Christophe Salon, Marion Prudent -How does pea (Pisum sativum) recover from water deficit?, ILS3 highlighted nice results and challenging opportunities for innovative research on grain legume. Legume Perspective, vol.18, 2019. ,
Vanessa Vernoud, Marion Prudent -Fine-tuning of nodulation is required for an efficient post-drought recovery in pea, 2019. ,
Christophe Salon -Analyse écophysiologique de la récupération après un stress hydrique chez la légumineuse à graine Pisum sativum -Forum Jeunes Chercheurs ,
Christophe Salon -How does pea (Pisum sativum) recover from drought, Journée des doctorants du département BAP de l'INRA ,
Christophe Salon -Analyse écophysiologique de la récupération après un stress hydrique chez la légumineuse à graine Pisum sativum -RFL #2 (2ème Rencontres Francophone des Légumineuses) ,
Christophe Salon, Marion Prudent -How does pea (Pisum sativum) recover from water deficit, Journée des doctorants de l'UMR Agroécologie ,
Christophe Salon, Marion Prudent -How does pea (Pisum sativum) recover from water deficit, Third international legume society (ILS #3) ,
, Le système racinaire nodulé du pois : un rôle pivot pour sa stabilité sous contraintes hydriques fluctuantes. Presented at Root Days, système racinaire, Interactions Rhizosphériques, Immunité végétale, 2019.
Christophe Salon -Comment la plante récupère-t-elle après un stress hydrique? Une étude écophysiologique et moléculaire chez la légumineuse à graines Pisum sativum -Journée des doctorants de l'UMR Agroécologie ,
, Christophe Salon, Vanessa Vernoud -Transcriptomic and metabolomic responses of the nodulated pea root system during water deficit recovery -Third International conference on legume genetics and genomics (ICLGG), p.13
Land-atmosphere coupling and climate change in Europe, Nature, vol.443, issue.7108, pp.205-214, 2006. ,
Abiotic stress responses in legumes: strategies used toCope with environmental challenges, Crit Rev Plant Sci, vol.34, issue.1-3, pp.237-80, 2015. ,
Coping mechanisms for crop plants in drought-prone environments, Ann Bot, vol.101, issue.7, pp.901-908, 2008. ,
Fate map of Medicago truncatula root nodules, Development, vol.141, issue.18, pp.3517-3545, 2014. ,
URL : https://hal.archives-ouvertes.fr/hal-02636064
Hormonal control of lateral root and nodule development in legumes, Plants, vol.4, issue.3, pp.523-570, 2015. ,
URL : https://hal.archives-ouvertes.fr/hal-02629771
Cell identity regulators link development and stress responses in the Arabidopsis root, Dev Cell, vol.21, issue.4, pp.770-82, 2011. ,
Root traits contributing to plant productivity under drought, Front Plant Sci, vol.4, p.442, 2013. ,
Plasma membrane and abiotic stress, Plant Cell Monogr, vol.19, pp.457-70, 2011. ,
Cold acclimation in plants: relationship between the lipid composition and the cryostability of the plasma membrane, J Plant Res, vol.112, pp.245-54, 1106. ,
Rehydration of dried systems: membranes and the nuclear genome, pp.343-64, 2002. ,
Sensing the environment: key roles of membrane-localized kinases in plant perception and response to abiotic stress, J Exp Bot, vol.64, issue.2, pp.445-58, 2013. ,
Fatty acid specificity and selectivity of the chloroplast sn-glycerol 3-phosphate acyltransferase of the chilling sensitive plant, Amaranthus lividus, Plant Physiol, vol.83, issue.3, pp.676-80, 1987. ,
Lateral and rotational Mobilities of lipids in specific cellular membranes Couchoud et al, BMC Plant Biology, vol.19, p.221, 2019. ,
, Eucalyptus gunnii cultivars exhibiting different freezing tolerance, Plant Physiol, vol.100, issue.1, pp.246-54, 1992.
