Palese P, Schulman J L
J Virol. 1976 Mar;17(3):876-84. doi: 10.1128/JVI.17.3.876-884.1976.
Analysis of the segmented RNAs of influenza A viruses by electrophoresis on polyacrylamide urea slab gels has provided a method for sharper resolution of the number and migration rates of different segments than previously has been possible. Using this system, the RNA genome of influenza A/WSN (HON1) virus can be separated into seven to nine separate bands, depending on whether virus is obtained after high or low multiplicity of infection, and the genome of influenza A/PR/8 (HON1) virus can be resolved into eight bands, six of which migrate differently from comparable RNA bands of WSN virus. Comparision of the RNA patterns produced by influenza A/PR/8 (HON1) and A/England/42/72 (H8n2) virus also reveals major differences in migration speeds of different bands, and analysis of the RNAs of the RNAs of an HON2 recombinant virus derived from these two strains permits the identification of RNA segments which have been derived from one particular parent. By extension of these techniques, it may be possible to define which RNA segment codes for each viral protein and to analyze recombinant strains to identify which genes have been derived from each of its parents.
通过在聚丙烯酰胺尿素平板凝胶上进行电泳分析甲型流感病毒的分段RNA,提供了一种比以往更清晰地分辨不同片段数量和迁移速率的方法。使用该系统,甲型流感病毒A/WSN(H1N1)的RNA基因组可根据感染复数高低分为七至九条不同的条带,甲型流感病毒A/PR/8(H1N1)的基因组可分为八条带,其中六条与WSN病毒的可比RNA带迁移不同。比较甲型流感病毒A/PR/8(H1N1)和A/England/42/72(H8N2)产生的RNA图谱也揭示了不同条带迁移速度的主要差异,对源自这两个毒株的H1N2重组病毒的RNA分析允许识别来自一个特定亲本的RNA片段。通过扩展这些技术,有可能确定每个病毒蛋白由哪个RNA片段编码,并分析重组毒株以识别其每个亲本的哪些基因。