School of Human Sciences, University of Western Australia, Crawley, Western Australia, 6009; Harry Perkins Institute of Medical Research, Nedlands, Western Australia, Australia; School of Molecular Sciences, University of Western Australia, Crawley, Western Australia, 6009, Australia.
Faculty of Pharmaceutical Sciences, Hokkaido University, Hokkaido, Japan.
Trends Biochem Sci. 2018 Feb;43(2):124-135. doi: 10.1016/j.tibs.2017.12.001. Epub 2017 Dec 27.
Long noncoding RNA (lncRNA) molecules are some of the newest and least understood players in gene regulation. Hence, we need good model systems with well-defined RNA and protein components. One such system is paraspeckles - protein-rich nuclear organelles built around a specific lncRNA scaffold. New discoveries show how paraspeckles are formed through multiple RNA-protein and protein-protein interactions, some of which involve extensive polymerization, and others with multivalent interactions driving phase separation. Once formed, paraspeckles influence gene regulation through sequestration of component proteins and RNAs, with subsequent depletion in other compartments. Here we focus on the dual aspects of paraspeckle structure and function, revealing an emerging role for these dynamic bodies in a multitude of cellular settings.
长链非编码 RNA (lncRNA) 分子是基因调控中最新且了解最少的参与者之一。因此,我们需要具有明确 RNA 和蛋白质成分的良好模型系统。一个这样的系统是核斑点 - 富含蛋白质的核细胞器,围绕特定的 lncRNA 支架构建。新的发现表明核斑点是如何通过多个 RNA-蛋白质和蛋白质-蛋白质相互作用形成的,其中一些涉及广泛的聚合,而另一些则涉及多价相互作用驱动相分离。一旦形成,核斑点通过隔离组成蛋白和 RNA 来影响基因调控,随后在其他隔室中耗尽。在这里,我们关注核斑点结构和功能的双重方面,揭示了这些动态体在多种细胞环境中的新兴作用。