Membrane fluidity and the perception of environmental signals in cyanobacteria and plants, Prog Lipid Res, vol.42, issue.6, pp.527-570, 2003. ,
Plasticity of plasma membrane compartmentalization during plant immune responses, Front Plant Sci, vol.3, p.181, 2012. ,
Lipids of plant membrane rafts, Prog Lipid Res, vol.51, issue.3, pp.272-99, 2012. ,
URL : https://hal.archives-ouvertes.fr/hal-02647225
Interactions between lipids and proteins are critical for organization of plasma membrane-ordered domains in tobacco BY-2 cells, J Exp Bot, vol.69, issue.15, pp.3545-57, 2018. ,
URL : https://hal.archives-ouvertes.fr/hal-02629167
Knowns and unknowns of plasma membrane protein degradation in plants, Plant Sci, vol.272, pp.55-61, 2018. ,
Neglecting legumes has compromised human health and sustainable food production, Nat Plants, vol.2, p.16112, 2016. ,
Comparative proteomic analysis of alfalfa revealed new salt and drought stress-related factors involved in seed germination, Mol Biol Rep, vol.44, issue.3, pp.261-72, 2017. ,
Proteomic analysis of the enhancement of seed vigour in osmoprimed alfalfa seeds germinated under salinity stress, Seed Sci Res, vol.23, issue.2, pp.99-110, 2013. ,
Physiological and proteomic responses of contrasting alfalfa (Medicago sativa L.) varieties to PEG-induced osmotic stress, Front Plant Sci, vol.9, p.242, 2018. ,
Water potential of aqueous polyethylene glycol, Plant Physiol, vol.67, issue.1, pp.64-71, 1981. ,
Plant roots use a patterning mechanism to position lateral root branches toward available water, Proc Natl Acad Sci, vol.111, issue.25, pp.9319-9343, 2014. ,
URL : https://hal.archives-ouvertes.fr/hal-02636761
PEG-mediated osmotic stress induces premature differentiation of the root apical meristem and outgrowth of lateral roots in wheat, J Exp Bot, vol.65, issue.17, pp.4863-72, 2014. ,
Microsatellite diversity and broad scale geographic structure in a model legume: building a set of nested core collection for studying naturally occurring variation in Medicago truncatula, BMC Plant Biol, vol.6, p.28, 2006. ,
URL : https://hal.archives-ouvertes.fr/hal-02659572
,
, Genome-wide association of drought-related and biomass traits with HapMap SNPs in Medicago truncatula, Plant Cell Environ, vol.38, issue.10, pp.1997-2011, 2015.
Cell Wall heterogeneity in root development of Arabidopsis, Front Plant Sci, vol.7, p.1242, 2016. ,
Constitutive expression of clathrin hub hinders elicitor-induced clathrinmediated endocytosis and defense gene expression in plant cells, FEBS Lett, vol.586, issue.19, pp.3293-3301, 2012. ,
URL : https://hal.archives-ouvertes.fr/hal-02646052
High lipid order of Arabidopsis cell-plate membranes mediated by sterol and DYNAMIN-RELATED PROTEIN1A function, Plant J, vol.80, issue.5, pp.745-57, 2014. ,
Modification of plasma membrane organization in tobacco cells elicited by cryptogein, Plant Physiol, vol.164, issue.1, pp.273-86, 2014. ,
URL : https://hal.archives-ouvertes.fr/hal-02638760
Di-4-ANEPPDHQ, a fluorescent probe for the visualisation of membrane microdomains in living Arabidopsis thaliana cells, Plant Physiol Bioch, vol.87, pp.53-60, 2015. ,
Mapping of membrane lipid order in root apex zones of Arabidopsis thaliana, Front Plant Sci, vol.6, p.1151, 2015. ,
Characterization and application of a new optical probe for membrane lipid domains, Biophys J, vol.90, issue.7, pp.2563-75, 2006. ,
Quantitative imaging of membrane lipid order in cells and organisms, Nat Protoc, vol.7, issue.1, pp.24-35, 2012. ,
Shaping a root system: regulating lateral versus primary root growth, Trends Plant Sci, vol.19, issue.7, pp.426-457, 2014. ,
Vesicular trafficking and salinity responses in plants, IUBMB Life, vol.67, issue.9, pp.677-86, 2015. ,
Regulation of endocytosis by external stimuli in plant cells, Plant Biosyst, vol.143, issue.3, pp.630-635, 2009. ,
URL : https://hal.archives-ouvertes.fr/hal-00508287
Endocytosis and signaling cascades: a close encounter, FEBS Lett, vol.498, issue.2-3, pp.190-196, 2001. ,
The crossroads of receptor-mediated signaling and endocytosis in plants, J Integr Plant Biol, vol.60, issue.9, pp.827-867, 2018. ,
FMdyes as experimental probes for dissecting vesicle trafficking in living plant cells, J Microsc-Oxford, vol.214, pp.159-73, 2004. ,
URL : https://hal.archives-ouvertes.fr/hal-00122335
