Harrison G P, Hunter E, Lever A M
Department of Medicine, Addenbrooke's Hospital, University of Cambridge, United Kingdom.
J Virol. 1995 Apr;69(4):2175-86. doi: 10.1128/JVI.69.4.2175-2186.1995.
A stable secondary structure model is presented for the region 3' of the primer-binding site to 130 bases into the gag sequence of the prototype type D retrovirus Mason-Pfizer monkey virus. Using biochemical probing of RNA from this region in association with free energy minimization, we have identified a stem-loop structure in the region, which from other studies has been shown to be important for genomic RNA encapsidation. The structure involves a highly stable stem of five G-C pairs terminating in a heptaloop. Comparison of the Mason-Pfizer monkey virus structure with one predicted for squirrel monkey retrovirus demonstrates an identical stem and a common ACC motif in the loop. Free energy studies of the secondary structure of the 5' regions of eight other retroviruses predict stem loops which have similar GAYC motifs. We believe this may represent a common structural and sequence motif which among other functions may be involved in genomic RNA packaging in these viruses.
本文提出了原型D型逆转录病毒梅森- Pfizer猴病毒引物结合位点3'端至gag序列中130个碱基区域的稳定二级结构模型。通过对该区域RNA进行生化探测并结合自由能最小化分析,我们确定了该区域的一个茎环结构,其他研究表明该结构对基因组RNA的包装很重要。该结构包含一个由五个G-C对组成的高度稳定的茎,末端为一个七核苷酸环。将梅森- Pfizer猴病毒的结构与松鼠猴逆转录病毒预测的结构进行比较,发现茎相同且环中存在共同的ACC基序。对其他八种逆转录病毒5'区域二级结构的自由能研究预测出具有相似GAYC基序的茎环。我们认为这可能代表一种共同的结构和序列基序,在这些病毒的基因组RNA包装等功能中可能发挥作用。