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Godin, C.

Publications and source records attributed to Godin, C..

At least 19 recordsLinked to original sources

CLEAR-FORCE: A reservoir computing framework for closed-loop brain stimulation

Electrical stimulation of brain activity has emerged as a key therapeutic intervention for neurological diseases. The success of these approaches relies on precisely tuned stimulation parameters. A major challenge is that these parameters should ideally be adjusted in real-time based on changes in brain activity. Closed-loop controllers address this challenge by monitoring brain activity and adapting stimulation according to ongoing changes in neural dynamics. While machine learning has been helpful in this context, closed-loop controllers typically do not adapt in real-time to fluctuations in brain activity. Here, we propose a novel framework based on reservoir computing to train a closed-loop, real-time neural controller. This approach, termed CLEAR-FORCE, trains the output weights of a recurrent network based on a combination of target signals and feedback from brain activity. Two series of simulations were performed, where the controller was successful at (1) inducing neural oscillations in a population of spiking neurons and (2) suppressing pathological oscillations. This framework provides a promising avenue for the implementation of neural controllers in low-powered, real-time, and adaptive hardware that harnesses machine learning for the personalized treatment of brain disorders.

neuroscience↗

Tree-to-cycle transition scale characterizes trade-off between dissipation and construction cost in adaptive transport networks

Biological transport networks range from tree-like to highly reticulated architectures, which have been proposed to reflect different balances between viscous dissipation and metabolic cost. This balance cannot currently be inferred from structure: available descriptors either discard edge width entirely or preserve it only as a hierarchical decomposition that has not been mapped to the dissipation--cost trade-off. Here we introduce the tree-to-cycle transition scale, a single number given by the radius of the thickest edge outside the maximum spanning tree, which we interpret as the highest cost a network accepts for redundancy. We compute it for networks adapting to spatially correlated load fluctuations, whose correlation length sets their position on the Pareto front. The transition scale decreases linearly with dissipation and increases linearly with metabolic cost. Its scatter is largest in the regime where some networks end up off the front, and adding a growth term removes the scatter but splits the correlation into two branches. A single quantity read off the static network architecture thus characterizes where a network sits on the Pareto front, and is sensitive to the trajectory the network took through the optimization landscape. This suggests a route to comparing observed networks, for example leaf venations across species or growth conditions, by the trade-off they realize.

biophysics↗

Near-equiprobable binary branching decisions underlie filament patterning in the moss Physcomitrium patens

Branching forms are ubiquitous in nature and have evolved repeatedly across scales and species. An important goal of developmental biology remains to identify similarities and differences in the regulatory mechanisms underlying branching. Here, we investigate the branching filaments that form upon spore germination in mosses, using Physcomitrium patens as a model species. To identify the macroscopic rules governing filament patterning, we developed a pipeline to acquire high-resolution 3D images of whole sporelings, reconstruct filament architecture at single-cell resolution, and formalize cell organization using mathematical tree representations. Our quantitative analysis reveals that branch patterning in moss filaments can be captured by a simple probabilistic model in which subapical cells have a near-equal probability of producing - or not producing - a side-branch between successive apical cell divisions. This framework provides a quantitative basis for comparing the developmental rules driving branching morphogenesis within and beyond the plant kingdom.

plant biology↗

Branching Varies with Light Limitation Scenarios in relation with Changes in Carbon Source-Sink Dynamics.

