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PLoS Comput Biol. Jan 2008; 4(1): e8.
Published online Jan 4, 2008. Prepublished online Dec 5, 2007. doi:  10.1371/journal.pcbi.0040008
PMCID: PMC2174979

Noise Propagation and Signaling Sensitivity in Biological Networks: A Role for Positive Feedback

Adam P Arkin, Editor

Abstract

Interactions between genes and proteins are crucial for efficient processing of internal or external signals, but this connectivity also amplifies stochastic fluctuations by propagating noise between components. Linear (unbranched) cascades were shown to exhibit an interplay between the sensitivity to changes in input signals and the ability to buffer noise. We searched for biological circuits that can maintain signaling sensitivity while minimizing noise propagation, focusing on cases where the noise is characterized by rapid fluctuations. Negative feedback can buffer this type of noise, but this buffering comes at the expense of an even greater reduction in signaling sensitivity. By systematically analyzing three-component circuits, we identify positive feedback as a central motif allowing for the buffering of propagated noise while maintaining sensitivity to long-term changes in input signals. We show analytically that noise reduction in the presence of positive feedback results from improved averaging of rapid fluctuations over time, and discuss in detail a particular implementation in the control of nutrient homeostasis in yeast. As the design of biological networks optimizes for multiple constraints, positive feedback can be used to improve sensitivity without a compromise in the ability to buffer propagated noise.

Author Summary

Biological circuits need to be sensitive to changes in environmental signals but at the same time buffer rapid fluctuations (noise) that might be imposed on this input. In this paper, we analyze the interplay between sensitivity to signals and the ability to buffer noise. Previous studies reported that negative feedback attenuates noise. We show, however, that this ability comes at the expense of an even more dramatic reduction in sensitivity. In fact, when comparing systems of the same sensitivity, a system with negative feedback is more amenable to noise than a system without such feedback. We searched for small biological circuits that can buffer noise while maintaining high sensitivity, and found that positive feedback exhibits this property. This ability of positive feedback to buffer noise reflects its slowed-down dynamics. We discuss general requirements for the function of positive feedback as a noise-filtering device and describe a particular implementation that appears to function in yeast nutrient homeostasis. Our study emphasizes the need to consider multiple constraints when analyzing the design logic of biological networks.

Introduction

Cells sense and process information using biochemical networks of interacting genes and proteins. Typically, a signal is sensed at a specific point of the network (input) and is propagated to modulate the activity or abundance of other network components (output). Reliable information processing requires high sensitivity to changes in the input signal but low sensitivity to random fluctuations in the transmitted signal. Since the detection of signal is inherently stochastic [1], and the microenvirnment of the cell is also fluctuating randomly, understanding the principles of noise propagation in biochemical and genetic networks is of interest [25].

Linear (unbranched) cascades present the simplest instance of biochemical networks. Recent studies have shown that such cascades display an interplay between sensitivity to changes in input signal and the ability to buffer stochastic fluctuations [69]. Indeed, an increase in the sensitivity toward input signals results also in elevated sensitivity to noise in the input. A key question is whether network connectivity, e.g., the presence of positive or negative feedbacks, can modulate this interplay, reducing propagated noise while maintaining high sensitivity. Previous studies argued that negative feedbacks can buffer noise relative to linear cascades [1012]. These studies, however, did not consider the associated changes in signaling sensitivity.

In general, the fine line that separates “noise” from “signal” is established functionally. Nevertheless, in many systems such as the sensing of temperature, nutrient levels, ligand concentration, etc., the signal is interpreted as a long-term change in the input, whereas noise is characterized by rapid stochastic fluctuations. In this study, we focus on this particular class of systems.

We explore for gene circuits that can buffer propagated noise while maintaining signaling sensitivity. We consider a large set of networks that are differentially designed but are equally sensitive to long-term changes in the input, and compare their ability to buffer propagated noise. Systematic analysis of all three-gene circuits revealed that negative feedback amplifies propagated noise. In contrast, positive feedback appears to be a necessary element for buffering such noise. Analytical analysis demonstrated that positive feedback contributes to noise buffering by slowing down the dynamics, thus providing a longer averaging time. A detailed analysis of a recurrent network design, found in systems controlling nutrient homeostasis, suggests that it functions as a noise-reduction device based on the principles identified in our analysis.

