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Section: New Results
Multi-scale models and analysis: from cells to plant architecture (and back)
Modeling water transport in roots
Participants : Mikaël Lucas [IRD] , Christophe Pradal, Christophe Godin, Yann Boursiac [BPMP] , Christophe Maurel [BPMP] .
This research theme is supported by the ANR project HydroRoot.
A model of Arabidopsis thaliana root hydraulics at the cellular level was developed in the OpenAlea modeling platform. The model relies on the integration throughout root architecture of elementary hydraulic components. Each component integrates local radial and axial water flows. Axial hydraulic conductivity is calculated according to Poiseuille’s law, based on local size of xylem vessels. Radial hydraulic conductivity is determined in part by aquaporin activity and was set constant throughout root architecture in the first model versions. In its current state, the model is parameterized using architectural, tissular and physiological data that were experimentally determined in the Aquaporin group at UMR BPMP. The architectural reconstruction of the root system is based on a tridimensional multi-scale tree graph (MTG). The current model is capable of predicting the water flow that is transported by a root system in the standard experimental conditions used in the Aquaporin group. This model was used to perform sensitivity analyses and determine the respective contributions to root hydraulic dynamics of various biological parameters (axial and radial hydraulic conductivites, root architecture). One major finding is that the root hydraulic conductivity (Lpr) computed from the model is highly dependent on root architecture. This is due to the limiting role of axial (xylem) conductance, one feature that had been neglected in previous representations of root water transport. The radial hydraulic conductivity may primarily be limiting in conditions of Lpr inhibition, since its increase from values in control roots has marginal effects on Lpr. A new set of experimental data including root diameter repartitions in wild-type plants, and xylem vessel diameters in mutants with altered xylem morphology (irx3, esk1) will be used to challenge the model. Root cell hydraulic conductivities will also be measured in these and aquaporin mutant phenotypes. Our aim is to check whether, based on anatomical and morphological data, the model can properly predict the radial hydraulic conductivity of these genotypes.
As the simulations may be time consuming and results sometimes difficult to interpret on complex branching systems, we started to investigate new methods to compute efficiently hydraulic conductivities and corresponding flows on complex root systems using architecture compression technics developed in the 1st axis of the project. First results show that very efficient computations of complex hydraulic architectures can be derived from the use of these compression techniques on idealized root architectures. These encouraging results provide a new abstraction that will be used in combination with the detailed modeling approach described above to break down the complexity of the analysis these huge branching systems.
Mechanical modeling of fruit growth
Participants : Ibrahim Cheddadi [Inra, Avignon] , Mik Cieslak [U. Calgary] , Frédéric Boudon, Valentina Baldazzi [Inra, Avignon] , Nadia Bertin [Inra, Avignon] , Michel Genard [Inra, Avignon] , Christophe Godin.
This research theme is supported by the Agropolis project MecaFruit3D.
Fruits and plants in general are large scale hydraulic systems in which growth is closely linked to water fluxes: thanks to osmotic pressure difference, the cells are able to absorb water from their environment and therefore increase their volume; as the cells are bounded by rigid walls, this results in both hydrostatic pressure (the so-called turgor pressure) in the cell and tension in the cell walls; above a threshold, synthesis of new cell wall material occurs and relaxes the tension. This process allows cells to grow, and along with cell division, is responsible for plant growth. In fruits, phloem and xylem vascular networks provide the water fluxes necessary for growth, while the osmotic pressure is mainly regulated by sugar intake from the phloem. The goal of this project is to combine a description of water and sugar fluxes at the fruit scale (see section 4) with a modelling of growth at cell level, as described above.
As a first step in this direction, we have developed a bidimensional multicellular model that couples, on the one hand, water fluxes between cells (symplastic pathway) and between cells and intercellular space (apoplastic pathway), and on the other hand, mechanical properties of the cell walls and mechanical equilibrium of this complex system. Existing multicellular models for plant growth overlook this coupling. From a mathematical point of view, it corresponds to a coupling between (1) the ordinary differential equations that describe fluxes and cell walls properties and (2) the highly non linear system of equations that describes the mechanical equilibrium of the cell walls.
