A novel sRNA component of the carbon storage regulatory system of Escherichia coli

被引:309
作者
Weilbacher, T
Suzuki, K
Dubey, AK
Wang, X
Gudapaty, S
Morozov, I
Baker, CS
Georgellis, D
Babitzke, P
Romeo, T [1 ]
机构
[1] Univ N Texas, Dept Mol Biol & Immunol, Ctr Hlth Sci, Ft Worth, TX 76107 USA
[2] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[3] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
[4] Univ Nacl Autonoma Mexico, Dept Mol Genet, Inst Fisiol Celular, Mexico City 04510, DF, Mexico
关键词
D O I
10.1046/j.1365-2958.2003.03459.x
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
Small untranslated RNAs (sRNAs) perform a variety of important functions in bacteria. The 245 nucleotide sRNA of Escherichia coli , CsrC, was discovered using a genetic screen for factors that regulate glycogen biosynthesis. CsrC RNA binds multiple copies of CsrA, a protein that post-transcriptionally regulates central carbon flux, biofilm formation and motility in E. coli . CsrC antagonizes the regulatory effects of CsrA, presumably by sequestering this protein. The discovery of CsrC is intriguing, in that a similar sRNA, CsrB, performs essentially the same function. Both sRNAs possess similar imperfect repeat sequences (18 in CsrB, nine in CsrC), primarily localized in the loops of predicted hairpins, which may serve as CsrA binding elements. Transcription of csrC increases as the culture approaches the stationary phase of growth and is indirectly activated by CsrA via the response regulator UvrY. Because CsrB and CsrC antagonize CsrA activity and depend on CsrA for their synthesis, a csrB null mutation causes a modest compensatory increase in CsrC levels and vice versa. Homologues of csrC are apparent in several Enterobacteriaceae. The regulatory and evolutionary implications of these findings are discussed.
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收藏
页码:657 / 670
页数:14
相关论文
共 51 条
[41]   Disruption of a global regulatory gene to enhance central carbon flux into phenylalanine biosynthesis in Escherichia coli [J].
Tatarko, M ;
Romeo, T .
CURRENT MICROBIOLOGY, 2001, 43 (01) :26-32
[42]   6S RNA regulates E-coli RNA polymerase activity [J].
Wassarman, KM ;
Storz, G .
CELL, 2000, 101 (06) :613-623
[43]  
Wassarman KM, 1999, TRENDS MICROBIOL, V7, P37
[44]   Small RNAs in bacteria: Diverse regulators of gene expression in response to environmental changes [J].
Wassarman, KM .
CELL, 2002, 109 (02) :141-144
[45]   Identification of novel small RNAs using comparative genomics and microarrays [J].
Wassarman, KM ;
Repoila, F ;
Rosenow, C ;
Storz, G ;
Gottesman, S .
GENES & DEVELOPMENT, 2001, 15 (13) :1637-1651
[46]   Global regulatory mutations in csrA and rpoS cause severe central carbon stress in Escherichia coli in the presence of acetate [J].
Wei, BD ;
Shin, S ;
LaPorte, D ;
Wolfe, AJ ;
Romeo, T .
JOURNAL OF BACTERIOLOGY, 2000, 182 (06) :1632-1640
[47]   Positive regulation of motility and flhDC expression by the RNA-binding protein CsrA of Escherichia coli [J].
Wei, BDL ;
Brun-Zinkernagel, AM ;
Simecka, JW ;
Prüss, BM ;
Babitzke, P ;
Romeo, T .
MOLECULAR MICROBIOLOGY, 2001, 40 (01) :245-256
[48]   Effects of mutations in the L-tryptophan binding pocket of the trp RNA-binding attenuation protein of Bacillus subtilis [J].
Yakhnin, AV ;
Trimble, JJ ;
Chiaro, CR ;
Babitzke, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (06) :4519-4524
[49]   Coordinate genetic regulation of glycogen catabolism and biosynthesis in Escherichia coli via the CsrA gene product [J].
Yang, HH ;
Liu, MY ;
Romeo, T .
JOURNAL OF BACTERIOLOGY, 1996, 178 (04) :1012-1017
[50]   The Sm-like Hfq protein increases OxyS RNA interaction with target mRNAs [J].
Zhang, AX ;
Wassarman, KM ;
Ortega, J ;
Steven, AC ;
Storz, G .
MOLECULAR CELL, 2002, 9 (01) :11-22