Results

Negative Feedback Amplifies Propagated Noise When Sensitivity Is Controlled for

To begin analyzing the effect of network architecture on the interplay between sensitivity and noise buffering, we considered a two-component cascade with a negative feedback loop. This cascade is composed of an input node, n0, which activates an output node, n1. The output node feeds back to repress its own expression (Figure 1A). Formally, this system is described by

equation image

where β1 denotes the maximal rate of n1 production, An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex001.jpg denotes the rate of n1 degradation, and h0, h1 are Hill coefficients. Note that n0 and n1 are normalized by their respective dissociation constants from the gene promoter.

Figure 1
Comparison of a System with Negative Feedback and without Negative Feedback

We consider an input signal n0(t) = left angle bracketn0right angle bracket + σ0(t) which fluctuates around some mean level left angle bracketn0right angle bracket. The fluctuating component σ0(t) has a zero mean and some autocorrelation time τ0. Figure 1B depicts the temporal fluctuations of n1 for a system with a strong negative feedback (Hill coefficient h1 = 4). The analogous dynamics for a system that lacks such feedback (h1 = 0) is also shown. Consistent with previous studies [1012], output noise is lower in the presence of negative feedback. Nevertheless, negative feedback also significantly lowers the sensitivity of the system to a two-fold change in the level of the mean input (Figure 1C).

To rigorously quantify the interplay between the sensitivity of the input–output relation and the buffering of propagated noise, we define two measures for the sensitivity and noise-amplification of the system. The steady-state sensitivity is captured by the susceptibility, s, [3,13,14] (also termed gain [9]) defined as the relative change in output following a change in the input:

equation image

with all quantities measured at steady state. The measure for noise amplification An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex002.jpg is defined as the ratio between the output and input noise:

equation image

As before, all quantities are measured at steady state. Both s and An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex003.jpg depend on the different parameters of the system, including the Hill coefficients and mean input levels.

Figure 1D depicts the noise amplification versus susceptibility for different levels of mean input. The case of no feedback (h1 = 0) is compared to that of increasing feedback cooperativity (h1 = 1 and 2). Again, a clear interplay between susceptibility and noise buffering is observed, with systems that are more sensitive to changes in the input level being also more vulnerable to noise. Notably, this interplay seems to be more severe in the presence of negative feedback. Thus, for a given level of susceptibility, propagated noise is amplified to a greater extent in the presence of a negative feedback. This result is consistent with the theoretical arguments for a two-node model [3]: with negligible intrinsic noise, and when controlling for sensitivity, negative feedback enhances, rather then represses, propagated noise.

Formulation of a Systematic Screen of All Three-Nodes Networks

Our analysis implies that negative feedback cannot be used to buffer against rapidly varying propagated noise in systems which require a sensitive response to long-term changes in their input. To identify network architectures that can buffer noise while maintaining sensitivity, we characterized systematically the relation between susceptibility and noise-buffering of all three-node circuits (Figure 2A). A three-node circuit is composed of an input node (n0), an output node (n2), and an intermediate node (n1), connected via activating or repressing interactions (arrows). We allowed for all incoming or outgoing arrows, with the exception of the input n0 which could affect both n1 and n2 (outgoing arrows), but was not subject to feedback regulation (no incoming arrows). Each arrow was assigned a positive sign (activation) or a negative sign (repression), thus leading to a total of 324 networks (Text S1, Section IV). To ensure controlled comparison between networks, we assume that degradation is not regulated and that all proteins degrade at the same rate (e.g., by dilution).

Figure 2
Screen for Networks with High Susceptibility and Low Noise Amplification

Each specific circuit supports a range of dynamic behaviors, depending on the precise value of the interaction parameters. Following the formalism presented by Paulsson [3,13], we used the Fluctuation Dissipation Theorem (FDT [15]) to derive an analytical formula for susceptibility and noise-amplification (Methods). Briefly, the system of equations that describe the dynamics of the three-node network was

equation image

The degradation terms were assumed to be first-order, and we considered τi = 1 to maintain a mathematically controlled comparison. This system of equations was linearized around the steady state. The linearization process excludes from the analysis possible noise-filtering mechanisms that show very sharp functions such as AND or OR gates [16] as well as oscillations or transitions between multiple steady states (such as the study on positive feedback loops and noise in [17]). Note also that the steady state n0 = n1 = n2 = 0 is not formally part of our analysis, because it renders the relative fluctuation η infinite.

