Smith M W, Ito M, Yamada T, Suzuki T, Komamine A
Biological Institute, Faculty of Science, Tohoku University, Sendai, Japan.
Plant Physiol. 1993 Mar;101(3):809-17. doi: 10.1104/pp.101.3.809.
A cDNA clone was isolated from a carrot (Daucus carota L.) cDNA expression library using monoclonal antibody 21D7, which recognizes a nuclear antigen associated with cell division in plant cells. To show that the isolated cDNA encodes the 21D7 antigen, a polyclonal antiserum was raised against a recombinant fusion protein specified by the cDNA. Both the polyclonal antiserum and the monoclonal antibody 21D7 recognized the same plant protein on immunoblots, in immunoprecipitation experiments, and in peptide mapping. Analysis of the cDNA revealed that the deduced amino acid sequence has 45% identity to the predicted sequence of the mouse transplantation antigen P91A from mutant tumor cells that is responsible for the immune rejection of the corresponding cell clone in a syngeneic mouse. The expression of the plant cDNA at the mRNA level was highly correlated with cell proliferation. In suspension cultures of Catharanthus roseus (L.) G Don. cells, the highest level of expression was observed during the midlogarithmic phase of growth. When auxin was added to stimulate cell division of auxin-starved cells arrested in the G1 phase, transcription was immediately enhanced, and the level of expression remained high throughout the G1 and S phases and dropped dramatically at the end of DNA replication.
利用单克隆抗体21D7从胡萝卜(Daucus carota L.)cDNA表达文库中分离出一个cDNA克隆,该抗体可识别与植物细胞中细胞分裂相关的核抗原。为了证明分离出的cDNA编码21D7抗原,制备了针对该cDNA所指定的重组融合蛋白的多克隆抗血清。在免疫印迹、免疫沉淀实验和肽图谱分析中,多克隆抗血清和单克隆抗体21D7都识别同一种植物蛋白。对该cDNA的分析表明,推导的氨基酸序列与来自突变肿瘤细胞的小鼠移植抗原P91A的预测序列有45%的同一性,P91A负责同基因小鼠中相应细胞克隆的免疫排斥。植物cDNA在mRNA水平的表达与细胞增殖高度相关。在长春花(Catharanthus roseus (L.) G Don.)细胞的悬浮培养中,在生长的对数中期观察到最高表达水平。当添加生长素以刺激停滞在G1期的生长素饥饿细胞进行细胞分裂时,转录立即增强,并且表达水平在整个G1和S期都保持较高,在DNA复制结束时急剧下降。