Wagner J D, Jankowsky E, Company M, Pyle A M, Abelson J N
Division of Biology, California Institute of Technology, Pasadena, CA 91125, USA.
EMBO J. 1998 May 15;17(10):2926-37. doi: 10.1093/emboj/17.10.2926.
Of the proteins required for pre-mRNA splicing, at least four, the DEAH-box proteins, are closely related due to the presence of a central 'RNA helicase-like' region, and extended homology through a large portion of the protein. A major unresolved question is the function of these proteins. Indirect evidence suggests that several of these proteins are catalysts for important structural rearrangements in the spliceosome. However, the mechanism for the proposed alterations is presently unknown. We present evidence that PRP22, a DEAH-box protein required for mRNA release from the spliceosome, unwinds RNA duplexes in a concentration- and ATP-dependent manner. This demonstrates that PRP22 can modify RNA structure directly. We also show that the PRP22-dependent release of mRNA from the spliceosome is an ATP-dependent process and that recombinant PRP22 is an ATPase. Non-hydrolyzable ATP analogs did not substitute for ATP in the RNA-unwinding reaction, suggesting that ATP hydrolysis is required for this reaction. Specific mutation of a putative ATP phosphate-binding motif in the recombinant protein eliminated the ATPase and RNA-unwinding capacity. Significantly, these data suggest that the DEAH-box proteins act directly on RNA substrates within the spliceosome.
在前体mRNA剪接所需的蛋白质中,至少有四种DEAH框蛋白由于存在一个中央“RNA解旋酶样”区域以及在蛋白质的大部分区域具有广泛的同源性而密切相关。一个主要未解决的问题是这些蛋白质的功能。间接证据表明,其中几种蛋白质是剪接体中重要结构重排的催化剂。然而,目前尚不清楚所提出的改变的机制。我们提供证据表明,PRP22是一种从剪接体释放mRNA所需的DEAH框蛋白,它以浓度和ATP依赖的方式解开RNA双链体。这表明PRP22可以直接修饰RNA结构。我们还表明,PRP22依赖的mRNA从剪接体的释放是一个ATP依赖的过程,并且重组PRP22是一种ATP酶。不可水解的ATP类似物在RNA解旋反应中不能替代ATP,这表明该反应需要ATP水解。重组蛋白中假定的ATP磷酸结合基序的特定突变消除了ATP酶和RNA解旋能力。重要的是,这些数据表明DEAH框蛋白直接作用于剪接体内的RNA底物。