We have developed a numerical method for this coupled system, that allows to simulate in a reasonable amount of time a hundred of connected cells. Numerical simulations exhibit a highly non linear behaviour with respect to the governing parameters. Thanks to the detailed analysis of a simplified setup, we have identified two clearly distinct growth regimes: one regime that allows large growth heterogeneities by amplifying the effect of differences between cells, and conversely another regime that smoothes differences out and yields a homogeneous growth. On the biological level, the first regime is well adapted to morphogenesis, whereas the second one is well adapted to homothetic growth after the differentiated tissues have been created. A publication of these completely new results is in preparation.
We have developped a collaboration with biophysicists in RDP laboratory in Lyon (Arezki Boudaoud and Yuchen Long) in order to compare the results of this model to experiments at the microscopic scale of the meristem. A publication is in preparation.
In the longer term, we plan extend this model to the larger scale of tissues and organs in order to model fruit growth.
Analyzing root growth and branching
Participants : Beatriz Moreno Ortega, Sixtine Passot, Yann Guédon, Laurent Laplaze [IRD, DIADE] , Mikaël Lucas [IRD, DIADE] , Bertrand Muller [INRA, LEPSE] .
This research theme is supported by two PhD programmes.
New 2D and 3D root phenotyping plateforms are emerging with associated image analysis toolbox (e.g. SmartRoot, RhizoScan) and the identification of developmental patterns within these complex phenotyping data requires new approaches. Here, we aim at developing a pipeline of methods for analyzing root systems at three scales:
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tissular scale to identify and characterize the division, elongation and mature zones along a root apex using piecewise heteroscedastic linear models for segmenting epidermal cell length profiles [35].
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individual root scale to analyze the dynamics of lateral root elongation. We in particular applied semi-Markov switching linear models for classifying roots on the basis of the identification of phases within growth rate profiles,
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root system scale to analyze the primary root branching structure.
This pipeline of analysis methods was applied to different species (maize, Pearl millet [23]) with contrasting biological objectives (study of genetic diversity for Pearl millet and of metabolic and hormonal controls of morphogenesis for maize).
Analyzing shoot and leaf elongation
Participants : Maryline Lièvre, Yann Guédon, Leo Guignard, Christine Granier [INRA, LEPSE] .
This research theme is supported by the labex Agro project "Integrated model of plant organ growth".
This study is based on the observation that there is a lack of methods enabling the integrated analysis of the processes controling the vegetative development in Arabidopsis thaliana.
The change in leaf size and shape during ontogeny associated with heteroblastic development is a composite trait for which extensive spatio-temporal data can be acquired using phenotyping platforms. However, only part of the information contained in such data is exploited, and developmental phases are usually defined using a selected organ trait. We introduced new methods for identifying developmental phases in the Arabidopsis rosette using various traits and minimum a priori assumptions [21]. A first pipeline of analysis was developed combining image analysis and statistical models to integrate morphological, shape, dimensional and expansion dynamics traits for the successive leaves of the Arabidopsis rosette. Dedicated segmentation models called semi-Markov switching models were built for selected genotypes in order to identify rosette developmental phases. Four successive developmental phases referred to as seedling, juvenile, transition and adult were identified for the different genotypes. We show that the degree of covering of the leaf abaxial surface with trichomes is insufficient to define these developmental phases. Using our pipeline of analysis, we were able to identify the supplementary seedling phase and to uncover the structuring role of various leaf traits. This enabled us to compare on a more objective basis the vegetative development of Arabidopsis mutants.
