Cargando…

Exploiting combinatorial cultivation conditions to infer transcriptional regulation

BACKGROUND: Regulatory networks often employ the model that attributes changes in gene expression levels, as observed across different cellular conditions, to changes in the activity of transcription factors (TFs). Although the actual conditions that trigger a change in TF activity should form an in...

Descripción completa

Detalles Bibliográficos
Autores principales: Knijnenburg, Theo A, de Winde, Johannes H, Daran, Jean-Marc, Daran-Lapujade, Pascale, Pronk, Jack T, Reinders, Marcel JT, Wessels, Lodewyk FA
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797021/
https://www.ncbi.nlm.nih.gov/pubmed/17241460
http://dx.doi.org/10.1186/1471-2164-8-25
_version_ 1782132284274507776
author Knijnenburg, Theo A
de Winde, Johannes H
Daran, Jean-Marc
Daran-Lapujade, Pascale
Pronk, Jack T
Reinders, Marcel JT
Wessels, Lodewyk FA
author_facet Knijnenburg, Theo A
de Winde, Johannes H
Daran, Jean-Marc
Daran-Lapujade, Pascale
Pronk, Jack T
Reinders, Marcel JT
Wessels, Lodewyk FA
author_sort Knijnenburg, Theo A
collection PubMed
description BACKGROUND: Regulatory networks often employ the model that attributes changes in gene expression levels, as observed across different cellular conditions, to changes in the activity of transcription factors (TFs). Although the actual conditions that trigger a change in TF activity should form an integral part of the generated regulatory network, they are usually lacking. This is due to the fact that the large heterogeneity in the employed conditions and the continuous changes in environmental parameters in the often used shake-flask cultures, prevent the unambiguous modeling of the cultivation conditions within the computational framework. RESULTS: We designed an experimental setup that allows us to explicitly model the cultivation conditions and use these to infer the activity of TFs. The yeast Saccharomyces cerevisiae was cultivated under four different nutrient limitations in both aerobic and anaerobic chemostat cultures. In the chemostats, environmental and growth parameters are accurately controlled. Consequently, the measured transcriptional response can be directly correlated with changes in the limited nutrient or oxygen concentration. We devised a tailor-made computational approach that exploits the systematic setup of the cultivation conditions in order to identify the individual and combined effects of nutrient limitations and oxygen availability on expression behavior and TF activity. CONCLUSION: Incorporating the actual growth conditions when inferring regulatory relationships provides detailed insight in the functionality of the TFs that are triggered by changes in the employed cultivation conditions. For example, our results confirm the established role of TF Hap4 in both aerobic regulation and glucose derepression. Among the numerous inferred condition-specific regulatory associations between gene sets and TFs, also many novel putative regulatory mechanisms, such as the possible role of Tye7 in sulfur metabolism, were identified.
format Text
id pubmed-1797021
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-17970212007-02-16 Exploiting combinatorial cultivation conditions to infer transcriptional regulation Knijnenburg, Theo A de Winde, Johannes H Daran, Jean-Marc Daran-Lapujade, Pascale Pronk, Jack T Reinders, Marcel JT Wessels, Lodewyk FA BMC Genomics Research Article BACKGROUND: Regulatory networks often employ the model that attributes changes in gene expression levels, as observed across different cellular conditions, to changes in the activity of transcription factors (TFs). Although the actual conditions that trigger a change in TF activity should form an integral part of the generated regulatory network, they are usually lacking. This is due to the fact that the large heterogeneity in the employed conditions and the continuous changes in environmental parameters in the often used shake-flask cultures, prevent the unambiguous modeling of the cultivation conditions within the computational framework. RESULTS: We designed an experimental setup that allows us to explicitly model the cultivation conditions and use these to infer the activity of TFs. The yeast Saccharomyces cerevisiae was cultivated under four different nutrient limitations in both aerobic and anaerobic chemostat cultures. In the chemostats, environmental and growth parameters are accurately controlled. Consequently, the measured transcriptional response can be directly correlated with changes in the limited nutrient or oxygen concentration. We devised a tailor-made computational approach that exploits the systematic setup of the cultivation conditions in order to identify the individual and combined effects of nutrient limitations and oxygen availability on expression behavior and TF activity. CONCLUSION: Incorporating the actual growth conditions when inferring regulatory relationships provides detailed insight in the functionality of the TFs that are triggered by changes in the employed cultivation conditions. For example, our results confirm the established role of TF Hap4 in both aerobic regulation and glucose derepression. Among the numerous inferred condition-specific regulatory associations between gene sets and TFs, also many novel putative regulatory mechanisms, such as the possible role of Tye7 in sulfur metabolism, were identified. BioMed Central 2007-01-22 /pmc/articles/PMC1797021/ /pubmed/17241460 http://dx.doi.org/10.1186/1471-2164-8-25 Text en Copyright © 2007 Knijnenburg 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
Knijnenburg, Theo A
de Winde, Johannes H
Daran, Jean-Marc
Daran-Lapujade, Pascale
Pronk, Jack T
Reinders, Marcel JT
Wessels, Lodewyk FA
Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title_full Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title_fullStr Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title_full_unstemmed Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title_short Exploiting combinatorial cultivation conditions to infer transcriptional regulation
title_sort exploiting combinatorial cultivation conditions to infer transcriptional regulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1797021/
https://www.ncbi.nlm.nih.gov/pubmed/17241460
http://dx.doi.org/10.1186/1471-2164-8-25
work_keys_str_mv AT knijnenburgtheoa exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT dewindejohannesh exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT daranjeanmarc exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT daranlapujadepascale exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT pronkjackt exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT reindersmarceljt exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation
AT wesselslodewykfa exploitingcombinatorialcultivationconditionstoinfertranscriptionalregulation