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通过无效剪接对基因表达进行转录后调控。

Post-transcriptional Regulation of Gene Expression via Unproductive Splicing.

作者信息

Zavileyskiy L G, Pervouchine D D

机构信息

Lomonosov Moscow State University, Moscow, 119192 Russian Federation.

Skolkovo Institute of Science and Technology, Moscow, 121205 Russian Federation.

出版信息

Acta Naturae. 2024 Jan-Mar;16(1):4-13. doi: 10.32607/actanaturae.27337.

Abstract

Unproductive splicing is a mechanism of post-transcriptional gene expression control in which premature stop codons are inserted into protein-coding transcripts as a result of regulated alternative splicing, leading to their degradation via the nonsense-mediated decay pathway. This mechanism is especially characteristic of RNA-binding proteins, which regulate each other's expression levels and those of other genes in multiple auto- and cross-regulatory loops. Deregulation of unproductive splicing is a cause of serious human diseases, including cancers, and is increasingly being considered as a prominent therapeutic target. This review discusses the types of unproductive splicing events, the mechanisms of auto- and cross-regulation, nonsense-mediated decay escape, and problems in identifying unproductive splice isoforms. It also provides examples of deregulation of unproductive splicing in human diseases and discusses therapeutic strategies for its correction using antisense oligonucleotides and small molecules.

摘要

无效剪接是一种转录后基因表达调控机制,在该机制中,由于受调控的可变剪接,过早的终止密码子被插入到蛋白质编码转录本中,导致它们通过无义介导的衰变途径被降解。这种机制是RNA结合蛋白的一个特别特征,这些蛋白在多个自调控和交叉调控环中相互调节彼此的表达水平以及其他基因的表达水平。无效剪接失调是包括癌症在内的严重人类疾病的一个病因,并且越来越被视为一个重要的治疗靶点。本综述讨论了无效剪接事件的类型、自调控和交叉调控的机制、无义介导的衰变逃逸以及识别无效剪接异构体的问题。它还提供了人类疾病中无效剪接失调的例子,并讨论了使用反义寡核苷酸和小分子对其进行纠正的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1e4/11062102/e20a2c8240eb/AN20758251-16-01-004-g001.jpg

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