Department of Pediatric Oncology, Hematology and Immunology, University of Heidelberg, Im Neuenheimer Feld 430, 69120 Heidelberg, Germany.
Molecular Medicine Partnership Unit, University of Heidelberg and European Molecular Biology Laboratory, Im Neuenheimer Feld 350, 69120 Heidelberg, Germany.
Biomolecules. 2020 Jul 4;10(7):999. doi: 10.3390/biom10070999.
Nonsense-mediated RNA decay (NMD) is the prototype example of a whole family of RNA decay pathways that unfold around a common central effector protein called UPF1. While NMD in yeast appears to be a linear pathway, NMD in higher eukaryotes is a multifaceted phenomenon with high variability with respect to substrate RNAs, degradation efficiency, effector proteins and decay-triggering RNA features. Despite increasing knowledge of the mechanistic details, it seems ever more difficult to define NMD and to clearly distinguish it from a growing list of other UPF1-mediated RNA decay pathways (UMDs). With a focus on mammalian, we here critically examine the prevailing NMD models and the gaps and inconsistencies in these models. By exploring the minimal requirements for NMD and other UMDs, we try to elucidate whether they are separate and definable pathways, or rather variations of the same phenomenon. Finally, we suggest that the operating principle of the UPF1-mediated decay family could be considered similar to that of a computing cloud providing a flexible infrastructure with rapid elasticity and dynamic access according to specific user needs.
无义介导的 RNA 衰减(NMD)是一类 RNA 衰减途径的原型范例,这些途径围绕着一种称为 UPF1 的常见中央效应蛋白展开。虽然酵母中的 NMD 似乎是一种线性途径,但高等真核生物中的 NMD 是一个多方面的现象,在底物 RNA、降解效率、效应蛋白和触发 RNA 特征方面具有高度的可变性。尽管对机制细节的了解不断增加,但似乎越来越难以定义 NMD,并清楚地区分它与越来越多的其他 UPF1 介导的 RNA 衰减途径(UMDs)。本文重点关注哺乳动物,批判性地审查了现有的 NMD 模型以及这些模型中的差距和不一致之处。通过探索 NMD 和其他 UMD 的最小要求,我们试图阐明它们是独立的、可定义的途径,还是同一现象的变体。最后,我们建议 UPF1 介导的衰减家族的工作原理可以被认为类似于云计算,它根据特定用户的需求提供了一个灵活的基础设施,具有快速的弹性和动态访问。