The plant defense elicitor cryptogein stimulates clathrin-mediated endocytosis correlated with reactive oxygen species production in bright yellow-2 tobacco cells, Plant Physiol, vol.146, issue.3, pp.1255-66, 2008. ,
URL : https://hal.archives-ouvertes.fr/hal-02665878
Live cell imaging of FM4-64, a tool for tracing the endocytic pathways in Arabidopsis root cells, Methods Mol Biol, vol.1242, pp.93-103, 2015. ,
Osmotically evoked shrinking of guardcell protoplasts causes vesicular retrieval of plasma membrane into the cytoplasm, Planta, vol.210, issue.3, pp.423-454, 2000. ,
Freeze/thaw-induced destabilization of the plasma membrane and the effects of cold acclimation, J Bioenerg Biomembr, vol.21, issue.1, pp.21-41, 1989. ,
Uptake of an endocytic marker by rice cells: variations related to osmotic and saline stress, Plant Cell Physiol, vol.44, issue.10, pp.1100-1111, 2003. ,
Stimulus-induced downregulation of root water transport involves reactive oxygen species-activated cell signalling and plasma membrane intrinsic protein internalization, Plant J, vol.56, issue.2, pp.207-225, 2008. ,
URL : https://hal.archives-ouvertes.fr/hal-00330107
Osmotic stress modulates the balance between exocytosis and Clathrin-mediated endocytosis in Arabidopsis thaliana, Mol Plant, vol.8, issue.8, pp.1175-87, 2015. ,
Halotropism is a response of plant roots to avoid a saline environment, Curr Biol, vol.23, issue.20, pp.2044-50, 2013. ,
URL : https://hal.archives-ouvertes.fr/hal-02649039
Clathrin-mediated endocytosis: the gateway into plant cells, Curr Opin Plant Biol, vol.14, issue.6, pp.674-82, 2011. ,
Elucidation of crosstalk and specificity of early response mechanisms to salt and PEG-simulated drought stresses in Brassica napus using comparative proteomic analysis, PLoS One, vol.10, issue.10, p.138974, 2015. ,
Salt stress induces internalization of plasma membrane aquaporin into the vacuole in Arabidopsis thaliana, Biochem Bioph Res Co, vol.474, issue.4, pp.742-748, 2016. ,
Single-molecule analysis of PIP2;1 dynamics and partitioning reveals multiple modes of Arabidopsis plasma membrane aquaporin regulation, Plant Cell, vol.23, issue.10, pp.3780-97, 2011. ,
URL : https://hal.archives-ouvertes.fr/hal-00662232
Salt-induced remodeling of spatially restricted clathrin-independent endocytic pathways in Arabidopsis root, Plant Cell, vol.27, issue.4, pp.1297-315, 2015. ,
Phospholipid composition of a plasma membraneenriched fraction from developing soybean roots, Plant Physiol, vol.79, issue.2, pp.494-502, 1985. ,
High-mass-resolution MALDI mass spectrometry imaging reveals detailed spatial distribution of metabolites and lipids in roots of barley seedlings in response to salinity stress, Metabolomics, vol.14, issue.5, p.63, 2018. ,
Osmoregulated ABC-transport system of Lactococcus lactis senses water stress via changes in the physical state of the membrane, Proc Natl Acad Sci, vol.97, issue.13, pp.7102-7108, 2000. ,
Osmosensing by bacteria: signals and membrane-based sensors, Microbiol Mol Biol Rev, vol.63, issue.1, pp.230-62, 1999. ,
Influence of water stress on the lipid physical state of plasma membranes from P. betuloefolia Bqe leaves, Colloid Surface B, vol.19, issue.2, pp.181-186, 2000. ,
Reorganization of Azospirillum brasilense cell membrane is mediated by lipid composition adjustment to maintain optimal fluidity during water deficit, J Appl Microbiol, vol.120, issue.1, pp.185-94, 2016. ,
Dynamic analysis of Arabidopsis AP2 sigma subunit reveals a key role in clathrin-mediated endocytosis and plant development, Development, vol.140, issue.18, pp.3826-3863, 2013. ,
Distinct endocytic pathways identified in tobacco pollen tubes using charged nanogold, J Cell Sci, vol.120, pp.3804-3823, 2007. ,
Aquaporin trafficking in plant cells: an emerging membrane-protein model, Traffic, vol.14, issue.6, pp.629-664, 2013. ,
URL : https://hal.archives-ouvertes.fr/hal-00874122
Genetic diversity of root system architecture in response to drought stress in grain legumes, J Exp Bot, vol.69, issue.13, pp.3267-77, 2018. ,
Medicago truncatula handbook Ardmore. USA: The samuel Roberts Noble Fondation, pp.1-26, 2006. ,
Evaluation of the water potentials of solutions of polyethylene Glycol-8000 both in the absence and presence of other solutes, Plant Physiol, vol.72, issue.1, pp.66-70, 1983. ,
A novel image-analysis toolbox enabling quantitative analysis of root system architecture, Plant Physiol, vol.157, issue.1, pp.29-39, 2011. ,
URL : https://hal.archives-ouvertes.fr/hal-02646938