Markowitz R B, Tolbert S, Dynan W S
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215.
J Virol. 1990 May;64(5):2411-5. doi: 10.1128/JVI.64.5.2411-2415.1990.
The archetypal strain of BK virus directed very little early gene expression compared with rearranged laboratory strains of the virus. One laboratory strain that was analyzed in detail contained newly created AP-1 binding enhancer modules spanning the junction between adjacent sequence repeats. Introduction of these sequences into the archetype activated the previously quiescent early promoter.
与病毒的重排实验室菌株相比,BK病毒的原型菌株早期基因表达非常少。详细分析的一种实验室菌株包含跨越相邻序列重复之间连接处的新创建的AP-1结合增强子模块。将这些序列导入原型激活了先前静止的早期启动子。