Casey J L, Hentze M W, Koeller D M, Caughman S W, Rouault T A, Klausner R D, Harford J B
Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, Bethesda, MD 20892.
Science. 1988 May 13;240(4854):924-8. doi: 10.1126/science.2452485.
The biosynthetic rates for both the transferrin receptor (TfR) and ferritin are regulated by iron. An iron-responsive element (IRE) in the 5' untranslated portion of the ferritin messenger RNA (mRNA) mediates iron-dependent control of its translation. In this report the 3' untranslated region of the mRNA for the human TfR was shown to be necessary and sufficient for iron-dependent control of mRNA levels. Deletion studies identified a 678-nucleotide fragment of the TfR complementary DNA that is critical for this iron regulation. Five potential stem-loops that resemble the ferritin IRE are contained within the region critical for TfR regulation. Each of two of the five TfR elements was independently inserted into the 5' untranslated region of an indicator gene transcript. In this location they conferred iron regulation of translation. Thus, an mRNA element has been implicated in the mediation of distinct regulatory phenomena dependent on the context of the element within the transcript.
转铁蛋白受体(TfR)和铁蛋白的生物合成速率均受铁的调节。铁蛋白信使核糖核酸(mRNA)5'非翻译区中的铁反应元件(IRE)介导对其翻译的铁依赖性控制。在本报告中,人TfR的mRNA的3'非翻译区被证明对mRNA水平的铁依赖性控制是必要且充分的。缺失研究确定了TfR互补DNA的一个678个核苷酸的片段,该片段对这种铁调节至关重要。在对TfR调节至关重要的区域内包含五个类似于铁蛋白IRE的潜在茎环结构。五个TfR元件中的两个分别独立插入到指示基因转录本的5'非翻译区。在这个位置,它们赋予了翻译的铁调节作用。因此,一个mRNA元件已被证明参与介导依赖于该元件在转录本中的上下文的不同调节现象。