1,449 research outputs found

    Module-Based Analysis of Robustness Tradeoffs in the Heat Shock Response System

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    Biological systems have evolved complex regulatory mechanisms, even in situations where much simpler designs seem to be sufficient for generating nominal functionality. Using module-based analysis coupled with rigorous mathematical comparisons, we propose that in analogy to control engineering architectures, the complexity of cellular systems and the presence of hierarchical modular structures can be attributed to the necessity of achieving robustness. We employ the Escherichia coli heat shock response system, a strongly conserved cellular mechanism, as an example to explore the design principles of such modular architectures. In the heat shock response system, the sigma-factor σ(32) is a central regulator that integrates multiple feedforward and feedback modules. Each of these modules provides a different type of robustness with its inherent tradeoffs in terms of transient response and efficiency. We demonstrate how the overall architecture of the system balances such tradeoffs. An extensive mathematical exploration nevertheless points to the existence of an array of alternative strategies for the existing heat shock response that could exhibit similar behavior. We therefore deduce that the evolutionary constraints facing the system might have steered its architecture toward one of many robustly functional solutions

    Synthetic control of a fitness tradeoff in yeast nitrogen metabolism

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    Background: Microbial communities are involved in many processes relevant to industrial and medical biotechnology, such as the formation of biofilms, lignocellulosic degradation, and hydrogen production. The manipulation of synthetic and natural microbial communities and their underlying ecological parameters, such as fitness, evolvability, and variation, is an increasingly important area of research for synthetic biology. Results: Here, we explored how synthetic control of an endogenous circuit can be used to regulate a tradeoff between fitness in resource abundant and resource limited environments in a population of Saccharomyces cerevisiae. We found that noise in the expression of a key enzyme in ammonia assimilation, Gdh1p, mediated a tradeoff between growth in low nitrogen environments and stress resistance in high ammonia environments. We implemented synthetic control of an endogenous Gdh1p regulatory network to construct an engineered strain in which the fitness of the population was tunable in response to an exogenously-added small molecule across a range of ammonia environments. Conclusion: The ability to tune fitness and biological tradeoffs will be important components of future efforts to engineer microbial communities

    Precise Regulation of Gene Expression Dynamics Favors Complex Promoter Architectures

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    Promoters process signals through recruitment of transcription factors and RNA polymerase, and dynamic changes in promoter activity constitute a major noise source in gene expression. However, it is barely understood how complex promoter architectures determine key features of promoter dynamics. Here, we employ prototypical promoters of yeast ribosomal protein genes as well as simplified versions thereof to analyze the relations among promoter design, complexity, and function. These promoters combine the action of a general regulatory factor with that of specific transcription factors, a common motif of many eukaryotic promoters. By comprehensively analyzing stationary and dynamic promoter properties, this model-based approach enables us to pinpoint the structural characteristics underlying the observed behavior. Functional tradeoffs impose constraints on the promoter architecture of ribosomal protein genes. We find that a stable scaffold in the natural design results in low transcriptional noise and strong co-regulation of target genes in the presence of gene silencing. This configuration also exhibits superior shut-off properties, and it can serve as a tunable switch in living cells. Model validation with independent experimental data suggests that the models are sufficiently realistic. When combined, our results offer a mechanistic explanation for why specific factors are associated with low protein noise in vivo. Many of these findings hold for a broad range of model parameters and likely apply to other eukaryotic promoters of similar structure

    Effects of Land-based Sources of Pollution on Coral Thermotolerance

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    Phenotypic plasticity is one way that species may cope with stressful environmental changes associated with climate change. Reef building corals present a good model for studying phenotypic plasticity because they have experienced rapid climate-driven declines in the past thirty years, often with differential survival among individuals during heat stress. One potential reason for underlying differences in thermotolerance may be due to differences in baseline levels of environmental stress. Stress associated with pollution has been shown to produce synergistic effects with heat stress, exacerbating the physiological damage of heat stress. Conversely, it is possible that mild pollution stress could prepare corals to better cope with heat stress via cross tolerance mechanisms. Cross tolerance occurs when a mild stressor prepares an organism for more extreme, subsequent stress, reducing the impact of that stressor on the organism. To examine these two possibilities, acute heat stress experiments were conducted on Acropora hyacinthus from five sites around Tutuila, American Samoa with differing pollution impact. Bleaching responses were measured visually, using photographic assessment to estimate chlorophyll content, and using pulse amplitude fluorometry to measure photosynthetic efficiency. Endosymbiont community composition was assessed at each site using quantitative PCR. RNA sequencing was used to compare differences in genes expression patterns prior to and during heat stress. Symbiont communities differed among sites, with heat tolerant Durusdinium dominating in areas with higher pollution impact and heat sensitive Cladocopium relatively more common in pristine areas. Pollution stress may induce a shift towards Durusdinium thereby enhancing resistance to subsequent heat stress in the near term. Gene expression patterns showed few differences correlating to site or pollution level. Thermotolerance, however, did correlate with gene expression patterns, both during heat stress and under control conditions. In this thesis, I present potential mechanisms underlying coral thermal tolerance in pollution-impacted areas. Our results highlight the importance of measuring pollution impacts on thermotolerance and identifying heat tolerant corals in “non-pristine” areas and their potential to seed nearby reefs following bleaching events

