Mitchell Sally A, Spriggs Keith A, Bushell Martin, Evans Joanne R, Stoneley Mark, Le Quesne John P C, Spriggs Ruth V, Willis Anne E
School of Pharmacy, University of Nottingham, University Park, Nottingham, NG7 2RD, UK.
Genes Dev. 2005 Jul 1;19(13):1556-71. doi: 10.1101/gad.339105.
We have identified a novel motif which consists of the sequence (CCU)(n) as part of a polypyrimidine-rich tract and permits internal ribosome entry. A number of constructs containing variations of this motif were generated and these were found to function as artificial internal ribosome entry segments (AIRESs) in vivo and in vitro in the presence of polypyrimidine tract-binding protein (PTB). The data show that for these sequences to function as IRESs the RNA must be present as a double-stranded stem and, in agreement with this, rather surprisingly, we show that PTB binds strongly to double-stranded RNA. All the cellular 5' untranslated regions (UTRs) tested that harbor this sequence were shown to contain internal ribosome entry segments that are dependent upon PTB for function in vivo and in vitro. This therefore raises the possibility that PTB or its interacting protein partners could provide a bridge between the IRES-RNA and the ribosome. Given the number of putative cellular IRESs that could be dependent on PTB for function, these data strongly suggest that PTB-1 is a universal IRES-trans-acting factor.
我们鉴定出了一种新型基序,它由序列(CCU)(n)组成,是富含嘧啶序列的一部分,并允许核糖体内部进入。构建了许多含有该基序变体的结构,发现在存在嘧啶序列结合蛋白(PTB)的情况下,这些结构在体内和体外均能作为人工核糖体内部进入片段(AIRESs)发挥作用。数据表明,对于这些序列要作为内部核糖体进入位点(IRESs)发挥作用,RNA必须以双链茎的形式存在,与此一致的是,相当令人惊讶的是,我们发现PTB能强烈结合双链RNA。所有测试的含有该序列的细胞5'非翻译区(UTRs)均显示含有核糖体内部进入片段,这些片段在体内和体外发挥功能均依赖于PTB。因此,这增加了PTB或其相互作用的蛋白伴侣可能在IRES-RNA和核糖体之间提供桥梁的可能性。鉴于可能依赖PTB发挥功能的假定细胞IRESs数量众多,这些数据强烈表明PTB-1是一种通用的IRES反式作用因子。