Following linearization, the combined effect of all interaction parameters (i.e., Hill coefficients and saturation levels) is captured by the elasticity [3,13]:

equation image

where An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex004.jpg is the rate of generating ni (e.g., via transcription) and An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex005.jpg is its degradation rate. With these definitions, the susceptibility of the output was (Text S1, Section I)

equation image

The absolute value facilitates a comparison between systems that increase or decrease their output when the input goes up.

Noise amplification was found by solving the matrix equation [3,13]

equation image

where the matrix η is composed of the normalized noise terms, the matrix M is related to the elasticities and time scales τi, and the matrix D contains a single term corresponding to noise input from n0. In the construction of D, we assume that the sole noise source is fluctuations in n0, and that these fluctuations die out exponentially with a time scale τ0 = 1 (autocorrelation time of one unit). The exact terms of Equation 7 are defined in Section II of Text S1 and in [3,13].

A particular choice of elasticity values for all arrows of the network defines a single point in the An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex006.jpg plane, and the general interplay between sensitivity and noise buffering was derived by considering a large number of different elasticity values (Figure 2A, Methods).

Positive Feedback Is an Essential Component When Buffering Noise without a Reduction in Sensitivity

As expected, noise amplification in linear (unbranched) cascades is precisely proportional to the susceptibility (Figure 2B). This case of no feedback provides the reference for comparison for other network architectures. Consistent with the analysis above, in the case of a negative feedback, all the points appear above the reference line (Figure 2C) implying an increase in noise for a given level of susceptibility. Noise amplification at constant susceptibilities is observed also for the coherent (Figure 2D) and incoherent (Figure 2E) feed-forward loops (FFLs) [16,18], probably reflecting the addition of nonsynchronous noise components mediated through the intermediate node. In contrast, for positive feedback the points in the An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex007.jpg plot appear below the reference line (Figure 2F). Thus, for a given level of sensitivity, positive feedback buffers propagated noise.

To further characterize the properties of all three-node circuits, we calculated for each network the fraction of parameter sets that produce a stable steady state (Text S1, Section III), following the paradigm of [19]. We then calculated the fraction of stable parameter sets (Methods, Section IV of Text S1) that display high susceptibility and low noise (Figure 2G). Notably, networks that were stable throughout the entire parameter range provided poor noise buffering for a given susceptibility. None of these circuits contained positive feedback loops. In sharp contrast, the circuits that enhanced noise buffering were amenable to instability and were all composed of positive feedback loops. Taken together, among the networks tested, positive feedback appears to be required for buffering propagated noise while maintaining sensitivity.

Positive Feedback Buffers Noise by Increasing Time Averaging

To better understand the reason underlying the ability of positive feedback to buffer propagated noise for a given susceptibility, we used the analytical description of a two-component system with an input n0 and an output n1, as was derived by Paulsson in [3,13] using the FDT approach [15]. In this framework (and while neglecting intrinsic noise), noise amplification was shown to be given by [3,13]:

equation image

where s = −H10/H11 denotes the susceptibility; τ0, τ1 denote the degradation time scales of n0 and n1, respectively; and H10, H11 are the elasticities (as defined in Equation 5 above). In the absence of feedback, H11 = 1. Negative feedback of n1 on itself implies H11 > 1, whereas positive feedback implies 0 < H11 < 1 (if H11 falls below zero, instability arises). As was shown by Paulsson [3], negative feedback impairs noise buffering at a given susceptibility by effectively accelerating the dynamics and reducing averaging of fluctuations over time. Similarly, positive feedback enhances noise buffering for constant susceptibility by slowing down the dynamics and allowing for better time-averaging of fluctuating components.

Notably, Equation 8 suggests that positive feedback is not the only way to reduce H11 [3,13]. Moving beyond the first-order degradation assumed in our study, H11 can also be decreased if the degradation is independent of n1 (An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex008.jpg in Equation 5). This, in fact, is likely to be the case for nondividing microorganisms. Hence, time averaging would also be improved if the degradation is close to zero-order and the synthesis is not influenced by n1.

