Department of Biochemistry, Inje University College of Medicine, Busan 50834, Korea.
Department of Biological and Chemical Engineering, Hongik University, 2639, Sejong-ro, Jochiwon-eup, Sejong-si 30016, Korea.
Int J Mol Sci. 2022 May 13;23(10):5451. doi: 10.3390/ijms23105451.
The relationship between transcription and aging is one that has been studied intensively and experimentally with diverse attempts. However, the impact of the nuclear mRNA export on the aging process following its transcription is still poorly understood, although the nuclear events after transcription are coupled closely with the transcription pathway because the essential factors required for mRNA transport, namely TREX, TREX-2, and nuclear pore complex (NPC), physically and functionally interact with various transcription factors, including the activator/repressor and pre-mRNA processing factors. Dysregulation of the mediating factors for mRNA export from the nucleus generally leads to the aberrant accumulation of nuclear mRNA and further impairment in the vegetative growth and normal lifespan and the pathogenesis of neurodegenerative diseases. The optimal stoichiometry and density of NPC are destroyed during the process of cellular aging, and their damage triggers a defect of function in the nuclear permeability barrier. This review describes recent findings regarding the role of the nuclear mRNA export in cellular aging and age-related neurodegenerative disorders.
转录与衰老之间的关系是一个经过深入研究和实验探索的关系。然而,核 mRNA 输出对转录后衰老过程的影响仍然知之甚少,尽管转录后核事件与转录途径密切相关,因为 mRNA 运输所需的基本因素,即 TREX、TREX-2 和核孔复合物 (NPC),在物理和功能上与各种转录因子相互作用,包括激活剂/抑制剂和前体 mRNA 加工因子。mRNA 从细胞核输出的中介因子的失调通常导致核内 mRNA 的异常积累,并进一步损害营养生长和正常寿命以及神经退行性疾病的发病机制。在细胞衰老过程中,NPC 的最佳化学计量和密度被破坏,其损伤会引发核通透性屏障功能缺陷。本综述描述了核 mRNA 输出在细胞衰老和与年龄相关的神经退行性疾病中的作用的最新发现。