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Results for “systems biology”

Search indexed bioRxiv preprints in genomics, neuroscience, cell biology and bioinformatics. Read source abstracts and check manuscript versions; preprints are not peer reviewed.

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At least 343 records · Page 19Linked to original sources

A neural-network framework for modelling auditory sensory cells and synapses

In classical computational neuroscience, analytical model descriptions are derived from neuronal recordings to mimic the underlying biological system. These neuronal models are typically slow to compute and cannot be integrated within large-scale neuronal simulation frameworks. We present a hybrid, machine-learning and computational-neuroscience approach that transforms analytical models of sensory neurons and synapses into deep-neural-network (DNN) neuronal units with the same biophysical properties. Our DNN-model architecture comprises parallel and differentiable equations that can be used for backpropagation in neuro-engineering applications, and offers a simulation run-time improvement factor of 70 and 280 on CPU or GPU systems respectively. We focussed our development on auditory neurons and synapses, and show that our DNN-model architecture can be extended to a variety of existing analytical models. We describe how our approach for auditory models can be applied to other neuron and synapse types to help accelerate the development of large-scale brain networks and DNN-based treatments of the pathological system.

systems biology↗

Global architecture of the nucleus in single cells by DNA seqFISH+ and multiplexed immunofluorescence

Identifying the relationships between chromosome structures, chromatin states, and gene expression is an overarching goal of nuclear organization studies. Because individual cells are highly variable at all three levels, it is essential to map all three modalities in the same single cell, a task that has been difficult to accomplish with existing tools. Here, we report the direct super-resolution imaging of over 3,660 chromosomal loci in single mouse embryonic stem cells (mESCs) by DNA seqFISH+, along with 17 chromatin marks by sequential immunofluorescence (IF) and the expression profile of 70 RNAs, in the same cells. We discovered that the nucleus is separated into zones defined by distinct combinatorial chromatin marks. DNA loci and nascent transcripts are enriched at the interfaces between specific nuclear zones, and the level of gene expression correlates with an association between active or nuclear speckle zones. Our analysis also uncovered several distinct mESCs subpopulations with characteristic combinatorial chromatin states that extend beyond known transcriptional states, suggesting that the metastable states of mESCs are more complex than previously appreciated. Using clonal analysis, we show that the global levels of some chromatin marks, such as H3K27me3 and macroH2A1 (mH2A1), are heritable over at least 3-4 generations, whereas other marks fluctuate on a faster time scale. The long-lived chromatin states may represent "hidden variables" that explain the observed functional heterogeneity in differentiation decisions in single mESCs. Our integrated spatial genomics approach can be used to further explore the existence and biological relevance of molecular heterogeneity within cell populations in diverse biological systems.

systems biology↗

Robust, sensitive, and quantitative single-cell proteomics based on ion mobility filtering

Unbiased single-cell proteomics (scProteomics) promises to advance our understanding of cell functions within complex biological systems. However, a major challenge for current methods is their ability to identify and provide accurate quantitative information for low abundance proteins. Herein, we describe an ion mobility-enhanced mass spectrometry acquisition and peptide identification method, TIFF (Transferring Identification based on FAIMS Filtering), designed to improve the sensitivity and accuracy of label-free scProteomics. TIFF significantly extends the ion accumulation times for peptide ions by filtering out singly charged background ions. The peptide identities are then assigned by a 3-dimensional MS1 feature matching approach (retention time, accurate mass, and FAIMS compensation voltage). The TIFF method enabled unbiased proteome analysis to a depth of >1,700 proteins in single HeLa cells with >1,100 proteins consistently quantified. As a demonstration, we applied the TIFF method to obtain temporal proteome profiles of >150 single murine macrophage cells during a lipopolysaccharide stimulation experiment and identified time-dependent proteome profiles.

systems biology↗

Understanding binary classifier model structure based on Shapley feature interaction patterns

There is increasing emphasis on the interpretability of machine learning models, including in understanding biological systems. The well-known Shapley value framework based on game theory works in principle with any models to attribute feature importance. While feature interactions are critical to understand and can be interpreted within this framework, much attention is paid in practice on global feature importance and general trends of interactions. The inter-relationships between underlying model structure and Shapley value and its decomposition is less clear. Here we use binary classifiers to systematically examine how logical and additive interactions affect marginal contributions. These decomposed main and interaction effects are reflected in resulting Shapley dependence plots. The directionality of inequalities or logical/additive operators influence independently the main and marginal/interaction effects. Lastly, we show that these principles are applicable for models with noise.