Bud outgrowth is a major component of plant architectural plasticity and is influenced by light conditions. While the inhibitory effect of low light intensity on branching is well documented, the underlying regulators remain debated and, especially, the role of sugar availability has never been thoroughly evaluated. Here, we combined experiments with a computational approach quantifying carbon source-sink balance in single-axis rose plants to investigate how continuous and transient light limitation regulate bud outgrowth. Continuous low light reduced photosynthesis, leading to decreased sugar availability and inhibited bud outgrowth. In contrast, a transient period of low light followed by high light unexpectedly stimulated bud outgrowth, shortened the delay between outgrowth of successive buds, and produced an over-branched phenotype. This response resulted from a non-reversible reduction in the growth of apical organs appearing under low light, which lowered carbon demand and caused sugar over-accumulation after the return to high light. Manipulating carbon supply and demand through leaf masking, photosynthetic inhibition, and targeted sucrose feeding causally confirmed the central role of sugar availability in these contrasting responses. Beyond these findings, key requirements for models simulating branching plasticity were identified and this work provides a basis for predicting branching responses under fluctuating and complex light environments. HighlightBud outgrowth, a key component of plant plasticity, is regulated by light intensity through sugar availability. Continuous and transient low light have opposite effects by limiting sugar production and use, respectively.

plant biology↗

Carbon-phosphorous exchange rate constrains growth of arbuscular mycorrhizal fungal networks

Symbiotic nutrient exchange between arbuscular mycorrhizal (AM) fungi and their host plants varies widely depending on their physical, chemical, and biological environment. Yet dissecting this context dependency remains challenging because we lack methods for tracking nutrients such as carbon (C) and phosphorus (P). Here, we developed a new approach to quantitatively estimate C and P fluxes in the AM symbiosis from comprehensive network morphology quantification, achieved by robotic imaging and machine learning based on roughly 100 million hyphal shape measurements. We found that rates of C transfer from the plant and P transfer from the fungus were, on average, related proportionally to one another. This ratio was nearly invariant across AM fungal strains despite contrasting growth phenotypes, but was strongly affected by plant host genotype. Fungal phenotype distributions were bounded by a Pareto front with a shape favoring specialization in an exploration-exploitation trade-off. This means AM fungi can be fast range expanders or fast resource extractors, but not both. Manipulating the C/P exchange rate by swapping the plant host genotype shifted this Pareto front, indicating that the exchange rate constrains possible AM fungal growth strategies. We show by mathematical modeling how AM fungal growth at fixed exchange rate leads to qualitatively different symbiotic outcomes depending on fungal traits and nutrient availability.

biophysics↗

Multi-physics modeling for ion homeostasis in multi-compartment plant cells using an energy function

Plant cells control their volume by regulating the osmotic potential of their cytoplasm and vacuole. Water is attracted into the cell as the result of a cascade of solute exchanges between the cell subcompartments and the cell surroundings, which are governed by chemical, electrostatic and mechanical forces. Due to this multi-physics aspect and to couplings between changes of volumes and chemical effects, modeling these exchanges remains a challenge that has only been partially adressed. In this paper, we introduce an energy-based approach to couple chemical, electrical and mechanical processes taking place between several subcompartments of a plant cell. The contributions of all physical effects are gathered in an energy function that allows us to derive the equations satisfied by each variable in a systematical way. This results in a modular, unified approach that can be interpreted analytically. We illustrate these properties on the modeling of ion and water transport in a guard cell during stoma opening. We represent the stoma opening process as a quasi-static evolution driven by hydrogen pumps in the plasma and vacuolar membranes, resulting in an interpretable model with few parameters. We perform numerical simulations to investigate the role of each hydrogen pump in this process. We show that this energy-based approach allows us to highlight a hierarchy between the forces involved in the system, that can be exploited to interpret the emergent properties of this complex multi-physics system.

biophysics↗

Geometry and cell wall mechanics guide early pollen tube growth in Arabidopsis thaliana

