scholarly journals Growth-Rate Dependent And Nutrient-Specific Gene Expression Resource Allocation In Fission Yeast

2021 ◽  
Author(s):  
Istvan T. Kleijn ◽  
Amalia Martínez-Segura ◽  
François Bertaux ◽  
Malika Saint ◽  
Holger Kramer ◽  
...  

Cellular resources are limited and their relative allocation to gene expression programmes determines physiological states and global properties such as the growth rate. Quantitative studies using various growth conditions have singled out growth rate as a major physiological variable explaining relative protein abundances. Here, we used the simple eukaryote Schizosaccharomyces pombe to determine the importance of growth rate in explaining relative changes in protein and mRNA levels during growth on a series of non-limiting nitrogen sources. Although half of fission yeast genes were significantly correlated with the growth rate, this came alongside wide-spread nutrient-specific regulation. Proteome and transcriptome often showed coordinated regulation but with notable exceptions, such as metabolic enzymes. Genes positively correlated with growth rate participated in every level of protein production with the notable exception of RNA polymerase II, whereas those negatively correlated mainly belonged to the environmental stress response programme. Critically, metabolic enzymes, which represent ~55-70% of the proteome by mass, showed mainly condition-specific regulation. Specifically, many enzymes involved in glycolysis and NAD-dependent metabolism as well as the fermentative and respiratory pathways were condition-dependent and not consistently correlated with growth. In summary, we provide a rich account of resource allocation to gene expression in a simple eukaryote, advancing our basic understanding of the interplay between growth-rate dependent and nutrient-specific gene expression.

2017 ◽  
Vol 43 (4) ◽  
pp. 1117-1130 ◽  
Author(s):  
Maria V. Churova ◽  
Olga V. Meshcheryakova ◽  
Aleksey E. Veselov ◽  
Denis A. Efremov ◽  
Nina N. Nemova

2010 ◽  
Vol 123 (24) ◽  
pp. 4374-4381 ◽  
Author(s):  
K. Papadopoulou ◽  
J.-S. Chen ◽  
E. Mead ◽  
A. Feoktistova ◽  
C. Petit ◽  
...  

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Francesca Lorenzin ◽  
Uwe Benary ◽  
Apoorva Baluapuri ◽  
Susanne Walz ◽  
Lisa Anna Jung ◽  
...  

Enhanced expression of the MYC transcription factor is observed in the majority of tumors. Two seemingly conflicting models have been proposed for its function: one proposes that MYC enhances expression of all genes, while the other model suggests gene-specific regulation. Here, we have explored the hypothesis that specific gene expression profiles arise since promoters differ in affinity for MYC and high-affinity promoters are fully occupied by physiological levels of MYC. We determined cellular MYC levels and used RNA- and ChIP-sequencing to correlate promoter occupancy with gene expression at different concentrations of MYC. Mathematical modeling showed that binding affinities for interactions of MYC with DNA and with core promoter-bound factors, such as WDR5, are sufficient to explain promoter occupancies observed in vivo. Importantly, promoter affinity stratifies different biological processes that are regulated by MYC, explaining why tumor-specific MYC levels induce specific gene expression programs and alter defined biological properties of cells.


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