Shalitin C, Weiser I
J Bacteriol. 1977 Sep;131(3):735-40. doi: 10.1128/jb.131.3.735-740.1977.
The synthesis of killer double-stranded ribonucleic acid (dsRNA) in Saccharomyces cerevisiae was examined in seven different cell division cycle mutants (cdc) that are defective in nuclear deoxyribonucleic acid replication and contain the "killer character." In cdc28, cdc4, and cdc7, which are defective in the initiation of nuclear deoxyribonucleic acid synthesis, and in cdc23 or in cdc14, defective in medial or late nuclear division, an overproduction of dsRNA at the restrictive temperature was observed. In contrast to the above mutants, the synthesis of killer dsRNA is not enhanced at the restrictive temperature in either cdc8 or cdc21, which are defective in deoxyribonucleic acid chain elongation. Examination of killer sensitive strains (cdc7 K- and cdc4 K-) has shown that the complete killer dsRNA genome is essential for the overproduction of dsRNA at the restrictive temperature.
在七个不同的细胞分裂周期突变体(cdc)中检测了酿酒酵母中杀伤性双链核糖核酸(dsRNA)的合成,这些突变体在核脱氧核糖核酸复制方面存在缺陷且具有“杀伤特性”。在cdc28、cdc4和cdc7中,它们在核脱氧核糖核酸合成起始方面存在缺陷;在cdc23或cdc14中,它们在核分裂中期或后期存在缺陷,在限制温度下观察到dsRNA过量产生。与上述突变体相反,在cdc8或cdc21中,它们在脱氧核糖核酸链延伸方面存在缺陷,在限制温度下杀伤性dsRNA的合成并未增强。对杀伤敏感菌株(cdc7 K-和cdc4 K-)的检测表明,完整的杀伤性dsRNA基因组对于在限制温度下dsRNA的过量产生至关重要。