Roovers D J, Young C S, Vos H L, Sussenbach J S
Laboratory for Physiological Chemistry, State University of Utrecht, The Netherlands.
Virus Genes. 1990 Jun;4(1):53-61. doi: 10.1007/BF00308565.
We have determined the exact nature of two thermosensitive (ts) adenovirus mutants, H5ts19 and H5ts149, which map to different genes in the E2 transcription unit. The H5ts19 mutation appears to stem from a single base-pair change of A-T to G-C at position 1840 (numbering as in ref. 1), corresponding to codon 154 of the gene coding for DBP. This results in a glutamine-to-arginine change in the amino-terminal domain of the protein. H5ts19 is defective in a late stage of infection, during virus assembly. This phenotype strongly differs from that described for the limited number of known DBP mutants, indicating that DBP is not only functional during DNA replication, but also plays a role in the late phase of the infection cycle. The defect of the (N group) mutant H5ts149 affects the initiation of viral DNA replication. Marker rescue experiments followed by nucleotide sequence analysis of H5ts149 DNA revealed a single point mutation in the gene coding for the Ad pol. A transition of C-G to A-T at position 7563 (numbering as in ref. 2) changes amino acid residue 411 of Ad pol, a leucine residue, to phenylalanine. This mutation is located in a region conserved among various DNA polymerases, which suggests an important role of this domain in DNA replication.
我们已经确定了两种温度敏感(ts)腺病毒突变体H5ts19和H5ts149的确切性质,它们定位于E2转录单元的不同基因。H5ts19突变似乎源于第1840位(编号如参考文献1)的A-T到G-C的单碱基对变化,对应于编码DBP的基因的第154密码子。这导致该蛋白质氨基末端结构域中的谷氨酰胺变为精氨酸。H5ts19在感染后期病毒组装过程中存在缺陷。这种表型与已知的有限数量的DBP突变体所描述的表型有很大不同,表明DBP不仅在DNA复制过程中起作用,而且在感染周期的后期也发挥作用。(N组)突变体H5ts149的缺陷影响病毒DNA复制的起始。对H5ts149 DNA进行核苷酸序列分析后进行的标记拯救实验揭示了编码腺病毒聚合酶(Ad pol)的基因中的一个单点突变。第7563位(编号如参考文献2)的C-G到A-T的转换将Ad pol的氨基酸残基411(一个亮氨酸残基)变为苯丙氨酸。该突变位于各种DNA聚合酶中保守的区域,这表明该结构域在DNA复制中起重要作用。