Cavanagh H M, Gallagher C F, Spibey N
Department of Veterinary Pathology, University of Glasgow Veterinary School, U.K.
J Gen Virol. 1991 Sep;72 ( Pt 9):2121-7. doi: 10.1099/0022-1317-72-9-2121.
The genomic DNA of a vaccine strain of canine adenovirus type 2 (Vaxitas; ICI Tasman) has been shown to contain two copies of the E1a region, the second being at the far right end of the genome. DNA sequence analysis of the right terminal 2.8 kbp of this vaccine strain showed that numerous point mutations have occurred in the second copy, which would preclude the synthesis of any functional products. However, expression vectors in which the E1a promoter from the right terminus were linked to the chloramphenicol acetyltransferase gene showed that the promoter was fully functional. Furthermore, the activity of the reiterated E1a promoter was considerably greater than that of the normal E4 promoter. This dramatic change in the regulation of E4 expression may be an important factor in determining the altered host cell specificity displayed by this vaccine strain virus.
犬腺病毒2型疫苗株(Vaxitas;ICI塔斯马尼亚)的基因组DNA已被证明含有两个E1a区域拷贝,第二个位于基因组的最右端。对该疫苗株右末端2.8kbp的DNA序列分析表明,第二个拷贝中发生了许多点突变,这将阻止任何功能性产物的合成。然而,将来自右末端的E1a启动子与氯霉素乙酰转移酶基因相连的表达载体表明该启动子具有完全功能。此外,重复的E1a启动子的活性明显高于正常的E4启动子。E4表达调控的这种显著变化可能是决定该疫苗株病毒所表现出的宿主细胞特异性改变的一个重要因素。