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
英国生物技术与生命科学研究理事会; 英国惠康基金;
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.
引用
收藏
页码:185 / U246
页数:7
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