Pellock B J, Lu A, Meagher R B, Weise M J, Miller L K
Department of Genetics, University of Georgia, Athens 30602-2603, USA.
Virology. 1996 Feb 1;216(1):146-57. doi: 10.1006/viro.1996.0041.
We have sequenced a 5.5-kb region of the DNA genome of the Spodoptera Ascovirus (SAV) containing a DNA polymerase gene. The gene codes for a 1104-amino-acid polypeptide with seven motifs characteristic of DNA polymerases and three additional motifs associated with polymerases possessing 3' to 5' exonuclease activity. The SAV DNA polymerase gene was able to functionally substitute for a baculovirus DNA polymerase gene in a transient assay that relies on origin-specific reporter plasmid DNA replication. Analysis of the predicted DNA polymerase sequence using neighbor-joining and protein parsimony algorithms indicated that this gene was only distantly related to other known viral and cellular DNA polymerases. The SAV DNA polymerase gene is the first ascovirus gene to be identified and sequenced. The molecular phylogenetic analyses of this gene supports the placement of insect ascoviruses in a separate virus family.
我们对含有DNA聚合酶基因的草地贪夜蛾正痘病毒(SAV)DNA基因组的一个5.5kb区域进行了测序。该基因编码一个1104个氨基酸的多肽,具有DNA聚合酶的七个特征基序以及与具有3'至5'核酸外切酶活性的聚合酶相关的另外三个基序。在依赖于特定原点报告质粒DNA复制的瞬时测定中,SAV DNA聚合酶基因能够功能性替代杆状病毒DNA聚合酶基因。使用邻接法和蛋白质简约算法对预测的DNA聚合酶序列进行分析表明,该基因与其他已知的病毒和细胞DNA聚合酶只有远缘关系。SAV DNA聚合酶基因是第一个被鉴定和测序的正痘病毒基因。对该基因的分子系统发育分析支持将昆虫正痘病毒置于一个单独的病毒科中。