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Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis

BACKGROUND: Network Component Analysis (NCA) is a network structure-driven framework for deducing regulatory signal dynamics. In contrast to principal component analysis, which can be employed to select the high-variance genes, NCA makes use of the connectivity structure from transcriptional regulat...

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Autores principales: Chen, Shun-Fu, Juang, Yue-Li, Chou, Wei-Kang, Lai, Jin-Mei, Huang, Chi-Ying F, Kao, Cheng-Yan, Wang, Feng-Sheng
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800846/
https://www.ncbi.nlm.nih.gov/pubmed/19943917
http://dx.doi.org/10.1186/1752-0509-3-110
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author Chen, Shun-Fu
Juang, Yue-Li
Chou, Wei-Kang
Lai, Jin-Mei
Huang, Chi-Ying F
Kao, Cheng-Yan
Wang, Feng-Sheng
author_facet Chen, Shun-Fu
Juang, Yue-Li
Chou, Wei-Kang
Lai, Jin-Mei
Huang, Chi-Ying F
Kao, Cheng-Yan
Wang, Feng-Sheng
author_sort Chen, Shun-Fu
collection PubMed
description BACKGROUND: Network Component Analysis (NCA) is a network structure-driven framework for deducing regulatory signal dynamics. In contrast to principal component analysis, which can be employed to select the high-variance genes, NCA makes use of the connectivity structure from transcriptional regulatory networks to infer dynamics of transcription factor activities. Using the budding yeast Saccharomyces cerevisiae as a model system, we aim to deduce regulatory actions of cytokinesis-related genes, using precise spatial proximity (midbody) and/or temporal synchronicity (cytokinesis) to avoid full-scale computation from genome-wide databases. RESULTS: NCA was applied to infer regulatory actions of transcription factor activity from microarray data and partial transcription factor-gene connectivity information for cytokinesis-related genes, which were a subset of genome-wide datasets. No literature has so far discussed the inferred results through NCA are independent of the scale of the gene expression dataset. To avoid full-scale computation from genome-wide databases, four cytokinesis-related gene cases were selected for NCA by running computational analysis over the transcription factor database to confirm the approach being scale-free. The inferred dynamics of transcription factor activity through NCA were independent of the scale of the data matrix selected from the four cytokinesis-related gene sets. Moreover, the inferred regulatory actions were nearly identical to published observations for the selected cytokinesis-related genes in the budding yeast; namely, Mcm1, Ndd1, and Fkh2, which form a transcription factor complex to control expression of the CLB2 cluster (i.e. BUD4, CHS2, IQG1, and CDC5). CONCLUSION: In this study, using S. cerevisiae as a model system, NCA was successfully applied to infer similar regulatory actions of transcription factor activities from two various microarray databases and several partial transcription factor-gene connectivity datasets for selected cytokinesis-related genes independent of data sizes. The regulated action for four selected cytokinesis-related genes (BUD4, CHS2, IQG1, and CDC5) belongs to the M-phase or M/G1 phase, consistent with the empirical observations that in S. cerevisiae, the Mcm1-Ndd1-Fkh2 transcription factor complex can regulate expression of the cytokinesis-related genes BUD4, CHS2, IQG1, and CDC5. Since Bud4, Iqg1, and Cdc5 are highly conserved between human and yeast, results obtained from NCA for cytokinesis in the budding yeast can lead to a suggestion that human cells should have the transcription regulator(s) as the budding yeast Mcm1-Ndd1-Fkh2 transcription factor complex in controlling occurrence of cytokinesis.
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spelling pubmed-28008462010-01-01 Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis Chen, Shun-Fu Juang, Yue-Li Chou, Wei-Kang Lai, Jin-Mei Huang, Chi-Ying F Kao, Cheng-Yan Wang, Feng-Sheng BMC Syst Biol Research article BACKGROUND: Network Component Analysis (NCA) is a network structure-driven framework for deducing regulatory signal dynamics. In contrast to principal component analysis, which can be employed to select the high-variance genes, NCA makes use of the connectivity structure from transcriptional regulatory networks to infer dynamics of transcription factor activities. Using the budding yeast Saccharomyces cerevisiae as a model system, we aim to deduce regulatory actions of cytokinesis-related genes, using precise spatial proximity (midbody) and/or temporal synchronicity (cytokinesis) to avoid full-scale computation from genome-wide databases. RESULTS: NCA was applied to infer regulatory actions of transcription factor activity from microarray data and partial transcription factor-gene connectivity information for cytokinesis-related genes, which were a subset of genome-wide datasets. No literature has so far discussed the inferred results through NCA are independent of the scale of the gene expression dataset. To avoid full-scale computation from genome-wide databases, four cytokinesis-related gene cases were selected for NCA by running computational analysis over the transcription factor database to confirm the approach being scale-free. The inferred dynamics of transcription factor activity through NCA were independent of the scale of the data matrix selected from the four cytokinesis-related gene sets. Moreover, the inferred regulatory actions were nearly identical to published observations for the selected cytokinesis-related genes in the budding yeast; namely, Mcm1, Ndd1, and Fkh2, which form a transcription factor complex to control expression of the CLB2 cluster (i.e. BUD4, CHS2, IQG1, and CDC5). CONCLUSION: In this study, using S. cerevisiae as a model system, NCA was successfully applied to infer similar regulatory actions of transcription factor activities from two various microarray databases and several partial transcription factor-gene connectivity datasets for selected cytokinesis-related genes independent of data sizes. The regulated action for four selected cytokinesis-related genes (BUD4, CHS2, IQG1, and CDC5) belongs to the M-phase or M/G1 phase, consistent with the empirical observations that in S. cerevisiae, the Mcm1-Ndd1-Fkh2 transcription factor complex can regulate expression of the cytokinesis-related genes BUD4, CHS2, IQG1, and CDC5. Since Bud4, Iqg1, and Cdc5 are highly conserved between human and yeast, results obtained from NCA for cytokinesis in the budding yeast can lead to a suggestion that human cells should have the transcription regulator(s) as the budding yeast Mcm1-Ndd1-Fkh2 transcription factor complex in controlling occurrence of cytokinesis. BioMed Central 2009-11-27 /pmc/articles/PMC2800846/ /pubmed/19943917 http://dx.doi.org/10.1186/1752-0509-3-110 Text en Copyright ©2009 Chen 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
Chen, Shun-Fu
Juang, Yue-Li
Chou, Wei-Kang
Lai, Jin-Mei
Huang, Chi-Ying F
Kao, Cheng-Yan
Wang, Feng-Sheng
Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title_full Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title_fullStr Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title_full_unstemmed Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title_short Inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
title_sort inferring a transcriptional regulatory network of the cytokinesis-related genes by network component analysis
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2800846/
https://www.ncbi.nlm.nih.gov/pubmed/19943917
http://dx.doi.org/10.1186/1752-0509-3-110
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