Kuge S, Nomoto A
J Virol. 1987 May;61(5):1478-87. doi: 10.1128/JVI.61.5.1478-1487.1987.
A number of deletion and insertion sequences were introduced into the 5' noncoding sequence (742 nucleotides long) of the genome of the Sabin strain of type 1 poliovirus by using an infectious cDNA clone of the virus strain. The genomes of all three poliovirus serotypes contained highly homologous sequences (nucleotide positions 509 to 639) as well as highly variable sequences (positions 640 to 742) in the 5' noncoding region. The viability of mutant viruses was tested by transfecting mutant cDNA clones into African green monkey kidney cells and then estimating the plaque sizes displayed on the cells. The results suggested that the highly variable sequence next to the VP4 coding region did not play an important role, at least in the in vitro culture system used, that the loci of highly conserved nucleotide sequences were not always expected to be the genome regions essential for viral replication, that the sequence between positions 564 and 599 carried genetic information to maintain the efficiency of certain steps in viral replication, and that the sequence between positions 551 to 563 might play an essential role in viral replication. Four-base deletion or insertion mutations were introduced into relatively variable sequences in the genome region upstream of position 509. The results suggest that variable sequences do not always indicate that the corresponding genome regions are less important. Apparent revertants (large-plaque variants) were easily generated from one of the viable mutants with the small-plaque phenotype. The determination of nucleotide sequences of the revertant genomes revealed the second mutation site. The results suggested that the different loci at around positions 200 and 500 might specifically interact with each other. This interaction may result in the formation of a functional structure that influences the efficiency of certain steps in the viral replication.
通过使用1型脊髓灰质炎病毒Sabin株的感染性cDNA克隆,将一些缺失和插入序列引入该病毒株基因组的5'非编码序列(742个核苷酸长)中。所有三种脊髓灰质炎病毒血清型的基因组在5'非编码区都包含高度同源序列(核苷酸位置509至639)以及高度可变序列(位置640至742)。通过将突变cDNA克隆转染到非洲绿猴肾细胞中,然后估计细胞上显示的噬斑大小来测试突变病毒的活力。结果表明,至少在所使用的体外培养系统中,VP4编码区旁边的高度可变序列没有发挥重要作用;高度保守核苷酸序列的位点并不总是预期为病毒复制所必需的基因组区域;564至599位之间的序列携带维持病毒复制某些步骤效率的遗传信息;551至563位之间的序列可能在病毒复制中起关键作用。在509位上游的基因组区域中相对可变的序列中引入了四碱基缺失或插入突变。结果表明,可变序列并不总是表明相应的基因组区域不太重要。从具有小噬斑表型的一种存活突变体中很容易产生明显的回复体(大噬斑变体)。回复体基因组核苷酸序列的测定揭示了第二个突变位点。结果表明,200位和500位左右的不同位点可能会特异性地相互作用。这种相互作用可能导致形成一种功能结构,影响病毒复制某些步骤的效率。