The Crp-Activated Small Noncoding Regulatory RNA CyaR (RyeE) Links Nutritional Status to Group Behavior

被引:139
作者
De Lay, Nicholas [1 ]
Gottesman, Susan [1 ]
机构
[1] NCI, Mol Biol Lab, Bethesda, MD 20892 USA
关键词
CATABOLITE REPRESSION CONTROL; ENVELOPE STRESS-RESPONSE; OUTER-MEMBRANE PROTEINS; AMP RECEPTOR PROTEIN; ESCHERICHIA-COLI; PSEUDOMONAS-PUTIDA; CARBON METABOLISM; GLOBAL REGULATOR; DOWN-REGULATION; SALMONELLA-TYPHIMURIUM;
D O I
10.1128/JB.01157-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Small noncoding regulatory RNAs (sRNAs) play a key role in regulating the expression of many genes in Escherichia coli and other bacteria. Many of the sRNAs identified in E. coli bind to mRNAs in an Hfq-dependent manner and stimulate or inhibit translation of the mRNAs. Several sRNAs are regulated by well-studied global regulators. Here, we report characterization of the CyaR (RyeE) sRNA, which was previously identified in a global search for sRNAs in E. coli. We demonstrated that CyaR is positively regulated by the global regulator Crp under conditions in which cyclic AMP levels are high. We showed by using microarray analysis and Northern blotting that several genes are negatively regulated by CyaR, including ompX, encoding a major outer membrane protein; luxS, encoding the autoinducer-2 synthase; nadE, encoding an essential NAD synthetase; and yqaE, encoding a predicted membrane protein with an unknown function. Using translational lacZ fusions to yqaE, ompX, nadE, and luxS, we demonstrated that the negative regulation of these genes by CyaR occurs at the posttranscriptional level and is direct. Different portions of a highly conserved 3' region of CyaR are predicted to pair with sequences near the ribosome binding site of each of these targets; mutations in this sequence affected regulation, and compensatory mutations in the target mRNA restored regulation, confirming that there is direct regulation by the sRNA. These results provide insight into the mechanisms by which Crp negatively regulates genes such as luxS and ompX and provide a link between catabolite repression, quorum sensing, and nitrogen assimilation in E. coli.
引用
收藏
页码:461 / 476
页数:16
相关论文
共 73 条
[1]   Vfr controls quorum sensing in Pseudomonas aeruginosa [J].
Albus, AM ;
Pesci, EC ;
RunyenJanecky, LJ ;
West, SEH ;
Iglewski, BH .
JOURNAL OF BACTERIOLOGY, 1997, 179 (12) :3928-3935
[2]   Novel small RNA-encoding genes in the intergenic regions of Escherichia coli [J].
Argaman, L ;
Hershberg, R ;
Vogel, J ;
Bejerano, G ;
Wagner, EGH ;
Margalit, H ;
Altuvia, S .
CURRENT BIOLOGY, 2001, 11 (12) :941-950
[3]   Insertion hot spot for horizontally acquired DNA within a bidirectional small-RNA locus in Salmonella enterica [J].
Balbontin, Roberto ;
Figueroa-Bossi, Nara ;
Casadesus, Josep ;
Bossi, Lionello .
JOURNAL OF BACTERIOLOGY, 2008, 190 (11) :4075-4078
[4]   Autoinducer 2 controls biofilm formation in Escherichia coli through a novel motility quorum-sensing regulator (MqsR, B3022) [J].
Barrios, AFG ;
Zuo, RJ ;
Hashimoto, Y ;
Yang, L ;
Bentley, WE ;
Wood, TK .
JOURNAL OF BACTERIOLOGY, 2006, 188 (01) :305-316
[5]   INTERCELLULAR SIGNALING IN VIBRIO-HARVEYI - SEQUENCE AND FUNCTION OF GENES REGULATING EXPRESSION OF LUMINESCENCE [J].
BASSLER, BL ;
WRIGHT, M ;
SHOWALTER, RE ;
SILVERMAN, MR .
MOLECULAR MICROBIOLOGY, 1993, 9 (04) :773-786
[6]   Cross-species induction of luminescence in the quorum-sensing bacterium Vibrio harveyi [J].
Bassler, BL ;
Greenberg, EP ;
Stevens, AM .
JOURNAL OF BACTERIOLOGY, 1997, 179 (12) :4043-4045
[7]   Differential regulation of twitching motility and elastase production by Vfr in Pseudomonas aeruginosa [J].
Beatson, SA ;
Whitchurch, CB ;
Sargent, JL ;
Levesque, RC ;
Mattick, JS .
JOURNAL OF BACTERIOLOGY, 2002, 184 (13) :3605-3613
[8]   A small RNA downregulates LamB maltoporin in Salmonella [J].
Bossi, Lionello ;
Figueroa-Bossi, Nara .
MOLECULAR MICROBIOLOGY, 2007, 65 (03) :799-810
[9]   Prophage insertion sites [J].
Campbell, A .
RESEARCH IN MICROBIOLOGY, 2003, 154 (04) :277-282
[10]   MicC, a second small-RNA regulator of Omp protein expression in Escherichia coli [J].
Chen, S ;
Zhang, AX ;
Blyn, LB ;
Storz, G .
JOURNAL OF BACTERIOLOGY, 2004, 186 (20) :6689-6697