Szabo E, Preis L H, Brown P H, Birrer M J
NCI-Navy Medical Oncology Branch, Bethesda, Maryland 20814.
Cell Growth Differ. 1991 Oct;2(10):475-82.
Terminal differentiation of the leukemic cell lines U-937 and HL-60 by 12-O-tetradecanoylphorbol-13-acetate is accompanied by marked changes in gene expression. In this study, we demonstrate that the expression of jun and fos gene family members is induced with variable kinetics during 12-O-tetradecanoylphorbol-13-acetate induced differentiation, with c-jun expression best paralleling differentiation. The generation of AP-1 complexes, as measured by DNA binding activity, closely parallels morphological differentiation. Furthermore, the ability of these complexes to regulate gene expression is demonstrated by increased transcription from an AP-1 driven reporter construct and marked increases in the expression of endogenous AP-1 regulated genes. Differentiation assays using water soluble phorbol esters reveal that differentiation becomes irreversible soon after AP-1 appears. This tight correlation between c-jun expression, the generation of AP-1 activity, and differentiation suggests a critical role for this gene and transcriptional complex during this process.
白血病细胞系U - 937和HL - 60经12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导发生终末分化时,伴随着基因表达的显著变化。在本研究中,我们证明在12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导分化过程中,jun和fos基因家族成员的表达以可变动力学被诱导,其中c - jun的表达与分化最为平行。通过DNA结合活性测定的AP - 1复合物的生成与形态学分化密切平行。此外,这些复合物调节基因表达的能力通过AP - 1驱动的报告构建体转录增加以及内源性AP - 1调节基因表达的显著增加得以证明。使用水溶性佛波酯的分化试验表明,在AP - 1出现后不久,分化就变得不可逆。c - jun表达、AP - 1活性的产生与分化之间的这种紧密相关性表明该基因和转录复合物在此过程中起关键作用。