TY - JOUR
T1 - Growth-rate regulated genes have profound impact on interpretation of transcriptome profiling in Saccharomyces cerevisiae
AU - Regenberg, Birgitte
AU - Grotkjaer, Thomas
AU - Winther, Ole
AU - Fausbøll, Anders
AU - Akesson, Mats
AU - Bro, Christoffer
AU - Hansen, Lars Kai
AU - Brunak, Søren
AU - Nielsen, Jens
PY - 2006
Y1 - 2006
N2 - BACKGROUND: Growth rate is central to the development of cells in all organisms. However, little is known about the impact of changing growth rates. We used continuous cultures to control growth rate and studied the transcriptional program of the model eukaryote Saccharomyces cerevisiae, with generation times varying between 2 and 35 hours.RESULTS: A total of 5930 transcripts were identified at the different growth rates studied. Consensus clustering of these revealed that half of all yeast genes are affected by the specific growth rate, and that the changes are similar to those found when cells are exposed to different types of stress (>80% overlap). Genes with decreased transcript levels in response to faster growth are largely of unknown function (>50%) whereas genes with increased transcript levels are involved in macromolecular biosynthesis such as those that encode ribosomal proteins. This group also covers most targets of the transcriptional activator RAP1, which is also known to be involved in replication. A positive correlation between the location of replication origins and the location of growth-regulated genes suggests a role for replication in growth rate regulation.CONCLUSION: Our data show that the cellular growth rate has great influence on transcriptional regulation. This, in turn, implies that one should be cautious when comparing mutants with different growth rates. Our findings also indicate that much of the regulation is coordinated via the chromosomal location of the affected genes, which may be valuable information for the control of heterologous gene expression in metabolic engineering.
AB - BACKGROUND: Growth rate is central to the development of cells in all organisms. However, little is known about the impact of changing growth rates. We used continuous cultures to control growth rate and studied the transcriptional program of the model eukaryote Saccharomyces cerevisiae, with generation times varying between 2 and 35 hours.RESULTS: A total of 5930 transcripts were identified at the different growth rates studied. Consensus clustering of these revealed that half of all yeast genes are affected by the specific growth rate, and that the changes are similar to those found when cells are exposed to different types of stress (>80% overlap). Genes with decreased transcript levels in response to faster growth are largely of unknown function (>50%) whereas genes with increased transcript levels are involved in macromolecular biosynthesis such as those that encode ribosomal proteins. This group also covers most targets of the transcriptional activator RAP1, which is also known to be involved in replication. A positive correlation between the location of replication origins and the location of growth-regulated genes suggests a role for replication in growth rate regulation.CONCLUSION: Our data show that the cellular growth rate has great influence on transcriptional regulation. This, in turn, implies that one should be cautious when comparing mutants with different growth rates. Our findings also indicate that much of the regulation is coordinated via the chromosomal location of the affected genes, which may be valuable information for the control of heterologous gene expression in metabolic engineering.
KW - Cell Growth Processes
KW - Chromosomes, Fungal/genetics
KW - Cluster Analysis
KW - Consensus Sequence
KW - Ethanol/metabolism
KW - Gene Expression Profiling
KW - Gene Expression Regulation, Fungal/genetics
KW - Genes, Fungal/genetics
KW - Open Reading Frames/genetics
KW - Promoter Regions, Genetic/genetics
KW - RNA, Messenger/genetics
KW - Replication Origin/genetics
KW - Saccharomyces cerevisiae/cytology
KW - Transcription, Genetic/genetics
U2 - 10.1186/gb-2006-7-11-r107
DO - 10.1186/gb-2006-7-11-r107
M3 - Journal article
C2 - 17105650
SN - 1474-760X
VL - 7
SP - R107
JO - Genome Biology (Online Edition)
JF - Genome Biology (Online Edition)
IS - 11
ER -