Publications

 2018

  • Berrabah F.,Ait Salem E.H., Garmier M., Ratet P. (2018a) The Multiple Faces of the Medicago-Sinorhizobium Symbiosis. In: Cañas L., Beltrán J. (eds) Functional Genomics in Medicago truncatula. Methods in Molecular Biology, vol 1822:241-260. Humana Press, New York, NY.  doi: 10.1007/978-1-4939-8633-0_16.
  • Berrabah F., Balliau T., Aït-Salem E.H., George J., Zivy M., Ratet P., Gourion B. (2018b) Control of the ethylene signaling pathway prevents plant defenses during intracellular accommodation of the rhizobia. New Phytologist 219(1): 310-323.  doi: 10.1111/nph.15142
  • Berrabah F., Ratet P., Gourion B. (2018c) Legume nodule: massive infection in the absence of defense induction. Mol Plant Microbe Interact. doi: 10.1094/MPMI-07-18-0205-FI [Epub ahead of print]
  • Garmier M., Gentzbittel L., Wen J., Mysore K.S., Ratet P. (2018) Genetic and genomic resources for the study of Medicago truncatula. Current Protocols in Plant Biology2(4): 318-349. doi: 10.1002/cppb.20058.
  • Magne K., Couzigou J.C., Schiessl K., Liu S., George J., Sahl L., Boyer F., Iantcheva A., Mysore K.S., Wen J., Zhukov V., Citerne S., Oldroyd G.E.D., RatetP.(2018a) MtNODULE ROOT1 and MtNODULE ROOT2 are essential for Medicago truncatula indeterminate nodule identity. Plant Physiology 178(1):295-316. doi: 10.1104/pp.18.00610.
  • Magne K., George J., Berbel Tornero A., Broquet B., Madueño F., Andersen S.U., Ratet P. (2018b) Lotus japonicus NOOT-BOP-COCH-LIKE1 is essential for nodule, nectary, leaf and flower development. Plant J. 94(5): 880-894. doi: 10.1111/tpj.13905.

 

2017

  • Brusamarello-Santos L.C., Gilard F., Brulé L., Quilleré I., Gourion B., Ratet P., Maltempi de Souza E., Lea P.J., Hirel B. (2017) Metabolic profiling of two maize (Zea mays L.) inbred lines inoculated with the nitrogen fixing plant-interacting bacteria Herbaspirillum seropedicae and Azospirillum brasilense. PLoS One 12(3):e0174576. doi: 10.1371/journal.pone.0174576. 
  • Domonkos Á., Kovács S., Gombár A., Kiss E., Horváth B., Kováts, G.Z., Farkas A., Tóth M.T., Ayaydin F., Bóka K., Fodor L., Ratet P., Kereszt A., Endre G., Kaló P. (2017) NAD1 controls defense-like responses in Medicago truncatula symbiotic nitrogen fixing nodules following rhizobial colonization in a BacA-independent manner. Genes 8(12) pii: E387. doi: 10.3390/genes8120387
  • Genot B., Lang J., Berriri S., Garmier M., Gilard F., Pateyron S., Haustraete K., Van Der Streaten D., Hirt H., Colcombet J. (2017) Constitutively Active Arabidopsis MAP Kinase 3 Triggers Defense Responses Involving Salicylic Acid and SUMM2 Resistance Protein. Plant Physiol. 174(2):1238-1249. doi: 10.1104/pp.17.00378.
  • Kazmierczak T., Nagymihály M., Lamouche F., Barrière Q., Guefrachi I., Alunni B., Ouadghiri M., Ibijbijen J., Kondorosi É., Mergaert P., Gruber V. (2017) Specific host-responsive associations between Medicago truncatula accessions and Sinorhizobium strains. Mol Plant Microbe Interact. 30(5):399-409. doi: 10.1094/MPMI-01-17-0009-R.
  • Nagymihály M., Vásarhely Bálint M., Barrière Q., Chong T.-M., Bálint B., Bihari P., Hong K.-W., Horváth B., Ibijbijen J., Amar M., Farkas A., Kondorosi É., Chan K.G., Gruber V., Ratet P., Mergaert P., Kereszt A.(2017) The complete genome sequence of Ensifer meliloti strain CCMM 1 B554 (FSM-MA), a highly effective nitrogen-fixing microsymbiont of Medicago truncatula Gaertn. Standards in Genomic Sciences 12:75. DOI 10.1186/s40793-017-0298-3.

