Felder Simon, Nelson Irma M, Hatfield Breanne M, Weeks Kevin M
Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599-3290, USA.
Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina 27599-3290, USA
RNA. 2025 Jan 22;31(2):143-149. doi: 10.1261/rna.080136.124.
Structures in the 5' untranslated regions (UTRs) of mRNAs can physically modulate translation efficiency by impeding the scanning ribosome or by sequestering the translational start site. We assessed the impact of stable protein binding in 5'- and 3'-UTRs on translation efficiency by targeting the MS2 coat protein to a reporter RNA via its hairpin recognition site. Translation was assessed from the reporter RNA when coexpressed with MS2 coat proteins of varying affinities for the RNA, and at different expression levels. Binding of high-affinity proteins in the 5'-UTR hindered translation, whereas no effect was observed when the coat protein was targeted to the 3'-UTR. Inhibition of translation increased with coat protein concentration and affinity, reaching a maximum of 50%-70%. MS2 proteins engineered to bind two reporter mRNA sites had a stronger effect than those binding a single site. Our findings demonstrate that protein binding in an mRNA 5'-UTR physically impedes translation, with the effect governed by affinity, concentration, and sterics.
信使核糖核酸(mRNA)5'非翻译区(UTR)中的结构可通过阻碍核糖体扫描或隔离翻译起始位点来物理调节翻译效率。我们通过将MS2外壳蛋白通过其发夹识别位点靶向报告RNA,评估了5'和3'UTR中稳定蛋白结合对翻译效率的影响。当与对RNA具有不同亲和力的MS2外壳蛋白共表达时,以及在不同表达水平下,从报告RNA评估翻译情况。5'UTR中高亲和力蛋白的结合阻碍了翻译,而当外壳蛋白靶向3'UTR时未观察到影响。翻译抑制随外壳蛋白浓度和亲和力的增加而增加,最高可达50%-70%。经工程改造以结合两个报告mRNA位点的MS2蛋白比结合单个位点的蛋白具有更强的作用。我们的研究结果表明,mRNA 5'UTR中的蛋白结合会物理阻碍翻译,其作用受亲和力、浓度和空间位阻的影响。