We developed a second pipeline of analysis methods combining a semi-automatic method for segmenting leaf epidermis images based on the ilastik software, and the analysis of the obtained cell areas using a gamma or inverse Gaussian mixture models whose component parameters are tied by a scaling rule. These mixture models allowed us to estimate the distribution of the number of endocycles. We highlighted in this way that the mean number of endocycles changes drastically with leaf rank. We extended the inference approach to take into account not only complete cell areas but also censored cell areas (corresponding to cells that intercept the edges of the images). We also investigated possible temporal interpretations of endoreduplication using stochastic processes.
A stochastic model of phyllotaxis
Participants : Yassin Refahi, Christophe Godin, Etienne Farcot, Teva Vernoux [RDP, ENS] .
This research theme has been supported by IBC and the Inria Project Lab Morphogenetics.
The geometric arrangement of lateral organs along plant stems, named phyllotaxis, shows a variety of striking patterns with remarkable regularities and symmetries. This has interested biologists, physicists, mathematicians and computer scientists for decades. These studies have lead to a commonly accepted standard interpretation of phyllotaxis that postulates that organs inhibit the formation of new organs in their vicinity. At a molecular scale, these inhibitory fields have been shown to result from the spatio-temporal distribution of the plant hormone auxin. This model theoretically explains a large part of the diversity of phyllotactic patterns observed in plants.
Recently, our colleagues from ENS-Lyon observed intriguing perturbation in arabidopsis mutants. These perturbations were also present, to a lesser extent in the wild type. In a series of works [79], [69], [1], we could show that these perturbations patterns in both wild-type and mutant plants could be explained by permutations in the order of insertion along the stem of 2 or 3 consecutive organs. After closer inspection, we realized that the mutated gene encodes a protein diffusing from the organs and creating a field around the organs that regulates the plastochron. We could demonstrate that in the mutant, the absence of this field leads to co-initiations and subsequently to the observed permutations.
To proceed further and find a mechanistic interpretation of this phenomenon, we developed a stochastic extension of the standard model of phyllotaxis. We first analyzed the properties of the inhibitory fields created by the existing primordia on the initiation of new primordia, and concluded that the angular positions of organs are very robust to perturbations while plastochrons may be dramatically affected. This suggested that there exists a strong decoupling between space and time in the patterning process. To account for this observation, we modeled the perception of the initiation signal by cells using stochastic processes coupled with the intensity of inhibitory fields and showed that the observed permutation patterns emerge spontaneously from this purely local processes. This model recapitulates accurately the classical phyllotactic patterns and, in addition, produces realistic pattern disorders at higher organization levels as a result of stochasticity in signal perception. We show that these subtle disorders surprisingly reveal key information on the functioning of the developmental system and can therefore be regarded as biological watermarks of the system. In genetically or environmentally modified plants, these biological watermarks inform us on the molecular mechanisms that have been affected in the experiment. Our theoretical analysis allows us to predict the specific pattern variations that would arise from perturbations of the signaling pathways involved in lateral inhibition signaling at the shoot apex [27].
The role of auxin and sugar in rose bud outgrowth control
Participants : Jessica Bertheloot [INRA, Angers] , Frédéric Boudon, Christophe Godin.
Auxin in the stem is known to be a key regulator of apical dominance. Over the last decades, many studies have been undertaken to understand its action mode, which is indirect because auxin in the main stem does not enter into the bud. Recently, apical dominance over basal buds in pea has been related to low sugar availability caused by high sugar demand of growing apical organs. Auxin and sugar are two signals regulating the entrance of bud into sustained growth in opposite ways. In the last year, it has also been demonstrated that sugar effect on bud outgrowth was preceded by a modification of the hormonal levels involved in bud outgrowth, which suggests that auxin and sugar pathways do interact in a non- trivial way. However, auxin and sugar effects have been studied separately until now. In this work, we investigate what is the combined effect of sugar and auxin on bud outgrowth, and how they integrate to regulate bud entrance into sustained growth. For this, a series of experiments has been carried out on a single-node cuttings of Rosa hybrida grown in vitro in which different combinations of sugar and auxin levels have been tested. A model of the regulatory networks controlling stem-bud molecular interaction has been developed.