Lipsick J S
J Virol. 1987 Oct;61(10):3284-7. doi: 10.1128/JVI.61.10.3284-3287.1987.
The v-myb oncogene of avian myeloblastosis virus transforms myeloid cells exclusively, both in vivo and in vitro. The c-myb proto-oncogene from which v-myb arose is expressed at relatively high levels in immature hematopoietic cells of the lymphoid, erythroid, and myeloid lineages but not in myeloblasts transformed by v-myb. This finding suggested that the nuclear v-myb gene product p48v-myb might act directly to inhibit the normal expression of the c-myb gene. I have therefore used a selectable avian retroviral vector to express p48v-myb in avian erythroblasts which normally express high levels of the c-myb gene product p75c-myb. The results demonstrate that p48v-myb and p75c-myb can be coexpressed in the nuclei of cloned cells. Therefore, p48v-myb does not invariably prevent the expression of p75c-myb.
禽成髓细胞瘤病毒的v-myb癌基因在体内和体外均仅转化髓样细胞。v-myb起源的c-myb原癌基因在淋巴、红系和髓系谱系的未成熟造血细胞中相对高水平表达,但在v-myb转化的成髓细胞中不表达。这一发现表明,核v-myb基因产物p48v-myb可能直接作用以抑制c-myb基因的正常表达。因此,我使用了一种可选择的禽逆转录病毒载体在通常表达高水平c-myb基因产物p75c-myb的禽成红细胞中表达p48v-myb。结果表明,p48v-myb和p75c-myb可以在克隆细胞核中共表达。因此,p48v-myb并非总是阻止p75c-myb的表达。