共 55 条
A processed noncoding RNA regulates an altruistic bacterial antiviral system
被引:105
作者:
Blower, Tim R.
[1
]
Pei, Xue Y.
[1
]
Short, Francesca L.
[1
]
Fineran, Peter C.
[2
]
Humphreys, David P.
[3
]
Luisi, Ben F.
[1
]
Salmond, George P. C.
[1
]
机构:
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
[3] UCB, Slough, Berks, England
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:
PHAGE ABORTIVE INFECTION;
TOXIN-ANTITOXIN SYSTEMS;
CRYSTAL-STRUCTURE;
PLASMID MAINTENANCE;
TERTIARY INTERACTIONS;
STRUCTURAL BASIS;
HIGH-LEVEL;
PROTEIN;
RECOGNITION;
INTERFERASES;
D O I:
10.1038/nsmb.1981
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:
The >= 10(30) bacteriophages on Earth relentlessly drive adaptive coevolution, forcing the generation of protective mechanisms in their bacterial hosts. One such bacterial phage-resistance system, ToxIN, consists of a protein toxin (ToxN) that is inhibited in vivo by a specific RNA antitoxin (ToxI); however, the mechanisms for this toxicity and inhibition have not been defined. Here we present the crystal structure of the ToxN-ToxI complex from Pectobacterium atrosepticum, determined to 2.75-angstrom resolution. ToxI is a 36-nucleotide noncoding RNA pseudoknot, and three ToxI monomers bind to three ToxN monomers to generate a trimeric ToxN-ToxI complex. Assembly of this complex is mediated entirely through extensive RNA-protein interactions. Furthermore, a 2'-3' cyclic phosphate at the 3' end of ToxI, and catalytic residues, identify ToxN as an endoRNase that processes ToxI from a repetitive precursor but is regulated by its own catalytic product.
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页码:185 / U246
页数:7
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