A Noise-Buffering Circuit in the Control of Nutrient Homeostasis

While positive feedback appears to be important for buffering propagated noise (when sensitivity is controlled for), such a mechanism needs to comply with several requirements. First, the feedback loop itself should produce low internal noise because intrinsic noise is not buffered. Second, the effective elasticity H11 (Equation 8) should be of intermediate magnitude: when it is too high (H11 → 1) the effect of the positive feedback is negligible, but when it is too low (H11 → 0) the system is on the verge of instability, and the steady state will no longer resist small fluctuations. Finally, to avoid decrease in susceptibility due to saturation effects, H11 must be maintained constant over a large range of parameters.

A class of mechanisms that complies with the above requirements is based on a combination of positive and negative feedbacks. Fast-acting negative feedback functions to ensure stability, while positive feedback provides the required noise buffering. A specific example for such a network is involved in nitrogen homeostasis in yeast [2022] (Figure 3A). Here, a transcription factor (Gat1p), which is activated by nuclear Gln3p, feeds back to enhance its own transcription, and in addition induces a transcriptional repressor (DAL80) that competes with Gat1p for the same DNA binding sites. This competition effectively weakens the positive feedback and ensures stability. Denoting the input signal to the system by n0, the output Gat1p by n1 and the repressor Dal80p by n2, the system can be modeled by the following two differential equations:

equation image

equation image

Figure 3
A Mechanism To Robustly Amplify a Signal and Average Noise

Here αi and βi denote the degradation and transcription rate constants, respectively, and l is a low rate of basal transcription required to prevent the shutdown of the system, n1 = n2 = 0. We will neglect this factor in subsequent analysis. The Kij coefficients in the protein production terms are dissociation constants, with n2/Ki2 describing the competitive inhibition of Dal80p. The Hill coefficient of n2 binding to its own promoter is 2 because Dal80p binds as a dimer [21,22]. The Hill coefficient of n2 binding to the n1 promoter is set to 1 to enhance noise buffering and susceptibility (although a value of 2 would still increase noise averaging).

For the system described by Equations 9 and 10 to operate as a sensitive noise buffer, it must work in a regime where all interactions are unsaturated. Hence, all the binding constants of the repressor, Ki2, must be small, and all binding constants of the activator, Ki1, must be large. In this regime, Equation 9 and 10 reduce to

equation image

and

equation image

Finally, if n2 responds more rapidly than n1 and n0 (H22α2 [dbl greater-than sign] H11α1, 1/τ0), then it can be assumed to be at quasi-steady state, and Equations 11 and 12 are combined to

equation image

The power law dependence of the transcription rate on n1 results in an almost-constant elasticity An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex009.jpg = 1/3 (An external file that holds a picture, illustration, etc.
Object name is pcbi.0040008.ex010.jpg + in Equation 5). Hence, this network can buffer noise and maintain susceptibility for a large range of concentrations at which it remains unsaturated. A more rigorous analysis of the system is presented in Section VI of Text S1.

Detailed simulations confirm that this system can indeed buffer propagated noise, as compared to a loop-free system with the same levels of susceptibility (Figure 3B and and3C).3C). Furthermore, the noise buffering capacity and the susceptibility of this system are maintained over a large range of input levels (Text S1, Section VI).

Discussion

The ability to distinguish input signals from stochastic fluctuations is crucial for reliable information processing. Yet, being processed by the same computation device, signal and noise are inherently coupled. It thus comes as no surprise that increasing the ability to buffer propagated noise comes typically at the expense of reducing the sensitivity toward the input signal. We study this interplay in the context of a special class of systems where the signal is retained for long time periods, whereas the noise fluctuates rapidly. Such systems are ubiquitous in the adjustment of cells to aspects of their extracellular environment.

Previous studies reported that negative feedback buffers gene expression noise [1012]. Nonetheless, when considering propagated noise that originates upstream of the feedback loop, this noise filtering merely reflects the reduction in the ability of the system to respond to changes in its input. Moreover, when parameters are chosen to preserve system sensitivity, negative feedback in fact amplifies, rather than reduces, propagated noise. By the same token, positive feedback, which appears to both increase the sensitivity of the system to changes in its input and to amplify intrinsic noise, reduces propagated noise when susceptibility (steady-state sensitivity) is controlled for.

