Bonatti S, Sonenberg N, Shatkin A J, Cancedda R
J Biol Chem. 1980 Dec 10;255(23):11473-7.
Sindbis 42 S genome RNA was isolated from virions and translated in vitro before and after purification by oligo(dT)-cellulose chromatography and sucrose density gradient centrifugation under denaturing conditions. In intact 42 S RNA, only the 5'-proximal initiation site for the synthesis of nonstructural proteins was used. The internally located start site for viral structural protein formation was active in broken genome RNA molecules where, as a consequence of fragmentation, it was closer to a 5' end. The results of several kinds of experiments indicate that the fragmentation-dependent synthesis of structural proteins directed by virion RNA was not due to the presence of 26 S subgenomic messenger RNA.
辛德毕斯病毒42S基因组RNA从病毒粒子中分离出来,在变性条件下,通过寡聚(dT)-纤维素柱层析和蔗糖密度梯度离心纯化前后进行体外翻译。在完整的42S RNA中,仅使用非结构蛋白合成的5'-近端起始位点。病毒结构蛋白形成的内部起始位点在破碎的基因组RNA分子中具有活性,由于片段化,该起始位点更靠近5'端。多种实验结果表明,病毒粒子RNA指导的结构蛋白的片段化依赖性合成并非由于26S亚基因组信使RNA的存在。