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过氧化氢胁迫对核仁氧化还原环境及前体核糖体RNA成熟的影响

Effects of Hydrogen Peroxide Stress on the Nucleolar Redox Environment and Pre-rRNA Maturation.

作者信息

Sapio Russell T, Burns Chelsea J, Pestov Dimitri G

机构信息

Graduate School of Biomedical Sciences, Rowan University School of Osteopathic Medicine, Stratford, NJ, United States.

Department of Cell Biology and Neuroscience, Rowan University School of Osteopathic Medicine, Stratford, NJ, United States.

出版信息

Front Mol Biosci. 2021 Apr 26;8:678488. doi: 10.3389/fmolb.2021.678488. eCollection 2021.

Abstract

Identifying biologically relevant molecular targets of oxidative stress may provide new insights into disease mechanisms and accelerate development of novel biomarkers. Ribosome biogenesis is a fundamental prerequisite for cellular protein synthesis, but how oxidative stress affects ribosome biogenesis has not been clearly established. To monitor and control the redox environment of ribosome biogenesis, we targeted a redox-sensitive roGFP reporter and catalase, a highly efficient HO scavenger, to the nucleolus, the primary site for transcription and processing of rRNA in eukaryotic cells. Imaging of mouse 3T3 cells exposed to non-cytotoxic HO concentrations revealed increased oxidation of the nucleolar environment accompanied by a detectable increase in the oxidative damage marker 8-oxo-G in nucleolar RNA. Analysis of pre-rRNA processing showed a complex pattern of alterations in pre-rRNA maturation in the presence of HO, including inhibition of the transcription and processing of the primary 47S transcript, accumulation of 18S precursors, and inefficient 3'-end processing of 5.8S rRNA. This work introduces new tools for studies of the redox biology of the mammalian nucleolus and identifies pre-rRNA maturation steps sensitive to HO stress.

摘要

识别氧化应激的生物学相关分子靶点可能为疾病机制提供新见解,并加速新型生物标志物的开发。核糖体生物发生是细胞蛋白质合成的基本前提,但氧化应激如何影响核糖体生物发生尚未明确。为了监测和控制核糖体生物发生的氧化还原环境,我们将一种对氧化还原敏感的roGFP报告基因和过氧化氢酶(一种高效的HO清除剂)靶向到核仁,核仁是真核细胞中rRNA转录和加工的主要场所。对暴露于无细胞毒性HO浓度的小鼠3T3细胞进行成像,结果显示核仁环境的氧化增加,同时核仁RNA中的氧化损伤标志物8-氧代-G可检测到增加。对前体rRNA加工的分析表明,在HO存在下,前体rRNA成熟存在复杂的变化模式,包括对初级47S转录本转录和加工的抑制、18S前体的积累以及5.8S rRNA 3'-末端加工效率低下。这项工作为研究哺乳动物核仁的氧化还原生物学引入了新工具,并确定了对HO应激敏感的前体rRNA成熟步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bc1/8107432/753dc6bdd67f/fmolb-08-678488-g001.jpg

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