MacFarlane Stuart A, McGavin Wendy J
Plant Pathology Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, UK.
J Gen Virol. 2009 Mar;90(Pt 3):747-753. doi: 10.1099/vir.0.007195-0.
Two sets of infectious cDNA clones of raspberry bushy dwarf virus (RBDV) have been constructed, enabling either the synthesis of infectious RNA transcripts or the delivery of infectious binary plasmid DNA by infiltration of Agrobacterium tumefaciens. In whole plants and in protoplasts, inoculation of RBDV RNA1 and RNA2 transcripts led to a low level of infection, which was greatly increased by the addition of RNA3, a subgenomic RNA coding for the RBDV coat protein (CP). Agroinfiltration of RNA1 and RNA2 constructs did not produce a detectable infection but, again, inclusion of a construct encoding the CP led to high levels of infection. Thus, RBDV replication is greatly stimulated by the presence of the CP, a mechanism that also operates with ilarviruses and alfalfa mosaic virus, where it is referred to as genome activation. Mutation to remove amino acids from the N terminus of the CP showed that the first 15 RBDV CP residues are not required for genome activation. Other experiments, in which overlapping regions at the CP N terminus were fused to the monomeric red fluorescent protein, showed that sequences downstream of the first 48 aa are not absolutely required for genome activation.
已经构建了两组树莓矮化病毒(RBDV)的感染性cDNA克隆,这使得通过根癌农杆菌浸润来合成感染性RNA转录本或传递感染性二元质粒DNA成为可能。在整株植物和原生质体中,接种RBDV RNA1和RNA2转录本导致低水平的感染,而添加RNA3(一种编码RBDV外壳蛋白(CP)的亚基因组RNA)后感染水平大大提高。RNA1和RNA2构建体的农杆菌浸润未产生可检测到的感染,但同样,包含编码CP的构建体导致高水平的感染。因此,CP的存在极大地刺激了RBDV的复制,这种机制也在等轴不稳环斑病毒和苜蓿花叶病毒中起作用,在这些病毒中被称为基因组激活。去除CP N端氨基酸的突变表明,RBDV CP的前15个残基对于基因组激活不是必需的。其他实验中,CP N端的重叠区域与单体红色荧光蛋白融合,结果表明,前48个氨基酸下游的序列对于基因组激活不是绝对必需的。