Structural basis for 5′-end-specific recognition of guide RNA by the A. fulgidus Piwi protein

Jin-Biao Ma, Yu-Ren Yuan, Gunter Meister, Yi Pei, Thomas Tuschl and Dinshaw J. Patel ()
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Jin-Biao Ma: Memorial Sloan-Kettering Cancer Center
Yu-Ren Yuan: Memorial Sloan-Kettering Cancer Center
Gunter Meister: The Rockefeller University
Yi Pei: The Rockefeller University
Thomas Tuschl: The Rockefeller University
Dinshaw J. Patel: Memorial Sloan-Kettering Cancer Center

Nature, 2005, vol. 434, issue 7033, 666-670

Abstract: Abstract RNA interference (RNAi) is a conserved sequence-specific gene regulatory mechanism1,2,3 mediated by the RNA-induced silencing complex (RISC), which is composed of a single-stranded guide RNA and an Argonaute protein. The PIWI domain, a highly conserved motif within Argonaute, has been shown to adopt an RNase H fold4,5 critical for the endonuclease cleavage activity of RISC4,5,6. Here we report the crystal structure of Archaeoglobus fulgidus Piwi protein bound to double-stranded RNA, thereby identifying the binding pocket for guide-strand 5′-end recognition and providing insight into guide-strand-mediated messenger RNA target recognition. The phosphorylated 5′ end of the guide RNA is anchored within a highly conserved basic pocket, supplemented by the carboxy-terminal carboxylate and a bound divalent cation. The first nucleotide from the 5′ end of the guide RNA is unpaired and stacks over a conserved tyrosine residue, whereas successive nucleotides form a four-base-pair RNA duplex. Mutation of the corresponding amino acids that contact the 5′ phosphate in human Ago2 resulted in attenuated mRNA cleavage activity. Our structure of the Piwi–RNA complex, and that determined elsewhere7, provide direct support for the 5′ region of the guide RNA serving as a nucleation site for pairing with target mRNA and for a fixed distance separating the RISC-mediated mRNA cleavage site from the anchored 5′ end of the guide RNA.

Date: 2005
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DOI: 10.1038/nature03514

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