Ihara S, Takekoshi M, Mori N, Sakuma S, Hashimoto J, Watanabe Y
Division of Molecular Life Science, Tokai University, School of Medicine, Kanagawa, Japan.
Arch Virol. 1994;137(3-4):263-75. doi: 10.1007/BF01309474.
The human cytomegalovirus (strain Towne) temperature-sensitive mutant ts 256 exhibits a virus specific DNA polymerase-negative phenotype. The position of the mutation of ts 256 was determined by three step marker-rescue assays to be within a 5.1 kb XbaI-BamHI fragment between map unit 0.33 and 0.35 in a HindIII-D fragment located in a long unique region. Nucleotide sequencing showed that the 5.1 kb fragment contained three open reading frames corresponding to those of the genes for UL52, UL53 and UL54 (DNA polymerase gene), respectively, of strain AD169. The functions of UL52 and UL53 are unknown. Comparison of the DNA sequences of the 5.1 kb fragments of the wild-type and ts 256 mutant revealed two base changes within UL53 and UL54, respectively, which result in amino acid substitutions. The mutation in the UL54 gene was located within a distinct conserved region VI common to alpha-like DNA polymerases, suggesting that this base change would be responsible for DNA negative phenotype.
人巨细胞病毒(汤氏株)温度敏感突变体ts 256表现出病毒特异性DNA聚合酶阴性表型。通过三步标记拯救试验确定ts 256的突变位置在位于长单一区域的HindIII-D片段中、图谱单位0.33至0.35之间的一个5.1 kb XbaI-BamHI片段内。核苷酸测序表明,该5.1 kb片段分别包含与AD169株的UL52、UL53和UL54(DNA聚合酶基因)基因相对应的三个开放阅读框。UL52和UL53的功能尚不清楚。野生型和ts 256突变体的5.1 kb片段的DNA序列比较分别揭示了UL53和UL54内的两个碱基变化,这导致了氨基酸取代。UL54基因中的突变位于α样DNA聚合酶共有的一个独特保守区域VI内,表明这种碱基变化可能是DNA阴性表型的原因。