Department of Biochemistry and Cell Biology, Max F. Perutz Laboratories, University of Vienna, Vienna, Austria.
RNA Biol. 2013 Jan;10(1):71-82. doi: 10.4161/rna.22492. Epub 2012 Oct 12.
RNA folding is an essential aspect underlying RNA-mediated cellular processes. Many RNAs, including large, multi-domain ribozymes, are capable of folding to the native, functional state without assistance of a protein cofactor in vitro. In the cell, trans-acting factors, such as proteins, are however known to modulate the structure and thus the fate of an RNA. DEAD-box proteins, including Mss116p, were recently found to assist folding of group I and group II introns in vitro and in vivo. The underlying mechanism(s) have been studied extensively to explore the contribution of ATP hydrolysis and duplex unwinding in helicase-stimulated intron splicing. Here we summarize the ongoing efforts to understand the novel role of DEAD-box proteins in RNA folding.
RNA 折叠是 RNA 介导的细胞过程的一个基本方面。许多 RNA,包括大型多结构域核酶,能够在没有蛋白质辅助因子的情况下在体外折叠成天然的、有功能的状态。然而,在细胞中,反式作用因子,如蛋白质,已知可以调节 RNA 的结构,从而影响其命运。最近发现 DEAD -box 蛋白,包括 Mss116p,在体外和体内有助于 I 组和 II 组内含子的折叠。为了探索 ATP 水解和双链解开在解旋酶刺激的内含子剪接中的贡献,人们对其潜在机制进行了广泛研究。在这里,我们总结了理解 DEAD 盒蛋白在 RNA 折叠中新颖作用的正在进行的努力。