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Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling

BACKGROUND: In nonlinear dynamic systems, synchrony through oscillation and frequency modulation is a general control strategy to coordinate multiple modules in response to external signals. Conversely, the synchrony information can be utilized to infer interaction. Increasing evidence suggests that...

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Autores principales: Gao, Shouguo, Hartman IV, John L, Carter, Justin L, Hessner, Martin J, Wang, Xujing
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017040/
https://www.ncbi.nlm.nih.gov/pubmed/21129191
http://dx.doi.org/10.1186/1752-0509-4-167
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author Gao, Shouguo
Hartman IV, John L
Carter, Justin L
Hessner, Martin J
Wang, Xujing
author_facet Gao, Shouguo
Hartman IV, John L
Carter, Justin L
Hessner, Martin J
Wang, Xujing
author_sort Gao, Shouguo
collection PubMed
description BACKGROUND: In nonlinear dynamic systems, synchrony through oscillation and frequency modulation is a general control strategy to coordinate multiple modules in response to external signals. Conversely, the synchrony information can be utilized to infer interaction. Increasing evidence suggests that frequency modulation is also common in transcription regulation. RESULTS: In this study, we investigate the potential of phase locking analysis, a technique to study the synchrony patterns, in the transcription network modeling of time course gene expression data. Using the yeast cell cycle data, we show that significant phase locking exists between transcription factors and their targets, between gene pairs with prior evidence of physical or genetic interactions, and among cell cycle genes. When compared with simple correlation we found that the phase locking metric can identify gene pairs that interact with each other more efficiently. In addition, it can automatically address issues of arbitrary time lags or different dynamic time scales in different genes, without the need for alignment. Interestingly, many of the phase locked gene pairs exhibit higher order than 1:1 locking, and significant phase lags with respect to each other. Based on these findings we propose a new phase locking metric for network reconstruction using time course gene expression data. We show that it is efficient at identifying network modules of focused biological themes that are important to cell cycle regulation. CONCLUSIONS: Our result demonstrates the potential of phase locking analysis in transcription network modeling. It also suggests the importance of understanding the dynamics underlying the gene expression patterns.
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spelling pubmed-30170402011-01-10 Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling Gao, Shouguo Hartman IV, John L Carter, Justin L Hessner, Martin J Wang, Xujing BMC Syst Biol Research Article BACKGROUND: In nonlinear dynamic systems, synchrony through oscillation and frequency modulation is a general control strategy to coordinate multiple modules in response to external signals. Conversely, the synchrony information can be utilized to infer interaction. Increasing evidence suggests that frequency modulation is also common in transcription regulation. RESULTS: In this study, we investigate the potential of phase locking analysis, a technique to study the synchrony patterns, in the transcription network modeling of time course gene expression data. Using the yeast cell cycle data, we show that significant phase locking exists between transcription factors and their targets, between gene pairs with prior evidence of physical or genetic interactions, and among cell cycle genes. When compared with simple correlation we found that the phase locking metric can identify gene pairs that interact with each other more efficiently. In addition, it can automatically address issues of arbitrary time lags or different dynamic time scales in different genes, without the need for alignment. Interestingly, many of the phase locked gene pairs exhibit higher order than 1:1 locking, and significant phase lags with respect to each other. Based on these findings we propose a new phase locking metric for network reconstruction using time course gene expression data. We show that it is efficient at identifying network modules of focused biological themes that are important to cell cycle regulation. CONCLUSIONS: Our result demonstrates the potential of phase locking analysis in transcription network modeling. It also suggests the importance of understanding the dynamics underlying the gene expression patterns. BioMed Central 2010-12-03 /pmc/articles/PMC3017040/ /pubmed/21129191 http://dx.doi.org/10.1186/1752-0509-4-167 Text en Copyright ©2010 Gao et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gao, Shouguo
Hartman IV, John L
Carter, Justin L
Hessner, Martin J
Wang, Xujing
Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title_full Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title_fullStr Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title_full_unstemmed Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title_short Global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
title_sort global analysis of phase locking in gene expression during cell cycle: the potential in network modeling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3017040/
https://www.ncbi.nlm.nih.gov/pubmed/21129191
http://dx.doi.org/10.1186/1752-0509-4-167
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