Ibanez C E, Lipsick J S
Department of Pathology, University of California, San Diego, La Jolla 92093.
J Virol. 1988 Jun;62(6):1981-8. doi: 10.1128/JVI.62.6.1981-1988.1988.
The v-myb oncogene of avian myeloblastosis virus causes acute myelomonocytic leukemia in vivo and transforms only myeloid cells in vitro. Its product, p48v-myb, is a nuclear protein of unknown function. To determine structure-function relationships for this protein, we constructed a series of deletion mutants of v-myb, expressed them in retroviral vectors, and studied their biochemical and biological properties. We used these mutants to identify two separate domains of p48v-myb which had distinct roles in its accumulation in the cell nucleus. We showed that the viral sequences which normally encode both termini of p48v-myb were dispensible for transformation. In contrast, both copies of the highly conserved v-myb amino-terminal repeat were required for transformation. We also identified a carboxyl-terminal domain of p48v-myb which was required for the growth of v-myb-transformed myeloblasts in soft agar but not for morphological transformation.
禽成髓细胞瘤病毒的v-myb癌基因在体内可引发急性髓单核细胞白血病,在体外仅能转化髓系细胞。其产物p48v-myb是一种功能未知的核蛋白。为确定该蛋白的结构-功能关系,我们构建了一系列v-myb缺失突变体,将它们在逆转录病毒载体中表达,并研究其生化和生物学特性。我们利用这些突变体鉴定出p48v-myb的两个不同结构域,它们在该蛋白在细胞核中的积累过程中发挥着不同作用。我们发现,通常编码p48v-myb两端的病毒序列对于转化并非必需。相反,高度保守的v-myb氨基末端重复序列的两个拷贝对于转化是必需的。我们还鉴定出p48v-myb的一个羧基末端结构域,它对于v-myb转化的成髓细胞在软琼脂中的生长是必需的,但对于形态转化并非必需。