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Tracing dynamic biological processes during phase transition

BACKGROUND: Phase transition widely exists in the biological world, such as transformation of cell cycle phases, cell differentiation stages, disease development, and so on. Such a nonlinear phenomenon is considered as the conversion of a biological system from one phenotype/state to another. Studie...

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Autores principales: Zeng, Tao, Chen, Luonan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403121/
https://www.ncbi.nlm.nih.gov/pubmed/23046764
http://dx.doi.org/10.1186/1752-0509-6-S1-S12
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author Zeng, Tao
Chen, Luonan
author_facet Zeng, Tao
Chen, Luonan
author_sort Zeng, Tao
collection PubMed
description BACKGROUND: Phase transition widely exists in the biological world, such as transformation of cell cycle phases, cell differentiation stages, disease development, and so on. Such a nonlinear phenomenon is considered as the conversion of a biological system from one phenotype/state to another. Studies on the molecular mechanisms of biological phase transition have attracted much attention, in particular, on different genotypes (or expression variations) in a specific phase, but with less of focus on cascade changes of genes' functions (or system state) during the phase shift or transition process. However, it is a fundamental but important mission to trace the temporal characteristics of a biological system during a specific phase transition process, which can offer clues for understanding dynamic behaviors of living organisms. RESULTS: By overcoming the hurdles of traditional time segmentation and temporal biclustering methods, a causal process model (CPM) in the present work is proposed to study the biological phase transition in a systematic manner, i.e. first, we make gene-specific segmentation on time-course expression data by developing a new boundary gene estimation scheme, and then infer functional cascade dynamics by constructing a temporal block network. After the computational validation on synthetic data, CPM was used to analyze the well-known Yeast cell cycle data. It was found that the dynamics of the boundary genes are periodic and consistent with the phases of the cell cycle, and the temporal block network indeed demonstrates a meaningful cascade structure of the enriched biological functions. In addition, we further studied protein modules based on the temporal block network, which reflect temporal features in different cycles. CONCLUSIONS: All of these results demonstrate that CPM is effective and efficient comparing to traditional methods, and is able to elucidate essential regulatory mechanism of a biological system even with complicated nonlinear phase transitions.
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spelling pubmed-34031212012-07-25 Tracing dynamic biological processes during phase transition Zeng, Tao Chen, Luonan BMC Syst Biol Research BACKGROUND: Phase transition widely exists in the biological world, such as transformation of cell cycle phases, cell differentiation stages, disease development, and so on. Such a nonlinear phenomenon is considered as the conversion of a biological system from one phenotype/state to another. Studies on the molecular mechanisms of biological phase transition have attracted much attention, in particular, on different genotypes (or expression variations) in a specific phase, but with less of focus on cascade changes of genes' functions (or system state) during the phase shift or transition process. However, it is a fundamental but important mission to trace the temporal characteristics of a biological system during a specific phase transition process, which can offer clues for understanding dynamic behaviors of living organisms. RESULTS: By overcoming the hurdles of traditional time segmentation and temporal biclustering methods, a causal process model (CPM) in the present work is proposed to study the biological phase transition in a systematic manner, i.e. first, we make gene-specific segmentation on time-course expression data by developing a new boundary gene estimation scheme, and then infer functional cascade dynamics by constructing a temporal block network. After the computational validation on synthetic data, CPM was used to analyze the well-known Yeast cell cycle data. It was found that the dynamics of the boundary genes are periodic and consistent with the phases of the cell cycle, and the temporal block network indeed demonstrates a meaningful cascade structure of the enriched biological functions. In addition, we further studied protein modules based on the temporal block network, which reflect temporal features in different cycles. CONCLUSIONS: All of these results demonstrate that CPM is effective and efficient comparing to traditional methods, and is able to elucidate essential regulatory mechanism of a biological system even with complicated nonlinear phase transitions. BioMed Central 2012-07-16 /pmc/articles/PMC3403121/ /pubmed/23046764 http://dx.doi.org/10.1186/1752-0509-6-S1-S12 Text en Copyright ©2012 Zeng and Chen; 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
Zeng, Tao
Chen, Luonan
Tracing dynamic biological processes during phase transition
title Tracing dynamic biological processes during phase transition
title_full Tracing dynamic biological processes during phase transition
title_fullStr Tracing dynamic biological processes during phase transition
title_full_unstemmed Tracing dynamic biological processes during phase transition
title_short Tracing dynamic biological processes during phase transition
title_sort tracing dynamic biological processes during phase transition
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3403121/
https://www.ncbi.nlm.nih.gov/pubmed/23046764
http://dx.doi.org/10.1186/1752-0509-6-S1-S12
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