Analytical analysis [3,13] revealed that noise propagation depends on two factors: the sensitivity to changes in input (susceptibility) on the one hand, and the averaging time [3,13] on the other hand. In the absence of feedback, this averaging time depends only on degradation rate. However, both negative and positive feedbacks impact this averaging time: negative feedback accelerates the dynamics [23] and consequently it reduces time averaging and does not buffer against noise. In contrast, positive feedback delays the kinetics leading to attenuation of propagated noise. If we view the feedback modules as low-pass frequency filters [12,24,25] and define a critical frequency [25] above which fluctuations are eliminated, then negative feedback increases this critical frequency, allowing more propagated noise to pass, whereas positive feedback decreases this frequency, thus reducing the amount of noise.

Whereas our study illustrates the effect of positive feedbacks, additional mechanisms could be used for reducing propagated noise by similarly increasing the averaging time. Such mechanisms include long linear cascades; cascades with an intermediate component that has a relatively large half-life [3,26]; or scenarios where both synthesis and degradation are essentially zero-order (from the definition of H11 in Equation 5). Finally, we note that systems that exhibit time delays together with bistability were not included in our screen but could also attenuate noise [17].

Positive feedbacks did not emerge as a recurrent network motif in several of the transcriptional networks analyzed [19]. One possibility is that designing the proper feedback that will maintain stability while providing noise buffering is evolutionarily difficult for the small size networks considered in these studies [19], due to the requirement it imposes on the extent of nonlinearities (Hill-coefficients) of the interactions. A simple realization of this concept, however, can easily be implemented by somewhat larger networks, as exemplified by the coupled positive–negative feedback we described. This and similar implementations function over a broad range of parameters and do not require strict tuning. Further analysis will be required to assess the abundance of this positive feedback–based noise-reduction scheme in different biological systems.

Methods

Simulations.

All simulations were based on the Gibson-Bruck [27] modification of Gillespie [28] algorithm. Input noise was implemented via transcription from a low copy mRNA with a short half life. No other mRNAs were explicitly considered. Simulation parameters are detailed in Section VII of Text S1. Simulations were carried out using Dizzy [29].

Parameter screen.

The interaction parameters of each arrow in each network are captured by the interaction elasticities Hij. The susceptibility (Equation 2) for each network is calculated from the elasticities using Equation 6 (for a general derivation of the susceptibility, see Text S1, Section I). The noise amplification is connected to the elasticities through the solution of Equation 7. Definitions for the terms in Equation 7 appear in Section II of Text S1. Equation 7 was solved symbolically for all three node networks using Maple (MapleSoft, Waterloo Maple). Solutions for specific network architectures are shown in Table S1.

The values for the elasticities were randomly assigned to each network. To control for similar distribution of positive and negative interactions, we defined the synthesis elasticity Sij by Hii = 1 − Sii and Hij = −Sij. When i enhances the synthesis of j, then Sij > 0, and vice versa. Positive feedback of i on itself implies Sii > 0 and vice-versa. The synthesis elasticity values were sampled from a uniform distribution between zero and four and assigned to the arrows in each network. Different sampling ranges did not have a significant effect on the conclusions (Text S1, Section IV). We sampled 20,000 random sets of parameters for each circuit. The time constants were held fixed at a value of one, but different values did not change the results (Text S1, Section IV).

Analysis of stability.

Stability criteria were established via the sign of the eigenvalues of the interaction matrix (Text S1, Section III).

Supporting Information

Table S1

Properties of Several Networks:

(54 KB DOC)

Text S1

Mathematical and Numerical Details:

(280 KB PDF)

Acknowledgments

We are grateful to Moshe Oren for support and encouragement throughout the work. We thank Andreas Doncic for helping with the screen design and critical review of the manuscript, and Nitzan Rosenfeld, Sagi Levi, Ran Kafri and members of our lab for comments and discussion.

Abbreviations

FFL
feed-forward loop
FDT
Fluctuation Dissipation Theorem

Footnotes

A previous version of this article appeared as an Early Online Release on December 5, 2007 (doi:10.1371/journal.pcbi.0040008.eor).

Author contributions. GH and NB conceived and designed the experiments and wrote the paper.

Funding. This work was supported by the Helen and Martin Kimmel award for innovative investigation, the Kahn fund for Systems Biology, the Tauber fund, and the US National Institutes of Health (GM068763 to the Center for Modular Biology).

Competing interests. The authors have declared that no competing interests exist.

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