6,210 research outputs found
The effect of scale-free topology on the robustness and evolvability of genetic regulatory networks
We investigate how scale-free (SF) and Erdos-Renyi (ER) topologies affect the
interplay between evolvability and robustness of model gene regulatory networks
with Boolean threshold dynamics. In agreement with Oikonomou and Cluzel (2006)
we find that networks with SFin topologies, that is SF topology for incoming
nodes and ER topology for outgoing nodes, are significantly more evolvable
towards specific oscillatory targets than networks with ER topology for both
incoming and outgoing nodes. Similar results are found for networks with SFboth
and SFout topologies. The functionality of the SFout topology, which most
closely resembles the structure of biological gene networks (Babu et al.,
2004), is compared to the ER topology in further detail through an extension to
multiple target outputs, with either an oscillatory or a non-oscillatory
nature. For multiple oscillatory targets of the same length, the differences
between SFout and ER networks are enhanced, but for non-oscillatory targets
both types of networks show fairly similar evolvability. We find that SF
networks generate oscillations much more easily than ER networks do, and this
may explain why SF networks are more evolvable than ER networks are for
oscillatory phenotypes. In spite of their greater evolvability, we find that
networks with SFout topologies are also more robust to mutations than ER
networks. Furthermore, the SFout topologies are more robust to changes in
initial conditions (environmental robustness). For both topologies, we find
that once a population of networks has reached the target state, further
neutral evolution can lead to an increase in both the mutational robustness and
the environmental robustness to changes in initial conditions.Comment: 16 pages, 15 figure
Emergence of switch-like behavior in a large family of simple biochemical networks
Bistability plays a central role in the gene regulatory networks (GRNs)
controlling many essential biological functions, including cellular
differentiation and cell cycle control. However, establishing the network
topologies that can exhibit bistability remains a challenge, in part due to the
exceedingly large variety of GRNs that exist for even a small number of
components. We begin to address this problem by employing chemical reaction
network theory in a comprehensive in silico survey to determine the capacity
for bistability of more than 40,000 simple networks that can be formed by two
transcription factor-coding genes and their associated proteins (assuming only
the most elementary biochemical processes). We find that there exist reaction
rate constants leading to bistability in ~90% of these GRN models, including
several circuits that do not contain any of the TF cooperativity commonly
associated with bistable systems, and the majority of which could only be
identified as bistable through an original subnetwork-based analysis. A
topological sorting of the two-gene family of networks based on the presence or
absence of biochemical reactions reveals eleven minimal bistable networks
(i.e., bistable networks that do not contain within them a smaller bistable
subnetwork). The large number of previously unknown bistable network topologies
suggests that the capacity for switch-like behavior in GRNs arises with
relative ease and is not easily lost through network evolution. To highlight
the relevance of the systematic application of CRNT to bistable network
identification in real biological systems, we integrated publicly available
protein-protein interaction, protein-DNA interaction, and gene expression data
from Saccharomyces cerevisiae, and identified several GRNs predicted to behave
in a bistable fashion.Comment: accepted to PLoS Computational Biolog
Dynamics of Unperturbed and Noisy Generalized Boolean Networks
For years, we have been building models of gene regulatory networks, where
recent advances in molecular biology shed some light on new structural and
dynamical properties of such highly complex systems. In this work, we propose a
novel timing of updates in Random and Scale-Free Boolean Networks, inspired by
recent findings in molecular biology. This update sequence is neither fully
synchronous nor asynchronous, but rather takes into account the sequence in
which genes affect each other. We have used both Kauffman's original model and
Aldana's extension, which takes into account the structural properties about
known parts of actual GRNs, where the degree distribution is right-skewed and
long-tailed. The computer simulations of the dynamics of the new model compare
favorably to the original ones and show biologically plausible results both in
terms of attractors number and length. We have complemented this study with a
complete analysis of our systems' stability under transient perturbations,
which is one of biological networks defining attribute. Results are
encouraging, as our model shows comparable and usually even better behavior
than preceding ones without loosing Boolean networks attractive simplicity.Comment: 29 pages, publishe
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Network Topologies That Can Achieve Dual Function of Adaptation and Noise Attenuation.
Many signaling systems execute adaptation under circumstances that require noise attenuation. Here, we identify an intrinsic trade-off existing between sensitivity and noise attenuation in the three-node networks. We demonstrate that although fine-tuning timescales in three-node adaptive networks can partially mediate this trade-off in this context, it prolongs adaptation time and imposes unrealistic parameter constraints. By contrast, four-node networks can effectively decouple adaptation and noise attenuation to achieve dual function without a trade-off, provided that these functions are executed sequentially. We illustrate ideas in seven biological examples, including Dictyostelium discoideum chemotaxis and the p53 signaling network and find that adaptive networks are often associated with a noise attenuation module. Our approach may be applicable to finding network design principles for other dual and multiple functions
A stochastic and dynamical view of pluripotency in mouse embryonic stem cells
Pluripotent embryonic stem cells are of paramount importance for biomedical
research thanks to their innate ability for self-renewal and differentiation
into all major cell lines. The fateful decision to exit or remain in the
pluripotent state is regulated by complex genetic regulatory network. Latest
advances in transcriptomics have made it possible to infer basic topologies of
pluripotency governing networks. The inferred network topologies, however, only
encode boolean information while remaining silent about the roles of dynamics
and molecular noise in gene expression. These features are widely considered
essential for functional decision making. Herein we developed a framework for
extending the boolean level networks into models accounting for individual
genetic switches and promoter architecture which allows mechanistic
interrogation of the roles of molecular noise, external signaling, and network
topology. We demonstrate the pluripotent state of the network to be a broad
attractor which is robust to variations of gene expression. Dynamics of exiting
the pluripotent state, on the other hand, is significantly influenced by the
molecular noise originating from genetic switching events which makes cells
more responsive to extracellular signals. Lastly we show that steady state
probability landscape can be significantly remodeled by global gene switching
rates alone which can be taken as a proxy for how global epigenetic
modifications exert control over stability of pluripotent states.Comment: 11 pages, 7 figure
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