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红细胞分化过程中的mRNA沉默:异质性核糖核蛋白K和异质性核糖核蛋白E1从3'端调控15-脂氧合酶的翻译。

mRNA silencing in erythroid differentiation: hnRNP K and hnRNP E1 regulate 15-lipoxygenase translation from the 3' end.

作者信息

Ostareck D H, Ostareck-Lederer A, Wilm M, Thiele B J, Mann M, Hentze M W

机构信息

Gene Expression Programme, European Molecular Biology Laboratory, Meyerhofstrasse, Heidelberg, Germany.

出版信息

Cell. 1997 May 16;89(4):597-606. doi: 10.1016/s0092-8674(00)80241-x.

Abstract

Although LOX mRNA accumulates early during differentiation, a differentiation control element in its 3' untranslated region confers translational silencing until late stage erythropoiesis. We have purified two proteins from rabbit reticulocytes that specifically mediate LOX silencing and identified them as hnRNPs K and E1. Transfection of hnRNP K and hnRNP E1 into HeLa cells specifically silenced the translation of reporter mRNAs bearing a differentiation control element in their 3' untranslated region. Silenced LOX mRNA in rabbit reticulocytes specifically coimmunoprecipitated with hnRNP K. In a reconstituted cell-free translation system, addition of recombinant hnRNP K and hnRNP E1 recapitulates this regulation via a specific inhibition of 80S ribosome assembly on LOX mRNA. Both proteins can control cap-dependent and internal ribosome entry site-mediated translation by binding to differentiation control elements. Our data suggest a specific cytoplasmic function for hnRNPs as translational regulatory proteins.

摘要

尽管LOX mRNA在分化早期积累,但其3'非翻译区的一个分化控制元件会导致翻译沉默,直至红细胞生成后期。我们从兔网织红细胞中纯化了两种特异性介导LOX沉默的蛋白质,并将它们鉴定为hnRNPs K和E1。将hnRNP K和hnRNP E1转染到HeLa细胞中,可特异性沉默其3'非翻译区带有分化控制元件的报告mRNA的翻译。兔网织红细胞中沉默的LOX mRNA与hnRNP K特异性共免疫沉淀。在重构的无细胞翻译系统中,添加重组hnRNP K和hnRNP E1通过对LOX mRNA上80S核糖体组装的特异性抑制来重现这种调控。这两种蛋白质都可以通过与分化控制元件结合来控制帽依赖性和内部核糖体进入位点介导的翻译。我们的数据表明hnRNPs作为翻译调节蛋白具有特定的细胞质功能。

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