Datta R, Sherman M L, Stone R M, Kufe D
Laboratory of Clinical Pharmacology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115.
Cell Growth Differ. 1991 Jan;2(1):43-9.
The AP-1 protein complex binds to specific DNA sequences that regulate transcription of genes responsive to certain growth factors and phorbol esters. This complex is composed of products of the jun and fos gene families. The present studies have examined the effects of 12-O-tetradecanoylphorbol-13-acetate (TPA) on the regulation of jun-B gene expression during induction of monocytic differentiation. Low levels of jun-B transcripts were present in uninduced HL-60 promyelocytic leukemia cells. In contrast, treatment with TPA was associated with rapid increases in jun-B mRNA levels that were maximal at 3 h and remained elevated at 48 h. The induction of jun-B expression by TPA in these cells preceded that of the c-jun and c-fos genes. Similar increases in jun-B transcripts were detectable in TPA-treated THP-1 and U-937 myeloid leukemia cells, although expression of this gene was transient in the more differentiated THP-1 cells. Run-on assays demonstrated low levels of jun-B gene activation in untreated HL-60 cells, whereas TPA treatment was associated with a 6-fold increase in the transcription rate of this gene. This induction of jun-B expression occurred in the absence of de novo protein synthesis. In contrast, inhibition of protein synthesis was associated with superinduction of TPA-induced jun-B mRNA levels and an increase in stability of this transcript. These findings suggest that jun-B gene expression is regulated at both the transcriptional and posttranscriptional levels during induction of monocytic differentiation.(ABSTRACT TRUNCATED AT 250 WORDS)
AP-1蛋白复合物与特定的DNA序列结合,这些序列可调节对某些生长因子和佛波酯有反应的基因的转录。该复合物由jun和fos基因家族的产物组成。本研究检测了12-O-十四酰佛波醇-13-乙酸酯(TPA)在单核细胞分化诱导过程中对jun-B基因表达调控的影响。未诱导的HL-60早幼粒细胞白血病细胞中存在低水平的jun-B转录本。相比之下,用TPA处理后,jun-B mRNA水平迅速升高,在3小时时达到最高,并在48小时时仍保持升高。TPA在这些细胞中诱导jun-B表达先于c-jun和c-fos基因。在TPA处理的THP-1和U-937髓系白血病细胞中也可检测到类似的jun-B转录本增加,尽管该基因在分化程度更高的THP-1细胞中的表达是短暂的。核转录分析表明,未处理的HL-60细胞中jun-B基因的激活水平较低,而TPA处理使该基因的转录速率增加了6倍。jun-B表达的这种诱导在没有从头合成蛋白质的情况下发生。相反,蛋白质合成的抑制与TPA诱导的jun-B mRNA水平的超诱导以及该转录本稳定性的增加有关。这些发现表明,在单核细胞分化诱导过程中,jun-B基因的表达在转录和转录后水平均受到调控。(摘要截短于250字)