TY - JOUR
T1 - Yeast glucose pathways converge on the transcriptional regulation of trehalose biosynthesis
AU - Apweiler, Eva
AU - Sameith, Katrin
AU - Margaritis, Thanasis
AU - Brabers, Nathalie
AU - van de Pasch, Loes
AU - Bakker, Linda V.
AU - van Leenen, Dik
AU - Holstege, Frank C.P.
AU - Kemmeren, Patrick
N1 - Funding Information:
We thank Marian Groot Koerkamp, Cheuk Ko and Diane Bouwmeester for technical assistance; Tony Miles, Sake van Wageningen, Ines de Castro Genebra de Jesus, Mariel Brok, Joris Benschop, Tineke Lenstra, Virginia Taliadouros, and Selma Waaijers for contributing data; Philip Lijnzaad and Sander van Hooff for bioinformatics support; all group members for useful advice and comments. We thank Johan Thevelein for his valuable advice and comments on the project. This work was supported by the Netherlands Bioinformatics Centre (NBIC) and the Netherlands Organization of Scientific Research (NWO), grants 016.108.607, 817.02.015, 050.71.057, 911.06.009, 863.07.007 (P.K.).
PY - 2012/6/14
Y1 - 2012/6/14
N2 - Background: Cellular glucose availability is crucial for the functioning of most biological processes. Our understanding of the glucose regulatory system has been greatly advanced by studying the model organism Saccharomyces cerevisiae, but many aspects of this system remain elusive. To understand the organisation of the glucose regulatory system, we analysed 91 deletion mutants of the different glucose signalling and metabolic pathways in Saccharomyces cerevisiae using DNA microarrays.Results: In general, the mutations do not induce pathway-specific transcriptional responses. Instead, one main transcriptional response is discerned, which varies in direction to mimic either a high or a low glucose response. Detailed analysis uncovers established and new relationships within and between individual pathways and their members. In contrast to signalling components, metabolic components of the glucose regulatory system are transcriptionally more frequently affected. A new network approach is applied that exposes the hierarchical organisation of the glucose regulatory system.Conclusions: The tight interconnection between the different pathways of the glucose regulatory system is reflected by the main transcriptional response observed. Tps2 and Tsl1, two enzymes involved in the biosynthesis of the storage carbohydrate trehalose, are predicted to be the most downstream transcriptional components. Epistasis analysis of tps2Δ double mutants supports this prediction. Although based on transcriptional changes only, these results suggest that all changes in perceived glucose levels ultimately lead to a shift in trehalose biosynthesis.
AB - Background: Cellular glucose availability is crucial for the functioning of most biological processes. Our understanding of the glucose regulatory system has been greatly advanced by studying the model organism Saccharomyces cerevisiae, but many aspects of this system remain elusive. To understand the organisation of the glucose regulatory system, we analysed 91 deletion mutants of the different glucose signalling and metabolic pathways in Saccharomyces cerevisiae using DNA microarrays.Results: In general, the mutations do not induce pathway-specific transcriptional responses. Instead, one main transcriptional response is discerned, which varies in direction to mimic either a high or a low glucose response. Detailed analysis uncovers established and new relationships within and between individual pathways and their members. In contrast to signalling components, metabolic components of the glucose regulatory system are transcriptionally more frequently affected. A new network approach is applied that exposes the hierarchical organisation of the glucose regulatory system.Conclusions: The tight interconnection between the different pathways of the glucose regulatory system is reflected by the main transcriptional response observed. Tps2 and Tsl1, two enzymes involved in the biosynthesis of the storage carbohydrate trehalose, are predicted to be the most downstream transcriptional components. Epistasis analysis of tps2Δ double mutants supports this prediction. Although based on transcriptional changes only, these results suggest that all changes in perceived glucose levels ultimately lead to a shift in trehalose biosynthesis.
KW - Gene expression profiling
KW - Glucose signalling
KW - Regulatory networks
KW - Saccharomyces cerevisiae
KW - Trehalose biosynthesis
UR - http://www.scopus.com/inward/record.url?scp=84862232768&partnerID=8YFLogxK
U2 - 10.1186/1471-2164-13-239
DO - 10.1186/1471-2164-13-239
M3 - Article
C2 - 22697265
AN - SCOPUS:84862232768
SN - 1471-2164
VL - 13
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 239
ER -