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2016

  • Chaintreuil C., Rivallan R., Bertioli D.J., Klopp C., Gouzy J., Courtois B., Leleux P., Martin G., Rami J.F., Gully D., Parrinello H., Séverac D., Patrel D., Fardoux J., Ribière W., Boursot M., Cartieaux F., Czernic P., Ratet P., Mournet P., Giraud E., Arrighi J.F. (2016). A gene-based map of the Nod factor-independent Aeschynomene evenia sheds new light on the evolution of nodulation and legume genomes. DNA Res. 23(4):365-376. doi: 10.1093/dnares/dsw020.
  • Couzigou J.M., Magne K., Mondy S., Cosson V., Clements J., Ratet P. (2016). The legume NOOT-BOP-COCH-LIKE genes are conserved regulators of abscission, a major agronomical trait in cultivated crops. New Phytol. 209(1):228-40. doi: 10.1111/nph.13634.
  • Hamoum H., Bouznad A., Mekhaldi A., Ratet P., Djibaoui R. (2016). Free-living diazotrophic rhizobacteria with plant growth promoting traits isolated from the rhizosphere of wheat grown on saline soil in west Algeria. J. Appl. Environ. Biol. Sci. 6(11):1-10.
  • Iantcheva A., Revalska M., Zehirov G., Boycheva I., Magne K., Radkova M., Ratet P., Vassileva V. (2016). Tnt1 retrotransposon as an efficient tool for development of an insertional mutant collection of Lotus japonicus. In Vitro Cellular and Developmental Biology Plant 52 (3):338-47. doi : 10.1007/s11627-016-9768-3.
  • Vialette-Guiraud A.C.M., Chauvet A., Gutierrez-Mazariegos J., Eschstruth A., Ratet P., Scutt C.P. (2016). A conserved role for the NAM/miR164 developmental module reveals a common mechanism underlying carpel margin fusion in monocarpous and syncarpous eurosids. Front. Plant Sci. 6:1239. doi: 10.3389/fpls.2015.01239.

 

 2015

  • Araújo S.S., Beebe S., Crespi M., Delbreil B., González E.M., Gruber V., Lejeune-Henaut I., Link W., Monteros M.J., Prats E., Rao I., Vadez V., Vaz Patto M.C. (2015). Abiotic Stress Responses in Legumes: Strategies Used to Cope with Environmental Challenges. Critical Reviews in Plant Sciences 34(1-3): 237-280. DOI: 10.1080/07352689.2014.898450.
  • Berrabah F., Ratet P., Gourion B. (2015). Multiple steps control immunity during the intracellular accommodation of rhizobia. J Exp Bot. 66(7):1977-85. doi: 10.1093/jxb/eru545.
  • Bruggeman Q., Prunier F., Mazubert C., de Bont L., Garmier M., Lugan R., Benhamed M., Bergounioux C., Raynaud C., Delarue M. (2015). Involvement of Arabidopsis Hexokinase1 in Cell Death Mediated by Myo-Inositol Accumulation. Plant Cell 27(6): 1801-14. doi: 10.1105/tpc.15.00068.
  • Cosson V., Eschstruth A., Ratet P. (2015). Medicago truncatula transformation using leaf explants. Methods Mol Biol. 1223:43-56. doi: 10.1007/978-1-4939-1695-5_4.
  • Faure D, et al. 2015. Environmental microbiology as a mosaic of explored ecosystems and issues. Environ. Sci. Pollut. Res. Int. 22:13577-13598. doi: 10.1007/s11356-015-5164-5.
  • Gourion, B., Berrabah, F., Ratet, P., and Stacey, G. (2015). Rhizobium-legume symbioses: the crucial role of plant immunity. Trends Plant Sci. 20:186–194. doi: 10.1016/j.tplants.2014.11.008.
  • Lauressergues D., André O., Peng J., Wen J., Chen R., Ratet P., Tadege M., Mysore K.S., Rochange S.F. (2015). Strigolactones contribute to shoot elongation and to the formation of leaf margin serrations in Medicago truncatula R108. J Exp Bot.  66(5):1237-44. doi: 10.1093/jxb/eru471.
  • Niu L., Lin H., Zhang F., Watira T.W., Li G., Tang Y., Wen J., Ratet P., Mysore K.S., Tadege M. (2015). LOOSE FLOWER, a WUSCHEL-like Homeobox gene, is required for lateral fusion of floral organs in Medicago truncatula. Plant J. 81(3): 480-92. doi: 10.1111/tpj.12743.

