GEARBOX GENE-EXPRESSION AND GROWTH-RATE

被引:8
作者
ALDEA, M
GARRIDO, T
TORMO, A
机构
[1] Department de Ciències Mèdiques Bàsiques, Universitat de Lleida, Lleida, 25006, Rovira Roure
[2] Centro de Investigaciones Biológicas, Consejo Superior de Investigaciones Cientificas, Madrid, 28006
[3] Departamento de Bioquímica y Biología Molecular I, Facultad de Biología, Universidad Complutense de Madrid, Madrid
关键词
CELL DIVISION; GEARBOX PROMOTER; GENE EXPRESSION REGULATION; GROWTH RATE;
D O I
10.1007/BF00328029
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Regulation of gene expression in prokaryotic cells usually takes place at the level of transcription initiation. Different forms of RNA polymerase recognizing specific promoters are engaged in the control of many prokaryotic regulons. This also seems to be the case for some Escherichia coli genes that are induced at low growth rates and by nutrient starvation. Their gene products are synthesized at levels inversely proportional to growth rate, and this mode of regulation has been termed gearbox gene expression. This kind of growth-rate modulation is exerted by specific transcriptional initiation signals, the gearbox promoters, and some of them depend on a putative new sigma factor (RpoS). Gearbox promoters drive expression of morphogenetic and cell division genes at constant levels per cell and cycle to meet the demands of cell division and septum formation. A mechanism is proposed that could sense the growth rate of the cell to alter gene expression by the action of specific sigma factors
引用
收藏
页码:414 / 420
页数:7
相关论文
共 43 条
[11]  
Genilloud O., Moreno F., Kolter R., DNA sequence, products and transcriptional pattern of the genes involved in production of the DNA replication inhibitor microcin B17, Journal of Bacteriology, 171, pp. 1126-1135, (1989)
[12]  
Gourse R.L., De Boer H.A., Nomura M., DNA determinants of rRNA synthesis in E. coli: growth rate dependent regulation, feedback inhibition, upstream activation, antitermination, Cell, 44, pp. 197-205, (1986)
[13]  
Hengge-Aronis R., Klein W., Lange R., Rimmele M., Boos W., Trehalose synthesis genes are controlled by the putative sigma factor encoded by rpoS and are involved in stationary-phase thermotolerance in Escherichia coli, Journal of Bacteriology, 173, pp. 7918-7924, (1991)
[14]  
Hernandez-Chico C., San Millan J.L., Kolter R., Moreno F., Growth phase and OmpR regulation of transcription of the microcin B17 genes, Journal of Bacteriology, 167, pp. 1058-1065, (1986)
[15]  
Jensen K.F., Pedersen S., Metabolic growth rate control in Escherichia coli may be a consequence of subsaturation of the macromolecular biosynthetic apparatus with substrates and catalytic components, Microbiological Reviews, 54, pp. 89-100, (1990)
[16]  
Jung J.U., Gutierrez C., Martin F., Ardourel M., Villarejo M., Transcription of osmB, a gene encoding an Escherichia coli lipoprotein, is regulated by dual signals, Journal of Biological Chemistry, 265, pp. 10574-10581, (1990)
[17]  
Kaasen I., Falkenberg P., Styrvold O.B., Strom A.R., Molecular cloning and physical mapping of the otsBA genes, which encode the osmoregulatory trehalose pathway of Escherichia coli: evidence that transcription is activated by KatF (AppR), Journal of Bacteriology, 174, pp. 889-898, (1992)
[18]  
Kolter R., Life and death in stationary phase, ASM News, 58, pp. 75-79, (1992)
[19]  
Laere A.V., Trehalose, reserve and/or stress metabolite?, FEMS Microbiological Reviews, 63, pp. 201-210, (1989)
[20]  
Lange R., Hengge-Aronis R., Growth phase-regulated expression of bolA and morphology of stationary-phase Escherichia coli cells are controlled by the novel sigma factor σ<sup>S</sup>, Journal of Bacteriology, 173, pp. 4474-4481, (1991)