Hong Y, Cole T E, Brasier C M, Buck K W
Department of Biology, Imperial College of Science, Technology, and Medicine, London, United Kingdom.
Virology. 1998 Mar 1;242(1):80-9. doi: 10.1006/viro.1997.8999.
The nucleotide sequences of 2 of the 10 mitochondrial double-stranded (ds) RNA segments in a diseased isolate, Log 1/3-8d2 (Ld), of Ophiostoma novo-ulmi, RNA-7 (1057 nucleotides) and RNA-10 (317-330 nucleotides), have been determined. Both RNAs are A-U-rich, but in Southern and Northern blots, no hybridization with mitochondrial DNA or RNA could be detected. Only very short open reading frames were found in both RNAs. As most of its sequence is unrelated to any of the other Ld dsRNAs, RNA-7 may be regarded as a satellite RNA. Northern blotting detected a full-length single-stranded (ss) form of RNA-7 in nucleic acid extracts from Ld. The 5'- and 3'-terminal 39 nucleotides of ssRNA-7 are imperfect inverted complementary repeats of each other, which could cause ssRNA-7 to form a panhandle structure. In addition, the 5'-terminal nucleotides 1-28 and 3'-terminal nucleotides 1032-1057 of ssRNA-7 each contained inverted complementary sequences, allowing the possibility for each terminus to form separate stem-loop structures. The combination of these two structural features has not been found previously in any dsRNA or ssRNA virus. RNA-10 was shown to have an unusual structure, consisting of a mosaic of sequences derived from regions of the 5'- and 3'-termini, or just the 5'-terminus, of RNA-7, RNA-10 has a high degree of inverted complementarity, with the potential to be folded into a very stable hairpin structure. A model for the formation of RNA-10 is presented, involving replicase-driven strand switching between (-)-strand and (+)-strand templates during RNA synthesis, followed by utilization of the nascent strand as a primer and template to form a snap-back RNA.
已测定了新榆枯萎病菌(Ophiostoma novo-ulmi)患病分离株Log 1/3 - 8d2(Ld)的10个线粒体双链(ds)RNA片段中的2个片段,即RNA - 7(1057个核苷酸)和RNA - 10(317 - 330个核苷酸)的核苷酸序列。这两种RNA都富含A - U,但在Southern和Northern印迹分析中,未检测到与线粒体DNA或RNA的杂交信号。在这两种RNA中仅发现了非常短的开放阅读框。由于RNA - 7的大部分序列与其他Ld双链RNA均无关联,因此可将其视为一种卫星RNA。Northern印迹分析在Ld的核酸提取物中检测到了全长单链(ss)形式的RNA - 7。ssRNA - 7的5'端和3'端的39个核苷酸彼此为不完全反向互补重复序列,这可能导致ssRNA - 7形成锅柄状结构。此外,ssRNA - 7的5'端核苷酸1 - 28和3'端核苷酸1032 - 1057各自包含反向互补序列,使得每个末端都有可能形成单独的茎环结构。这两种结构特征的组合在之前的任何双链RNA或单链RNA病毒中均未发现。RNA - 10显示出一种不寻常的结构,由源自RNA - 7的5'端和3'端区域或仅5'端区域的序列镶嵌而成,RNA - 10具有高度的反向互补性,有可能折叠成非常稳定的发夹结构。本文提出了一个RNA - 10形成的模型,该模型涉及在RNA合成过程中,复制酶驱动的负链和正链模板之间的链交换,随后利用新生链作为引物和模板形成回折RNA。