Kemp L M, Latchman D S
Department of Biochemistry, University College, London, UK.
EMBO J. 1988 Dec 20;7(13):4239-44. doi: 10.1002/j.1460-2075.1988.tb03321.x.
The gene encoding the U3 SnRNA is transcriptionally induced early in infection with herpes simplex virus (HSV). This effect is due to the action of the HSV virion protein Vmw65 and is dependent upon the octamer motif in the U3 promoter. In contrast the U1 SnRNA gene which also contains an octamer is not activated by Vmw65 in infections or transfections. We show that this is due to sequence differences between the octamers in the U1 and U3 genes. Thus the U3 octamer can confer responsiveness to Vmw65 to truncated U1 or U3 promoters whereas the U1 octamer cannot. The use of Vmw65 as a tool to analyse the role of the octamer sequence in mediating a variety of expression patterns in different genes is discussed.
编码U3 SnRNA的基因在单纯疱疹病毒(HSV)感染早期会被转录诱导。这种效应是由于HSV病毒体蛋白Vmw65的作用,并且依赖于U3启动子中的八聚体基序。相比之下,同样含有八聚体的U1 SnRNA基因在感染或转染过程中不会被Vmw65激活。我们发现这是由于U1和U3基因中八聚体之间的序列差异所致。因此,U3八聚体可以赋予截短的U1或U3启动子对Vmw65的反应性,而U1八聚体则不能。本文讨论了使用Vmw65作为工具来分析八聚体序列在介导不同基因的多种表达模式中的作用。