Calothy G, Laugier D, Cross F R, Jove R, Hanafusa T, Hanafusa H
J Virol. 1987 May;61(5):1678-81. doi: 10.1128/JVI.61.5.1678-1681.1987.
Previous studies showed that the amino-terminal domain of Rous sarcoma virus p60v-src involved in myristylation and membrane association of the protein is required for morphological transformation and anchorage independence. Analysis of src delection mutants revealed that the amino-terminal one-third of p60v-src, including the membrane-binding domain, is not essential for induction of cell proliferation. These results demonstrated that, in contrast to the cellular target(s) involved in morphological transformation and anchorage independence, the target(s) involved in mitogenic activity is accessible to nonmyristylated src proteins.
先前的研究表明,劳氏肉瘤病毒p60v-src的氨基末端结构域参与蛋白质的肉豆蔻酰化和膜结合,是形态转化和锚定非依赖性所必需的。对src缺失突变体的分析表明,p60v-src的氨基末端三分之一,包括膜结合结构域,对于诱导细胞增殖并非必需。这些结果表明,与参与形态转化和锚定非依赖性的细胞靶点相反,参与有丝分裂活性的靶点可被非肉豆蔻酰化的src蛋白所作用。