Clerx-Van Haaster C M, Clewley J P, Bishop D H
J Virol. 1980 Feb;33(2):807-17. doi: 10.1128/JVI.33.2.807-817.1980.
RNase T(1) oligonucleotide fingerprint analyses of three vesicular stomatitis virus Indiana serotype small defective interfering (DI) particle RNA species indicate that they only have oligonucleotides derived from the 5' region of the viral genome. These studies also indicate that these three DI RNAs have partial L gene sequences as well as two 5' viral oligonucleotides (59 and 70) that are not transcribed into L (or other) mRNA species (J. P. Clewley and D. H. L. Bishop, J. Virol. 30:116-123, 1979). Analyses of the large DI RNA (LT DI) reveal a different origin. The LT DI RNA has oligonucleotides derived from both the 3' end of the genome (including all the large oligonucleotides identified for N, NS, M, and G genes), in addition to at least one of the 5'-proximal L gene oligonucleotides (47), as well as all seven oligonucleotides (3, 38, 42, 43, 44B, 59, and 70) that are not protected from nuclease digestion after the formation of mRNA-viral RNA duplexes (Clewley and Bishop). It appears therefore that the genesis of LT RNA involves a deletion of internal L gene sequences from the viral RNA. Oligonucleotide sequence analyses have been undertaken on several of the vesicular stomatitis viral RNA oligonucleotides, including all seven (3, 38, 42, 43, 44B, 59, and 70) that are not transcribed into mRNA. The analyses confirm that oligonucleotides 59 [3'...GAACACCAAAAAUAAAAAAUA(G)...5'] and 70 [3'...GACCAAAACACCA(G)...5'] are at the 5'-end region of the viral genome. Oligonucleotide 38 [3'...GAAAUUCAUACUUUUUU(U)(G)...5'] may represent the termination signal for L mRNA synthesis (R. A. Lazzarini, personal communication). Oligonucleotide 43 [3'...GUAUACUUUUUUU(G)...5'] corresponds to the sequence shown to be the N gene mRNA polyadenylation signal (D. J. McGeoch, Cell 17:673-681, 1979). The other three oligonucleotides share a common feature with oligonucleotides 43 and 38, viz., a stretch of 6 or 7 U residues preceded by an AUAC sequence. Thus the sequence of oligonucleotide 3 is 3'...GAAUUAAUAUAAAAUUAAAAAUUAAAAAUACUUUUUU(U)(G)...5', whereas that of oligonucleotide 42 is 3'...GAUACUUUUUUUCAU(U)(G)...5', and that of oligonucleotide 44B is 3'...G(U)AUACUUUUUU(G)...5'. These sequence analyses suggest a common polyadenylation signal for the synthesis of all vesicular stomatitis virus mRNA species, i.e., the sequence (3')...AUACUUUUUU(U)...(5').
对三种水泡性口炎病毒印第安纳血清型小缺陷干扰(DI)颗粒RNA进行核糖核酸酶T(1)寡核苷酸指纹分析表明,它们仅具有源自病毒基因组5'区域的寡核苷酸。这些研究还表明,这三种DI RNA具有部分L基因序列以及两个未转录成L(或其他)mRNA种类的5'病毒寡核苷酸(59和70)(J.P. 克莱利和D.H.L. 毕晓普,《病毒学杂志》30:116 - 123,1979年)。对大DI RNA(LT DI)的分析揭示了不同的起源。LT DI RNA除了至少一个5'-近端L基因寡核苷酸(47)外,还具有源自基因组3'端的寡核苷酸(包括为N、NS、M和G基因鉴定的所有大寡核苷酸),以及在mRNA - 病毒RNA双链体形成后未被核酸酶消化保护的所有七个寡核苷酸(3、38、42、43、44B、59和70)(克莱利和毕晓普)。因此,LT RNA的起源似乎涉及从病毒RNA中删除内部L基因序列。已对几种水泡性口炎病毒RNA寡核苷酸进行了寡核苷酸序列分析,包括未转录成mRNA的所有七个(3、38、42、43、44B、59和70)。分析证实寡核苷酸59 [3'...GAACACCAAAAAUAAAAAAUA(G)...5']和70 [3'...GACCAAAACACCA(G)...5']位于病毒基因组的5'-末端区域。寡核苷酸38 [¾...GAAAUUCAUACUUUUUU(U)(G)...5']可能代表L mRNA合成的终止信号(R.A. 拉扎里尼个人交流)。寡核苷酸43 [3'...GUAUACUUUUUUU(G)...5']对应于显示为N基因mRNA聚腺苷酸化信号的序列(D.J. 麦吉奥克,《细胞》17:673 - 681,1979年)。其他三个寡核苷酸与寡核苷酸43和38具有共同特征,即一段6或7个U残基,前面是AUAC序列。因此,寡核苷酸3的序列是3'...GAAUUAAUAUAAAAUUAAAAAUUAAAAAUACUUUUUU(U)(G)...5',而寡核苷酸42的序列是3'...GAUACUUUUUUUCAU(U)(G)...5',寡核苷酸44B的序列是3'...G(U)AUACUUUUUU(G)...5'。这些序列分析表明所有水泡性口炎病毒mRNA种类合成具有共同的聚腺苷酸化信号,即序列(3')...AUACUUUUUU(U)...(5')。