Gruss Oliver J, Meduri Rajyalakshmi, Schilling Maximilian, Fischer Utz
Department of Genetics, Rheinische Friedrich-Wilhelms-Universität Bonn, Karlrobert-Kreiten-Str. 13, 53115, Bonn, Germany.
Department of Biochemistry, University of Würzburg, Biozentrum, Am Hubland, D-97074, Würzburg, Germany.
Chromosoma. 2017 Oct;126(5):577-593. doi: 10.1007/s00412-017-0637-6. Epub 2017 Aug 1.
Macromolecular complexes composed of proteins or proteins and nucleic acids rather than individual macromolecules mediate many cellular activities. Maintenance of these activities is essential for cell viability and requires the coordinated production of the individual complex components as well as their faithful incorporation into functional entities. Failure of complex assembly may have fatal consequences and can cause severe diseases. While many macromolecular complexes can form spontaneously in vitro, they often require aid from assembly factors including assembly chaperones in the crowded cellular environment. The assembly of RNA protein complexes implicated in the maturation of pre-mRNAs (termed UsnRNPs) has proven to be a paradigm to understand the action of assembly factors and chaperones. UsnRNPs are assembled by factors united in protein arginine methyltransferase 5 (PRMT5)- and survival motor neuron (SMN)-complexes, which act sequentially in the UsnRNP production line. While the PRMT5-complex pre-arranges specific sets of proteins into stable intermediates, the SMN complex displaces assembly factors from these intermediates and unites them with UsnRNA to form the assembled RNP. Despite advanced mechanistic understanding of UsnRNP assembly, our knowledge of regulatory features of this essential and ubiquitous cellular function remains remarkably incomplete. One may argue that the process operates as a default biosynthesis pathway and does not require sophisticated regulatory cues. Simple theoretical considerations and a number of experimental data, however, indicate that regulation of UsnRNP assembly most likely happens at multiple levels. This review will not only summarize how individual components of this assembly line act mechanistically but also why, how, and when the UsnRNP workflow might be regulated by means of posttranslational modification in response to cellular signaling cues.
由蛋白质或蛋白质与核酸组成的大分子复合物而非单个大分子介导了许多细胞活动。维持这些活动对于细胞存活至关重要,需要各个复合物组分的协同产生以及它们忠实地整合到功能实体中。复合物组装失败可能会产生致命后果并导致严重疾病。虽然许多大分子复合物在体外可以自发形成,但在拥挤的细胞环境中,它们通常需要包括组装伴侣在内的组装因子的帮助。参与前体mRNA成熟的RNA蛋白复合物(称为UsnRNP)的组装已被证明是理解组装因子和伴侣作用的一个范例。UsnRNP由联合在蛋白质精氨酸甲基转移酶5(PRMT5)和存活运动神经元(SMN)复合物中的因子组装而成,这些复合物在UsnRNP生产线中依次发挥作用。虽然PRMT5复合物将特定的蛋白质组预排列成稳定的中间体,但SMN复合物将组装因子从这些中间体中置换出来,并将它们与UsnRNA结合形成组装好的RNP。尽管对UsnRNP组装有了先进的机制理解,但我们对这一基本且普遍存在的细胞功能的调控特征的了解仍然非常不完整。有人可能会认为这个过程作为一个默认的生物合成途径运行,不需要复杂的调控线索。然而,简单的理论思考和一些实验数据表明,UsnRNP组装的调控很可能发生在多个层面。这篇综述不仅将总结这条生产线的各个组分如何在机制上发挥作用,还将总结为什么、如何以及何时UsnRNP工作流程可能通过翻译后修饰来响应细胞信号线索进行调控。