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Staphylococcus aureus RNAIII and the endoribonuclease III coordinately regulate spa gene expression
被引:263
作者:
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
机构:
[1] CNRS, Inst Biol Mol & Cellulaire, UPR 9002, F-67084 Strasbourg, France
[2] Fac Med Laennec, Natl Reference Ctr Staphylococci, INSERM E0230, F-69372 Lyon, France
[3] CNRS Genet Interact Macromol, URA2171, Paris, France
[4] Inst Pasteur, Paris, France
关键词:
mRNA degradation;
post-transcriptional control;
regulatory RNA;
RNase III;
Staphylococcus aureus;
D O I:
10.1038/sj.emboj.7600572
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:
Staphylococcus aureus RNAIII is one of the largest regulatory RNAs, which controls several virulence genes encoding exoproteins and cell- wall- associated proteins. One of the RNAIII effects is the repression of spa gene ( coding for the surface protein A) expression. Here, we show that spa repression occurs not only at the transcriptional level but also by RNAIII- mediated inhibition of translation and degradation of the stable spa mRNA by the double-strand-specific endoribonuclease III ( RNase III). The 30 end domain of RNAIII, partially complementary to the 50 part of spa mRNA, efficiently anneals to spa mRNA through an initial loop - loop interaction. Although this annealing is sufficient to inhibit in vitro the formation of the translation initiation complex, the coordinated action of RNase III is essential in vivo to degrade the mRNA and irreversibly arrest translation. Our results further suggest that RNase III is recruited for targeting the paired RNAs. These findings add further complexity to the expression of the S. aureus virulon.
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页码:824 / 835
页数:12
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