Schilders Geurt, van Dijk Erwin, Raijmakers Reinout, Pruijn Ger J M
Department of Biochemistry, Nijmegen Center for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.
Int Rev Cytol. 2006;251:159-208. doi: 10.1016/S0074-7696(06)51005-8.
The identification and characterization of the exosome complex has shown that the exosome is a complex of 3' --> 5' exoribonucleases that plays a key role in the processing and degradation of a wide variety of RNA substrates. Advances in the understanding of exosome function have led to the identification of numerous cofactors that are required for a selective recruitment of the exosome to substrate RNAs, for their structural alterations to facilitate degradation, and to aid in their complete degradation/processing. Structural data obtained by two-hybrid interaction analyses and X-ray crystallography show that the core of the exosome adopts a doughnut-like structure and demonstrates that probably not all exosome subunits are active exoribonucleases. Despite all data obtained on the structure and function of the exosome during the last decade, there are still a lot of unanswered questions. What is the molecular mechanism by which cofactors select and target substrate RNAs to the exosome and modulate its function for correct processing or degradation? How can the exosome discriminate between processing or degradation of a specific substrate RNA? What is the precise structure of exosome subunits and how do they contribute to its function? Here we discuss studies that provide some insight to these questions and speculate on the mechanisms that control the exosome.
外泌体复合物的鉴定和特性表明,外泌体是一种3'→5'外切核糖核酸酶复合物,在多种RNA底物的加工和降解中起关键作用。对外泌体功能理解的进展导致了众多辅助因子的鉴定,这些辅助因子是外泌体选择性募集到底物RNA、使其结构改变以促进降解以及协助其完全降解/加工所必需的。通过双杂交相互作用分析和X射线晶体学获得的结构数据表明,外泌体的核心呈甜甜圈状结构,并表明可能并非所有外泌体亚基都是活性外切核糖核酸酶。尽管在过去十年中获得了关于外泌体结构和功能的所有数据,但仍有许多未解决的问题。辅助因子选择底物RNA并将其靶向外泌体并调节其功能以进行正确加工或降解的分子机制是什么?外泌体如何区分特定底物RNA的加工或降解?外泌体亚基的确切结构是什么,它们如何对其功能做出贡献?在这里,我们讨论为这些问题提供一些见解的研究,并推测控制外泌体的机制。