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Construction of viable deletion and insertion mutants of the Sabin strain of type 1 poliovirus: function of the 5 noncoding sequence in viral replication.

机译:1型脊髓灰质炎病毒Sabin株可行的缺失和插入突变体的构建:5非编码序列在病毒复制中的功能。

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摘要

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.
机译:通过使用病毒株的传染性cDNA克隆,将许多缺失和插入序列引入到1型脊髓灰质炎病毒的萨宾株的基因组的5'非编码序列(长742个核苷酸)中。所有这三种脊髓灰质炎病毒血清型的基因组在5'非编码区均包含高度同源的序列(核苷酸位置509至639)以及高度可变的序列(位置640至742)。通过将突变的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,来测试突变病毒的生存能力。结果表明,至少在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,并非总是期望高度保守的核苷酸序列的基因座是基因组区域。病毒复制,位置564和599之间的序列携带遗传信息以维持某些步骤在病毒复制中的效率,并且位置551至563之间的序列可能在病毒复制中起重要作用。四碱基缺失或插入突变被引入到位置509上游的基因组区域的相对可变序列中。结果表明,可变序列并不总是表明相应的基因组区域重要性较低。从具有小噬斑表型的可行突变体之一容易产生表观回复株(大噬斑变体)。回复基因组核苷酸序列的确定揭示了第二个突变位点。结果表明,位置200和500附近的不同基因座可能会特异性地相互作用。这种相互作用可能导致功能结构的形成,该功能结构影响病毒复制中某些步骤的效率。

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