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程序性核糖体移码的生物学意义与治疗前景

Biological Significance and Therapeutic Promise of Programmed Ribosomal Frameshifting.

作者信息

Ramamonjiharisoa Miora Bruna Marielle, Liu Sen

机构信息

Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Key Laboratory of Fermentation Engineering (Ministry of Education), Wuhan 430068, China.

Hubei Key Laboratory of Industrial Microbiology, National "111" Center for Cellular Regulation and Molecular Pharmaceutics, School of Life and Health Sciences, Hubei University of Technology, Wuhan 430068, China.

出版信息

Int J Mol Sci. 2025 Feb 3;26(3):1294. doi: 10.3390/ijms26031294.

Abstract

Programmed Ribosomal Frameshifting (PRF) is a mechanism that alters the mRNA reading frame during translation, resulting in the production of out-of-frame proteins. PRF plays crucial roles in maintaining cellular homeostasis and contributes significantly to disease pathogenesis, particularly in viral infections. Notably, PRF can induce immune responses in the SARS-CoV-2 mRNA vaccine, further extending its biological significance. These multiple aspects of PRF highlight its potential as a therapeutic target. Since PRF efficiency can be modulated by cellular factors, its expression or silencing is context-dependent. Therefore, a deeper understanding of PRF is essential for harnessing its therapeutic potential. This review explores PRF biological significance in disease and homeostasis. Such knowledge would serve as a foundation to advance therapeutic strategies targeting PRF modulation, especially in viral infections and vaccine development.

摘要

程序性核糖体移码(PRF)是一种在翻译过程中改变mRNA阅读框的机制,导致产生框外蛋白。PRF在维持细胞稳态中起关键作用,并对疾病发病机制有重大贡献,尤其是在病毒感染中。值得注意的是,PRF可在SARS-CoV-2 mRNA疫苗中诱导免疫反应,进一步扩展了其生物学意义。PRF的这些多方面特性突出了其作为治疗靶点的潜力。由于PRF效率可受细胞因子调节,其表达或沉默取决于具体情况。因此,深入了解PRF对于发挥其治疗潜力至关重要。本综述探讨了PRF在疾病和稳态中的生物学意义。这些知识将为推进针对PRF调节的治疗策略奠定基础,特别是在病毒感染和疫苗开发方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dbd/11818727/72d01231967b/ijms-26-01294-g001.jpg

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