Ostareck D H, Ostareck-Lederer A, Shatsky I N, Hentze M W
Gene Expression Programme, European Molecular Biology Laboratory, Meyerhofstrasse 1, D-69117, Heidelberg, Germany.
Cell. 2001 Jan 26;104(2):281-90. doi: 10.1016/s0092-8674(01)00212-4.
15-lipoxygenase (LOX) expression is translationally silenced in early erythroid precursor cells by a specific mRNA-protein complex formed between the differentiation control element in the 3' untranslated region (UTR) and hnRNPs K and E1. The 3'UTR regulatory complex prevents translation initiation by an unknown mechanism. We demonstrate that the 40S ribosomal subunit can be recruited and scan to the translation initiation codon even when the silencing complex is bound to the 3'UTR. However, the joining of the 60S ribosomal subunit at the AUG codon to form a translation competent 80S ribosome is inhibited, unless initiation is mediated by the IGR-IRES of the cricket paralysis virus. These findings identify the critical step at which LOX mRNA translation is controlled and reveal that 60S subunit joining can be specifically regulated.
15-脂氧合酶(LOX)的表达在早期红系前体细胞中通过3'非翻译区(UTR)中的分化控制元件与hnRNPs K和E1之间形成的特定mRNA-蛋白质复合物而发生翻译沉默。3'UTR调控复合物通过未知机制阻止翻译起始。我们证明,即使沉默复合物与3'UTR结合,40S核糖体亚基也可以被招募并扫描到翻译起始密码子。然而,除非由蟋蟀麻痹病毒的IGR-IRES介导起始,否则60S核糖体亚基在AUG密码子处的加入以形成具有翻译活性的80S核糖体受到抑制。这些发现确定了LOX mRNA翻译被控制的关键步骤,并揭示了60S亚基的加入可以被特异性调节。