Nakamura H, Yoshimura K, Bajocchi G, Trapnell B C, Pavirani A, Crystal R G
Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health Bethesda, MD 20892.
FEBS Lett. 1992 Dec 21;314(3):366-70. doi: 10.1016/0014-5793(92)81507-i.
Based on the knowledge that expression of the cystic fibrosis transmembrane conductance regulator (CFTR) gene can be modulated at the transcriptional level, and that the CFTR gene promoter contains sequences homologous to elements in other promoters that respond to tumor necrosis factor-alpha (TNF), we evaluated the hypothesis that TNF might modulate CFTR gene expression in epithelial cells. Studies with HT-29 cells, a colon epithelium-derived tumor cell line known to express the CFTR gene, demonstrated that TNF downregulated CFTR mRNA transcript levels in a dose- and time-dependent fashion. Interestingly, nuclear run-on analyses demonstrated that TNF did not affect the rate of transcription of CFTR gene, but exposure of the cells to TNF did modify the stability of CFTR mRNA transcripts, resulting in a mRNA half-life that was reduced to 65% of the resting level. These observations suggest that CFTR gene expression can be modulated by TNF, at least in part, at the posttranscriptional level.
基于囊性纤维化跨膜传导调节因子(CFTR)基因的表达可在转录水平受到调控,以及CFTR基因启动子含有与其他对肿瘤坏死因子-α(TNF)有反应的启动子中的元件同源的序列这一认识,我们评估了TNF可能调节上皮细胞中CFTR基因表达的假说。对HT-29细胞(一种已知表达CFTR基因的结肠上皮来源的肿瘤细胞系)的研究表明,TNF以剂量和时间依赖性方式下调CFTR mRNA转录水平。有趣的是,核转录分析表明TNF不影响CFTR基因的转录速率,但将细胞暴露于TNF确实改变了CFTR mRNA转录本的稳定性,导致mRNA半衰期降至静息水平的65%。这些观察结果表明,CFTR基因表达至少部分可在转录后水平受到TNF的调控。