McGeoch D J, Dalrymple M A, Dolan A, McNab D, Perry L J, Taylor P, Challberg M D
Institute of Virology, University of Glasgow, United Kingdom.
J Virol. 1988 Feb;62(2):444-53. doi: 10.1128/JVI.62.2.444-453.1988.
Recently, a method has been developed to identify regions in the genome of herpes simplex virus type 1 (HSV-1) which contain genes required for DNA synthesis from an HSV-1 origin of DNA replication, and seven genomic loci have been identified as representing the necessary and sufficient gene set for such replication (C. A. Wu, N. J. Nelson, D. J. McGeoch, and M. D. Challberg, J. Virol. 62:435-443, 1988). Two of the loci represent the well-known genes for DNA polymerase and major DNA-binding protein, but the remainder had little or no previous characterization. In this report we present the DNA sequences of the five newly identified genes and their deduced transcript organizations and encoded amino acid sequences. These genes were designated UL5, UL8, UL9, UL42, and UL52 and were predicted to encode proteins with molecular weights of, respectively, 99,000, 80,000, 94,000, 51,000, and 114,000. All of these genes had clear counterparts in the genome of the related alphaherpesvirus varicella-zoster virus, but only UL5 and UL52 were detectably conserved in the distantly related gammaherpesvirus Epstein-Barr virus, as judged by amino acid sequence similarity. The sequence of the UL5 protein, and of its counterparts in the other viruses, contained a region closely resembling known ATP-binding sites; this could be indicative, for instance, of a helicase or primase activity.
最近,已开发出一种方法来鉴定单纯疱疹病毒1型(HSV-1)基因组中包含从HSV-1 DNA复制起点进行DNA合成所需基因的区域,并且已鉴定出七个基因组位点代表了这种复制所需的必要且充分的基因集(C.A. Wu、N.J. Nelson、D.J. McGeoch和M.D. Challberg,《病毒学杂志》62:435 - 443,1988年)。其中两个位点代表了众所周知的DNA聚合酶基因和主要DNA结合蛋白基因,但其余位点此前几乎没有或没有任何特征描述。在本报告中,我们展示了五个新鉴定基因的DNA序列及其推导的转录本结构和编码的氨基酸序列。这些基因被命名为UL5、UL8、UL9、UL42和UL52,预计分别编码分子量为99,000、80,000、94,000、51,000和114,000的蛋白质。所有这些基因在相关的α疱疹病毒水痘带状疱疹病毒的基因组中都有明确的对应物,但根据氨基酸序列相似性判断,在远缘相关的γ疱疹病毒爱泼斯坦 - 巴尔病毒中,只有UL5和UL52可检测到保守。UL5蛋白及其在其他病毒中的对应物的序列包含一个与已知ATP结合位点非常相似的区域;例如,这可能表明具有解旋酶或引发酶活性。