Underproduction of σ70 mimics a stringent response -: A proteome approach

被引:39
作者
Magnusson, LU [1 ]
Nyström, T [1 ]
Farewell, A [1 ]
机构
[1] Univ Gothenburg, Dept Cell & Mol Biol Microbiol, S-40530 Gothenburg, Sweden
关键词
D O I
10.1074/jbc.M209881200
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
When Escherichia coli cells enter stationary phase due to carbon starvation the synthesis of ribosomal proteins is rapidly repressed. In a DeltarelA DeltaspoT mutant, defective in the production of the alarmone guanosine tetraphosphate (ppGpp), this regulation of the levels of the protein synthesizing system is abolished. Using a proteomic approach we demonstrate that the production of the vast majority of detected E. coli proteins are decontrolled during carbon starvation in the DeltarelA DeltaspoT strain and that the starved cells behave as if they were growing exponentially. In addition we show that the inhibition of ribosome synthesis by the stringent response can be qualitatively mimicked by artificially lowering the levels of the housekeeping sigma factor, sigma(70). In other words, genes encoding the protein-synthesizing system are especially sensitive to reduced availability of sigma(70) programmed RNA polymerase. This effect is not dependent on ppGpp since lowering the levels of sigma(70) gives a similar but less pronounced effect in a ppGpp(0) strain. The data is discussed in view of the models advocating for a passive control of gene expression during stringency based on alterations in RNA polymerase availability.
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收藏
页码:968 / 973
页数:6
相关论文
共 40 条
[1]   Construction and initial characterization of Escherichia coli strains with few or no intact chromosomal rRNA operons [J].
Asai, T ;
Condon, C ;
Voulgaris, J ;
Zaporojets, D ;
Shen, BH ;
Al-Omar, M ;
Squires, C ;
Squires, CL .
JOURNAL OF BACTERIOLOGY, 1999, 181 (12) :3803-3809
[2]  
BARACCHINI E, 1988, J BIOL CHEM, V263, P2597
[3]   DETERMINATION OF SYNTHESIS RATE AND LIFETIME OF BACTERIAL MESSENGER-RNAS [J].
BARACCHINI, E ;
BREMER, H .
ANALYTICAL BIOCHEMISTRY, 1987, 167 (02) :245-260
[4]   Mechanism of regulation of transcription initiation by ppGpp.: I.: Effects of ppGpp on transcription initiation in vivo and in vitro [J].
Barker, MM ;
Gaal, T ;
Josaitis, CA ;
Gourse, RL .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 305 (04) :673-688
[5]   Mechanism of regulation of transcription initiation by ppGpp. II. Models for positive control based on properties of RNAP mutants and competition for RNAP [J].
Barker, MM ;
Gaal, T ;
Gourse, RL .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 305 (04) :689-702
[6]  
Cashel M, 1996, ESCHERICHIA COLI SAL, P1458
[7]   Gene expression profiling of Escherichia coli growth transitions:: an expanded stringent response model [J].
Chang, DE ;
Smalley, DJ ;
Conway, T .
MOLECULAR MICROBIOLOGY, 2002, 45 (02) :289-306
[8]   The study of guanosine 5′-diphosphate 3′-diphosphate-mediated transcription regulation in vitro using a coupled transcription-translation system [J].
Choy, HE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (10) :6783-6789
[9]  
Daniels Lacy, 1994, P512
[10]   One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products [J].
Datsenko, KA ;
Wanner, BL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) :6640-6645