    Multicriteria global optimization for biocircuit design

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    One of the challenges in Synthetic Biology is to design circuits with increasing levels of complexity. While circuits in Biology are complex and subject to natural tradeoffs, most synthetic circuits are simple in terms of the number of regulatory regions, and have been designed to meet a single design criterion. In this contribution we introduce a multiobjective formulation for the design of biocircuits. We set up the basis for an advanced optimization tool for the modular and systematic design of biocircuits capable of handling high levels of complexity and multiple design criteria. Our methodology combines the efficiency of global Mixed Integer Nonlinear Programming solvers with multiobjective optimization techniques. Through a number of examples we show the capability of the method to generate non intuitive designs with a desired functionality setting up a priori the desired level of complexity. The presence of more than one competing objective provides a realistic design setting where every design solution represents a trade-off between different criteria. The tool can be useful to explore and identify different design principles for synthetic gene circuits

    Optimality principles in the regulation of metabolic networks.

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    One of the challenging tasks in systems biology is to understand how molecular networks give rise to emergent functionality and whether universal design principles apply to molecular networks. To achieve this, the biophysical, evolutionary and physiological constraints that act on those networks need to be identified in addition to the characterisation of the molecular components and interactions. Then, the cellular “task” of the network—its function—should be identified. A network contributes to organismal fitness through its function. The premise is that the same functions are often implemented in different organisms by the same type of network; hence, the concept of design principles. In biology, due to the strong forces of selective pressure and natural selection, network functions can often be understood as the outcome of fitness optimisation. The hypothesis of fitness optimisation to understand the design of a network has proven to be a powerful strategy. Here, we outline the use of several optimisation principles applied to biological networks, with an emphasis on metabolic regulatory networks. We discuss the different objective functions and constraints that are considered and the kind of understanding that they provide

    Computer-aided rational design of the phosphotransferase system for enhanced glucose uptake in Escherichia coli

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    The phosphotransferase system (PTS) is the sugar transportation machinery that is widely distributed in prokaryotes and is critical for enhanced production of useful metabolites. To increase the glucose uptake rate, we propose a rational strategy for designing the molecular architecture of the Escherichia coli glucose PTS by using a computer-aided design (CAD) system and verified the simulated results with biological experiments. CAD supports construction of a biochemical map, mathematical modeling, simulation, and system analysis. Assuming that the PTS aims at controlling the glucose uptake rate, the PTS was decomposed into hierarchical modules, functional and flux modules, and the effect of changes in gene expression on the glucose uptake rate was simulated to make a rational strategy of how the gene regulatory network is engineered. Such design and analysis predicted that the mlc knockout mutant with ptsI gene overexpression would greatly increase the specific glucose uptake rate. By using biological experiments, we validated the prediction and the presented strategy, thereby enhancing the specific glucose uptake rate

    Architecture, Design, and Tradeoffs in Biomolecular Feedback Systems

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    A core pursuit in systems and synthetic biology is the analysis of the connection between the low-level structure and parameters of a biomolecular network and its high-level function and performance. Elucidating this mapping has become increasingly feasible as precise measurements of both input parameters and output dynamics become abundant. At the same time, cross-pollination between biology and engineering has led to the realization that many of the mathematical tools from control theory are well-suited to analyze biological processes. The goal of this thesis is to use tools from control theory to analyze a variety of biomolecular systems from both natural and synthetic settings, and subsequently yield insight into the architecture, tradeoffs, and limitations of biological network. In Chapter 2, I demonstrate how allosteric proteins can be used to respond logarithmically to changes in signal. In Chapter 3, I show how control theoretic techniques can be used to inform the design of synthetic integral feedback networks that implement feedback with a sequestration mechanism. Finally, in Chapter 4 I present a novel simplified model of the E. coli heat shock response system and show how the the mapping of circuit parameters to function depends on the network's architecture. The unifying theme of this research is that the conceptual framework used to study engineered systems is remarkably well-suited to biology. That being said, it is important to apply these tools in a way that is informed by the molecular details of biological processes. By combining structural and biochemical data with the functional perspective of engineering, it is possible to understand the architectural principles that underlie living systems.</p
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