A structural view of microRNA-target recognition

被引:12
作者
Leoni, Guido [1 ]
Tramontano, Anna [1 ,2 ]
机构
[1] Univ Roma La Sapienza, Dept Phys, Piazzale Aldo Moro 5, I-00184 Rome, Italy
[2] Fdn Cenci Bolognetti, Ist Pasteur, Viale Regina Elena 291, I-00161 Rome, Italy
关键词
AGO SILENCING COMPLEXES; MESSENGER-RNAS; BINDING-SITES; MIRNA; IDENTIFICATION; REPERTOIRE; PREDICTION; CLEAVAGE; PIPELINE; PROTEIN;
D O I
10.1093/nar/gkw043
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
It is well established that the correct identification of the messenger RNA targeted by a given microRNA (miRNA) is a difficult problem, and that available methods all suffer from low specificity. We hypothesize that the correct identification of the pairing should take into account the effect of the Argonaute protein (AGO), an essential catalyst of the recognition process. Therefore, we developed a strategy named MiREN for building and scoring three-dimensional models of the ternary complex formed by AGO, a miRNA and 22 nt of a target mRNA that putatively interacts with it. We show here that MiREN can be used to assess the likelihood that an RNA molecule is the target of a given miRNA and that this approach is more accurate than other existing methods, usually based on sequence or sequence-related features. Our results also suggest that AGO plays a relevant role in the selection of the miRNA targets. Our method can represent an additional step for refining predictions made by faster but less accurate classical methods for the identification of miRNA targets.
引用
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页数:8
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