Newman A M, Elliott S G, McLaughlin C S, Sutherland P A, Warner R C
J Virol. 1981 Apr;38(1):263-71. doi: 10.1128/JVI.38.1.263-271.1981.
The mode of replication of the L double-stranded RNA (dsRNA) present in virus-like particles in Saccharomyces cerevisiae was examined by density transfer experiments. After transfer to light medium, significant amounts of fully heavy dsRNA persisted over a number of cell doublings. In addition, very little material of hybrid density was ever formed, and the accumulation of fully light material began as early as 0.5 doubling after transfer to light medium. Our results are compatible with a conservative mode of replication or with a semiconservative mode of replication carried out by a small portion of the total dsRNA population. In additional experiments the synthesis of dsRNA relative to the cell cycle was studied. This was done by determining the ratio of short-term to long-term radioactive label in size-separated cell fractions of a prelabeled exponential culture. The ratio of short-term to long-term label remained constant for all fractions, implying that dsRNA is synthesized throughout the cell cycle, increasing through the cell cycle at an exponential rate.
通过密度转移实验研究了酿酒酵母中病毒样颗粒中存在的L双链RNA(dsRNA)的复制模式。转移到轻培养基后,大量完全重的dsRNA在多个细胞倍增过程中持续存在。此外,几乎没有形成杂交密度的物质,并且早在转移到轻培养基后0.5个倍增时就开始积累完全轻的物质。我们的结果与保守复制模式或由总dsRNA群体的一小部分进行的半保守复制模式一致。在另外的实验中,研究了dsRNA相对于细胞周期的合成。这是通过确定预标记指数培养物的大小分离细胞组分中短期与长期放射性标记的比率来完成的。所有组分的短期与长期标记比率保持恒定,这意味着dsRNA在整个细胞周期中合成,并以指数速率在细胞周期中增加。