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Free RNA polymerase and modeling global transcription in Escherichia coli
被引:70
|作者:
Bremer, H
Dennis, P
Ehrenberg, M
机构:
[1] Uppsala Univ, BMC, Dept Cell & Mol Biol, S-75124 Uppsala, Sweden
[2] Univ Texas, Dept Mol & Cell Biol, Richardson, TX 75083 USA
[3] Natl Sci Fdn, Div Mol & Cellular Biosci, Arlington, VA 22230 USA
来源:
关键词:
E;
coli;
RNA polymerase;
promoters;
rrn;
ppGpp;
D O I:
10.1016/S0300-9084(03)00105-6
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Growth rate-dependent changes in the cytoplasmic concentration of free functional RNA polymerase, [R-f], affect the activity of all bacterial genes. Since [R-f] is not accessible to direct experimental quantitation, it can only be found indirectly from an evaluation of promoter activity data. Here, a theory has been derived to calculate [R-f] from the concentrations of total RNA polymerase and promoters in a model system with known Michaelis-Menten constants for the polymerase-promoter interactions. The theory takes transcript lengths and elongation rates into account and predicts how [R-f] changes with varying gene dosages. From experimental data on total concentrations of RNA polymerase and kinetic properties of different classes of promoters, the theory was developed into a mathematical model that reproduces the global transcriptional control in Escherichia coli growing at different rates. The model allows an estimation of the concentrations of free and DNA-bound RNA polymerase, as well as the partitioning of RNA polymerase into mRNA and stable RNA synthesizing fractions. According to this model, [R-f] is about 0.4 and 1.2 muM at growth rates corresponding to 1.0 and 2.5 doublings/h, respectively. The model accurately reflects a number of further experimental observations and suggests that the free RNA polymerase concentration increases with increasing growth rate. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
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页码:597 / 609
页数:13
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