Andersen Christian B F, Ballut Lionel, Johansen Jesper S, Chamieh Hala, Nielsen Klaus H, Oliveira Cristiano L P, Pedersen Jan Skov, Séraphin Bertrand, Le Hir Hervé, Andersen Gregers Rom
Department of Molecular Biology, University of Aarhus, DK-8000 Aarhus, Denmark.
Science. 2006 Sep 29;313(5795):1968-72. doi: 10.1126/science.1131981. Epub 2006 Aug 24.
In higher eukaryotes, a multiprotein exon junction complex is deposited on spliced messenger RNAs. The complex is organized around a stable core, which serves as a binding platform for numerous factors that influence messenger RNA function. Here, we present the crystal structure of a tetrameric exon junction core complex containing the DEAD-box adenosine triphosphatase (ATPase) eukaryotic initiation factor 4AIII (eIF4AIII) bound to an ATP analog, MAGOH, Y14, a fragment of MLN51, and a polyuracil mRNA mimic. eIF4AIII interacts with the phosphate-ribose backbone of six consecutive nucleotides and prevents part of the bound RNA from being double stranded. The MAGOH and Y14 subunits lock eIF4AIII in a prehydrolysis state, and activation of the ATPase probably requires only modest conformational changes in eIF4AIII motif I.
在高等真核生物中,一种多蛋白外显子连接复合体沉积在剪接后的信使核糖核酸(mRNA)上。该复合体围绕一个稳定的核心组织而成,这个核心作为众多影响信使核糖核酸功能的因子的结合平台。在此,我们展示了一种四聚体外显子连接核心复合体的晶体结构,该复合体包含与一种ATP类似物结合的DEAD盒腺苷三磷酸酶(ATP酶)真核起始因子4AIII(eIF4AIII)、MAGOH、Y14、MLN51的一个片段以及一个聚尿嘧啶mRNA模拟物。eIF4AIII与六个连续核苷酸的磷酸核糖骨架相互作用,并阻止部分结合的RNA形成双链。MAGOH和Y14亚基将eIF4AIII锁定在预水解状态,而ATP酶的激活可能仅需要eIF4AIII基序I发生适度的构象变化。