Computational Models of the Notch Network Elucidate Mechanisms of Context-dependent Signaling

The Notch signaling pathway controls numerous cell fate decisions during development and adulthood through diverse mechanisms. Thus, whereas it functions as an oscillator during somitogenesis, it can mediate an all-or-none cell fate switch to influence pattern formation in various tissues during development. Furthermore, while in some contexts continuous Notch signaling is required, in others a transient Notch signal is sufficient to influence cell fate decisions. However, the signaling mechanisms that underlie these diverse behaviors in different cellular contexts have not been understood. Notch1 along with two downstream transcription factors hes1 and RBP-Jk forms an intricate network of positive and negative feedback loops, and we have implemented a systems biology approach to computationally study this gene regulation network. Our results indicate that the system exhibits bistability and is capable of switching states at a critical level of Notch signaling initiated by its ligand Delta in a particular range of parameter values. In this mode, transient activation of Delta is also capable of inducing prolonged high expression of Hes1, mimicking the “ON” state depending on the intensity and duration of the signal. Furthermore, this system is highly sensitive to certain model parameters and can transition from functioning as a bistable switch to an oscillator by tuning a single parameter value. This parameter, the transcriptional repression constant of hes1, can thus qualitatively govern the behavior of the signaling network. In addition, we find that the system is able to dampen and reduce the effects of biological noise that arise from stochastic effects in gene expression for systems that respond quickly to Notch signaling

Noise Reduction by Diffusional Dissipation in a Minimal Quorum Sensing Motif

Cellular interactions are subject to random fluctuations (noise) in quantities of interacting molecules. Noise presents a major challenge for the robust function of natural and engineered cellular networks. Past studies have analyzed how noise is regulated at the intracellular level. Cell–cell communication, however, may provide a complementary strategy to achieve robust gene expression by enabling the coupling of a cell with its environment and other cells. To gain insight into this issue, we have examined noise regulation by quorum sensing (QS), a mechanism by which many bacteria communicate through production and sensing of small diffusible signals. Using a stochastic model, we analyze a minimal QS motif in Gram-negative bacteria. Our analysis shows that diffusion of the QS signal, together with fast turnover of its transcriptional regulator, attenuates low-frequency components of extrinsic noise. We term this unique mechanism “diffusional dissipation” to emphasize the importance of fast signal turnover (or dissipation) by diffusion. We further show that this noise attenuation is a property of a more generic regulatory motif, of which QS is an implementation. Our results suggest that, in a QS system, an unstable transcriptional regulator may be favored for regulating expression of costly proteins that generate public goods

Stability of Systems with Stochastic Delay

Stability of systems with stochastic delays is addressed in this dissertation. A linear delay differential equation is considered where the delay takes values from a finite set of numbers according to a probability distribution function. Exact stability conditions for the resulting system are obtained. These conditions depend on the parameters of the system, the delay values and the probability distribution function governing the delay. The stability criteria are first obtained in a discretetime setting after discretizing the continuous-time system. Then, the stability conditions are obtained in a continuous-time setting where an operator description of delay differential equations is used. The stability results are applied to models of gene regulatory networks. The results can determine whether a steady state protein production is stable or oscillations in protein levels may arise as a result of stochastic fluctuations in reaction times. Finally, the interplay between noise in the gene expression level and noise in the population level in microbial consortia is investigated. The results suggest a mechanism for creating robust oscillations in multicellular environments.PHDMechanical EngineeringUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttps://deepblue.lib.umich.edu/bitstream/2027.42/144051/1/mehsad_1.pd

