Ribas J C, Wickner R B
Section on Genetics of Simple Eukaryotes, National Institute of Diabetes, Digestive and Kidney Diseases, NIH, Bethesda, MD 20892-0830, USA.
Yeast. 1996 Sep 30;12(12):1219-28. doi: 10.1002/(SICI)1097-0061(19960930)12:12%3C1219::AID-YEA14%3E3.0.CO;2-N.
Saccharomyces cerevisiae contains two double-stranded RNA (dsRNA) viruses (L-A and L-BC) and two different single-stranded (ssRNA) replicons (20S RNA and 23S RNA). Replicase (dsRNA synthesis on a ssRNA template) and transcriptase (ssRNA synthesis on a dsRNA template) activities have been described for L-A and L-BC viruses, but not for 20S or 23S RNA. We report the characterization of a new in vitro RNA replicase activity in S. cerevisiae. This activity is detected after partial purification of a particulate fraction in CsCl gradients where it migrates at the density of free protein. The activity does not require the presence of L-A or L-BC viruses or 23S RNA, and its presence or absence is correlated with the presence or absence of the 20S RNA replicon. Strains lacking both this RNA polymerase activity and 20S RNA acquire this activity when they acquire 20S RNA by cytoduction (cytoplasmic mixing). This polymerase activity converts added ssRNA to dsRNA by synthesis of the complementary strand, but has no specificity for the 3' end or internal template sequence. Although it replicates all tested RNA templates, it has a template size requirement, being unable to replicate templates larger than 1 kb. The replicase makes dsRNA from a ssRNA template, but many single-stranded products due to a terminal transferase activity are also formed. These results suggest that, in contrast to the L-A and L-BC RNA polymerases, dissociation of 20S RNA polymerase from its RNA (or perhaps some cellular factor) makes the enzyme change its specificity.
酿酒酵母含有两种双链RNA(dsRNA)病毒(L-A和L-BC)以及两种不同的单链(ssRNA)复制子(20S RNA和23S RNA)。已报道L-A和L-BC病毒具有复制酶(在ssRNA模板上合成dsRNA)和转录酶(在dsRNA模板上合成ssRNA)活性,但20S或23S RNA不具有这些活性。我们报道了酿酒酵母中一种新的体外RNA复制酶活性的特性。在CsCl梯度中对颗粒部分进行部分纯化后可检测到这种活性,其在游离蛋白质的密度下迁移。该活性不需要L-A或L-BC病毒或23S RNA的存在,其存在与否与20S RNA复制子的存在与否相关。缺乏这种RNA聚合酶活性和20S RNA的菌株在通过细胞融合(细胞质混合)获得20S RNA时会获得这种活性。这种聚合酶活性通过合成互补链将添加的ssRNA转化为dsRNA,但对3'端或内部模板序列没有特异性。虽然它能复制所有测试的RNA模板,但有模板大小要求,无法复制大于1 kb的模板。该复制酶从ssRNA模板合成dsRNA,但也会由于末端转移酶活性形成许多单链产物。这些结果表明,与L-A和L-BC RNA聚合酶不同,20S RNA聚合酶与其RNA(或可能是某些细胞因子)的解离会使该酶改变其特异性。