Stringent control of bacterial transcription
Stringent control of bacterial transcription
复制标题
严格控制细菌转录
DOI:
10.1016/0092-8674(85)90050-9
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发表时间:
1985
期刊:
影响因子:
64.5
通讯作者:
A. Travers
中科院分区:
文献类型:
--
作者:
A. Lamond;A. Travers
When bacterial cells experience starvation caused by limited availability of amino acids or by exhaustion of their primary carbon source, they halt further growth and make a rapid, complex, and varied set of adjustments to their metabolism. The rates of many disparate metabolic processes, including the accumulation of RNA, the replication of DNA, the biosynthesis of carbohydrates, lipids, nucleotides, peptidoglycans, and glycolytic intermediates, are all reduced, the total rate of intracellular proteolysis is increased, and the transport of many macromolecular precursors across the ceil membrane is inhibited. This spectrum of regulation, known for amino acid starvation as the stringent response, collectively enhances the viability of bacteria during periods of nutritional deprivation and, importantly, allows quick recovery and reinitiation of growth when the environmental conditions improve. In a rapidly growing bacterium, a major proportion of the available energy is required for the synthesis of ribosomes. Thus, cessation of this process in response to starvation and other environmental insults constitutes an important mode of energy conservation. The abrupt change in the rate of ribosome biosynthesis results from a highly specific inhibition of the synthesis of stable RNAs (ie, rRNA, tRNA) and mRNA for ribosomal proteins, the transcription rate of these genes falling by some lo-fold. By contrast, the rate of total mRNA synthesis is only modestly reduced after starvation, while that of certain species, such as his mRNA (Stephens et al., PNAS 72, 4389-4393, 1975), is actually stimulated. What is implicit in these observations is that E. coli cells can selectively regulate the genes encoding the components of the translational apparatus.A plethora of mechanisms have been proposed to explain this selective regulation: control of transcription initiation, arrest of RNA chain elongation(polymerase pausing), and even an increased turnover of nascent stable RNA. Although the evidence now shows that modulation of transcription initiation is the principal control, a contributory role for other mechanisms has not been excluded.