Shen Haihong, Zheng Xuexiu, Shen Jingping, Zhang Lingdi, Zhao Rui, Green Michael R
Department of Life Science, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Genes Dev. 2008 Jul 1;22(13):1796-803. doi: 10.1101/gad.1657308.
The essential splicing factor human UAP56 (hUAP56) is a DExD/H-box protein known to promote prespliceosome assembly. Here, using a series of hUAP56 mutants that are defective for ATP-binding, ATP hydrolysis, or dsRNA unwindase/helicase activity, we assess the relative contributions of these biochemical functions to pre-mRNA splicing. We show that prespliceosome assembly requires hUAP56's ATP-binding and ATPase activities, which, unexpectedly, are required for hUAP56 to interact with U2AF(65) and be recruited into splicing complexes. Surprisingly, we find that hUAP56 is also required for mature spliceosome assembly, which requires, in addition to the ATP-binding and ATPase activities, hUAP56's dsRNA unwindase/helicase activity. We demonstrate that hUAP56 directly contacts U4 and U6 snRNAs and can promote unwinding of the U4/U6 duplex, and that both these activities are dependent on U2AF(65). Our results indicate that hUAP56 first interacts with U2AF(65) in an ATP-dependent manner, and subsequently with U4/U6 snRNAs to facilitate stepwise assembly of the spliceosome.
必需剪接因子人UAP56(hUAP56)是一种DExD/H盒蛋白,已知其可促进剪接体前体组装。在此,我们使用一系列在ATP结合、ATP水解或双链RNA解旋酶/解旋酶活性方面存在缺陷的hUAP56突变体,评估这些生化功能对前体mRNA剪接的相对贡献。我们发现,剪接体前体组装需要hUAP56的ATP结合和ATP酶活性,而这些活性出人意料地是hUAP56与U2AF(65)相互作用并被招募到剪接复合物中所必需的。令人惊讶的是,我们发现hUAP56对于成熟剪接体的组装也是必需的,除了ATP结合和ATP酶活性外,成熟剪接体的组装还需要hUAP56的双链RNA解旋酶/解旋酶活性。我们证明hUAP56直接与U4和U6 snRNA接触,并可促进U4/U6双链体的解旋,且这两种活性均依赖于U2AF(65)。我们的结果表明,hUAP56首先以ATP依赖的方式与U2AF(65)相互作用,随后与U4/U6 snRNA相互作用,以促进剪接体的逐步组装。