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 2014

  • Berrabah F., Bourcy M., Cayrel A., Eschstruth A., Mondy S., Ratet P., Gourion B. (2014a). Growth Conditions Determine the DNF2 Requirement for Symbiosis. PLoS ONE 9(3): e91866. doi:10.1371/journal.pone.0091866.
  • Berrabah F., Bourcy M., Eschstruth A., Cayrel A., Guefrachi I., Mergaert P., Wen J., Cosson V., Mysore K.S, Gourion B., Ratet P. (2014b). A non-RD receptor-like kinase prevents nodule early senescence and defense-like reactions during symbiosis. New Phytologist, 203(4): 1305-14. doi: 10.1111/nph.12881.
  • Cheng X., Wang M., Lee H.K., Tadege M., Ratet P., Udvardi M., Mysore K.S. Wen J., (2014). An efficient reverse genetics platform in the model legume Medicago truncatula. New Phytologist, 201(3):1065-76. doi: 10.1111/nph.12575.
  • Couzigou J.M., Ratet P. (2014). NOOT-dependent control of nodule identity: nodule homeosis and meristem perturbation. Biological Nitrogen Fixation. F.J. de Bruijn editor., Vol 2, section, chapter 49.
  • Guefrachi I., Nagymihaly M., Pislariu C.I., Van de Velde W., Ratet P., Mars M., Udvardi M.K., Kondorosi E., Mergaert P., Alunni B. (2014). Extreme specificity of NCR gene expression in Medicago truncatula. BMC Genomics, 15:712. doi:10.1186/1471-2164-15-712.
  • Hopkins J, Pierre O, Kazmierczak T, Gruber V, Frugier F, Clement M, Frendo P, Herouart D, Boncompagni (2014).  MtZR1, a PRAF protein, is involved in the development of roots and symbiotic root nodules in Medicago truncatula. Plant Cell Environ. 37(3):658-69. doi: 10.1111/pce.12185.
  • Huault E., Laffont C., Wen J., Mysore K.S., Ratet P., Duc G., Frugier F. (2014). Local and systemic regulation of plant root system architecture and symbiotic nodulation by a receptor-like kinase. PLoS Genet. 10(12):e1004891. doi: 10.1371/journal.pgen.1004891.
  • Mondy S., Lenglet A., Beury-Cirou A., Libanga C., Ratet P., Faure D., Dessaux Y. (2014a). An increasing opine carbon bias in artificial exudation systems and genetically modified plant rhizospheres leads to an increasing reshaping of bacterial populations. Molecular Ecology, 23(19):4846-61. doi: 10.1111/mec.12890.
  • Mondy S., Lenglet A., Cosson V., Pelletier S., Pateyron S., Gilard F., Scholte M., Brocard L., Couzigou J.-M., Tcherkez G., Péan M., and Ratet P. (2014b). GOLLUM [FeFe]-hydrogenase-like proteins are essential for plant development in normoxic conditions and modulate energy metabolism. Plant Cell Env. 37(1): 54-69. doi: 10.1111/pce.12128.
  • Wang E., Yu N., Bano S.A., Liu C., Miller A.J., Cousins D., Zhang X., Ratet P., Tadege M., Mysore K.S., Downie J.A., Murray J.D., Oldroyd G.E., Schultze M. (2014). A H+-ATPase that energizes nutrient uptake during mycorrhizal symbioses in rice and Medicago truncatula. Plant Cell. 26(4): 1818-1830.

 

 2013

  • Bourcy M., Berrabah F., Ratet P., Gourion B. (2013a). Failure of self-control : Defense like reactions during legume/rhizobia symbiosis. Plant Signal Behav. 8(4). doi:pii: e23915.
  • Bourcy M., Brocard L., Pislariu C.I., Cosson V., Mergaert P., Tadege M., Mysore K.S., Udvardi M.K., Gourion B., Ratet P. (2013b). Medicago truncatula DNF2 is a PI-PLC-XD-containing protein required for bacteroid persistence and prevention of nodule early senescence and defense-like reactions. New Phytologist, 197(4), 1250-61.
  • Couzigou JM, Mondy S., Sahl L., Gourion B., Ratet P. (2013). To be or noot to be: evolutionary tinkering for symbiotic organ identity. Plant Signal Behav. 8(8). doi:pii: e24969.
  • Iantcheva A., Mysore K.S., Ratet P. (2013). Transformation of leguminous plants to study symbiotic interactions. Int. J. Dev. Biol. 57(6-8): 577-586.
  • Jaudal M., Yeoh C.C., Zhang L., Stockum C., Mysore K.S., Ratet P., Putterill J. (2013). Retroelement insertions at the Medicago FTa1 locus in spring mutants eliminate vernalisation but not long day requirements for early flowering. Plant J. 76(4): 580-591 doi: 10.1111/tpj.12315.
  • Yeoh C.C., Balcerowicz M., Zhang L., Jaudal J., Brocard L., Ratet P., Putterill J. (2013). Fine mapping links the FTa1 flowering time regulator to the dominant spring1 locus in Medicago. PLoS One 8(1):e53467. doi: 10.1371/journal.pone.0053467.

 

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