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Biology subjects

Jönsson, H.

Publications and source records attributed to Jönsson, H..

6 recordsLinked to original sources

Learning a mechanical growth model of flower morphogenesis

Morphogenesis, the process by which organs take their shape, is a fundamental problem in biology and requires a complex combination of genetic, biochemical, and mechanical signals. The data that we collect for this process are usually multi-scale and multi-modal, typically image timeseries of tissue morphology and transcription data. As the data becomes larger and more diverse, the harder it becomes to gain meaningful understanding in terms of theoretical models. Here, and tackling this problem in the developing flower organ, we learn a mechanical model of growth starting from combined morphology and transcription data across the tissue by firstly learning and connecting independent representations for the two spaces and secondly refining the representation using the mechanical state of the tissue to learn a mechanical growth model. This approach can link multiple scales, in this case proposing the physical action of genes, and can act as a vehicle to accommodate diverse data and hypotheses in developmental biology of plants and beyond.

developmental biology↗

Sugar signaling modulates SHOOT MERISTEMLESS expression and meristem function in Arabidopsis

In plants, development of all above-ground tissues is controlled by the shoot apical meristem (SAM) which balances cell proliferation and differentiation to allow life-long growth. To maximize fitness and survival, meristem activity is adjusted to the prevailing conditions through a poorly understood integration of developmental signals with environmental and nutritional information. Here, we show that sugar signals influence SAM function by altering the protein levels of SHOOT MERISTEMLESS (STM), a key regulator of meristem maintenance. STM is less abundant in the inflorescence meristems of plants grown or treated under limiting light conditions, with lower STM levels correlating with lower sugar content in these meristems. Additionally, sucrose but not light is sufficient to sustain STM accumulation in excised inflorescences. Plants overexpressing the 1-subunit of SUCROSE-NON-FERMENTING1-RELATED KINASE 1 (SnRK1) accumulate less STM protein under optimal light conditions, despite higher sugar accumulation in the meristem. Furthermore, SnRK11 interacts physically with STM, suggesting a direct local repression. Surprisingly, silencing SnRK1 in the meristem leads to reduced STM expression and severe developmental phenotypes previously associated with STM loss-of-function. Altogether, we demonstrate that sugars promote STM accumulation and that the SnRK1 sugar sensor plays a dual role in the SAM, limiting STM abundance under unfavorable conditions but being required for overall meristem organization and integrity. This highlights the importance of sugars and SnRK1 signaling for the proper coordination of meristem activities.

plant biology↗

It’s about time: Analysing an alternative approach for reductionist modelling of linear pathways in systems biology

Thoughtful use of simplifying assumptions is crucial to make systems biology models tractable while still representative of the underlying biology. A useful simplification can elucidate the core dynamics of a system. A poorly chosen assumption can, however, either render a model too complicated for making conclusions or it can prevent an otherwise accurate model from describing experimentally observed dynamics.\n\nHere, we perform a computational investigation of linear pathway models that contain fewer pathway steps than the system they are designed to emulate. We demonstrate when such models will fail to reproduce data and how detrimental truncation of a linear pathway leads to detectable signatures in model dynamics and its optimised parameters.\n\nAn alternative assumption is suggested for simplifying linear pathways. Rather than assuming a truncated number of pathway steps, we propose to use the assumption that the rates of information propagation along the pathway is homogeneous and instead letting the length of the pathway be a free parameter. This results in a three-parameter representation of arbitrary linear pathways which consistently outperforms its truncated rival and a delay differential equation alternative in recapitulating observed dynamics.\n\nOur results provide a foundation for well-informed decision making during model simplifications.\n\n1 Author summaryMathematical modelling can be a highly effective way of condensing our understanding of biological processes and highlight the most important aspects of them. Effective models are based on simplifying assumptions that reduce complexity while still retaining the core dynamics of the original problem. Finding such assumptions is, however, not trivial.\n\nIn this paper, we explore ways in which one can simplify long chains of simple reactions wherein each step is linearly dependent on its predecessor. After generating synthetic data from models that describe such chains in explicit detail, we compare how well different simplifications retain the original dynamics. We show that the most common such simplification, which is to ignore parts of the chain, often renders models unable to account for time delays. However, we also show that when such a simplification has had a detrimental effect, it leaves a detectable signature in its optimal parameter values. We also propose an alternative assumption which leads to a highly effective model with only three parameters. By comparing the effects of these simplifying assumptions in thousands of different cases and for different conditions we are able to clearly show when and why one is preferred over the other.