In Arabidopsis thaliana, successful fertilization relies on the precise guidance of the pollen tube tip as it navigates through the female pistil tissues to deliver non-motile sperm cells to ovules. While prior studies have unveiled the role of the pistil in directing pollen tubes to ovules, growth guidance mechanisms within the stigmatic epidermis during the initial phase of the pollen tubes journey remains elusive. A recent analysis comparing wild-type (WT) pollen tube paths in WT and ktn1-5 stigmatic cells revealed a tight connection between directed pollen tube growth and the mechanical properties of the invaded stigmatic cell. Building upon these observations, we constructed here a mathematical model to explore the mechanisms guiding early pollen tube growth through the papilla cell wall (CW). We found that in ktn1-5, the pollen tube moves freely on the curved papilla surface, following geodesics, while the WT papilla exerts directional guidance on the pollen tube. An order of magnitude analysis of the mechanical forces involved in pollen tube growth in papillae suggests a guidance mechanism, where the elongated papilla geometry and the CW elasticity combine to efficiently direct pollen tube growth towards the papilla base.

plant biology↗

Water fluxes contribute to growth patterning in shoot meristems

In multicellular organisms, localized tissue outgrowth creates a new water sink thereby modifying hydraulic patterns at the organ level. These fluxes are often considered passive by-products of development and their patterning and potential contribution to morphogenesis remains largely unexplored. Here, we generated a complete map of cell volumetric growth and deformation across the shoot apex in Arabidopsis thaliana. Within the organ-meristem boundary, we found that a subpopulation of cells next to fast-growing cells experiences volumetric shrinkage. To understand this process, we used a vertex-based model integrating mechanics and hydraulics, informed by the measured growth rates. Organ outgrowth simulations revealed the emerging water fluxes and predicted water deficit with volume loss for a few cells at the boundary. Consistently, in planta, a water-soluble dye is preferentially allocated to fast-growing tissues and fails to enter the boundary domain. Analysis of intact meristems further validated our model by revealing cell shrinkage next to fast-growing cells in different contexts of tissue surface curvature and cell deformation. A molecular signature of water deficit at the boundary further confirmed our conclusion. Taken together, we propose a model where the differential sink strength of emerging organs prescribes the hydraulic patterns that define the boundary domain at the shoot apex.

plant biology↗

The post-transcriptional regulation of TFs in immature motoneurons shapes the axon-muscle connectome

Temporal factors expressed sequentially in neural stem cells, such as RNA binding proteins (RBPs) or transcription factors (TFs), are key elements in the generation of neuronal diversity. The molecular mechanism underlying how the temporal identity of stem cells is decoded into their progeny to generate neuronal diversity is largely unknown. Here, we used genetic and new computational tools to study with precision the unique fates of the progeny of a stem cell producing 29 morphologically distinct leg motoneurons (MNs) in Drosophila. We identified 40 TFs expressed in this MN lineage, 15 of which are expressed in a combinatorial manner in immature MNs just before their morphological differentiation. By following TF expression patterns at an earlier developmental stages, we discovered 19 combinatorial codes of TFs that were progressively established in immature MNs as a function of their birth order. The comparison of the RNA and protein expression profiles of 6 TFs revealed that post-transcriptional regulation plays an essential role in shaping these TF codes. We found that the two known RBPs, Imp and Syp, expressed sequentially in neuronal stem cells, are upstream regulators of the TF codes. Both RBPs are key players in the construction of axon-muscle connectome through the post-transcriptional regulation of 5 of the 6 TFs examined. By deciphering the function of Imp in the immature MNs with respect to the stem cell of the same lineage, we propose a model where RBPs shape the morphological fates of MNs through post-transcriptional regulation of TF codes in immature MNs. Taken together, our study reveals that immature MNs are plastic cells that have the potential to acquire many morphological fates. The molecular basis of MN plasticity originates in the broad expression of different TF mRNA, that are post-transcriptionally shaped into TF codes by Imp and Syp, and potentially by other RBPs that remain to be discovered, to determine their morphological fates.

developmental biology↗

Assessment of deep learning algorithms for 3D instance segmentation of confocal image datasets

