Shanks M, Tomenius K, Clapham D, Huskisson N S, Barker P J, Wilson I G, Maule A J, Lomonossoff G P
John Innes Institute, Norwich, United Kingdom.
Virology. 1989 Dec;173(2):400-7. doi: 10.1016/0042-6822(89)90552-7.
To investigate the mode of gene expression of red clover mottle virus (RCMV) middle component (M) RNA, we have synthesized an oligopeptide corresponding to the predicted carboxy-terminus of the RCMV counterparts of the cowpea mosaic virus (CPMV) 48K and 58K proteins. Using an antiserum raised against this synthetic oligopeptide, we have detected a 43-kDa protein in the 30,000 g pellet from extracts of RCMV-infected cowpea protoplasts. Immunogold cytochemistry further localized this protein to the plasmodesmata of RCMV-infected pea tissue. This subcellular location, taken together with other evidence, suggests that this 43-kDa protein has a role in the cell-to-cell spread of RCMV.
为了研究红三叶草斑驳病毒(RCMV)中间组分(M)RNA的基因表达模式,我们合成了一种寡肽,该寡肽对应于豇豆花叶病毒(CPMV)48K和58K蛋白的RCMV对应物预测的羧基末端。使用针对这种合成寡肽产生的抗血清,我们在RCMV感染的豇豆原生质体提取物的30,000 g沉淀中检测到一种43 kDa的蛋白质。免疫金细胞化学进一步将该蛋白质定位到RCMV感染的豌豆组织的胞间连丝中。这种亚细胞定位,连同其他证据,表明这种43 kDa的蛋白质在RCMV的细胞间传播中起作用。