A., Gueunier, M., Cromer, L., Giraudet, D., Formey, D., Niebel, A., Martinez, E.A., Driguez, H., Bécard, G. and Dénarié, J. 2011. An arbuscular mycorrhizal fungus secretes lipochitooligosaccharidic symbiotic signals. Nature 469, 58-64. 
    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., Ott, T. 2010. A remorin protein interacts with symbiotic receptors and regulates bacterial infection. Proc Nat Acad Sci USA 107, 2343-48. 
    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., and 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
  • Yendrek, C.R., Lee, Y.C., Morris, V., Liang, Y., Pislariu, C.I., Burkart, G., Meckfessel, H., Salehin, M., Kessler, H., Wessler, H., Lloyd, M., Lutton, H., Teillet, A., Sherrier, D.J., Journet, E.P., Harris, J.M. and Dickstein, R. 2010. A putative transporter is essential for integrating nutrient and hormone signaling with lateral root growth and nodule development in Medicago truncatula. Plant J 62, 100-12. 
    PubMed
  • Jeudy, C., Ruffel, S., Freixes, S., Tillard, P., Santoni, AL., Morel, S., Journet, E.P., Duc, G., Gojon, A., Lepetit, M., and Salon, C. 2010. Adaptation of Medicago truncatula to nitrogen limitation is modulated via local and systemic nodule developmental responses. New Phytol 185, 817-28. 
    PubMed
  • Svistoonoff, S., Sy, MO., Diagne, N., Barker, D.G., Bogusz, D. and Franche, C. 2010. Infection-Specific Activation of the Medicago truncatula Enod11 Early Nodulin Gene Promoter During Actinorhizal Root Nodulation. Mol Plant-Microbe Interact 23, 740-47. 
    PubMed
  • Bonaldi, K., Gherbi, H., Franche, C., Bastien, G., Fardoux, J., Barker, D.G., Giraud, E. and Cartiaux, F. 2010. The Nod factor-independent symbiotic signaling pathway: development of Agrobacterium rhizogenes-mediated transformation for the legume Aeschynomene indica. Mol Plant-Microbe Interact 23, 1537-44.
    PubMed
  • Sieberer, B.J., Chabaud, M., Timmers, A.C., Monin, A., Fournier, J. and Barker, D.G. 2009. A nuclear-targeted cameleon demonstrates intranuclear calcium spiking in Medicago truncatula root hairs in response to rhizobial nodulation factors. Plant Physiol 151, 1197-206. 
    PubMed
  • Iantcheva, A., Chabaud, M., Cosson, V., Barascud, M., Schutz, B, Primard-Brisset, C, Durand, P, Barker, D.G., Vlahova, M., Ratet, P. 2009. Osmotic shock improves Tnt1 transposition in Medicago truncatula cv Jemalong during in vitro regeneration. Plant Cell Rep 28, 1563-72. 
    PubMed
  • Salon, C., Lepetit, M., Gamas, P., Jeudy, C., Moreau, S., Moreau, D., Voisin, A.S., Duc, G., Bourion, V., Munier-Jolain, N. 2009. Analysis and modeling of the integrative response of Medicago truncatula to nitrogen constraints. C R Biol 332, 1022-1033. 
    PubMed
  • Gimeno-Gilles, C., Lelievre, E., Viau, L., Malik-Ghulam, M., Ricoult, C., Niebel, A., Leduc, N., and Limami, A.M. 2009. ABA-Mediated Inhibition of Germination Is Related to the Inhibition of Genes Encoding Cell-Wall Biosynthetic and Architecture: Modifying Enzymes and Structural Proteins in Medicago truncatula Embryo Axis. Mol Plant 2, 108-19. 
    PubMed
  • Talukdar, T., Gorecka, K.M., de Carvalho-Niebel, F., Downie, J.A., Cullimore, J. and Pikula, S. 2009. Annexins – calcium- and membrane-binding proteins in the plant kingdom. Potential role in nodulation and mycorrhization in Medicago truncatula. Acta Biochim Polonica 56, 199-210. 
    PubMed

Other selected publications

  • Combier, J.P., de Billy, F., Gamas, P., Niebel, A., and Rivas, S. 2008. Trans-regulation of the expression of the transcription factor MtHAP2-1 by a uORF controls root nodule development. Genes Dev 22, 1549-59. 
    PubMed
  • Genre, A., Chabaud, M., Faccio, A., Barker, D.G. and Bonfante, P.  2008. Prepenetration apparatus assembly precedes and predicts the colonization patterns of arbuscular mycorrhizal fungi within the root cortex of both Medicago truncatula and Daucus carota. Plant Cell 20, 1407-20. 
    PubMed
  • Vernié, T., Moreau, S., de Billy, F., Plet, J., Combier, J.P., Rogers, C., Oldroyd, G., Frugier, F., Niebel, A., and Gamas, P. 2008. EFD Is an ERF transcription factor involved in the control of nodule number and differentiation in Medicago truncatula. Plant Cell 20, 2696-713. 
    PubMed
  • Fournier, J., Timmers, A.C.J., Sieberer, B.J., Jauneau, A., Chabaud, M. and Barker, D.G. 2008. Mechanism of infection thread elongation in root hairs of Medicago truncatula and dynamic interplay with associated rhizobial colonization. Plant Physiol 148, 1985-95. 