Segmenting three dimensional microscopy images is essential for understanding phenomena like morphogenesis, cell division, cellular growth and genetic expression patterns. Recently, deep learning (DL) pipelines have been developed which claim to provide high accuracy segmentation of cellular images and are increasingly considered as the state-of-the-art for image segmentation problems. However, it remains difficult to define their relative performances as the concurrent diversity and lack of uniform evaluation strategies makes it difficult to know how their results compare. In this paper, we first made an inventory of the available DL methods for 3 dimensional (3D) cell segmentation. We next implemented and quantitatively compared a number of representative DL pipelines, alongside a highly efficient non-DL method named MARS. The DL methods were trained on a common dataset of 3D cellular confocal microscopy images. Their segmentation accuracies were also tested in the presence of different image artifacts. A specific method for segmentation quality evaluation was adopted which isolates segmentation errors due to under/over segmentation. This is complemented with a 3D visualization strategy for interactive exploration of segmentation quality. Our analysis shows that the DL pipelines have different levels of accuracy. Two of them, which are end to end 3D and were originally designed for cell boundary detection, show high performance, and offer clear advantages in terms of adaptability to new data. Author summaryIn recent years a number of deep learning (DL) algorithms based on computational neural networks have been developed which claim to achieve high accuracy and automatic segmentation of 3D microscopy images. Although these algorithms have received considerable attention in the literature, it is difficult to evaluate their relative performances, while it remains unclear whether they really perform better than other, more classical segmentation methods. To clarify these issues, we performed a detailed, quantitative analysis of a number of representative DL pipelines for cell instance segmentation from 3D confocal microscopy image datasets. We developed a protocol for benchmarking the performances of such DL based segmentation pipelines using common training and test datasets, evaluation metrics and visualizations. Using this protocol, we evaluated and compared four different DL pipelines to identify their strengths and limitations. A high performance non-DL method was also included in the evaluation. We show that DL pipelines may show significant differences in their performances depending on their model architecture and pipeline components but overall show excellent adaptability to unseen data. We also show that our benchmarking protocol could be extended to a variety of segmentation pipelines and datasets.

bioinformatics↗

The making of cauliflowers: the story of unsuccessful flowers

The arrangement of plant organs, called phyllotaxis, produce remarkable spiral or whorled patterns. Cauliflowers present a unique phyllotaxis with a multitude of spirals over a wide range of scales. How such a self-similar fractal organization emerges from developmental mechanisms has remained elusive. Combining experimental assays with modeling, we found that cauliflowers arise due to the hysteresis of the bistable floral network that generates inflorescences imprinted by a transient floral state. We further show how additional mutations affecting meristem growth dynamics can induce the production of conical phyllotactic structures reminiscent of the conspicuous fractal Romanesco shape. This study reveals how the spectacular morphological modification of the inflorescences in cauliflower and Romanesco shape arises from the hysteresis of the genetic programs controlling inflorescence development. One Sentence SummaryThe molecular making of cauliflowers

plant biology↗

A multiscale analysis of early flower development in Arabidopsis provides an integrated view of molecular regulation and growth control

The link between gene regulation and morphogenesis of multicellular organisms is a fundamental problem in biology. We address this question in the floral meristem of Arabidopsis, which generates new tissues and organs through complex changes in growth patterns. Starting from high-resolution time-lapse images, we generated a comprehensive 4-D atlas of early flower development including cell lineage, cellular growth rates and the expression patterns of 28 regulatory genes. This information was introduced in MorphoNet, a web-based open-access platform. The application of mechanistic computational models indicated that the molecular network based on the literature only explained a minority of the expression patterns. This was substantially improved by adding single regulatory hypotheses for individual genes. We next used the integrated information to correlate growth with the combinatorial expression of multiple genes. This led us to propose a set of hypotheses for the action of individual genes in morphogenesis, not visible by simply correlating gene expression and growth. This identified the central transcription factor LEAFY as a potential regulator of heterogeneous growth, which was supported by quantifying growth patterns in a leafy mutant. By providing an integrated, multiscale view of flower development, this atlas should represent a fundamental step towards mechanistic multiscale-scale models of flower development.

