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

被引:443
作者
Ostareck, DH
OstareckLederer, A
Wilm, M
Thiele, BJ
Mann, M
Hentze, MW
机构
[1] EUROPEAN MOL BIOL LAB,GENE EXPRESS PROGRAMME,D-69117 HEIDELBERG,GERMANY
[2] EUROPEAN MOL BIOL LAB,PROT & PEPTIDE GRP,D-69117 HEIDELBERG,GERMANY
[3] HUMBOLDT UNIV BERLIN,INST BIOCHEM,D-10115 BERLIN,GERMANY
关键词
D O I
10.1016/S0092-8674(00)80241-X
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
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.
引用
收藏
页码:597 / 606
页数:10
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