Niman H L
Nature. 1984;307(5947):180-3. doi: 10.1038/307180a0.
It has recently been reported that the sequences of the sis oncogene of simian sarcoma virus (SSV) and of human platelet-derived growth factor (PDGF) are very similar, establishing the most solid link yet between the mitogenic actions of growth factors and the transforming proteins of retroviruses. To investigate molecular mechanisms of transformation I have produced antisera against synthetic peptides corresponding to segments of the protein sequences predicted by the nucleotide sequences of viral oncogenes. Applying this approach to the case of sis and PDGF, I report here the results of probing outdated human platelets with an antiserum directed against a synthetic peptide representing residues 139-155 of the predicted sequence of the SSV transforming protein, p28sis (ref. 3). I detected peptides of apparent molecular weights (MWs) 30,000 to 31,000 (30-31K) and 16-18K, which correspond to the apparent molecular weights of nonreduced and reduced PDGF. In addition, a peptide of MW 21,000 was detected in platelets and a protein of MW 56,000 was detected in SSV-infected marmoset cells.
最近有报道称,猿猴肉瘤病毒(SSV)的sis癌基因与人血小板衍生生长因子(PDGF)的序列非常相似,这在生长因子的促有丝分裂作用与逆转录病毒的转化蛋白之间建立了迄今为止最确凿的联系。为了研究转化的分子机制,我制备了针对合成肽的抗血清,这些合成肽对应于病毒癌基因核苷酸序列预测的蛋白质序列片段。将这种方法应用于sis和PDGF的情况,我在此报告用针对代表SSV转化蛋白p28sis预测序列第139 - 155位残基的合成肽的抗血清探测过期人血小板的结果。我检测到表观分子量(MW)为30,000至31,000(30 - 31K)和16 - 18K的肽段,它们分别对应于非还原和还原型PDGF的表观分子量。此外,在血小板中检测到一个分子量为21,000的肽段,在感染SSV的狨猴细胞中检测到一个分子量为56,000的蛋白质。