Tu Jun, Sunter Garry
Department of Biology, The University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249, USA.
Virology. 2007 Oct 10;367(1):117-25. doi: 10.1016/j.virol.2007.04.018. Epub 2007 May 25.
We have identified a nine base pair sequence in Tomato golden mosaic virus that is required for binding of nuclear proteins from tobacco and Arabidopsis to viral DNA. The sequence is located within the promoter for a 0.7 kb complementary sense mRNA (AL-1629). Mutation of the binding site results in a two- to six-fold reduction in the accumulation of AL-1629 mRNA, leading to reduced AL2 and AL3 gene expression. Viral sequences located immediately adjacent to the core binding site appear to influence AL2 and AL3 expression, but retain some binding affinity to a soluble host protein(s). The ability of a nuclear protein(s) to bind sequences within the AL-1629 promoter correlates with efficient viral DNA replication, as mutation of these sequences results in reduced viral DNA levels. Analysis of begomo- and curtoviruses indicates extensive conservation of this binding site, which suggests a common mechanism regulating expression of two viral genes involved in replication and suppression of host defense responses.
我们在番茄金色花叶病毒中鉴定出一段9个碱基对的序列,烟草和拟南芥的核蛋白与病毒DNA结合需要该序列。该序列位于一个0.7 kb互补有义mRNA(AL-1629)的启动子内。结合位点的突变导致AL-1629 mRNA积累减少两到六倍,从而导致AL2和AL3基因表达降低。紧邻核心结合位点的病毒序列似乎会影响AL2和AL3的表达,但仍保留对一种或多种可溶性宿主蛋白的一些结合亲和力。一种或多种核蛋白与AL-1629启动子内序列结合的能力与有效的病毒DNA复制相关,因为这些序列的突变会导致病毒DNA水平降低。对菜豆金色花叶病毒属病毒和矮缩病毒属病毒的分析表明,该结合位点具有广泛的保守性,这表明存在一种共同机制来调节参与复制和抑制宿主防御反应的两个病毒基因的表达。