systems biology↗

Incoherent modulation of bi-stable dynamics orchestrates the Mushroom and Isola bifurcations

In biological networks, steady state dynamics of cell-fate regulatory genes often exhibit Mushroom and Isola kind of bifurcations. How these complex bifurcations emerge for these complex networks, and what are the minimal network structures that can generate these bifurcations, remain elusive. Herein, by employing Waddingtons landscape theory and bifurcation analysis, we have shown that both Mushroom and Isola bifurcations can be realized with four minimal network motifs that are constituted by combining positive feedback motifs with different types of incoherent feedback motifs. Our study demonstrates that the intrinsic bi-stable dynamics due to the presence of the positive feedback motif can be fine-tuned by altering the extent of the incoherence of these proposed minimal networks to orchestrate these complex bifurcations. These modeling insights will be useful in identifying and analyzing possible network motifs that may give rise to either Mushroom or Isola bifurcation in other biological systems.

systems biology↗

Single-cell gene regulatory network inference atscale: The Inferelator 3.0

MotivationGene regulatory networks define regulatory relationships between transcription factors and target genes within a biological system, and reconstructing them is essential for understanding cellular growth and function. Methods for inferring and reconstructing networks from genomics data have evolved rapidly over the last decade in response to advances in sequencing technology and machine learning. The scale of data collection has increased dramatically; the largest genome-wide gene expression datasets have grown from thousands of measurements to millions of single cells, and new technologies are on the horizon to increase to tens of millions of cells and above. ResultsIn this work, we present the Inferelator 3.0, which has been significantly updated to integrate data from distinct cell types to learn context-specific regulatory networks and aggregate them into a shared regulatory network, while retaining the functionality of the previous versions. The Inferelator is able to integrate the largest single-cell datasets and learn cell-type specific gene regulatory networks. Compared to other network inference methods, the Inferelator learns new and informative Saccharomyces cerevisiae networks from single-cell gene expression data, measured by recovery of a known gold standard. We demonstrate its scaling capabilities by learning networks for multiple distinct neuronal and glial cell types in the developing Mus musculus brain at E18 from a large (1.3 million) single-cell gene expression dataset with paired single-cell chromatin accessibility data. AvailabilityThe inferelator software is available on GitHub (https://github.com/flatironinstitute/inferelator) under the MIT license and has been released as python packages with associated documentation (https://inferelator.readthedocs.io/).

systems biology↗

Relationships of diversity and evenness in adaptation strategies of the effect of protective coloration of animals

This study aims to investigate the relationship between the diversity and uniformity of the protective coloration of animals. The protective coloration of animals is the result of the formation of adaptation strategies. The aim of this study is to identify the colorimetric parameters that characterize the adaptive properties of the protective coloration of animals in relation to their natural habitat. The relevance of this study is related to the importance of the tasks of remote collection of information about various biological species; in particular, animals that carry dangerous infections. This is all the more important in light of the current epidemic problems facing humanity. The revealed colorimetric characteristics can be used to describe digital images and their further recognition. They can be classifying features in machine learning algorithms. We give an example of digital image processing of a duck (Anas platyrhynchos). The analysis of the distribution of the found colorimetric parameter makes it possible to identify the image segments corresponding to the Anas platyrhynchos. The results thus obtained are also of interest from the point of view of the problem of the adaptive role of the diversity of biological systems in relation to the problem of the mechanisms of functioning of the protective coloration of animals.

systems biology↗

MOFA: Multi-Objective Flux Analysis for the COBRA Toolbox

Multi-objective Optimization (MO) is an important tool for quantitative examination of the trade-offs faced by biological organisms. Using genome-scale constraint-based models of metabolism (GSMs), Multi-Objective Flux Analysis (MOFA) allows MO analyses of trade-offs among key biological tasks. The leading software package for conducting a plethora of different types of constraint-based analyses using GSMs is the COBRA Toolbox for MATLAB. We have developed a new add-on tool for this toolbox using Normalized Normal Constraint (NNC) that performs MOFA for a number of objectives only limited by computation power (n [≤] 10). This development will facilitate MOFA analyses by COBRAs large user base and allow greater multi-faceted examination of metabolic trade-offs in complicated biological systems. Availability and ImplementationThe MOFA software is freely available for download from https://bbs.llnl.gov under the GPL v2 license. The program runs on MATLAB with the COBRA software on Windows, Linux, and MacOS. It includes a detailed manual explaining the input and output of a simulation, a listing of the codes functions, and an example MOFA run using a well-curated GSM model of E. coli. Contactgriesemer1@llnl.gov or navid1@llnl.gov

systems biology↗

Sequence analysis paradigm shift reveals unsuspected semantic properties of species proteomes

