无义介导的信使核糖核酸衰变:机制见解和生理意义。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Biotechnology Pub Date : 2024-11-01 Epub Date: 2023-11-06 DOI:10.1007/s12033-023-00927-4
Ipsita Patro, Annapurna Sahoo, Bilash Ranjan Nayak, Rutupurna Das, Sanjoy Majumder, Gagan Kumar Panigrahi
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引用次数: 0

摘要

无义介导的信使核糖核酸衰变(NMD)是真核生物进化上保守的监测机制,也调节生理转录物的表达,从而参与基因调控。它本质上确保了异常转录物的识别和去除。因此,NMD通过限制截短蛋白的合成来保护细胞系统,可能通过消除有缺陷的mRNA。NMD在真核生物中是一种进化上保守的监测机制,也调节生理转录物的表达,因此也参与基因调控。首先,NMD机制扫描并区分异常和非异常转录物。由于截短蛋白的产生,产生了大量的细胞功能障碍,因此NMD核心蛋白,即上移码因子(UPFs)识别出有缺陷的mRNA,并进一步募集导致mRNA降解的因子。NMD在调节细胞机制(包括病理和生理事件)方面表现出惊人的可变性。但是,NMD的详细潜在分子机制仍然模糊不清,需要进行广泛的研究才能深入了解细胞稳态。NMD通路的理解之所以复杂,是因为许多蛋白质、分子相互作用及其在该过程不同步骤中的作用。此外,选择性剪接等方法会产生大量的mRNA异构体,因此很难理解选择性剪接对NMD功能效率的影响。NMD在癌症发展中的作用是非常复杂的。研究表明,在某些情况下,癌症细胞利用NMD通路作为工具,利用NMD机制维持肿瘤微环境。对肿瘤如何利用NMD途径获得益处的复杂机制有了更深入的了解,就可以制定一种靶向和抑制参与促肿瘤活性的NMD因子的策略。关于NMD途径,以及它如何区分NMD靶向的mRNA和非靶向的信使核糖核酸,目前可获得的信息很少。这篇综述强调了我们目前对NMD的理解,特别是对监管机制的理解,并试图概述需要进一步调查的较少探索的问题。总的来说,对NMD机制的详细分子理解可以在改善细胞稳态和制定对抗病理性疾病的战略方面产生广泛的应用,从而朝着实现联合国可持续发展目标(SDG 3:良好健康和福祉)的方向迈进。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nonsense-Mediated mRNA Decay: Mechanistic Insights and Physiological Significance.

Nonsense-mediated mRNA decay (NMD) is an evolutionarily conserved surveillance mechanism across eukaryotes and also regulates the expression of physiological transcripts, thus involved in gene regulation. It essentially ensures recognition and removal of aberrant transcripts. Therefore, the NMD protects the cellular system by restricting the synthesis of truncated proteins, potentially by eliminating the faulty mRNAs. NMD is an evolutionarily conserved surveillance mechanism across eukaryotes and also regulates the expression of physiological transcripts, thus involved in gene regulation as well. Primarily, the NMD machinery scans and differentiates the aberrant and non-aberrant transcripts. A myriad of cellular dysfunctions arise due to production of truncated proteins, so the NMD core proteins, the up-frameshift factors (UPFs) recognizes the faulty mRNAs and further recruits factors resulting in the mRNA degradation. NMD exhibits astounding variability in its ability in regulating cellular mechanisms including both pathological and physiological events. But, the detailed underlying molecular mechanisms in NMD remains blurred and require extensive investigation to gain insights on cellular homeostasis. The complexity in understanding of NMD pathway arises due to the involvement of numerous proteins, molecular interactions and their functioning in different steps of this process. Moreover methods such as alternative splicing generates numerous isoforms of mRNA, so it makes difficulties in understanding the impact of alternative splicing on the efficiency of NMD functioning. Role of NMD in cancer development is very complex. Studies have shown that in some cases cancer cells use NMD pathway as a tool to exploit the NMD mechanism to maintain tumor microenvironment. A greater level of understanding about the intricate mechanism of how tumor used NMD pathway for their benefits, a strategy can be developed for targeting and inhibiting NMD factors involved in pro-tumor activity. There are very little amount of information available about the NMD pathway, how it discriminate mRNAs that are targeted by NMD from those that are not. This review highlights our current understanding of NMD, specifically the regulatory mechanisms and attempts to outline less explored questions that warrant further investigations. Taken as a whole, a detailed molecular understanding of the NMD mechanism could lead to wide-ranging applications for improving cellular homeostasis and paving out strategies in combating pathological disorders leaping forward toward achieving United Nations sustainable development goals (SDG 3: Good health and well-being).

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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