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c‐Myc Interferes with the Commitment to Differentiation of Murine Erythroleukemia Cells at a Reversible Point

机译:c‐Myc在可逆点干扰小鼠红细胞白血病细胞分化的承诺

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摘要

When murine erythroleukemia (MEL) cells, containing the transferred rat c‐myc gene under the control of human metallothionein II gene promoter, are induced to differentiate with dimethyl sulfoxide, the level of differentiation is dependent on the c‐Myc level, which is modulated by the addition of Zn ions. In this work, we examined the point of inhibition of differentiation by elevated levels of c‐Myc in one (clone 38‐2) of the typical transformants. Commitment assay indicated that elevated levels of c‐Myc interfere with entry of the transformant into the commitment event, but when c‐myc expression was reduced by removing Zn ions from the medium, the cells could reenter the commitment program. However, once the cells were committed, such cells could not return to the uncommitted state. In addition, time‐dependent expression of two erythroid specific genes was inhibited by elevated levels of c‐Myc in time‐dependent manner. These results suggest that c‐Myc modulates MEL cell differentiation at a reversible point of commitment.
机译:当含有在人类金属硫蛋白II基因启动子控制下转移的大鼠c-myc基因的鼠红细胞白血病(MEL)细胞被二甲基亚砜诱导分化时,分化水平取决于c-Myc水平,该水平受到调节通过添加锌离子。在这项工作中,我们研究了一个典型克隆(克隆38-2)中c-Myc水平升高对分化的抑制作用。承诺分析表明,升高的c-Myc水平会干扰转化子进入承诺事件,但是当通过从培养基中去除Zn离子降低c-myc表达时,细胞可以重新进入承诺程序。但是,一旦提交了单元,则此类单元将无法返回未提交状态。此外,c-Myc水平的升高以时间依赖的方式抑制了两个红系特异基因的时间依赖表达。这些结果表明,c-Myc在可逆的承诺点调节MEL细胞分化。

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