Alignment-based methods dominate molecular biology. However, by primarily allowing one-to-one comparisons, these methods are focused on a gene-centered viewpoint and lack the broad context essential to analyze how complex biological systems function and evolve. In actuality, a gene is part of genome where more than one sequence contributes to the functional network and evolutionary trajectory of the cell. The need for conservation of established interactions, is arguably more important to the evolutionary success of species than conservation of individual function. To test whether such contextual information exists, a distributional semantics method - Latent Semantic Analysis (LSA), was applied to thousands of species proteomes. Using natural language processing, Latent Taxonomic Signatures (LTSs) were identified that outperformed existing alignment-based BLAST methods when random protein sequences were being mapped to annotated taxonomy according to GenBank. LTSs are a novel proteome distributed feature, suggesting the existence of evolutionary constraints imposed on individual proteins by their proteome context. Even orphan proteins are exhibiting LTSs, which makes their uniqueness linked to a specific taxonomic level questionable. Unlike more simple bias, LTSs represent a self-similarity pattern, where random sets of species proteins show the same statistical properties of a complete proteome at many scales. Natural language processing and machine learning provide insights not easily discernable using alignment based methods suggestive there is more to species related differences than just translational optimization.

systems biology↗

Quantifying Cellular Pluripotency and Pathway Robustness through Forman-Ricci Curvature

In stem cell biology, cellular pluripotency describes the capacity of a given cell to differentiate into multiple cell types. From a statistical physics perspective, entropy provides a statistical measure of randomness and has been demonstrated as a way to quantitate pluripotency when considering biological gene networks. Furthermore, recent theoretical work has established a relationship between Ricci curvature (a geometric measure of "flatness") and entropy (also related to robustness), which one can exploit to link the geometric quantity of curvature to the statistical quantity of entropy. Therefore, this study seeks to explore Ricci curvature in biological gene networks as a descriptor of pluripotency and robustness among gene pathways. Here, we investigate Forman-Ricci curvature, a combinatorial discretization of Ricci curvature, along with network entropy, to explore the relationship of the two quantities as they occur in gene networks. First, we demonstrate our approach on an experiment of stem cell gene expression data. As expected, we find Ricci curvature directly correlates with network entropy, suggesting Ricci curvature could serve as an indicator for cellular pluripotency much like entropy. Second, we measure Forman-Ricci curvature in a dataset of cancer and non-cancer cells from melanoma patients. We again find Ricci curvature is increased in the cancer state, reflecting increased pluripotency or "stemness". Further, we locally examine curvature on the gene level to identify several genes and gene pathways with known relevance to melanoma. In turn, we conclude Forman-Ricci curvature provides valuable biological information related to pluripotency and pathway functionality. In particular, the advantages of this geometric approach are promising for extension to higher-order topological structures in order to represent more complex features of biological systems.

systems biology↗

Cell Wall Biochemistry Drives Pollen Tube Mechanics and Affects Growth Rate

Pollen tubes maintain cell wall integrity as they rapidly grow towards the ovule, yet need to rupture at a precise moment to release the sperm cells. This biomechanical balance is critical for fertilization and relies on the interplay between turgor pressure and cell wall rigidity. How cell wall composition affects its mechanical properties is, however, not well understood. In this study, we combine experimental and simulation techniques to determine key mechanical parameters using Arabidopsis cell wall mutants. We integrated cellular force microscopy with a Finite Element Method-based model to predict growth rates of different mutant pollen tubes. The Finite Element Method-based model allowed us to quantify the effects of cell wall mutations on the time-independent turgor pressure and cell wall elasticity, while cellular force microscopy enabled determination of time-dependent viscoelastic properties of the cell wall. This novel approach can be applied across biological systems and advances mechanical studies of cell and tissue morphogenesis.

