Campbell Zachary T, Wickens Marvin
Department of Biochemistry, University of Wisconsin-Madison, 433 Babcock Drive, Madison, WI 53706, USA.
Department of Biochemistry, University of Wisconsin-Madison, 433 Babcock Drive, Madison, WI 53706, USA.
Trends Biochem Sci. 2015 Mar;40(3):157-64. doi: 10.1016/j.tibs.2015.01.003. Epub 2015 Jan 27.
RNA-protein interactions are pervasive. The specificity of these interactions dictates which RNAs are controlled by what protein. Here we describe a class of revolutionary new methods that enable global views of RNA-binding specificity in vitro, for both single proteins and multiprotein complexes. These methods provide insight into central issues in RNA regulation in living cells, including understanding the balance between free and bound components, the basis for exclusion of binding sites, detection of binding events in the absence of discernible regulatory elements, and new approaches to targeting endogenous transcripts by design. Comparisons of in vitro and in vivo binding provide a foundation for comprehensive understanding of the biochemistry of protein-mediated RNA regulatory networks.
RNA与蛋白质的相互作用广泛存在。这些相互作用的特异性决定了哪些RNA受何种蛋白质的调控。在此,我们描述了一类全新的革命性方法,这些方法能够在体外对单个蛋白质和多蛋白复合物的RNA结合特异性进行全局性观察。这些方法为深入了解活细胞中RNA调控的核心问题提供了思路,包括理解游离成分与结合成分之间的平衡、结合位点被排除的基础、在缺乏可识别调控元件的情况下检测结合事件,以及通过设计靶向内源性转录本的新方法。体外和体内结合的比较为全面理解蛋白质介导的RNA调控网络的生物化学提供了基础。