Hastings K E, Millward S
J Virol. 1978 Nov;28(2):490-8. doi: 10.1128/JVI.28.2.490-498.1978.
During in vitro synthesis of reovirus mRNA by viral cores, methyl groups from S-adenosylmethionine are incorporated only into 5'-terminal cap structures, i.e., m7GpppGmCp.... Thus, mRNA synthesized in the presence of S-adenosyl-[methyl-3H]methionine is 3H labeled specifically at the 5' terminus. This circumstance was exploited in the determination of 5'-terminal nucleotide sequences. Seven 5'-terminal fragments derived by complete RNase T1, digestion of methyl-3Hlabeled mRNA were partially degraded with RNase T2, and the products were separated by electrophoresis-homochromatography. From the patterns formed by the methyl-3H-labeled RNase T2 products, the sequences of the seven RNase T1-generated fragments were deduced. All seven fragments started with the sequence m7GpppGmCUA, after which the sequences diverged, with a tendency to be either U-rich or A-rich. Their chain lengths ranged from 7 to 10 nucleotides (excluding the m7G residue), and none of them contained an initiator AUG triplet. The sequences obtained support the hypothesis that virion-associated oligonucleotides arise through abortive transcription of the viral genome. There is no apparent 5'-terminal sequence feature distinctive of early versus late mRNA species within the small-mRNA size class.
在病毒核心进行呼肠孤病毒mRNA的体外合成过程中,来自S-腺苷甲硫氨酸的甲基仅掺入5'-末端帽结构,即m7GpppGmCp.... 因此,在S-腺苷-[甲基-3H]甲硫氨酸存在下合成的mRNA在5'末端被特异性地3H标记。这种情况被用于确定5'-末端核苷酸序列。通过用RNase T1完全消化甲基-3H标记的mRNA得到的七个5'-末端片段用RNase T2进行部分降解,产物通过电泳-同系层析法分离。根据甲基-3H标记的RNase T2产物形成的图谱,推导了七个RNase T1产生的片段的序列。所有七个片段均以m7GpppGmCUA序列起始,此后序列 diverged,倾向于富含U或富含A。它们的链长范围为7至10个核苷酸(不包括m7G残基),并且它们均不包含起始AUG三联体。获得的序列支持这样的假设,即病毒体相关的寡核苷酸通过病毒基因组的流产转录产生。在小mRNA大小类别中,早期与晚期mRNA种类之间没有明显的5'-末端序列特征。