Harel-Bellan A, Brini A T, Farrar W L
Laboratory of Molecular Immunoregulation, National Cancer Institute, Frederick Cancer Research Facility, MD 21701.
J Immunol. 1988 Aug 1;141(3):1012-7.
Proliferation of NSF-60.8 cells, a CSF-dependent murine myeloid cell line, is strongly inhibited by murine IFN-gamma. Northern analysis of growth arrested, NSF-60.8 cells activated by addition of CSF in the presence or absence of IFN-gamma indicated that IFN-gamma inhibited the induction of c-myc mRNA steady state level by CSF. The effect was observed as early as 30 min after induction and the inhibition was complete after 20 h. IFN-gamma did not impair the transcriptional activation of c-myc gene, and it had only a slight destabilizing effect on the mature c-myc message. Study of the processing steps of c-myc mRNA precursor indicated that in the presence of IFN-gamma, a putative 3.6-kb splice intermediate accumulated instead of the mature message, suggesting that IFN-gamma inhibits the splicing of c-myc precursor.
NSF-60.8细胞是一种依赖集落刺激因子(CSF)的小鼠髓样细胞系,其增殖受到小鼠γ干扰素(IFN-γ)的强烈抑制。对在添加或不添加IFN-γ的情况下添加CSF激活的生长停滞的NSF-60.8细胞进行Northern分析表明,IFN-γ抑制了CSF对c-myc mRNA稳态水平的诱导。该效应在诱导后30分钟就可观察到,20小时后抑制作用完全。IFN-γ不会损害c-myc基因的转录激活,并且它对成熟的c-myc信使RNA只有轻微的去稳定化作用。对c-myc mRNA前体加工步骤的研究表明,在存在IFN-γ的情况下,一个假定的3.6 kb剪接中间体积累,而不是成熟的信使RNA,这表明IFN-γ抑制了c-myc前体的剪接。