The Seed Region of a Small RNA Drives the Controlled Destruction of the Target mRNA by the Endoribonuclease RNase E

被引:169
作者
Bandyra, Katarzyna J. [2 ]
Said, Nelly [3 ]
Pfeiffer, Verena [3 ]
Gorna, Maria W. [2 ]
Vogel, Joerg [1 ,3 ]
Luisi, Ben F. [2 ]
机构
[1] Univ Wurzburg, Inst Mol Infect Biol, D-97080 Wurzburg, Germany
[2] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[3] Max Planck Inst Infect Biol, RNA Biol Grp, D-10115 Berlin, Germany
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
SMALL REGULATORY RNA; DEPENDENT SMALL RNA; ESCHERICHIA-COLI; HFQ-BINDING; TRANSLATIONAL INITIATION; PROTEIN-SYNTHESIS; BIOFILM FORMATION; RIBONUCLEASE E; NONCODING RNA; SOLUBLE-RNAS;
D O I
10.1016/j.molcel.2012.07.015
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
Numerous small non-coding RNAs (sRNAs) in bacteria modulate rates of translation initiation and degradation of target mRNAs, which they recognize through base-pairing facilitated by the RNA chaperone Hfq. Recent evidence indicates that the ternary complex of Hfq, sRNA and mRNA guides endoribonuclease RNase E to initiate turnover of both the RNAs. We show that a sRNA not only guides RNase E to a defined site in a target RNA, but also allosterically activates the enzyme by presenting a monophosphate group at the 5'-end of the cognate-pairing "seed." Moreover, in the absence of the target the 5'-monophosphate makes the sRNA seed region vulnerable to an attack by RNase E against which Hfq confers no protection. These results suggest that the chemical signature and pairing status of the sRNA seed region may help to both 'proofread' recognition and activate mRNA cleavage, as part of a dynamic process involving cooperation of RNA, Hfq and RNase E.
引用
收藏
页码:943 / 953
页数:11
相关论文
共 53 条
[1]   Both RNase E and RNase III control the stability of sodB mRNA upon translational inhibition by the small regulatory RNA RyhB [J].
Afonyushkin, T ;
Vecerek, B ;
Moll, I ;
Bläsi, U ;
Kaberdin, VR .
NUCLEIC ACIDS RESEARCH, 2005, 33 (05) :1678-1689
[2]   Mechanism of RNA silencing by Hfq-binding small RNAs [J].
Aiba, Hiroji .
CURRENT OPINION IN MICROBIOLOGY, 2007, 10 (02) :134-139
[3]   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
[4]   Recognition of heptameric seed sequence underlies multi-target regulation by RybB small RNA in Salmonella enterica [J].
Balbontin, Roberto ;
Fiorini, Francesca ;
Figueroa-Bossi, Nara ;
Casadesus, Josep ;
Bossi, Lionello .
MOLECULAR MICROBIOLOGY, 2010, 78 (02) :380-394
[5]   The Base-Pairing RNA Spot 42 Participates in a Multioutput Feedforward Loop to Help Enact Catabolite Repression in Escherichia coli [J].
Beisel, Chase L. ;
Storz, Gisela .
MOLECULAR CELL, 2011, 41 (03) :286-297
[6]   Small RNA Binding to 5′ mRNA Coding Region Inhibits Translational Initiation [J].
Bouvier, Marie ;
Sharma, Cynthia M. ;
Mika, Franziska ;
Nierhaus, Knud H. ;
Vogel, Joerg .
MOLECULAR CELL, 2008, 32 (06) :827-837
[7]   Structure of Escherichia coli RNase E catalytic domain and implications for RNA turnover [J].
Callaghan, AJ ;
Marcaida, MJ ;
Stead, JA ;
McDowall, KJ ;
Scott, WG ;
Luisi, BF .
NATURE, 2005, 437 (7062) :1187-1191
[8]   Small RNA-mediated regulation at the level of transcript stability [J].
Caron, Marie-Pier ;
Lafontaine, Daniel A. ;
Masse, Eric .
RNA BIOLOGY, 2010, 7 (02) :140-144
[9]   The RNA degradosome of Escherichia coli:: An mRNA-degrading machine assembled on RNase E [J].
Carpousis, Agamemnon J. .
ANNUAL REVIEW OF MICROBIOLOGY, 2007, 61 :71-87
[10]   The bacterial enzyme RppH triggers messenger RNA degradation by 5' pyrophosphate removal [J].
Deana, Atilio ;
Celesnik, Helena ;
Belasco, Joel G. .
NATURE, 2008, 451 (7176) :355-U14