Inhibition of rot translation by RNAIII, a key feature of agr function

被引:186
作者
Geisinger, Edward
Adhikari, Rajan P.
Jin, Ruzhong
Ross, Hope F.
Novick, Richard P. [1 ]
机构
[1] NYU, Med Ctr, Dept Microbiol, Skirball Inst, New York, NY 10016 USA
[2] NYU, Med Ctr, Dept Med, New York, NY 10016 USA
关键词
D O I
10.1111/j.1365-2958.2006.05292.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
RNAIII is a 514 nt regulatory RNA that is the effector molecule of the staphylococcal agr quorum-sensing system, regulating a large set of virulence and other accessory genes at the level of transcription. RNAIII was discovered nearly 20 years ago and we long ago hypothesized that it would function by regulating the synthesis or activity of one or more intermediary transcription factors. We have finally confirmed this hypothesis, showing that Staphylococcus aureus RNAIII regulates the synthesis of a major pleiotropic transcription factor, Rot, by blocking its translation. RNAIII has a complex secondary structure with several stable hairpins that have highly C-rich end loops, unusual in an AT-rich organism. We noted that these loops are complementary to two G-rich stem loops of the rot mRNA translation initiation region (TIR). Pairing of the complementary RNAs would be predicted to occlude the rot Shine-Dalgarno (SD) site and to block rot translation. Through a combination of transcriptional and translational fusions and Northern and Western blot hybridization analyses, we show that RNAIII does, indeed, block rot translation. Through alterations in the C-rich loops of RNAIII and the G-rich loops of rot, we show that the sequences of these loops are critical for inhibition of rot translation and suggest that this inhibition is affected by pairing between the complementary stem loops, followed by the cleavage of rot mRNA. We propose that the RNAIII-rot mRNA interaction plays a key role in agr regulation of staphylococcal virulence.
引用
收藏
页码:1038 / 1048
页数:11
相关论文
共 28 条
[1]  
[Anonymous], [No title captured]
[2]   fhlA repression by OxyS RNA:: Kissing complex formation at two sites results in a stable antisense-target RNA complex [J].
Argaman, L ;
Altuvia, S .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (05) :1101-1112
[3]  
AZAVEDO JC, 1985, INFECT IMMUN, V50, P304
[4]   trans-Complementation of a Staphylococcus aureus agr mutant by Staphylococcus lugdunensis agr RNAIII [J].
Benito, Y ;
Lina, G ;
Greenland, T ;
Etienne, J ;
Vandenesch, F .
JOURNAL OF BACTERIOLOGY, 1998, 180 (21) :5780-5783
[5]   Probing the structure of RNAIII, the Staphylococcus aureus agr regulatory RNA, and identification of the RNA domain involved in repression of protein A expression [J].
Benito, Y ;
Kolb, FA ;
Romby, P ;
Lina, G ;
Etienne, J ;
Vandenesch, F .
RNA, 2000, 6 (05) :668-679
[6]   Novel cassette-based shuttle vector system for gram-positive bacteria [J].
Charpentier, E ;
Anton, AI ;
Barry, P ;
Alfonso, B ;
Fang, Y ;
Novick, RP .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (10) :6076-6085
[7]   Transcription profiling-based identification of Staphylococcus aureus genes regulated by the agr and/or sarA loci [J].
Dunman, PM ;
Murphy, E ;
Haney, S ;
Palacios, D ;
Tucker-Kellogg, G ;
Wu, S ;
Brown, EL ;
Zagursky, RJ ;
Shlaes, D ;
Projan, SJ .
JOURNAL OF BACTERIOLOGY, 2001, 183 (24) :7341-7353
[8]   Global virulence regulation in Staphylococcus aureus:: Pinpointing the roles of ClpP and ClpX in the sar/agr regulatory network [J].
Frees, D ;
Sorensen, K ;
Ingmer, H .
INFECTION AND IMMUNITY, 2005, 73 (12) :8100-8108
[9]   Staphylococcus aureus RNAIII and the endoribonuclease III coordinately regulate spa gene expression [J].
Huntzinger, E ;
Boisset, S ;
Saveanu, C ;
Benito, Y ;
Geissmann, T ;
Namane, A ;
Lina, G ;
Etienne, J ;
Ehresmann, B ;
Ehresmann, C ;
Jacquier, A ;
Vandenesch, FO ;
Romby, P .
EMBO JOURNAL, 2005, 24 (04) :824-835
[10]   Bacterial interference caused by autoinducing peptide variants [J].
Ji, GY ;
Beavis, R ;
Novick, RP .
SCIENCE, 1997, 276 (5321) :2027-2030