systems biology↗

Parameter estimation in the age of degeneracy and unidentifiability

Parameter estimation from observable or experimental data is a crucial stage in any modeling study. Identifiability refers to ones ability to uniquely estimate the model parameters from the available data. Structural unidentifiability in dynamic models, the opposite of identifiability, is associated with the notion of degeneracy where multiple parameter sets produce the same pattern. Therefore, the inverse function of determining the model parameters from the data is not well defined. Degeneracy is not only a mathematical property of models, but it has also been reported in biological experiments. Classical studies on structural unidentifiability focused on the notion that one can at most identify combinations of unidentifiable model parameters. We have identified a different type of structural degeneracy/unidentifiability present in a family of models, which we refer to as the Lambda-Omega ({Lambda}-{Omega}) models. These are an extension of the classical lambda-omega ({lambda}-{omega}) models that have been used to model biological systems, and display a richer dynamic behavior and waveforms that range from sinusoidal to square-wave to spike-like. We show that the {Lambda}-{Omega} models feature infinitely many parameter sets that produce identical stable oscillations, except possible for a phase-shift (reflecting the initial phase). These degenerate parameters are not identifiable combinations of unidentifiable parameters as is the case in structural degeneracy. In fact, reducing the number of model parameters in the {Lambda}-{Omega} models is minimal in the sense that each one controls a different aspect of the model dynamics and the dynamic complexity of the system would be reduced by reducing the number of parameters. We argue that the family of {Lambda}-{Omega} models serves as a framework for the systematic investigation of degeneracy and identifiability in dynamic models and for the investigation of the interplay between structural and other forms of unidentifiability resulting on the lack of information from the experimental/observational data.

systems biology↗

Validation that human microbiome phages use alternative genetic coding with TAG stop read as Q

Metagenomic findings suggesting that bacteriophages (phages) can use genetic codes different from those of their host bacteria reveal a new dimension of phage-host interaction dynamics. Whereas reassignment of stop codons to code for amino acids has been predicted, there has been no proteomic validation of alternative coding in phages. In fact, one code where the stop codon TAG is reassigned to glutamine (code 15) has never been experimentally validated in any biological system. Here, we characterized stop codon reassignment in two crAss-like phages found in the human gut microbiome using LC-MS/MS-based metaproteomics. The proteome data from several phage structural proteins clearly demonstrates reassignment of the TAG stop codon to glutamine, establishing for the first time the expression of genetic code 15. One-Sentence SummaryMass spectrometry confirms protein expression of predicted alternate genetic coding in phage genomes from human microbiomes.

systems biology↗

CELLoGeNe - an Energy Landscape Framework for Logical Networks Controlling Cell Decisions

Experimental and computational efforts are constantly made to elucidate mechanisms controlling cell fate decisions during development and cell reprogramming. One powerful method is to consider cell commitment and reprogramming as movements in an energy landscape. Here, we develop CELLoGeNe (Computation of Energy Landscapes of Logical Gene Networks), which maps Boolean implementation of gene regulatory networks (GRNs) into energy landscapes. CELLoGeNe removes inadvertent symmetries in the energy landscapes normally arising from standard Boolean operators. Furthermore, CELLoGeNe provides a tool for visualising multi-dimensional energy landscapes and a platform to stochastically probe and analyse the shapes of the computed landscapes corresponding to the epigenetic landscapes for development and reprogramming. We demonstrate CELLoGeNe on a GRN governing maintenance and self-renewal of pluripotency, identifying attractors experimentally validated. We also apply CELLoGeNe on a network controlling reprogramming from mouse embryonic fibroblast (MEF) to induced pluripotent stem cells (iPSCs) where we identify potential roadblocks as attractors. CELLoGeNe is a general framework that can be applied to various biological systems offering a broad picture of intracellular dynamics otherwise inaccessible with existing methods.

systems biology↗

Bayesian multi-model-based 13C15N-metabolic flux analysis quantifies carbon-nitrogen metabolism in mycobacteria

Metabolic flux is the final output of cellular regulation and has been extensively studied for carbon but much less is known about nitrogen, which is another important building block for living organisms. For the pathogen Mycobacterium tuberculosis (Mtb), this is particularly important in informing the development of effective drugs targeting Mtbs metabolism. Here we performed 13C15N dual isotopic labelling of mycobacterial steady state cultures and quantified intracellular carbon-nitrogen (CN) and nitrogen (N) fluxes in addition to carbon (C) fluxes and inferred their reaction bidirectionalities. The combination of 13C15N-MFA with a Bayesian multi-model approach allowed us to resolve C and N fluxes simultaneously which was not possible with classical 13C-MFA. We quantified CN fluxes for amino acid and, for the first time, nucleotide biosynthesis. Our analysis identified glutamate as the central CN and N node in mycobacteria, and improved resolution of the anaplerotic node. Our study describes a powerful platform to measure carbon and nitrogen metabolism in any biological system with statistical rigor.