systems biology↗

Anisotropic growth is achieved through the additive mechanical effect of material anisotropy and elastic asymmetry

Fast directional growth is a necessity for the young seedling: after germination, the seedling needs to quickly reach through the soil to begin its autotrophic life. In most dicot plants, this rapid escape is due to the anisotropic elongation of the hypocotyl, the columnar organ between the root and the shoot meristems. Such anisotropic growth is common in many plant organs and is canonically attributed to cell wall anisotropy produced by oriented cellulose fibers in the cell wall. More recently, a mechanism based on asymmetric cell wall elasticity has been proposed, produced by differential pectin biochemistry. Here we present a harmonizing model for anisotropic growth control in the dark-grown Arabidopsis hypocotyl: basic anisotropic information is provided by cellulose orientation (proxied by microtubules) and additive anisotropic information is provided by pectin-based elastic asymmetry in the epidermis. We demonstrate that hypocotyl growth was always anisotropic with axial and transverse walls growing differently, from germination. We present experimental evidence for pectin biochemical differences and wall mechanics underlying this differential growth. We demonstrate that pectin biochemical changes control the transition to rapid growth characteristic of Arabidopsis hypocotyl elongation, and provide evidence for a substantial mechanical role for pectin in the cell wall when microtubules are compromised. Lastly, our in silico modelling experiments indicate an additive combination for pectin biochemistry and cellulose orientation in promoting anisotropic growth.

plant biology↗

MoonFit, a minimal interface for fitting ODE dynamical models, bridging simulation by experimentalists and customization by C++ programmers

The modelling of biological systems often consists into differential equation models that need to be fitted to experimental data. During this complex process, the practical experience of the biologist and the theoretical abstraction of the modeller require back-and-forth refinements of the model, design of new experiments and inclusion of more data-points into the fitting procedure. Available optimization interfaces rarely simultaneously allow customizations by the programmer and the capacity for the biologist to perform simulations or optimizations with a simple interface.\n\nHere, we provide the C++ code of a graphical user interface based on a user defined minimal C++ ODE model class. The graphical interface allows to perform simulations and optimizations without any knowledge in programming. The code was designed minimal and modular to be easily modified, with maximal freedom to link customized optimization libraries, solver or hand-made scripts. Moonfit is powerful enough to fit and compare models with high dimensionality, multiple datasets, to automatize optimizations, and to perform iterative fittings using data interpolation. We believe this will ease the interaction between modellers and experimental partners.\n\nAvailability: Moonfit is freely available via c++ source code and accompanying scripts from gitlab.com/Moonfit/MoonLight.

systems biology↗

A model of protein interactions for regulating plant stem cells

The plant shoot apical meristem holds a stem cell niche from which all aerial organs originate. Using a computational approach we show that a mixture of monomers and heterodimers of the transcription factors WUSCHEL and HAIRY MERISTEM is sufficient to pattern the stem cell niche, and predict that immobile heterodimers form a regulatory pocket surrounding the stem cells. The model achieves to reproduce an array of perturbations, including mutants and tissue size modifications. We also show its ability to reproduce the recently observed dynamical shift of the stem cell niche during the development of an axillary meristem. The work integrates recent experimental results to answer the longstanding question of how the asymmetry of expression between the stem cell marker CLAVATA3 and its activator WUSCHEL is achieved, and recent findings of plasticity in the system.

plant biology↗