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转染的人c-myc癌基因的表达抑制小鼠红白血病细胞系的分化。

Expression of a transfected human c-myc oncogene inhibits differentiation of a mouse erythroleukaemia cell line.

作者信息

Dmitrovsky E, Kuehl W M, Hollis G F, Kirsch I R, Bender T P, Segal S

出版信息

Nature. 1986;322(6081):748-50. doi: 10.1038/322748a0.

Abstract

The Friend-virus-derived mouse erythroleukaemia (MEL) cell lines represent transformed early erythroid precursors that can be induced to differentiate into more mature erythroid cells by a variety of agents including dimethyl sulphoxide (DMSO). There is a latent period of 12 hours after inducer is added, when 80-90% of the cells become irreversibly committed to the differentiation programme, undergoing several rounds of cell division before permanently ceasing to replicate. After DMSO induction, a biphasic decline in steady-state levels of c-myc and c-myb messenger RNAs occurs. Following the initial decrease in c-myc mRNA expression, the subsequent increase occurs in, and is restricted to, the G1 phase of the cell cycle. We sought to determine whether the down-regulation is a necessary step in chemically induced differentiation. Experiments reported here indicate that expression in MEL cells of a transfected human c-myc gene inhibits the terminal differentiation process.

摘要

源自弗瑞德病毒的小鼠红白血病(MEL)细胞系代表了转化的早期红系前体细胞,这些细胞可被包括二甲基亚砜(DMSO)在内的多种试剂诱导分化为更成熟的红系细胞。添加诱导剂后有12小时的潜伏期,在此期间80%-90%的细胞会不可逆地进入分化程序,在永久停止复制前经历几轮细胞分裂。DMSO诱导后,c-myc和c-myb信使RNA的稳态水平呈双相下降。在c-myc mRNA表达最初下降之后,随后的增加发生在细胞周期的G1期,并局限于该期。我们试图确定这种下调是否是化学诱导分化的必要步骤。此处报道的实验表明,转染的人c-myc基因在MEL细胞中的表达会抑制终末分化过程。

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