developmental biology↗

Developmental constraints modulate reproductive fate and plasticity within the Arabidopsis ovule primordium

In multicellular organisms, sexual reproduction requires the separation of the germline from the soma. In flowering plants, the first cells of the germline, so-called spore mother cells (SMCs), differentiate as the reproductive organs form. Here, we explored how organ growth influences and contributes to SMC differentiation. We generated a collection of 92 annotated 3D images capturing ovule primordium ontogeny at cellular resolution in Arabidopsis. We identified a spatio-temporal pattern of cell divisions that acts in a domain-specific manner as the primordium forms, which is coupled with the emergence of a single SMC. Using tissue growth models, we uncovered plausible morphogenetic principles involving a spatially confined growth signal, differential mechanical properties, and cell growth anisotropy. Our analysis also reveals that SMC characteristics first arise in more than one cell but SMC fate becomes progressively restricted to a single cell during organ growth. Altered primordium geometry coincided with a delay in this fate restriction process in katanin mutants. Altogether, our study suggests that tissue geometry canalizes and modulates reproductive cell fate in the Arabidopsis ovule primordium.

plant biology↗

Skeletonization of Plant Point Cloud Data in Stochastic Optimization Framework

Skeleton extraction from 3D plant point cloud data is an essential prior for myriads of phenotyping studies. Although skeleton extraction from 3D shapes have been studied extensively in the computer vision and graphics literature, handling the case of plants is still an open problem. Drawbacks of the existing approaches include the zigzag structure of the skeleton, nonuniform density of skeleton points, lack of points in the areas having complex geometry structure, and most importantly the lack of biological relevance. With the aim to improve existing skeleton structures of state-of-the-art, we propose a stochastic framework which is supported by the biological structure of the original plant (we consider plants without any leaves). Initially we estimate the branching structure of the plant by the notion of {beta}-splines to form a curve tree defined as a finite set of curves joined in a tree topology with certain level of smoothness. In the next phase, we force the discrete points in the curve tree to move towards the original point cloud by treating each point in the curve tree as a center of Gaussian, and points in the input cloud data as observations from the Gaussians. The task is to find the correct locations of the Gaussian centroids by maximizing a likelihood. The optimization technique is iterative and is based on the Expectation Maximization (EM) algorithm. The E-step estimates which Gaussian the observed point cloud was sampled from, and the M-step maximizes the negative log-likelihood that the observed points were sampled from the Gaussian Mixture Model (GMM) with respect to the model parameters. We experiment with several real world and synthetic datasets and demonstrate the robustness of the approach over the state-of-the-art.

plant biology↗

Multiscale mechanical model for cell division orientation in developing biological systems

Developing biological structures are highly complex systems, within which shape dynamics at different places is tightly coordinated. One key process at play during development is the regulation of cell division orientation. In this work, through a reformulation of cell division in terms of its energetic cost, we propose that oriented cell division is one mechanism by which cells can read and react to mechanical forces propagating in a tissue even in the absence of interphase cellular elongation in the direction of these forces. This view reproduces standard geometric division long-axis rules as a special case of a more general behaviour, in which systematic deviations from these rules can emerge. We show that states of anisotropic tension in multicellular systems can be the cause of these deviations, as often experimentally found in living tissues. Our results provide a unifying view on the different intracellular mechanisms at play in orienting cell division: they are processes which minimize energy loss, reflecting a trade-off between local and long-range mechanical signals. The consequences of this competition are explored in simulated tissues and confirmed in vivo during both the development of the pupal epithelium of dorsal thorax in D. melanogaster and the epidermal morphogenesis of ascidian embryos. Author summaryIn this work we reformulate the process of cell division orientation in development as a mechanical-energy optimization. We show that classical rules for division orientation naturally emerge when a cell minimizes the work performed against its local environment. Moreover, when multicellular stress profiles are taken into account, observed systematic violations of these rules are explained in correlation with states of anisotropic tension within the tissue. We confirm our findings experimentally on developing systems imaged with cellular resolution. Our results provide a new paradigm to understand cell division in multicellular contexts and contribute to building a physical view of biological phenomena.

