Lipoxygenase mRNA silencing in erythroid differentiation:: The 3′UTR regulatory complex controls 60S ribosomal subunit joining

被引:212
作者
Ostareck, DH
Ostareck-Lederer, A
Shatsky, IN
Hentze, MW
机构
[1] European Mol Biol Lab, Gene Express Programme, D-69117 Heidelberg, Germany
[2] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow, Russia
基金
俄罗斯基础研究基金会;
关键词
D O I
10.1016/S0092-8674(01)00212-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:281 / 290
页数:10
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