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The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle
BACKGROUND: The G1-to-S transition of the cell cycle in the yeast Saccharomyces cerevisiae involves an extensive transcriptional program driven by transcription factors SBF (Swi4-Swi6) and MBF (Mbp1-Swi6). Activation of these factors ultimately depends on the G1 cyclin Cln3. RESULTS: To determine th...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911115/ https://www.ncbi.nlm.nih.gov/pubmed/20573214 http://dx.doi.org/10.1186/gb-2010-11-6-r67 |
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author | Ferrezuelo, Francisco Colomina, Neus Futcher, Bruce Aldea, Martí |
author_facet | Ferrezuelo, Francisco Colomina, Neus Futcher, Bruce Aldea, Martí |
author_sort | Ferrezuelo, Francisco |
collection | PubMed |
description | BACKGROUND: The G1-to-S transition of the cell cycle in the yeast Saccharomyces cerevisiae involves an extensive transcriptional program driven by transcription factors SBF (Swi4-Swi6) and MBF (Mbp1-Swi6). Activation of these factors ultimately depends on the G1 cyclin Cln3. RESULTS: To determine the transcriptional targets of Cln3 and their dependence on SBF or MBF, we first have used DNA microarrays to interrogate gene expression upon Cln3 overexpression in synchronized cultures of strains lacking components of SBF and/or MBF. Secondly, we have integrated this expression dataset together with other heterogeneous data sources into a single probabilistic model based on Bayesian statistics. Our analysis has produced more than 200 transcription factor-target assignments, validated by ChIP assays and by functional enrichment. Our predictions show higher internal coherence and predictive power than previous classifications. Our results support a model whereby SBF and MBF may be differentially activated by Cln3. CONCLUSIONS: Integration of heterogeneous genome-wide datasets is key to building accurate transcriptional networks. By such integration, we provide here a reliable transcriptional network at the G1-to-S transition in the budding yeast cell cycle. Our results suggest that to improve the reliability of predictions we need to feed our models with more informative experimental data. |
format | Text |
id | pubmed-2911115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29111152010-07-28 The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle Ferrezuelo, Francisco Colomina, Neus Futcher, Bruce Aldea, Martí Genome Biol Research BACKGROUND: The G1-to-S transition of the cell cycle in the yeast Saccharomyces cerevisiae involves an extensive transcriptional program driven by transcription factors SBF (Swi4-Swi6) and MBF (Mbp1-Swi6). Activation of these factors ultimately depends on the G1 cyclin Cln3. RESULTS: To determine the transcriptional targets of Cln3 and their dependence on SBF or MBF, we first have used DNA microarrays to interrogate gene expression upon Cln3 overexpression in synchronized cultures of strains lacking components of SBF and/or MBF. Secondly, we have integrated this expression dataset together with other heterogeneous data sources into a single probabilistic model based on Bayesian statistics. Our analysis has produced more than 200 transcription factor-target assignments, validated by ChIP assays and by functional enrichment. Our predictions show higher internal coherence and predictive power than previous classifications. Our results support a model whereby SBF and MBF may be differentially activated by Cln3. CONCLUSIONS: Integration of heterogeneous genome-wide datasets is key to building accurate transcriptional networks. By such integration, we provide here a reliable transcriptional network at the G1-to-S transition in the budding yeast cell cycle. Our results suggest that to improve the reliability of predictions we need to feed our models with more informative experimental data. BioMed Central 2010 2010-06-23 /pmc/articles/PMC2911115/ /pubmed/20573214 http://dx.doi.org/10.1186/gb-2010-11-6-r67 Text en Copyright ©2010 Ferrezuelo 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 Ferrezuelo, Francisco Colomina, Neus Futcher, Bruce Aldea, Martí The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title | The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title_full | The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title_fullStr | The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title_full_unstemmed | The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title_short | The transcriptional network activated by Cln3 cyclin at the G1-to-S transition of the yeast cell cycle |
title_sort | transcriptional network activated by cln3 cyclin at the g1-to-s transition of the yeast cell cycle |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2911115/ https://www.ncbi.nlm.nih.gov/pubmed/20573214 http://dx.doi.org/10.1186/gb-2010-11-6-r67 |
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