Usharani K S, Periasamy M, Malathi V G
Plant Virology Unit, Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi 110 012, India.
Virus Res. 2006 Aug;119(2):154-62. doi: 10.1016/j.virusres.2005.12.013. Epub 2006 Feb 3.
The AV promoter expressing AV1 and AV2 genes and AC1 promoter expressing AC1 gene are present in opposite orientation in the intergenic region of Mungbean yellow mosaic India virus (MYMIV). Transient Agrobacterium-mediated delivery of putative promoter constructs into Nicotiana benthamiana and different legumes, followed by reporter gene (beta-d-glucuronidase, GUS) assay, identified the promoter region of both AC1 and AV genes that is necessary for transcriptional initiation. Transcription activator protein-independent activity of AV promoter and differential regulation of AC1 promoter are unique to MYMIV. The AV promoter is a composite core promoter having both TATA box and Initiator elements (TATA(+)Inr(+)). Many transcription factor binding sites were identified in the upstream promoter sequences of both virion and complementary sense genes, which might be used in the transcription regulation studies of the host plant as well as the virus.
表达AV1和AV2基因的AV启动子以及表达AC1基因的AC1启动子,以相反的方向存在于印度绿豆黄花叶病毒(MYMIV)的基因间隔区。通过农杆菌介导将推定的启动子构建体瞬时导入本氏烟草和不同豆科植物,随后进行报告基因(β - D - 葡萄糖醛酸酶,GUS)检测,确定了AC1和AV基因启动子区域对于转录起始是必需的。AV启动子的转录激活蛋白非依赖性活性以及AC1启动子的差异调控是MYMIV所特有的。AV启动子是一个具有TATA盒和起始子元件(TATA(+)Inr(+))的复合核心启动子。在病毒粒子基因和互补链基因的上游启动子序列中鉴定出许多转录因子结合位点,这可能用于宿主植物以及病毒的转录调控研究。