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A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation

BACKGROUND: Green plant leaves have always fascinated biologists as hosts for photosynthesis and providers of basic energy to many food webs. Today, comprehensive databases of gene expression data enable us to apply increasingly more advanced computational methods for reverse-engineering the regulat...

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Autores principales: Street, Nathaniel Robert, Jansson, Stefan, Hvidsten, Torgeir R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030533/
https://www.ncbi.nlm.nih.gov/pubmed/21232107
http://dx.doi.org/10.1186/1471-2229-11-13
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author Street, Nathaniel Robert
Jansson, Stefan
Hvidsten, Torgeir R
author_facet Street, Nathaniel Robert
Jansson, Stefan
Hvidsten, Torgeir R
author_sort Street, Nathaniel Robert
collection PubMed
description BACKGROUND: Green plant leaves have always fascinated biologists as hosts for photosynthesis and providers of basic energy to many food webs. Today, comprehensive databases of gene expression data enable us to apply increasingly more advanced computational methods for reverse-engineering the regulatory network of leaves, and to begin to understand the gene interactions underlying complex emergent properties related to stress-response and development. These new systems biology methods are now also being applied to organisms such as Populus, a woody perennial tree, in order to understand the specific characteristics of these species. RESULTS: We present a systems biology model of the regulatory network of Populus leaves. The network is reverse-engineered from promoter information and expression profiles of leaf-specific genes measured over a large set of conditions related to stress and developmental. The network model incorporates interactions between regulators, such as synergistic and competitive relationships, by evaluating increasingly more complex regulatory mechanisms, and is therefore able to identify new regulators of leaf development not found by traditional genomics methods based on pair-wise expression similarity. The approach is shown to explain available gene function information and to provide robust prediction of expression levels in new data. We also use the predictive capability of the model to identify condition-specific regulation as well as conserved regulation between Populus and Arabidopsis. CONCLUSIONS: We outline a computationally inferred model of the regulatory network of Populus leaves, and show how treating genes as interacting, rather than individual, entities identifies new regulators compared to traditional genomics analysis. Although systems biology models should be used with care considering the complexity of regulatory programs and the limitations of current genomics data, methods describing interactions can provide hypotheses about the underlying cause of emergent properties and are needed if we are to identify target genes other than those constituting the "low hanging fruit" of genomic analysis.
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spelling pubmed-30305332011-01-29 A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation Street, Nathaniel Robert Jansson, Stefan Hvidsten, Torgeir R BMC Plant Biol Research Article BACKGROUND: Green plant leaves have always fascinated biologists as hosts for photosynthesis and providers of basic energy to many food webs. Today, comprehensive databases of gene expression data enable us to apply increasingly more advanced computational methods for reverse-engineering the regulatory network of leaves, and to begin to understand the gene interactions underlying complex emergent properties related to stress-response and development. These new systems biology methods are now also being applied to organisms such as Populus, a woody perennial tree, in order to understand the specific characteristics of these species. RESULTS: We present a systems biology model of the regulatory network of Populus leaves. The network is reverse-engineered from promoter information and expression profiles of leaf-specific genes measured over a large set of conditions related to stress and developmental. The network model incorporates interactions between regulators, such as synergistic and competitive relationships, by evaluating increasingly more complex regulatory mechanisms, and is therefore able to identify new regulators of leaf development not found by traditional genomics methods based on pair-wise expression similarity. The approach is shown to explain available gene function information and to provide robust prediction of expression levels in new data. We also use the predictive capability of the model to identify condition-specific regulation as well as conserved regulation between Populus and Arabidopsis. CONCLUSIONS: We outline a computationally inferred model of the regulatory network of Populus leaves, and show how treating genes as interacting, rather than individual, entities identifies new regulators compared to traditional genomics analysis. Although systems biology models should be used with care considering the complexity of regulatory programs and the limitations of current genomics data, methods describing interactions can provide hypotheses about the underlying cause of emergent properties and are needed if we are to identify target genes other than those constituting the "low hanging fruit" of genomic analysis. BioMed Central 2011-01-13 /pmc/articles/PMC3030533/ /pubmed/21232107 http://dx.doi.org/10.1186/1471-2229-11-13 Text en Copyright ©2011 Street et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Street, Nathaniel Robert
Jansson, Stefan
Hvidsten, Torgeir R
A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title_full A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title_fullStr A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title_full_unstemmed A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title_short A systems biology model of the regulatory network in Populus leaves reveals interacting regulators and conserved regulation
title_sort systems biology model of the regulatory network in populus leaves reveals interacting regulators and conserved regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3030533/
https://www.ncbi.nlm.nih.gov/pubmed/21232107
http://dx.doi.org/10.1186/1471-2229-11-13
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