Tacke E, Prüfer D, Salamini F, Rohde W
Max-Planck-Institut für Züchtungsforschung, Köln, F.R.G.
J Gen Virol. 1990 Oct;71 ( Pt 10):2265-72. doi: 10.1099/0022-1317-71-10-2265.
Northern blot analysis of Solanum tuberosum infected with potato leafroll luteovirus revealed the 6 kb genomic RNA and a major 2.3 kb subgenomic RNA. The 5' end of the subgenomic RNA was located at nucleotide 3653 in an intergenic region located at the centre of the viral genome upstream of three open reading frames (ORFs). Transient expression in tobacco and potato protoplasts of the beta-glucuronidase reporter gene fused to various putative regulatory sequences present in the subgenomic RNA was used to study their influence on expression levels. We observed a suppression of the amber stop codon separating the coat protein (CP) gene from a downstream ORF (56K protein), to a level of 0.9% to 1.3%. Translation initiation at the AUG of an ORF (17K protein) which is nested within the CP gene, exceeds translation of the CP gene itself by a factor of 7.
对感染马铃薯卷叶黄症病毒的马铃薯进行Northern印迹分析,结果显示出6 kb的基因组RNA和一个主要的2.3 kb亚基因组RNA。亚基因组RNA的5'端位于病毒基因组中心一个基因间隔区的核苷酸3653处,该基因间隔区位于三个开放阅读框(ORF)上游。将β-葡萄糖醛酸酶报告基因与亚基因组RNA中存在的各种假定调控序列融合,在烟草和马铃薯原生质体中进行瞬时表达,以研究它们对表达水平的影响。我们观察到,将外壳蛋白(CP)基因与下游一个开放阅读框(56K蛋白)分隔开的琥珀色终止密码子的抑制率为0.9%至1.3%。位于CP基因内的一个开放阅读框(17K蛋白)的AUG处的翻译起始,其效率比CP基因本身的翻译高出7倍。