Asseline U, Grasby J, Hamy F, Iwai S, Mann D A, Pritchard C, Karn J, Gait M J
MRC Laboratory of Molecular Biology, Cambridge, UK.
Nucleic Acids Symp Ser. 1993(29):113-4.
Synthetic oligoribonucleotides have been prepared and annealed to form model RNA duplexes that mimic the high affinity RNA recognition sites for the HIV-1 tat and rev proteins. The contributions of individual functional groups on the model RNAs to the specificity of binding by their respective proteins were studied by use of oligoribonucleotides containing site-specifically modified nucleotides. Both tat and rev appear to recognise specifically a limited number of functional groups in the major groove of an RNA double helix distorted by virtue of unpaired or non-Watson-Crick paired nucleotides.
已制备合成寡核糖核苷酸并使其退火以形成模拟HIV-1反式激活因子(tat)和调节蛋白(rev)高亲和力RNA识别位点的模型RNA双链体。通过使用含有位点特异性修饰核苷酸的寡核糖核苷酸,研究了模型RNA上各个官能团对其各自蛋白质结合特异性的贡献。tat和rev似乎都能特异性识别RNA双螺旋大沟中由于未配对或非沃森-克里克配对核苷酸而变形的有限数量的官能团。