Yang Quansheng, Jankowsky Eckhard
Department of Biochemistry and Center for RNA Molecular Biology, School of Medicine, Case Western Reserve University, 10900 Euclid Ave., Cleveland, Ohio 44106, USA.
Nat Struct Mol Biol. 2006 Nov;13(11):981-6. doi: 10.1038/nsmb1165. Epub 2006 Oct 29.
Helicases unwind RNA or DNA duplexes and displace proteins from nucleic acids in an ATP-dependent fashion. To unwind duplexes, helicases typically load onto one of the two nucleic acid strands, usually at a single-stranded region, and then translocate on this strand in a unidirectional fashion, thereby displacing the complementary DNA or RNA. Here we show that the DEAD-box RNA helicase Ded1 unwinds duplexes in a different manner. Ded1 uses the single-stranded region to gain access to the duplex. Strand separation is directly initiated from the duplex region and no covalent connection between the single strand and the duplex region is required. This new type of helicase activity explains observations with other DEAD-box proteins and may be the prototype for duplex-unwinding reactions in RNA metabolism.
解旋酶以ATP依赖的方式解开RNA或DNA双链,并将蛋白质从核酸上置换下来。为了解开双链,解旋酶通常加载到两条核酸链之一上,通常是在单链区域,然后以单向方式在这条链上移位,从而置换互补的DNA或RNA。在这里,我们表明DEAD-box RNA解旋酶Ded1以不同的方式解开双链。Ded1利用单链区域进入双链。链的分离直接从双链区域开始,单链和双链区域之间不需要共价连接。这种新型的解旋酶活性解释了对其他DEAD-box蛋白的观察结果,并且可能是RNA代谢中双链解开反应的原型。