Esteban R, Wickner R B
Mol Cell Biol. 1986 May;6(5):1552-61. doi: 10.1128/mcb.6.5.1552-1561.1986.
Killer strains of Saccharomyces cerevisiae bear at least two different double-stranded RNAs (dsRNAs) encapsidated in 39-nm viruslike particles (VLPs) of which the major coat protein is coded by the larger RNA (L-A dsRNA). The smaller dsRNA (M1 or M2) encodes an extracellular protein toxin (K1 or K2 toxin). Based on their densities on CsCl gradients, L-A- and M1-containing particles can be separated. Using this method, we detected a new type of M1 dsRNA-containing VLP (M1-H VLP, for heavy) that has a higher density than those previously reported (M1-L VLP, for light). M1-H and M1-L VLPs are present together in the same strains and in all those we tested. M1-H, M1-L, and L-A VLPs all have the same types of proteins in the same approximate proportions, but whereas L-A VLPs and M1-L VLPs have one dsRNA molecule per particle, M1-H VLPs contain two M1 dsRNA molecules per particle. Their RNA polymerase produces mainly plus single strands that are all extruded in the case of M1-H particles but are partially retained inside the M1-L particles to be used later for dsRNA synthesis. We show that M1-H VLPs are formed in vitro from the M1-L VLPs. We also show that the peak of M1 dsRNA synthesis is in fractions lighter than M1-L VLPs, presumably those carrying only a single plus M1 strand. We suggest that VLPs carrying two M1 dsRNAs (each 1.8 kilobases) can exist because the particle is designed to carry one L-A dsRNA (4.5 kilobases).
酿酒酵母的杀伤菌株携带至少两种不同的双链RNA(dsRNA),它们被包裹在39纳米的病毒样颗粒(VLP)中,其中主要的衣壳蛋白由较大的RNA(L-A dsRNA)编码。较小的dsRNA(M1或M2)编码一种细胞外蛋白毒素(K1或K2毒素)。根据它们在CsCl梯度上的密度,可以分离出含有L-A和M1的颗粒。利用这种方法,我们检测到一种新型的含有M1 dsRNA的VLP(M1-H VLP,重的),其密度高于先前报道的(M1-L VLP,轻的)。M1-H和M1-L VLP存在于同一菌株中,并且在我们测试的所有菌株中都同时存在。M1-H、M1-L和L-A VLP都含有相同类型的蛋白质,且比例大致相同,但是L-A VLP和M1-L VLP每个颗粒含有一个dsRNA分子,而M1-H VLP每个颗粒含有两个M1 dsRNA分子。它们的RNA聚合酶主要产生正单链,在M1-H颗粒的情况下,这些正单链全部被挤出,但在M1-L颗粒中部分保留在内部,供以后用于dsRNA合成。我们表明,M1-H VLP是由M1-L VLP在体外形成的。我们还表明,M1 dsRNA合成的峰值出现在比重于M1-L VLP的组分中,推测这些组分只携带一条正M1链。我们认为携带两条M1 dsRNA(每条1.8千碱基)的VLP能够存在,是因为该颗粒被设计用来携带一条L-A dsRNA(4.5千碱基)。