Xue Shifeng, Barna Maria
a Department of Developmental Biology, Stanford University ; Stanford , CA USA.
b Department of Genetics, Stanford University ; Stanford , CA USA.
RNA Biol. 2015;12(10):1083-7. doi: 10.1080/15476286.2015.1085149. Epub 2015 Sep 1.
Recent evidence has shown that the ribosome itself can play a highly regulatory role in the specialized translation of specific subpools of mRNAs, in particular at the level of ribosomal proteins (RP). However, the mechanism(s) by which this selection takes place has remained poorly understood. In our recent study, we discovered a combination of unique RNA elements in the 5'UTRs of mRNAs that allows for such control by the ribosome. These mRNAs contain a Translation Inhibitory Element (TIE) that inhibits general cap-dependent translation, and an Internal Ribosome Entry Site (IRES) that relies on a specific RP for activation. The unique combination of an inhibitor of general translation and an activator of specialized translation is key to ribosome-mediated control of gene expression. Here we discuss how these RNA regulatory elements provide a new level of control to protein expression and their implications for gene expression, organismal development and evolution.
最近的证据表明,核糖体本身在特定mRNA亚库的特异性翻译中可发挥高度调控作用,尤其是在核糖体蛋白(RP)水平上。然而,这种选择发生的机制仍知之甚少。在我们最近的研究中,我们在mRNA的5'UTR中发现了独特RNA元件的组合,其可实现核糖体的这种调控。这些mRNA含有抑制一般帽依赖性翻译的翻译抑制元件(TIE),以及依赖特定RP激活的内部核糖体进入位点(IRES)。一般翻译抑制剂和特异性翻译激活剂的独特组合是核糖体介导的基因表达调控的关键。在此,我们讨论这些RNA调控元件如何为蛋白质表达提供新的调控水平及其对基因表达、机体发育和进化的影响。