    PubMed
  • Teillet, A., Garcia, J., de Billy, F., Gherardi, M., Huguet, T., Barker, D.G., de Carvalho-Niebel, F., and Journet, E-P. 2008. api, a novel Medicago truncatula mutant impaired in nodule primordium invasion. Mol Plant-Microbe Interact 21, 535-46. 
    PubMed
  • Combier, J.P., Kuster, H., Journet, E.P., Hohnjec, N., Gamas, P., and Niebel, A. 2008. Evidence for the involvement in nodulation of the two small putative regulatory peptide-encoding genes MtRALFL1 and MtDVL1. Mol Plant-Microbe Interact 21, 1118-27. 
    PubMed
  • Andriankaja, A., Boisson-Dernier, A., Frances, L., Sauviac, L., Jauneau, A., Barker, D.G. and de Carvalho-Niebel, F. 2007. AP2-ERF transcription factors mediate Nod factor-dependent MtENOD11 activation in root hairs via a novel cis -regulatory motif. Plant Cell 19, 2866-85. 
    PubMed
  • Combier, J.P., Vernié, T., de Billy, F., El Yahyaoui, F., Mathis, R., and Gamas, P. 2007. The MtMMPL1 early nodulin is a novel member of the matrix metalloendoproteinase family with a role in Medicago truncatula infection by Sinorhizobium meliloti. Plant Physiol 144, 703-16. 
    PubMed
  • Raffaele, S., Mongrand, S., Gamas, P., Niebel, A., and Ott, T. 2007. Genome-wide annotation of remorins, a plant-specific protein family: evolutionary and functional perspectives. Plant Physiol 145, 593-600. 
    PubMed
  • Godiard, L., Niebel, A., Micheli, F., Gouzy, J., Ott, T., and Gamas, P. 2007. Identification of new potential regulators of the Medicago truncatula-Sinorhizobium meliloti symbiosis using a large-scale suppression subtractive hybridization approach. Mol Plant-Microbe Interact 20, 321-32. 
    PubMed
  • Combier, J.P., Frugier, F., de Billy, F., Boualem, A., El-Yahyaoui, F., Moreau, S., Vernié, T., Ott, T., Gamas, P., Crespi, M., and Niebel, A. 2006. MtHAP2-1 is a key transcriptional regulator of symbiotic nodule development regulated by microRNA169 in Medicago truncatula. Genes Dev 20, 3084-88. 
    PubMed
  • Genre, A., Chabaud, M., Timmers, T., Bonfante, P. and Barker, D.G. 2005. Arbuscular mycorrhizal fungi elicit a novel intracellular apparatus in Medicago truncatula root epidermal cells prior to infection. Plant Cell 17, 3489-99. 
    PubMed
  • Boisson-Dernier, A., Andriankaja, A., Chabaud, M., Niebel, A., Journet, E-P., Barker, D.G. and de Carvalho-Niebel, F. 2005. MtENOD11 gene activation during rhizobial infection and mycorrhizal arbuscule development requires a common AT-rich-containing regulatory sequence. Mol Plant-Microbe Interact 18, 1269-76. 
    PubMed
  • Küster, H., Hohnjec, N., Krajinski, F., El Yahyaoui, F., Manthey, K., Gouzy, J., Dondrup, M., Meyer, F., Kalinowski, J., Brechenmacher, L., van Tuinen, D., Gianinazzi-Pearson, V., Pühler, A., Gamas, P., Becker, A. 2004. Construction and validation of cDNA-based macro- and micro-arrays to explore root endosymbioses in the model legume Medicago truncatula. J. Biotechnology 108, 95-113. 
    PubMed
  • El Yahyaoui, F., Küster, H., Ben Amor, B., Hohnjec, N., Pühler, A., Becker, A., Gouzy, J., Vernié, T., Gough, C., Niebel, A., Godiard, L., Gamas, P. 2004. Expression profiling in Medicago truncatula identifies more than 750 genes differentially expressed during nodulation, including many potential regulators of the symbiotic program. Plant Physiol 136, 3159-76. 
    PubMed
  • Charron, D., Pingret, J.L., Chabaud, M., Journet, E.P. and Barker, D.G. 2004. Pharmacological evidence that multiple phospholipid signaling pathways link Rhizobium nodulation factor perception in Medicago truncatula root hairs to intracellular responses including calcium spiking and specific ENOD gene expression. Plant Physiol 136, 3582-93. 
    PubMed
  • Kosuta, S., Chabaud, M., Lougnon, G., Gough, C., Denarie, J., Barker, D.G. and Bécard, G. 2003. A diffusible factor from arbuscular mycorrhizal fungi induces symbiosis-specific MtENOD11 expression in roots of Medicago truncatula. Plant Physiol 131, 952-62. 
    PubMed
  • Journet, E-P., van Tuinen, D., Gouzy, J., Crespeau, H., Carreau, V., Farmer, M-J., Niebel, A., Schiex, T., Jaillon, O., Chatagnier, O., Godiard, L., Micheli, F., Kahn, D., Gianinazzi-Pearson, V., Gamas, P. 2002. Exploring root symbiotic programs in the model legume Medicago truncatula using EST analysis Nucl Acids Res 30, 5579-92. 
    PubMed
  • de Carvalho-Niebel, F., Timmers, A.C.J., Chabaud, M., Defaux-Petras, A. and Barker, D.G. 2002. The Nod factor-elicited annexin MtAnn1 is preferentially localised at the nuclear periphery in symbiotically-activated root tissues of Medicago truncatula. Plant J 32, 343-52. 
    PubMed
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