Evidence map›Paper›PMID 19769791›Full record

ArticleBMC systems biology2009

Inferring Drosophila gap gene regulatory network: a parameter sensitivity and perturbation analysis.

Yves Fomekong-Nanfack, Marten Postma, Jaap A Kaandorp

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Article in BMC systems biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
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  4. Review
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  9. Integrating heterogeneous gene expression data for gene regulatory network modelling.Theory in biosciences = Theorie in den Biowissenschaften · 2012
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  15. Dynamic models of immune responses: what is the ideal level of detail?Theoretical biology & medical modelling · 2010
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yves Fomekong-NanfackSection Computational Science, Faculty of Science, University of Amsterdam, Amsterdam, the Netherlands. Y.FomekongNanfack@uva.nl
Marten Postma
Jaap A Kaandorp

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInverse modelling of gene regulatory networks (GRNs) capable of simulating continuous spatio-temporal biological processes requires accurate data and a good description of the system. If quantitative relations between genes cannot be extracted from direct measurements, an efficient method to estimate the unknown parameters is mandatory. A model that has been proposed to simulate spatio-temporal gene expression patterns is the connectionist model. This method describes the quantitative dynamics of a regulatory network in space. The model parameters are estimated by means of model-fitting algorithms. The gene interactions are identified without making any prior assumptions concerning the network connectivity. As a result, the inverse modelling might lead to multiple circuits showing the same quantitative behaviour and it is not possible to identify one optimal circuit. Consequently, it is important to address the quality of the circuits in terms of model robustness.

resultsHere we investigate the sensitivity and robustness of circuits obtained from reverse engineering a model capable of simulating measured gene expression patterns. As a case study we use the early gap gene segmentation mechanism in Drosophila melanogaster. We consider the limitations of the connectionist model used to describe GRN Inferred from spatio-temporal gene expression. We address the problem of circuit discrimination, where the selection criterion within the optimization technique is based of the least square minimization on the error between data and simulated results.

conclusionParameter sensitivity analysis allows one to discriminate between circuits having significant parameter and qualitative differences but exhibiting the same quantitative pattern. Furthermore, we show that using a stochastic model derived from a deterministic solution, one can introduce fluctuations within the model to analyze the circuits' robustness. Ultimately, we show that there is a close relation between circuit sensitivity and robustness to fluctuation, and that circuit robustness is rather modular than global. The current study shows that reverse engineering of GRNs should not only focus on estimating parameters by minimizing the difference between observation and simulation but also on other model properties. Our study suggests that multi-objective optimization based on robustness and sensitivity analysis has to be considered.

Indexed as

Models, BiologicalAnimalsComputer SimulationDrosophila melanogasterDrosophila ProteinsGene Expression ProfilingGene Expression RegulationGTPase-Activating ProteinsSignal TransductionDrosophila ProteinsGTPase-Activating Proteins

Identifiers

PMID19769791
PMCPMC2761871

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.