Models of self-organization in biological development

Bibliography: p. 297-320.In this thesis we thus wish to consider the concept of self-organization as an overall paradigm within which various theoretical approaches to the study of development may be described and evaluated. In the process, an attempt is made to give a fair and reasonably comprehensive overview of leading modelling approaches in developmental biology, with particular reference to self-organization. The work proceeds from a physical or mathematical perspective, but not unduly so - the major mathematical derivations and results are relegated to appendices - and attempts to fill a perceived gap in the extant review literature, in its breadth and attempted impartiality of scope. A characteristic of the present account is its markedly interdisciplinary approach: it seeks to place self-organization models that have been proposed for biological pattern formation and morphogenesis both within the necessary experimentally-derived biological framework, and in the wider physical context of self-organization and the mathematical techniques that may be employed in its study. Hence the thesis begins with appropriate introductory chapters to provide the necessary background, before proceeding to a discussion of the models themselves. It should be noted that the work is structured so as to be read sequentially, from beginning to end; and that the chapters in the main text were designed to be understood essentially independently of the appendices, although frequent references to the latter are given. In view of the vastness of the available information and literature on developmental biology, a working knowledge of embryological principles must be assumed. Consequently, rather than attempting a comprehensive introduction to experimental embryology, chapter 2 presents just a few biological preliminaries, to 'set the scene', outlining some of the major issues that we are dealing with, and sketching an indication of the current status of knowledge and research on development. The chapter is aimed at furnishing the necessary biological, experimental background, in the light of which the rest of the thesis should be read, and which should indeed underpin and motivate any theoretical discussions. We encounter the different hierarchical levels of description in this chapter, as well as some of the model systems whose experimental study has proved most fruitful, some of the concepts of experimental embryology, and a brief reference to some questions that will not be addressed in this work. With chapter 3, we temporarily move away from developmental biology, and consider the wider physical and mathematical concepts related to the study of self-organization. Here we encounter physical and chemical examples of spontaneous structure formation, thermodynamic considerations, and different approaches to the description of complexity. Mathematical approaches to the dynamical study of self-organization are also introduced, with specific reference to reaction-diffusion equations, and we consider some possible chemical and biochemical realizations of self-organizing kinetics. The chapter may be read in conjunction with appendix A, which gives a somewhat more in-depth study of reaction-diffusion equations, their analysis and properties, as an example of the approach to the analysis of self-organizing dynamical systems and mathematically-formulated models. Appendix B contains a more detailed discussion of the Belousov-Zhabotinskii reaction, which provides a vivid chemical paradigm for the concepts of symmetry-breaking and self-organization. Chapter 3 concludes with a brief discussion of a model biological system, the cellular slime mould, which displays rudimentary development and has thus proved amenable to detailed study and modelling. The following two chapters form the core of the thesis, as they contain discussions of the detailed application of theoretical concepts and models, largely based on self-organization, to various developmental situations. We encounter a diversity of models which has arisen largely in the last quarter century, each of which attempts to account for some aspect of biological pattern formation and morphogenesis; an aim of the discussion is to assess the extent of the underlying unity of these models in terms of the self-organization paradigm. In chapter 4 chemical pre-patterns and positional information are considered, without the overt involvement of cells in the patterning. In chapter 5, on the other hand, cellular interactions and activities are explicitly taken into account; this chapter should be read together with appendix C, which contains a brief introduction to the mathematical formulation and analysis of some of the models discussed. The penultimate chapter, 6, considers two other approaches to the study of development; one of these has faded away, while the other is still apparently in the ascendant. The assumptions underlying catastrophe theory, the value of its applications to developmental biology and the reasons for its decline in popularity, are considered. Lastly, discrete approaches, including the recently fashionable cellular automata, are dealt with, and the possible roles of rule-based interactions, such as of the so-called L-systems, and of fractals and chaos are evaluated. Chapter 7 then concludes the thesis with a brief assessment of the value of the self-organization concept to the study of biological development

A Meshless Modelling Framework for Simulation and Control of Nonlinear Synthetic Biological Systems

Synthetic biology is a relatively new discipline that incorporates biology and engineering principles. It builds upon the advances in molecular, cell and systems biology and aims to transform these principles to the same effect that synthesis transformed chemistry. What distinguishes synthetic biology from traditional molecular or cellular biology is the focus on design and construction of components (e.g. parts of a cell) that can be modelled, characterised and altered to meet specific performance criteria. Integration of these parts into larger systems is a core principle of synthetic biology. However, unlike some areas of engineering, biology is highly non-linear and less predictable. In this thesis the work that has been conducted to combat some of the complexities associated with dynamic modelling and control of biological systems will be presented. Whilst traditional techniques, such as Orthogonal Collocation on Finite Elements (OCFE) are common place for dynamic modelling they have significant complexity when sampling points are increased and offer discrete solutions or solutions with limited differentiability. To circumvent these issues a meshless modelling framework that incorporates an Artificial Neural Network (ANN) to solve Ordinary Differential Equations (ODEs) and model dynamic processes is utilised. Neural networks can be considered as mesh-free numerical methods as they are likened to approximation schemes where the input data for a design of a network consists of a set of unstructured discrete data points. The use of the ANN provides a solution that is differentiable and is of a closed analytic form, which can be further utilised in subsequent calculations. Whilst there have been advances in modelling biological systems, there has been limited work in controlling their outputs. The benefits of control allow the biological system to alter its state and either upscale production of its primary output, or alter its behaviour within an integrated system. In this thesis a novel meshless Nonlinear Model Predictive Control (NLMPC) framework is presented to address issues related to nonlinearities and complexity. The presented framework is tested on a number of case studies. A significant case study within this work concerns simulation and control of a gene metabolator. The metabolator is a synthetic gene circuit that consists of two metabolite pools which oscillate under the influence of glycolytic flux (a combination of sugars, fatty acids and glycerol). In this work it is demonstrated how glycolytic flux can be used as a control variable for the metabolator. The meshless NLMPC framework allows for both Single-Input Single-Output (SISO) and Multiple-Input Multiple-Output (MIMO) control. The dynamic behaviour of the metabolator allows for both top-down control (using glycolytic flux) and bottom-up control (using acetate). The benefit of using MIMO (by using glycolytic flux and acetate as the control variables) for the metabolator is that it allows the system to reach steady state due to the interactions between the two metabolite pools. Biological systems can also encounter various uncertainties, especially when performing experimental validation. These can have profound effect on the system and can alter the dynamics or overall behaviour. In this work the meshless NLMPC framework addresses uncertainty through the use of Zone Model Predictive Control (Zone MPC), where the control profile is set as a range, rather than a fixed set point. The performance of Zone MPC under the presence of various magnitudes of random disturbances is analysed. The framework is also applied to biological systems architecture, for instance the development of biological circuits from well-characterised and known parts. The framework has shown promise in determining feasible circuits and can be extended in future to incorporate a full list of biological parts. This can give rise to new circuits that could potentially be used in various applications. The meshless NLMPC framework proposed in this work can be extended and applied to other biological systems and heralds a novel method for simulation and control