Bagby G C, Shaw G, Heinrich M C, Hefeneider S, Brown M A, DeLoughery T G, Segal G M, Band L
Molecular Hematology Laboratory, V.A. Medical Center, Portland, OR.
Prog Clin Biol Res. 1990;352:233-9.
To date, the notion that the AU rich motif in the 3' UT of GM-CSF mRNA can function as an IL-1 response element has not been adequately examined. We suspect that it must play some role because virtually all IL-1 inducible gene have AU rich 3' untranslated regions. Thus, we will continue to address these technical problems so that the hypothesis can be more clearly tested. Nonetheless, we can state with reasonable certainty that: 1) IL-1 induces expression of GM-CSF in EC by inducing accumulation of mRNA, 2) the GM-CSF gene is constitutively transcribed but the half life of the mRNA is short, 3) IL-1 induced mRNA accumulation results from stabilization of the transcript, 4) although most IL-1 responsive genes have AU-rich domains in their 3' untranslated regions, it is not yet clear that these AU-rich regions are sufficient to function as an IL-1 response element, and 5) murine L cells cannot be used for studies on the molecular biology of cytokine induction by IL-1.
迄今为止,GM-CSF mRNA 3'非翻译区中富含 AU 的基序可作为白细胞介素-1(IL-1)反应元件这一观点尚未得到充分研究。我们怀疑它必定发挥了某种作用,因为几乎所有 IL-1 诱导型基因的 3'非翻译区都富含 AU。因此,我们将继续解决这些技术问题,以便能更清晰地检验这一假说。尽管如此,我们可以有合理把握地指出:1)IL-1 通过诱导 mRNA 积累来诱导内皮细胞(EC)中 GM-CSF 的表达;2)GM-CSF 基因是组成型转录的,但 mRNA 的半衰期很短;3)IL-1 诱导的 mRNA 积累是转录本稳定化的结果;4)尽管大多数 IL-1 反应基因在其 3'非翻译区具有富含 AU 的结构域,但目前尚不清楚这些富含 AU 的区域是否足以作为 IL-1 反应元件发挥作用;5)小鼠 L 细胞不能用于 IL-1 诱导细胞因子分子生物学的研究。