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RNA与DNA的差异:机制、氧化应激、转录保真度及其对健康的影响

RNA-DNA Differences: Mechanisms, Oxidative Stress, Transcriptional Fidelity, and Health Implications.

作者信息

Stolc Viktor, Preto Ondrej, Karhanek Miloslav, Freund Friedemann, Griko Yuri, Loftus David J, Ohayon Maurice M

机构信息

NASA Ames Research Center, Moffett Field, CA 94035, USA.

Biomedical Research Center, Slovak Academy of Sciences, 845 05 Bratislava, Slovakia.

出版信息

Antioxidants (Basel). 2025 Apr 30;14(5):544. doi: 10.3390/antiox14050544.

Abstract

RNA-DNA differences (RDDs) challenge the traditional view of RNA as a faithful copy of DNA, arising through RNA editing, transcriptional errors, and oxidative damage. Reactive oxygen species (ROS) play a central role, inducing lesions like 8-oxo-guanine that compromise transcription and translation, leading to dysfunctional proteins. This review explores the biochemical basis of RDDs, their exacerbation under oxidative stress, and their dual roles in cellular adaptation and disease. RDDs contribute to genomic instability and are implicated in cancers, neurodegenerative disorders, and autoimmune diseases, while also driving phenotypic diversity. Drawing on terrestrial and spaceflight studies, we highlight the intersection of oxidative stress, RDD formation, and cellular dysfunction, proposing innovative mitigation approaches. Advancements in RDD detection and quantification, along with ROS management therapies, offer new avenues to restore cellular homeostasis and promote resilience. By positioning RDDs as a hallmark of genomic entropy, this review underscores the limits of biological adaptation. Furthermore, the prevalence of guanine-rich codons in antioxidant genes increases their susceptibility to ROS-induced oxidative lesions, linking redox stress, genomic instability, and constrained adaptation. These insights have profound implications for understanding aging, disease progression, and adaptive mechanisms in both terrestrial and space environments.

摘要

RNA- DNA差异(RDDs)对RNA是DNA忠实拷贝的传统观点提出了挑战,其产生原因包括RNA编辑、转录错误和氧化损伤。活性氧(ROS)起着核心作用,诱导诸如8-氧代鸟嘌呤等损伤,这些损伤会损害转录和翻译,导致蛋白质功能失调。本文综述探讨了RDDs的生化基础、在氧化应激下的加剧情况及其在细胞适应和疾病中的双重作用。RDDs会导致基因组不稳定,并与癌症、神经退行性疾病和自身免疫性疾病有关,同时也推动了表型多样性。借鉴地面和太空飞行研究,我们强调了氧化应激、RDD形成和细胞功能障碍之间的交叉点,提出了创新的缓解方法。RDD检测和定量的进展以及ROS管理疗法为恢复细胞稳态和提高恢复力提供了新途径。通过将RDDs定位为基因组熵的一个标志,本文综述强调了生物适应的局限性。此外,抗氧化基因中富含鸟嘌呤的密码子的普遍性增加了它们对ROS诱导的氧化损伤的易感性,将氧化还原应激、基因组不稳定和适应性受限联系起来。这些见解对于理解地球和太空环境中的衰老、疾病进展和适应机制具有深远意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9db8/12108522/e931e0cfc2d9/antioxidants-14-00544-g001.jpg

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