Da Rocha Gomes Sonia, Dausse Eric, Toulmé Jean-Jacques
INSERM U386, IFR 66, Université Victor Segalen Bordeaux 2, France and Institut Européen de Chimie et Biologie, Pessac, France.
Biochem Biophys Res Commun. 2004 Sep 24;322(3):820-6. doi: 10.1016/j.bbrc.2004.07.185.
Domain II of the hepatitis C virus internal ribosome entry site is a major RNA structure involved in the viral mRNA translation. It comprises four different structural domains. We performed in vitro selection against the apical loop of the domain II and we identified RNA aptamers folding as an imperfect hairpin with an internal loop of interacting with the apical loop of the domain II. This RNA-RNA interaction creates apical loop-internal loop complex. The aptamer binds the target with an apparent K(d) of 35nM. In this study, the main structural elements of the target and the aptamer involved in the formation of the complex are characterized by mutation, deletion, and RNase probing analysis. We demonstrate that a complementary loop flanked by G,C rich upper and lower stems are crucial for such RNA-RNA interactions.
丙型肝炎病毒内部核糖体进入位点的结构域II是参与病毒mRNA翻译的主要RNA结构。它由四个不同的结构域组成。我们针对结构域II的顶端环进行了体外筛选,鉴定出折叠成具有与结构域II顶端环相互作用的内环的不完美发夹结构的RNA适体。这种RNA-RNA相互作用形成了顶端环-内环复合物。该适体以35nM的表观解离常数(K(d))结合靶标。在本研究中,通过突变、缺失和核糖核酸酶探测分析对参与复合物形成的靶标和适体的主要结构元件进行了表征。我们证明,由富含G、C的上部和下部茎侧翼的互补环对于这种RNA-RNA相互作用至关重要。