Rodriguez-Cousiño N, Esteban R
Instituto de Microbiología Bioquímica, Consejo Superior de Investigaciones Científicas/Universidad de Salamanca, Spain.
Nucleic Acids Res. 1992 Jun 11;20(11):2761-6. doi: 10.1093/nar/20.11.2761.
Most yeast strains carry a cytoplasmic double-stranded RNA (dsRNA) molecule called W, of 2.5 kb in size. We have cloned and sequenced most of W genome (1), and we proposed that W (+) strands were identical to 20S RNA, a single-stranded RNA (ssRNA) species, whose copy number is highly induced under stress conditions. Recently it was proposed that 20S RNA was circular (2). In this paper, however, we demonstrate that both W dsRNA and 20S RNA are linear. Linearity of W dsRNA is shown by the stoichiometric labelling of both strands of W with 32P-pCp and T4 RNA ligase. The last 3' end nucleotide of both strands is about 70 to 80% C and 20 to 30% A. Linearity of 20S RNA is directly demonstrated by a site-specific cleavage of 20S RNA with RNase H, using an oligodeoxynucleotide complementary to an internal site of 20S RNA. The cleavage produced not one but two RNA fragments expected from the linearity of 20S RNA.
大多数酵母菌株携带一种名为W的细胞质双链RNA(dsRNA)分子,大小为2.5 kb。我们已经克隆并测序了W基因组的大部分(1),并且我们提出W(+)链与20S RNA相同,20S RNA是一种单链RNA(ssRNA),其拷贝数在应激条件下会高度诱导。最近有人提出20S RNA是环状的(2)。然而,在本文中,我们证明W双链RNA和20S RNA都是线性的。W双链RNA的线性通过用32P-pCp和T4 RNA连接酶对W的两条链进行化学计量标记来显示。两条链的最后一个3'末端核苷酸约70%至80%为C,20%至30%为A。使用与20S RNA内部位点互补的寡聚脱氧核苷酸,通过用RNase H对20S RNA进行位点特异性切割,直接证明了20S RNA的线性。切割产生的不是一个而是两个预期来自20S RNA线性的RNA片段。