Ness S A, Beug H, Graf T
Differentiation Programme, European Molecular Biology Laboratory, Heidelberg, Federal Republic of Germany.
Cell. 1987 Oct 9;51(1):41-50. doi: 10.1016/0092-8674(87)90008-0.
Chick myelomonocytic cells transformed by the v-myc oncogene resemble mature macrophages; those transformed by v-myb or v-myb,ets exhibit an immature phenotype. We have analyzed whether these oncogenes are capable of altering the differentiation phenotype of transformed cells by introducing both v-myc plus either v-myb or v-myb,ets into the same cells. Surprisingly, the doubly transformed cells were found to be essentially indistinguishable from cells transformed by v-myb or v-myb,ets alone even when they expressed a high level of v-myc protein. These results demonstrate that v-myb is dominant over v-myc and that, while v-myc induces cell proliferation without affecting differentiation, v-myb induces in the same target cells both proliferation and a block or reversal of differentiation.
由v-myc癌基因转化的鸡骨髓单核细胞类似于成熟巨噬细胞;由v-myb或v-myb、ets转化的细胞表现出未成熟表型。我们通过将v-myc与v-myb或v-myb、ets同时导入同一细胞,分析了这些癌基因是否能够改变转化细胞的分化表型。令人惊讶的是,即使双转化细胞表达高水平的v-myc蛋白,也发现它们与仅由v-myb或v-myb、ets转化的细胞基本无法区分。这些结果表明,v-myb对v-myc具有显性作用,并且,虽然v-myc诱导细胞增殖而不影响分化,但v-myb在相同的靶细胞中既诱导增殖又诱导分化阻滞或逆转。