Bosselman R A, Verma I M
J Virol. 1980 Jan;33(1):487-93. doi: 10.1128/JVI.33.1.487-493.1980.
Purified virions of Moloney murine leukemia virus can synthesize genome-length double-stranded DNA in vitro. Two predominant species of long DNA transcripts, with average sizes of 9.1 and 8.5 kilobases (kb) can be identified. Both species of DNA contain the negative (complementary to viral RNA) and positive (same polarity as viral RNA) strands. However, only the negative strand of the 8.5-kb species can be identified if the synthesis of DNA is carried out in the presence of the drug actinomycin D. The 9.1-kb species appears to be slightly larger than the genomic RNA. If the linear double-stranded 9.1-kb species is treated with Escherichia coli exonuclease III and allowed to anneal, circular DNA molecules can be observed. Furthermore, polyadenylate-containing short genomic RNA fragments (0.5 to 1.0 kb) can anneal to both the 5' and the 3' termini of 9.1-kb complementary DNA. The polyadenylate moiety of the RNA fragments can be identified by tagging it with circular polyoma DNA containing polydeoxybromouridylic acid tails. Thus, the 9.1-kb complementary DNA transcript with two circular polyoma DNA molecules at its termini can be observed. However, when similar annealings are performed with 8.5-kb complementary DNA species, only one end of the resulting molecule has circular polyoma DNA. We conclude that the 9.1-kb complementary DNA species has a large terminal redundancy. The sequences involved in terminal redundancy appear to be derived from the 3' end of the genomic RNA.
莫洛尼鼠白血病病毒的纯化病毒粒子能在体外合成基因组长度的双链DNA。可鉴定出两种主要的长DNA转录本,平均大小分别为9.1和8.5千碱基(kb)。这两种DNA都含有负链(与病毒RNA互补)和正链(与病毒RNA极性相同)。然而,如果在放线菌素D存在的情况下进行DNA合成,那么只能鉴定出8.5-kb转录本的负链。9.1-kb转录本似乎比基因组RNA稍大一点。如果用大肠杆菌核酸外切酶III处理线性双链9.1-kb转录本并使其退火,就能观察到环状DNA分子。此外,含聚腺苷酸的短基因组RNA片段(0.5至1.0 kb)能与9.1-kb互补DNA的5'和3'末端退火。RNA片段的聚腺苷酸部分可用含聚脱氧溴尿苷酸尾巴的环状多瘤DNA进行标记来鉴定。因此,能观察到在其末端带有两个环状多瘤DNA分子的9.1-kb互补DNA转录本。然而,当用8.5-kb互补DNA转录本进行类似退火时,所得分子只有一端带有环状多瘤DNA。我们得出结论,9.1-kb互补DNA转录本具有大量末端冗余。参与末端冗余的序列似乎源自基因组RNA的3'末端。