systems biology↗

A Novel Strategy for Dynamic Modelling of Genome-Scale Interaction Networks

BackgroundModern medicine is equipped with huge amounts of big biological datasets and a wide range of computational methods to understand the molecular events underlying complex disorders. The recent availability of omics data allows a holistic view towards the interactions of various biomolecule types. However, the constructed maps are static, ignoring the dynamicity of molecular processes. On the other hand, the dynamic models of biological systems are commonly generated in small scales. Hence, the construction of large scale dynamic models that can quantitatively predict the time-course cellular behaviors is a big challenge. This study was aimed at developing a pipeline for automatic construction of such models from time-course experimental data. ResultsInformation of interactions between input genes is retrieved from SIGNORE 2.0 database and an interaction network is constructed which then is translated to biochemistry language and converted to a biochemical reactions network. In the next step, a large-scale ODE system is constructed by generating the ODE equivalent of each biochemical reaction. To estimate the kinetics parameters of the ODE model, a novel large-scale parameter approximation method is proposed. This method gives an estimation of system parameters by fitting model outputs to time-course experimental measurements. The total pipeline is provided as a MATLAB toolbox called SPADAN, standing for Systematic Protein Association Dynamic ANalyzer. Using multilayer time-series experimental data, the performance of the pipeline was checked by modeling 4379 regulatory interactions between 768 molecules in colon cancer cells exposed to chemotherapy agents. ConclusionStarting from time-series experimental data, SPADAN automatically constructs map of interactions, generates an ODE system, and performs a parameter approximation procedure. It constructs genome-scale dynamic models, filling the gap between large-scale static and small-scale dynamic modeling strategies. This simulation approach allows for holistic quantitative predictions which is critical for the simulation of therapeutic interventions in precision medicine.

systems biology↗

Coupled mutual inhibition and mutual activation motifs as tools for cell-fate control

Multistability is central to biological systems as it plays a key role in adaptation, evolvability, and differentiation. Multistability can be achieved by integrating positive feedback loops into the regulation. The simplest of such feedback loops are a) a mutual inhibition (MI) loop, b) a mutual activation (MA) loop, and, c) self-activation. While it is established that all three motifs can give rise to bistability, the characteristic differences in the bistability exhibited by each of these motifs is relatively less understood. Here, we use ODE-based simulations across a large ensemble of parameter sets and initial conditions to study the characteristics of the bistability of these motifs and their limits in the parameter space. We also examine the behavior of these motifs under mutual degradation and self-activation. Finally, we investigate the utility of these motifs for achieving coordinated expression through cyclic and parallel coupling. Through our analysis, we found that MI-based architectures offer robustness in maintaining distinct multistability and allow for coordination among multiple genes. This coordination paves way for understanding the naturally occurring gene regulatory network and may also help in the better design of robust and controllable synthetic networks.

systems biology↗

Mitochondrial interactome remodeling in aging mouse skeletal muscle associated with functional decline.

Genomic, transcriptomic, and proteomic approaches have been employed to gain insight into molecular underpinnings of aging in laboratory animals and in humans. However, protein function in biological systems is under complex regulation and includes factors in addition to abundance levels, such as modifications, localization, conformation, and protein-protein interactions. We have applied new robust quantitative chemical cross-linking technologies to uncover changes muscle mitochondrial interactome contributing to functional decline in aging. Statistically significant age-related changes in protein cross-link levels relating to assembly of electron transport system complexes I and IV, activity of glutamate dehydrogenase, and coenzyme-A binding in fatty acid beta-oxidation and TCA enzymes were observed. These changes showed remarkable correlation with measured CI based respiration differences within the same young-old animal pairs, indicating these cross-link levels offer new molecular insight on commonly observed age-related phenotypic differences. Overall, these system-wide quantitative mitochondrial interactome data provide the first molecular-level insight on ETS complex and substrate utilization enzyme remodeling that occur during age-related mitochondrial dysfunction. Each observed cross-link can serve as a protein conformational or protein-protein interaction probe in future studies making this dataset a unique resource for many additional in-depth molecular studies that are needed to better understand complex molecular changes that occur with aging.

systems biology↗