ترغب بنشر مسار تعليمي؟ اضغط هنا

Dynamic change of gene-to-gene regulatory networks in response to SARS-CoV-2 infection

205   0   0.0 ( 0 )
 نشر من قبل Yoshihisa Tanaka
 تاريخ النشر 2020
  مجال البحث علم الأحياء
والبحث باللغة English
 تأليف Yoshihisa Tanaka




اسأل ChatGPT حول البحث

The current pandemic of SARS-CoV-2 has caused extensive damage to society. The characterization of SARS-CoV-2 profiles has been addressed by researchers globally with the aim of resolving this disruptive crisis. This investigation process is indispensable for an understanding of how SARS-CoV-2 behaves in human host cells. However, little is known about the systematic molecular mechanisms involved in the effect of SARS-CoV-2 infection on human host cells. Here, we have presented gene-to-gene regulatory networks in response to SARS-CoV-2 using a Bayesian network. We examined the dynamic changes of the SARS-CoV-2-purturbated networks established by our proposed framework for gene network analysis, revealing that interferon signaling gradually switches to the subsequent inflammatory-cytokine signaling cascades. Furthermore, we have succeeded in capturing a COVID-19 patient-specific network in which transduction of these signalings is coincidently induced. This enabled us to explore local regulatory systems influenced by SARS-CoV-2 in host cells more precisely at an individual level. Our panel of network analyses has provided new insight into SARS-CoV-2 research from the perspective of cellular systems.



قيم البحث

اقرأ أيضاً

Genes and proteins regulate cellular functions through complex circuits of biochemical reactions. Fluctuations in the components of these regulatory networks result in noise that invariably corrupts the signal, possibly compromising function. Here, w e create a practical formalism based on ideas introduced by Wiener and Kolmogorov (WK) for filtering noise in engineered communications systems to quantitatively assess the extent to which noise can be controlled in biological processes involving negative feedback. Application of the theory, which reproduces the previously proven scaling of the lower bound for noise suppression in terms of the number of signaling events, shows that a tetracycline repressor-based negative-regulatory gene circuit behaves as a WK filter. For the class of Hill-like nonlinear regulatory functions, this type of filter provides the optimal reduction in noise. Our theoretical approach can be readily combined with experimental measurements of response functions in a wide variety of genetic circuits, to elucidate the general principles by which biological networks minimize noise.
Gene regulatory networks (GRNs) control cellular function and decision making during tissue development and homeostasis. Mathematical tools based on dynamical systems theory are often used to model these networks, but the size and complexity of these models mean that their behaviour is not always intuitive and the underlying mechanisms can be difficult to decipher. For this reason, methods that simplify and aid exploration of complex networks are necessary. To this end we develop a broadly applicable form of the Zwanzig-Mori projection. By first converting a thermodynamic state ensemble model of gene regulation into mass action reactions we derive a general method that produces a set of time evolution equations for a subset of components of a network. The influence of the rest of the network, the bulk, is captured by memory functions that describe how the subnetwork reacts to its own past state via components in the bulk. These memory functions provide probes of near-steady state dynamics, revealing information not easily accessible otherwise. We illustrate the method on a simple cross-repressive transcriptional motif to show that memory functions not only simplify the analysis of the subnetwork but also have a natural interpretation. We then apply the approach to a GRN from the vertebrate neural tube, a well characterised developmental transcriptional network composed of four interacting transcription factors. The memory functions reveal the function of specific links within the neural tube network and identify features of the regulatory structure that specifically increase the robustness of the network to initial conditions. Taken together, the study provides evidence that Zwanzig-Mori projections offer powerful and effective tools for simplifying and exploring the behaviour of GRNs.
The complex dynamics of gene expression in living cells can be well-approximated using Boolean networks. The average sensitivity is a natural measure of stability in these systems: values below one indicate typically stable dynamics associated with a n ordered phase, whereas values above one indicate chaotic dynamics. This yields a theoretically motivated adaptive advantage to being near the critical value of one, at the boundary between order and chaos. Here, we measure average sensitivity for 66 publicly available Boolean network models describing the function of gene regulatory circuits across diverse living processes. We find the average sensitivity values for these networks are clustered around unity, indicating they are near critical. In many types of random networks, mean connectivity <K> and the average activity bias of the logic functions <p> have been found to be the most important network properties in determining average sensitivity, and by extension a networks criticality. Surprisingly, many of these gene regulatory networks achieve the near-critical state with <K> and <p> far from that predicted for critical systems: randomized networks sharing the local causal structure and local logic of biological networks better reproduce their critical behavior than controlling for macroscale properties such as <K> and <p> alone. This suggests the local properties of genes interacting within regulatory networks are selected to collectively be near-critical, and this non-local property of gene regulatory network dynamics cannot be predicted using the density of interactions alone.
85 - Yipei Guo , Ariel Amir 2020
Homeostasis of protein concentrations in cells is crucial for their proper functioning, and this requires concentrations (at their steady-state levels) to be stable to fluctuations. Since gene expression is regulated by proteins such as transcription factors (TFs), the full set of proteins within the cell constitutes a large system of interacting components. Here, we explore factors affecting the stability of this system by coupling the dynamics of mRNAs and protein concentrations in a growing cell. We find that it is possible for protein concentrations to become unstable if the regulation strengths or system size becomes too large, and that other global structural features of the networks can dramatically enhance the stability of the system. In particular, given the same number of proteins, TFs, number of interactions, and regulation strengths, a network that resembles a bipartite graph with a lower fraction of interactions that target TFs has a higher chance of being stable. By scrambling the $textit{E. coli.}$ transcription network, we find that the randomized network with the same number of regulatory interactions is much more likely to be unstable than the real network. These findings suggest that constraints imposed by system stability could have played a role in shaping the existing regulatory network during the evolutionary process. We also find that contrary to what one might expect from random matrix theory and what has been argued in the literature, the degradation rate of mRNA does not affect whether the system is stable.
Gene transcription is a stochastic process mostly occurring in bursts. Regulation of transcription arises from the interaction of transcription factors (TFs) with the promoter of the gene. The TFs, such as activators and repressors can interact with the promoter in a competitive or non-competitive way. Some experimental observations suggest that the mean expression and noise strength can be regulated at the transcription level. A Few theories are developed based on these experimental observations. Here we re-establish that experimental results with the help of our exact analytical calculations for a stochastic model with non-competitive transcriptional regulatory architecture and find out some properties of Noise strength (like sub-Poissonian fano factor) and mean expression as we found in a two state model earlier. Along with those aforesaid properties we also observe some anomalous characteristics in noise strength of mRNA and in variance of protein at lower activator concentrations.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا