Kowenz-Leutz E, Herr P, Niss K, Leutz A
Max-Delbrück-Centrum for Molecular Medicine, Berlin, Germany.
Cell. 1997 Oct 17;91(2):185-95. doi: 10.1016/s0092-8674(00)80401-8.
The homeobox gene GBX2 was identified as a target gene of the v-Myb oncoprotein encoded by the avian myeloblastosis virus (AMV). GBX2 activation by c-Myb requires signal transduction emanating from the cell surface while the leukemogenic AMV v-Myb constitutively induces the GBX2 gene. Mutations in the DNA binding domain of AMV-Myb render it independent of signaling events and concomitantly abrogate the collaboration between Myb and CCAAT Enhancer Binding Proteins (C/EBP), which are involved in granulocyte differentiation. Ectopic expression of GBX2 in growth factor-dependent myeloblasts induces monocytic features and independence from exogenous cytokines, reflecting distinct features of AMV-transformed cells. Our results suggest that Myb or factors it interacts with contribute to hematopoietic lineage choice and differentiation in a signal transduction-dependent fashion.
同源框基因GBX2被确定为禽成髓细胞瘤病毒(AMV)编码的v-Myb癌蛋白的靶基因。c-Myb对GBX2的激活需要细胞表面发出的信号转导,而致白血病的AMV v-Myb则组成性地诱导GBX2基因。AMV-Myb的DNA结合结构域中的突变使其独立于信号事件,并同时消除了Myb与参与粒细胞分化的CCAAT增强子结合蛋白(C/EBP)之间的协作。GBX2在生长因子依赖性成髓细胞中的异位表达诱导单核细胞特征并对外源细胞因子产生独立性,反映了AMV转化细胞的独特特征。我们的结果表明,Myb或与其相互作用的因子以信号转导依赖的方式促进造血谱系选择和分化。