RNA-protein interaction methods to study viral IRES elements

被引:19
|
作者
Francisco-Velilla, Rosario [1 ]
Fernandez-Chamorro, Javier [1 ]
Lozano, Gloria [1 ]
Diaz-Toledano, Rosa [1 ]
Martinez-Salas, Encarnacion [1 ]
机构
[1] Univ Autonoma Madrid, Consejo Super Invest Cient, Ctr Biol Mol Severo Ochoa, E-28049 Madrid, Spain
关键词
RNA virus; IRES elements; RNA-binding proteins; RNA structure; Translation control; RIBOSOME-ENTRY SITE; HEPATITIS-C-VIRUS; INTERNAL TRANSLATION INITIATION; IN-VIVO; AFFINITY-PURIFICATION; MEDIATED TRANSLATION; SECONDARY STRUCTURE; SHAPE CHEMISTRY; MESSENGER-RNAS; POLIOVIRUS RNA;
D O I
10.1016/j.ymeth.2015.06.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Translation control often takes place through the mRNA untranslated regions, involving direct interactions with RNA-binding proteins (RBPs). Internal ribosome entry site elements (IRESs) are cis-acting RNA regions that promote translation initiation using a cap-independent mechanism. A subset of positive-strand RNA viruses harbor IRESs as a strategy to ensure efficient viral protein synthesis. IRESs are organized in modular structural domains with a division of functions. However, viral IRESs vary in nucleotide sequence, secondary RNA structure, and transacting factor requirements. Therefore, in-depth studies are needed to understand how distinct types of viral IRESs perform their function. In this review we describe methods to isolate and identify RNA-binding proteins important for IRES activity, and to study the impact of RNA structure and RNA-protein interactions on IRES activity. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:3 / 12
页数:10
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