biophysics↗

Sugar availability suppresses the auxin-induced strigolactone pathway to promote bud outgrowth

O_LIApical dominance occurs when the growing shoot tip inhibits the outgrowth of axillary buds. Apically-derived auxin in the nodal stem indirectly inhibits bud outgrowth via cytokinins and strigolactones. Recently, sugar deprivation was found to contribute to this phenomenon.\nC_LIO_LIUsing rose and pea, we investigated whether sugar availability interacts with auxin in bud outgrowth control, and the role of cytokinins and strigolactones, in vitro and in planta.\nC_LIO_LIWe show that sucrose antagonizes auxins effect on bud outgrowth, in a dose-dependent and coupled manner. Sucrose also suppresses strigolactone-inhibition of outgrowth, and rms3 strigolactone-perception mutant is less affected by reducing sucrose supply; however, sucrose does not interfere with the regulation of cytokinin levels by auxin, and stimulates outgrowth even with optimal cytokinin supply. These observations were assembled into a computational model where sucrose represses bud response to strigolactones, largely independently of cytokinin levels. It quantitatively captures our observed dose-dependent sucrose-hormones effects on bud outgrowth, and allows us to express outgrowth response to various combinations of auxin and sucrose levels as a simple quantitative law.\nC_LIO_LIThis study places sugars in the bud outgrowth regulatory network, and paves the way for better understanding of branching plasticity in response to environmental and genotypic factors.\nC_LI

plant biology↗

A microtubule-mediated mechanical feedback controls leaf blade development in three dimensions

Many plant species have thin leaf blades, which is an important adaptation that optimizes the exchanges with the environment. Here, we provide evidence that their three-dimensional geometry is governed by microtubule alignment along mechanical stress patterns in internal walls. Depending on the primary shape of the primordium, this process has the potential to amplify an initial degree of flatness, or promote the formation of nearly axisymmetric, mostly elongating organs, such as stems and roots. This mechanism may explain leaf evolution from branches, which is alternative to Zimmermanns influential, but widely questioned, telome theory.\n\nOne Sentence SummaryMechanical feedback controls leaf development in three dimensions

developmental biology↗

Coupling water fluxes with cell wall mechanics in a multicellular model of plant development

The growth of plant organs is a complex process powered by osmosis that attracts water inside the cells; this influx induces simultaneously an elastic extension of the walls and pressure in the cells, called turgor pressure; above a threshold, the walls yield and the cells grow. Based on Lockharts seminal work, various models of plant morphogenesis have been proposed, either for single cells, or focusing on the wall mechanical properties. However, the synergistic coupling of fluxes and wall mechanics has not yet been fully addressed in a multicellular model. This work lays the foundations of such a model, by simplifying as much as possible each process and putting emphasis on the coupling itself. Its emergent properties are rich and can help to understand plant morphogenesis. In particular, we show that the model can display a new type of lateral inhibitory mechanism that could contribute to the amplification of growth heterogeneities, essential for shape differentiation.\n\nSignificance StatementPlant cells are surrounded by a rigid wall that prevents cell displacements and rearrangements as in animal tissues. Therefore, plant morphogenesis relies only on cell divisions, shape changes, and local modulation of growth rate. It has long been recognized that cell growth relies on the competition between osmosis that tends to attract water into the cells and wall mechanics that resists to it, but this interplay has never been fully explored in a multicellular model. The goal of this work is to analyze the theoretical consequences of this coupling. We show that the emergent behavior is rich and complex: among other findings, pressure and growth rate heterogeneities are predicted without any ad-hoc assumption; furthermore the model can display a new type of lateral inhibition based on fluxes that could complement and strengthen the efficiency of already known mechanisms.

biophysics↗