Kiberstis P A, Loesch-Fries L S, Hall T C
Department of Horticulture, University of Wisconsin, Madison, Wisconsin 53706, USA.
Virology. 1981 Jul 30;112(2):804-8. doi: 10.1016/0042-6822(81)90331-7.
When barley protoplasts were inoculated with brome mosaic virus (BMV) RNAs 1 and 2, there was a pronounced synthesis of the 110,000- and 100,000-dalton virally coded proteins. In contrast, there was no detectable synthesis of any viral proteins following inoculation with RNA 3 alone or RNA 4 alone. When RNAs 1 and 2 were recombined with RNA 3 in the inoculum, the profile of proteins synthesized was identical to that following inoculation with similar quantities of unfractionated BMV RNA; i.e., the 35,000-dalton virally coded protein and coat protein were synthesized in addition to the two high-molecular-weight viral polypeptides. RNAs 1 and 2 were shown not to be selectively bound (in preference to RNAs 3 or 4); hence, these data reveal that one or both of these RNAs encode proteins involved in early events of infection, perhaps replication.
当用雀麦花叶病毒(BMV)的RNA 1和RNA 2接种大麦原生质体时,会显著合成分子量为110,000和100,000道尔顿的病毒编码蛋白。相比之下,单独用RNA 3或单独用RNA 4接种后,未检测到任何病毒蛋白的合成。当在接种物中将RNA 1和RNA 2与RNA 3重组时,合成的蛋白质谱与用等量未分级的BMV RNA接种后的情况相同;即,除了两种高分子量病毒多肽外,还合成了分子量为35,000道尔顿的病毒编码蛋白和外壳蛋白。研究表明,RNA 1和RNA 2不会被选择性结合(相对于RNA 3或RNA 4);因此,这些数据表明,这些RNA中的一种或两种编码参与感染早期事件(可能是复制)的蛋白质。