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[无义介导的mRNA降解逃逸机制及其在疾病治疗中的应用]

[The NMD escape mechanism and its application in disease therapy].

作者信息

Cheng Miao Miao, Cao Yan Yan

机构信息

Department of Medical Genetics, Capital Institute of Pediatrics, Beijing 100020, China.

出版信息

Yi Chuan. 2020 Apr 20;42(4):354-362. doi: 10.16288/j.yczz.19-335.

Abstract

Nonsense-mediated mRNA decay (NMD) refers to the degradation of mRNA due to the presence of premature stop codon (PTC) on mRNA under pathological or physiological conditions. NMD is widely considered an mRNA-specific quality control process. Recently it was discovered that some PTCs do not trigger NMD in a variety of diseases - a process known as NMD escape; however, its exact mechanism remains unclear. At present, there are two widely accepted mechanistic hypotheses during NMD escape. The first is PTC read-through, in which protein translation undergoes PTC until the normal stop codon is encountered, producing a full-length protein. The second is translation reinitiation, in which protein translation recommences at the potential start codon downstream of PTC and terminates at the stop codon, producing an N-terminal truncated protein. Currently, an increasing number of drugs or small molecules that use PTC read-through have been successfully applied to treat nonsense variation-associated diseases. In this review, we summarize the NMD mechanism and discuss the application and progress in our understanding of NMD escape in disease therapy. This review should provide a useful framework to advance current understanding of the research and application of NMD escape.

摘要

无义介导的mRNA衰变(NMD)是指在病理或生理条件下,由于mRNA上存在提前终止密码子(PTC)而导致mRNA降解。NMD被广泛认为是一种mRNA特异性的质量控制过程。最近发现,在多种疾病中,一些PTC不会触发NMD——这一过程被称为NMD逃逸;然而,其确切机制仍不清楚。目前,在NMD逃逸过程中有两种被广泛接受的机制假说。第一种是PTC通读,即蛋白质翻译越过PTC继续进行,直到遇到正常终止密码子,从而产生全长蛋白质。第二种是翻译重新起始,即蛋白质翻译在PTC下游的潜在起始密码子处重新开始,并在终止密码子处终止,产生N端截短的蛋白质。目前,越来越多利用PTC通读的药物或小分子已成功应用于治疗无义变异相关疾病。在这篇综述中,我们总结了NMD机制,并讨论了在疾病治疗中对NMD逃逸的理解方面的应用和进展。这篇综述应为推进当前对NMD逃逸的研究和应用的理解提供一个有用的框架。

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